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<channel>
	<title>Izotóp Intézet Kft.</title>
	<link>http://www.izotop.hu</link>
	<description></description>
	<lastBuildDate>Thu, 19 Aug 2010 14:03:11 +0000</lastBuildDate>
	<docs>http://backend.userland.com/rss092</docs>
	<language>en</language>
	
	<item>
		<title>ISOGAMMA-LLCo</title>
		<description>Main features:


Self contained, large capacity laboratory irradiator
Dry storage
Co-60 (24 kCi), max. 48 pieces, Ø11x220 mm)
The irradiation chamber is separated by stainless steel lining from sources
The irradiation room has no doors, which disturbs the irradiation field
Large sized sample holders can be used (Ø150x280 mm)
Sources placed far from irradiation area, providing good ...</description>
		<link>http://www.izotop.hu/?p=658</link>
			</item>
	<item>
		<title>ISOGAMMA-SLCs</title>
		<description>Main features:


Self contained, small capacity laboratory irradiator
Dry storage
Cs-137 (1 kCi)
Different sample holders can be used (Ø300x75 mm)
Attenuators will set the required beam
Rotating sample-holder for good dose ratio
Mass: 1.5-2 tons


Source exchange can be done at site (replacement of the source holder)


 </description>
		<link>http://www.izotop.hu/?p=656</link>
			</item>
	<item>
		<title>ISOGAMMA-CAL</title>
		<description>Main features:


Panoramic laboratory irradiator for calibration
Dry storage
Max. 3 pcs of source
6-8 m long rail system for sample table
Each of the movements is controlled from central PLC
Mass: ~2 tons
Source exchange can be done at site



 </description>
		<link>http://www.izotop.hu/?p=654</link>
			</item>
	<item>
		<title>ISOGAMMA-MT</title>
		<description>Main features:


Multipurpose Commercial panoramic tote box irradiator
Safety features in accordance with IAEA recommendations
Wet storage
Tote box system, tote box sizes:480x480x900 mm
Max. 7 m3/h capacity with the above box
14 m3 of target material is irradiated at the same time
Continuous and batch mode of operation
Co-60 (1 MCi)



 </description>
		<link>http://www.izotop.hu/?p=652</link>
			</item>
	<item>
		<title>ISOGAMMA-MP</title>
		<description>Main features:


Multipurpose Commercial panoramic pallet irradiator
Safety features in accordance with IAEA recommendations
Wet storage
Tote box system for pallets of sizes 1280x1000x900 mm
Max. 20 m3/h capacity with the above box
9 m3 of target material is irradiated at the same time
Continuous and batch mode of operation
Co-60 (1 MCi)


 </description>
		<link>http://www.izotop.hu/?p=650</link>
			</item>
	<item>
		<title>ISOGAMMA HC</title>
		<description>Main features:


Working area 2400x1250 mm
Two working place, two windows, but only three manipulators
200-250 mm lead shielding
Mass: 60 tons
Could be installed in existing laboratory



 </description>
		<link>http://www.izotop.hu/?p=647</link>
			</item>
	<item>
		<title>Radiation technique services</title>
		<description>
Loading, unloading, reloading of gamma irradiation and medical sources
Commissioning, recommissioning, decommissioning of irradiators
Service, maintenance, repair of all kind of gamma irradiators
Equipment, tools for radiation technologies of radioactive material production
Handling of radioactive waste material (waste management)
Re-encapsulation of sources
Irradiation service
 </description>
		<link>http://www.izotop.hu/?p=645</link>
			</item>
	<item>
		<title>Egyéb C-14-gyel és tríciummal jelzett vegyületek</title>
		<description>Carbon-14



Code
Product (specific activity: 370 – 1850 MBq/mmol)
Unlabelled CAS number
*Availability


CC-509
[U-14C]Benzenesulfonyl chloride
98-11-3
1


CC-473
3-Bromo[ring-U-14C]thioanisole
33733-73-2
3


CC-528
i-[1-14C]Butyric acid hydrazide
3619-17-8
1


CC-38
[1-14C]Butyric acid, sodium salt
156-54-7
1


CC-14
[14C]Carbondisulfide
75-15-0
3


CC-502
2-Chloro[ring-U-14C]acetanilide
533-17-5
1


CC-504
2-Chloro[ring-U-14C]nitrobenzene
88-73-3
1


CC-439
Copper(I) [14C]cyanide
544-92-3
1


CC-16
1,2-Dibromo[U-14C]ethane
106-93-4
3


CC-488
Dibutyl [carboxyl-14C]phthalate
84-74-2
3


CC-527
2,5-Dichloro[U-14C]aniline
95-82-9
3


CC-526
1,4-Dichloro[U-14C]benzene
106-46-7
3


CC-507
2,4'-Dichloro[carbonyl-14C]benzophenone
85-29-0
1


CC-511
2,4'-Dichloro[4'-chlorophenyl-U-14C]benzophenone
85-29-0
1


CC-514
3,4-Dichloro[U-14C]phenyl isocyanate
102-36-3
1


CC-521
2,5-Dichloro[U14C]phenol
583-78-8
2


CC-506
3,4-Dimethyl[U-14C]aniline
95-64-7
1


CC-472
1,3-Dimethyl[14C]thiourea
39577-43-0
2


CC-520
4-Fluoro[ring-U-14C]acetanilide
351-83-7
2


CC-63
[1-14C]Glycine
56-40-6
1


CC-65
[2-14C]Glycine
56-40-6
1


CC-500
Z-[2-14C]Glycine
1138-80-3
1


CC-145
[14C]Guanidine hydrochloride
50-01-1
2


CC-515
[imidazole 2-14C]Medetomidine
86347-14-0
1


CC-517
[phenyl U-14C]Medetomidine
86347-14-0
1


CC-513
Methyl 2-pyrimidine[14C]carboxylate
34253-03-7
1


CC-240
1-[carboxyl-14C]Naphtoic acid
86-55-5
1


CC-519
[carboxyl-14C]Nicotinic acid
59-67-6
1


CC-501
2-Nitro-[ring-U-14C]acetanilide
552-32-9
1


CC-503
4-Nitro-[ring-U-14C]acetanilide
104-04-1
1


CC-518
4-Nitro-[U-14C]aniline
100-01-6
1


CC-505
4-Nitro-[formyl-14C]benzaldehyde
555-16-8
1


CC-18
4-Nitro[U-14C]phenol
100-02-7
3


CC-288
[U-14C]Oxalic acid
144-62-7
3


CC-516
trans-[cyclopropyl 1-14C]Permethrinic acid
55701-05-8 (mixture)
1


CC-469
3-Phenoxy[ring-U-14C]benzoic acid
3739-38-6
3


CC-524
3-Phenoxy[carboxyl-14C]benzoic acid
3739-38-6
1


CC-525
3-([U-14C]Phenoxy)benzoic acid
3739-38-6
3


CC-512
3-Phenoxy[benzyl ring-U-14C]benzyl alcohol
13826-35-2
1


CC-237
Phenyl[1-14C]acetic acid
103-82-2
1


CC-461
2-[ring-U-14C]Phenylpropionic acid
492-37-5
1


CC-471
2-Phenyl[1-14C]propionic acid
492-37-5
1


CC-113
[1,7-14C]Pimelic acid
111-16-0
3


CC-510
Potassium [14C]thiocyanate
333-20-0
1


CC-508
[2-14C]Propen-2-yl-triphenylphosphonium iodide
24470-78-8
1


CC-148
Sodium [14C]cyanide
143-33-9
1


CC-312
Sodium [14C]bicarbonate
144-55-8
1


CC-195
[1,4-14C]Succinic acid
110-15-6
1


CC-523
Sulfadiazine, [sulfanyl ring-U-14C]
68-35-9
1


CC-476
Sulfamethoxazole, [phenyl ring-U-14C]
723-46-6
2


CC-468
Tilmicosin, [3,5-dimethylpiperidin-1-yl 3,5-14C]
108050-54-0
2


CC-127
[14C]Thiourea
62-56-6
1


CC-522
4-[ring-U-14C]Toluic acid
99-94-5
3


CC-495
1,2,4-Trichloro[U-14C]benzene
120-82-1
3


CC-499
2-Trifluoromethyl[ring-U-14C]benzoic acid
433-97-6
2


CC-361
Troglitazone, ...</description>
		<link>http://www.izotop.hu/?p=623</link>
			</item>
	<item>
		<title>Tríciummal jelzett receptor ligandok</title>
		<description>Opiate alkaloids




HS-101
[3H]Buprenorphine


HS-102
[3H]Cyprodime


HS-105
[3H]Dihydromorphine


HS-140
[3H]14-Methoxymetopon NEW!


HS-108
[3H]Naloxone


HS-109
[3H]Naltrindole


HS-110
[3H]Nor-BNI



Opioid peptides




HS-141
[3H]DALDA, [Dmt1]- NEW!


HS-143
Acpc2-endomorphin-2, [3',4'-3H-Acpc]- NEW!


HS-144
Achc2-endomorphin-2, [Achc2-3,4-3H]- NEW!


HS-145
Ac-Arg-Tyr-Tyr-Arg-Ile-Lys-ol, [3,5-3H Tyr3,3,5- 3H-Tyr4]- NEW!


HS-118
[3H]Deltorphin I, [(S)Atc3, Ile5,6]-


HS-103
[3H]Deltorphin II


HS-104
[3H]Deltorphin II, [Ile5,6]-


HS-116
[3H]Deltorphin II, [(R)Atc3, Ile5,6]-


HS-119
[3H]Dermorphin


HS-120
[3H]Dmt(N,N-Me2)-Tic-OH


HS-121
[3H]Dynorphin A (1-17)


HS-122
[3H]Dynorphin A (1-11) amide


HS-123
[3H]Endomorphin-1


HS-115
[3H]Endomorphin-2


HS-124
[3H]Endomorphin-2


HS-132
[3H]Endomorphin-2


HS-142
[3H]Endomorphin-2, [Dmt1]- NEW!


HS-107
[3H]Leu-Enkephalin


HS-106
[3H]Leu-Enkephalin, [d-Ala2]-


HS-125
[3H]Met-Enkephalin


HS-126
[3H]Enkephalin-Arg-Phe, [d-Ala2, d-Nle5]-


HS-117
[3H]Met-Enkephalin-Arg-Phe


HS-127
[3H]VV-Hemorphin-7


HS-113
[3H]Nociceptin amide


HS-128
[3H]Nociceptin (1-13) amide


HS-129
[3H]TICP[Y]


HS-111
[3H]TIPP


HS-112
[3H]TIPP[Y]



Other receptor ligands




HS-130
[3H]l-Dihydroalprenolol


HS-131
[3H]GnRH-III



Producer:

Biological Research Center
Hungarian Academy of Sciences
Isotope Laboratory "B" level

H-6701 Szeged, P.O.B. 521
Phone: (36-62) ...</description>
		<link>http://www.izotop.hu/?p=622</link>
			</item>
	<item>
		<title>C-14 jelzett peszticidek (fungicidek, herbicidek, inszekticidek)</title>
		<description>


Acephate, [S-methyl-14C]
CC-368


Alachlor, [methoxy-14C]
CC-309


Aldicarb, [i-butyl-14C]
CC-326


Ametryn, [ring-U-14C]
CC-270


Asulam, [ring-U-14C]
CC-315


Atrazine, [ring-U-14C]
CC-298


Azocyclotin, [cyclohexyl-1-14C]
CC-402


Benfuracarb, [isopropyl-2-14C]
CC-370


Benfuracarb, [phenyl ring-U-14C]
CC-371


Bentazone, [carbonyl-14C]
CC-328


Bifenthrin, [benzyl ring-U-14C]
CC-350


Bifenthrin, [cyclopropane-1-14C]
CC-351


Bromoxynil octanoate, [ring-U-14C]
CC-333


Cadusafos, [sec-butyl-1-14C]
CC-373


Carbaryl, [ring-1-14C]
CC-255


Carbendazim, [imidazol-2-14C]
CC-305


Carbofuran, [(2,2-dimethyl,3)-14C3]
CC-239


Carbofuran, [phenyl ring-U-14C]
CC-339


Chlormequat, [ethyl-1,2-14C2]
CC-319


Chlorfenvinphos, [ethyl-1-14C2]
CC-242


Chlorpyrifos, [ethyl-1-14C2]
CC-243


Clodinafop-propargyl, [phenyl ring-U-14C]
CC-421


Clodinafop-propargyl, [pyridyl-2,6-14C2]
CC-424


Coumaphos, [coumarin-4-14C]
CC-253


Cyhexatin, [cyclohexyl-1-14C3]
CC-308


Beta-cypermethrin, [benzyl-7-14C]
CC-329


Beta-cypermethrin, [cyano-14C]
CC-447


Beta-cypermethrin, [cyclopropane-1-14C]
CC-446


Beta-cypermethrin, [benzyl ring-U-14C]
CC-445


Beta-cypermethrin, [phenyl ring-U-14C]
CC-369


Cypermethrin, [benzyl-7-14C]
CC-261


Cypermethrin, [carboxyl-14C]
CC-266


Cypermethrin, [cyano-14C]
CC-265


Cypermethrin, [cyclopropane-1-14C]
CC-267


Cypermethrin, [phenyl ring-14C]
CC-413


Cymoxanyl, [acetyl-2-14C]
CC-444


2,4-D, [carboxyl-14C]
CC-294


2,4-D, [ring-U-14C]
CC-292


2,4-DB, [ring-U-14C]
CC-367


DDE, [ring-U-14C]
CC-257


DDT, [ring-U-14C]
CC-256


Deltamethrin, ...</description>
		<link>http://www.izotop.hu/?p=621</link>
			</item>
	<item>
		<title>Nor-BNI, [1, 1-3H]-</title>
		<description>Norbinaltorphimine




C40H43N3O6


Descriptionk opioid antagonist


Molecular weightMW 661.81 (unlabelled free base)


Molar activity30-60 Ci/mmol


Product codeHS-110



Structural formula of nor-BNI:



Ref.: Kinouchi et al.  Evidence for kappa 1 opioid receptor multiplicity in the guinea pig cerebellum.  Eur. J. Pharmacol. 207, 135-141 (1991). Márki et al.  Tritiated kappa receptor antagonist norbinaltorphimine: synthesis and in vitro ...</description>
		<link>http://www.izotop.hu/?p=590</link>
			</item>
	<item>
		<title>Naltrindole, [1, 5-3H]-</title>
		<description>[1,5 -3H]-17-Cyclopropylmethyl-6,7-dehydro-4,5a -epoxy-3,14-dihydroxy-6,7-2 ,3 -indolo-morphinan




C26H26N2O3


DescriptionHighly selective, non-peptide d opioid receptor antagonist


Molecular weightMW 414.20 (unlabelled free base)


Molar activity30-50 Ci/mmol


Product codeHS-109



Structural formula of naltrindole:



Ref.: Portoghese et al.  Design of peptidomimetic d opioid receptor antagonists using the message-address concept.  J. Med. Chem. 33, 1714-1720 (1990). Yamamura et al.  Characterisation of ...</description>
		<link>http://www.izotop.hu/?p=589</link>
			</item>
	<item>
		<title>Naloxone, [N-allyl-2,3-3H]-</title>
		<description>[17-(2,3-3H-2-propenyl)]-4, 5a -epoxy-3,14-dihydroxymorphinan-6-one




C19H21NO4


DescriptionGeneral opioid antagonist


Molecular weightMW 327.38 (unlabelled free base)


Molar activity40-80 Ci/mmol


Product codeHS-108



Structural formula of naloxone:



Ref.: Lord et al. Endogenous opioid peptides: multiple agonists and receptors. Nature 267, 495-499 (1977). Sawynok et al. Minireview on the specificity of naloxone as an opiate antagonist. Life Sci. 25, 1621-1632 (1979). Tóth et ...</description>
		<link>http://www.izotop.hu/?p=588</link>
			</item>
	<item>
		<title>14-Methoxymetopon, [7,8-3H]-</title>
		<description>4, 5a -epoxy-3-hydroxy-14b-methoxy-5b,17-dimethylmorphinan-6-one




C19H23NO4


Descriptionm opioid agonist


Molecular weightMW 329.39 (unlabelled free base)


Molar activity15-40 Ci/mmol


Product codeHS-140



Structural formula of 14-Methoxymetopon:



Ref.: Schmidhammer et al. Synthesis and biological evaluation of 14-alkoxymorphinans. 8. 14-Methoxymetopon, an extremely potent opioid agonist. Helv. Chim. Acta 81, 1784-1787 (1990). Spetea et al. Binding characteristics of [3H]14-methoxymetopon, a high affinity m-opioid receptor ...</description>
		<link>http://www.izotop.hu/?p=587</link>
			</item>
	<item>
		<title>Dihydromorphine, [7,8-3H]-</title>
		<description>[7,8-3H]-3,6-dihydroxy-N-methyl-morphinan




C17H20NO3


Descriptionm opioid agonist


Molecular weightMW 286.35 (unlabelled free base)


Molar activity50-80 Ci/mmol


Product codeHS-105



Structural formula of dihydromorphine:



Ref.: Tóth et al. Preparation of 1,7,8-3H-dihydromorphine of high molecular activity and its application in opiate receptor binding experiments. Radiochem. Radioanal. Lett. 56, 209-216 (1982). Maggi et al. Antiprogestins inhibit the binding of opioids to mu-opioid receptors ...</description>
		<link>http://www.izotop.hu/?p=586</link>
			</item>
	<item>
		<title>Cyprodime, [1-3H]-</title>
		<description>[1-3H]-N-cyclopropylmethyl-3,14-dimethoxymorphinan-6-one




C22H26NO4


Descriptionm opioid antagonist


Molecular weightMW 368.45 (unlabelled free base)


Molar activity20-30 Ci/mmol


Product codeHS-102



Structural formula of cyprodime:



Ref.: Ötvös et al. Tritium labelling of cyprodime (= (-)17-(cyclopropylmethyl)-4,14-dimethoxymorphinan-6-one), a m receptor selective opioid antagonist. Helv. Chim. Acta 75, 1718-1720 (1992). Márki et al. Mu-opioid receptor specific antagonist cyprodime: characterisation by in vitro radioligand and [35S]GTPg ...</description>
		<link>http://www.izotop.hu/?p=585</link>
			</item>
	<item>
		<title>Buprenorphine, [15, 16-3H]-</title>
		<description>[15,16-3H]-N-cyclopropylmethyl-6,14-etheno-3-hydroxy-7-(1-hydroxy-1,2,2-trimethyl-propyl)-6-methoxy-morphinan




C29H41NO4


DescriptionNonselective partial opioid agonist/antagonist


Molecular weightMW 467.65 (unlabelled free base)


Molar activity40-60 Ci/mmol


Product codeHS-101



Structural formula of buprenorphine:



Ref.: Mello et al. Buprenorphin suppresses heroin use by heroin addicts. Science, 207, 657-659 (1980). Leander Buprenorphin has potent kappa opioid receptor antagonist activity. Neuropharmacology, 26, 1445-1447 (1987). Ötvös et al. Synthesis of high specific activity ...</description>
		<link>http://www.izotop.hu/?p=584</link>
			</item>
	<item>
		<title>Ziram, [methyl-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Ziram, [methyl-14C]

zinc bis(dimethyldithiocarbamate)


CC-352
C6H12N2S4Zn
137-30-4

 </description>
		<link>http://www.izotop.hu/?p=583</link>
			</item>
	<item>
		<title>Ziram, [carbamate-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Ziram, [carbamate-14C]

zinc bis(dimethyldithiocarbamate)


CC-324
C6H12N2S4Zn
137-30-4

 </description>
		<link>http://www.izotop.hu/?p=582</link>
			</item>
	<item>
		<title>Zineb, [ethylene-1,2-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Zineb, [ethylene-1,2-14C2]

zinc ethylenebis(dithiocarbamate) (polymeric)


CC-277
C4H6N2S4Zn
12122-67-7

 </description>
		<link>http://www.izotop.hu/?p=581</link>
			</item>
	<item>
		<title>Vinclozolin, [phenyl ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Vinclozolin, [phenyl ring-U-14C]

(RS)-3-(3,5-dichlorophenyl)-5-methyl-5-vinyl-1,3-oxazolidine-2,4-dione


CC-394
C12H9Cl2NO3
50471-44-8

 </description>
		<link>http://www.izotop.hu/?p=580</link>
			</item>
	<item>
		<title>Tri-allate, [allyl-1-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Tri-allate, [allyl-1-14C]

S-2,3,3-trichloroallyl diisopropyl(thiocarbamate)


CC-364
C10H16Cl3NOS
2303-17-5

 </description>
		<link>http://www.izotop.hu/?p=579</link>
			</item>
	<item>
		<title>Thiram, [carbamate-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Thiram, [carbamate-14C]

tetramethylthiuram disulfide


CC-441
C6H12N2S4
137-26-8

 </description>
		<link>http://www.izotop.hu/?p=578</link>
			</item>
	<item>
		<title>Terbutryn, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Terbutryn, [ring-U-14C]

N2-tert-butyl-N4-ethyl-6-methylthio-1,3,5-triazine-2,4-diamine


CC-448
C10H19N5S
886-50-0

 </description>
		<link>http://www.izotop.hu/?p=577</link>
			</item>
	<item>
		<title>Terbuthylazine, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Terbuthylazine, [ring-U-14C]

N2-tert-butyl-6-chloro-N4-ethyl-1,3,5-triazine-2,4-diamine


CC-437
C9H16ClN5
5915-41-3

 </description>
		<link>http://www.izotop.hu/?p=576</link>
			</item>
	<item>
		<title>Terbufos, [O-ethyl-1-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Terbufos, [O-ethyl-1-14C2]

S-tert-butylthiomethyl O,O-diethyl phosphorodithioate


CC-321
C9H21O2PS3
13071-79-9

 </description>
		<link>http://www.izotop.hu/?p=575</link>
			</item>
	<item>
		<title>Tebuthiuron, [ring-5-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Tebuthiuron, [ring-5-14C]

1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea


CC-272
C9H16N4OS
34014-18-1

 </description>
		<link>http://www.izotop.hu/?p=574</link>
			</item>
	<item>
		<title>Tebuconazole, [triazole ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Tebuconazole, [triazole ring-U-14C]

(RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol


CC-459
C16H22ClN3O
107534-96-3

 </description>
		<link>http://www.izotop.hu/?p=573</link>
			</item>
	<item>
		<title>Tebuconazole, [phenyl ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Tebuconazole, [phenyl ring-U-14C]

(RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol


CC-390
C16H22ClN3O
107534-96-3

 </description>
		<link>http://www.izotop.hu/?p=572</link>
			</item>
	<item>
		<title>Simazine, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Simazine, [ring-U-14C]

6-chloro-N2,N4-diethyl-1,3,5-triazine-2,4-diamine


CC-249
C7H12ClN5
122-34-9

 </description>
		<link>http://www.izotop.hu/?p=571</link>
			</item>
	<item>
		<title>SDDC, [carbamate-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


SDDC, [carbamate-14C]

Sodium-N,N-dimethyl ditiocarbamate


CC-442
C3H6NS2Na
128-04-1

 </description>
		<link>http://www.izotop.hu/?p=570</link>
			</item>
	<item>
		<title>Pyridaphenthion, [pyridazinyl-4,5-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Pyridaphenthion, [pyridazinyl-4,5-14C2]

O-(1,6-dihydro-6-oxo-1-phenylpyridazin-3-yl) O,O-diethyl phosphorothioate


CC-389
C14H17N2O4PS
119-12-0

 </description>
		<link>http://www.izotop.hu/?p=569</link>
			</item>
	<item>
		<title>Pyributicarb, [phenyl-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Pyributicarb, [phenyl-U-14C]

O-3-tert-butylphenyl 6-methoxy-2-pyridyl(methyl)thiocarbamate


CC-363
C18H22N2O2S
88678-67-5

 </description>
		<link>http://www.izotop.hu/?p=568</link>
			</item>
	<item>
		<title>Pyributicarb, [pyridyl-2,6-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Pyributicarb, [pyridyl-2,6-14C2]

O-3-tert-butylphenyl 6-methoxy-2-pyridyl(methyl)thiocarbamate


CC-362
C18H22N2O2S
88678-67-5

 </description>
		<link>http://www.izotop.hu/?p=567</link>
			</item>
	<item>
		<title>Prosulfocarb sulfoxide, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Prosulfocarb sulfoxide, [ring-U-14C]

1-(benzylsulfinyl)-N,N-dipropylmethanamide


CC-443
C14H21NO2S
n/a

 </description>
		<link>http://www.izotop.hu/?p=566</link>
			</item>
	<item>
		<title>Prosulfocarb, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Prosulfocarb, [ring-U-14C]

S-benzyl dipropyl(thiocarbamate)


CC-356
C14H21NOS
52888-80-9

 </description>
		<link>http://www.izotop.hu/?p=565</link>
			</item>
	<item>
		<title>Propisochlor, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Propisochlor, [ring-U-14C]

2-chloro-6'-ethyl-N-isopropoxymethylaceto-o-toluidide


CC-416
C15H22ClNO2
86763-47-5

 </description>
		<link>http://www.izotop.hu/?p=564</link>
			</item>
	<item>
		<title>Propisochlor, [2-chloroacetyl 1-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Propisochlor, [2-chloroacetyl 1-14C]

2-chloro-6'-ethyl-N-isopropoxymethylaceto-o-toluidide


CC-417
C15H22ClNO2
86763-47-5

 </description>
		<link>http://www.izotop.hu/?p=563</link>
			</item>
	<item>
		<title>Propiconazole, [triazol ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Propiconazole, [triazol ring-U-14C]

(2RS,4RS;2RS,4SR)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole


CC-387
C15H17Cl2N3O2
60207-90-1

 </description>
		<link>http://www.izotop.hu/?p=562</link>
			</item>
	<item>
		<title>Propiconazole, [mixture of dioxolane-4-14C, phenyl ring-U-14C, triazole ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Propiconazole, [mixture of dioxolane-4-14C, phenyl ring-U-14C, triazole ring-U-14C]

(2RS,4RS;2RS,4SR)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole


CC-268
C15H17Cl2N3O2
60207-90-1

 </description>
		<link>http://www.izotop.hu/?p=561</link>
			</item>
	<item>
		<title>Propiconazole, [dioxolane-4-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Propiconazole, [dioxolane-4-14C]

(2RS,4RS;2RS,4SR)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole


CC-323
C15H17Cl2N3O2
60207-90-1

 </description>
		<link>http://www.izotop.hu/?p=560</link>
			</item>
	<item>
		<title>Prochloraz, [phenyl ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Prochloraz, [phenyl ring-U-14C]

N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide


CC-248
C15H16Cl3N3O2
67747-09-5

 </description>
		<link>http://www.izotop.hu/?p=559</link>
			</item>
	<item>
		<title>Pirimiphos-methyl, [pyrimidinyl-2-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Pirimiphos-methyl, [pyrimidinyl-2-14C]

O-2-diethylamino-6-methylpyrimidin-4-yl O,O-dimethyl phosphorothioate


CC-248
C11H20N3O3PS
29232-93-7

 </description>
		<link>http://www.izotop.hu/?p=558</link>
			</item>
	<item>
		<title>GnRH-III, [prolyl9-3,4-3H]-</title>
		<description>Pyr-His-Trp-Ser-His-Asp-Trp-Lys-Pro-Gly-NH2




C59H74N18O14


DescriptionGnRH receptor agonist with antitumor activity


Molecular weightMW 1259.36 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-131



Ref.: Knox et al.  Characterization and localization of gonadotropin-releasing hormone receptors in the adult female sea lamprey, Petromyzon marinus.  Endocrinology 134, 492-498 (1994). Lovas et al.  Direct anticancer activity of gonadotropin-releasing hormone-III.  ...</description>
		<link>http://www.izotop.hu/?p=620</link>
			</item>
	<item>
		<title>l-Dihydroalprenolol, [ring, propyl-3H]-</title>
		<description>


C15H25NO2


DescriptionPotent competitive ß-adrenergic antagonist


Molecular weightMW 251.32 (unlabelled free base)


Molar activity50-80 Ci/mmol


Product codeHS-130



Structural formula of L-dihydroalprenolol:



Ref.: Williams et al.  Adipocyte beta-adrenergic receptors. Identification and subcellular localisation by (-)-[3H]dihydroalprenolol binding.  J. Biol. Chem. 251, 3096-3104 (1976). Randall et al.  Structure and biological activity of (-)-[3H]dihydroalprenolol, a radioligand for studies ...</description>
		<link>http://www.izotop.hu/?p=619</link>
			</item>
	<item>
		<title>TIPP[Y], [tyrosyl1-3,5-3H</title>
		<description>H-[3H]Tyr-TicY [CH2-NH]Phe-Phe-OH




C37H40N4O5


DescriptionHighly specific and stable d opioid antagonist


Molecular weightMW 620.75 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-112



Ref.: Visconti et al.  TIPP[Y], a highly selective delta ligand.  Neurosci. Lett. 181, 47-49 (1994). Nevin et al.  Synthesis and binding characteristics of tritiated TIPP[Y], a highly specific and stable delta ...</description>
		<link>http://www.izotop.hu/?p=618</link>
			</item>
	<item>
		<title>TIPP, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Tic-Phe-Phe-OH




C37H38N4O6


Descriptiond opioid antagonist with high affinity and extraordinary selectivity


Molecular weightMW 634.73 (unlabelled free peptide base)


Molar activity20-30 Ci/mmol


Product codeHS-111



Ref.: Nevin et al.  Synthesis and binding characteristics of the highly specific, tritiated delta opioid antagonist [3H]TIPP.  Life Sci. 53, PL57-62 (1993). </description>
		<link>http://www.izotop.hu/?p=617</link>
			</item>
	<item>
		<title>TICP[Y], [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-TicY [CH2-NH]Cha-Phe-OH




C37H46N4O5


DescriptionHighly specific and stable d opioid antagonist


Molecular weightMW 626.79 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-129



Ref.: Schiller et al.  Subtleties of structure-agonist versus antagonist relationship of opioid peptides and peptidomimetics.  J. Recept. Signal Transduct. Res. 19, 573-588 (1999). Szatmári et al.  Synthesis and binding characteristics of ...</description>
		<link>http://www.izotop.hu/?p=616</link>
			</item>
	<item>
		<title>Nociceptin (1-13) amide, [phenylalanyl1-4-3H]-</title>
		<description>H-[3H]Phe-Gly-Gly-Phe-Thr-Gly-Ala-Arg-Lys-Ser-Ala-Arg-Lys-NH2




C61H100N22O15


DescriptionAgonist for opioid receptor-like1 (ORL1) receptors


Molecular weightMW 1381.62 (unlabelled free peptide base)


Molar activity20-30 Ci/mmol


Product codeHS-128



Ref.: Guerrini et al.  Address and message sequences for the nociceptin receptor: a structure-activity study of nociceptin(1-13)-peptide amide.  J. Med. Chem. 40, 1789-1793 (1997). </description>
		<link>http://www.izotop.hu/?p=615</link>
			</item>
	<item>
		<title>Nociceptin amide, [phenylalanyl1-4-3H]-</title>
		<description>H-[3H]Phe-Gly-Gly-Phe-Thr-Gly-Ala-Arg-Lys-Ser-Ala-Arg-Lys-Leu-Ala-Asn-Gln-NH2
Orphanin FQ




C79H130N28O21


DescriptionPutative endogenous agonist for opioid receptor-like1 (ORL1) receptors


Molecular weightMW 1808.07 (unlabelled free peptide base)


Molar activity20-30 Ci/mmol


Product codeHS-113



Ref.: Meunier et al.  Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor.  Nature 377, 532-535 (1995). Benyhe et al.  Nociceptin binding sites in frog (Rana esculenta) ...</description>
		<link>http://www.izotop.hu/?p=614</link>
			</item>
	<item>
		<title>VV-Hemorphin-7, [tyrosyl3-3,5-3H]-</title>
		<description>H-Val-Val-[3H]Tyr-Pro-Trp-Thr-Glu-Arg-Phe-OH




C59H82N14O13


Molecular weightMW 1195.40 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-127



Ref.: Garreau et al.  VV-hemorphin-7 and LVV-hemorphin-7 released during in vitro peptic haemoglobin hydrolysis are morphinomimetic peptides.  Neuropeptides 28, 243-250 (1995). Szikra et al.  Receptor binding properties of a hemorphin analogue in rat brain membrane preparation.  Neurobiology ...</description>
		<link>http://www.izotop.hu/?p=613</link>
			</item>
	<item>
		<title>Met-Enkephalin-Arg-Phe, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Gly-Gly-Phe-Met-Arg-Phe-OH
MERF




C42H56N10O9S


Descriptionk opioid agonist


Molecular weightMW 877.04 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-117



Ref.: Wollemann et al.  Characterisation of [3H]Met-Enkephalin-Arg6-Phe7 Binding to Opioid Receptors in Frog Brain Membrane Preparations.  J. Neurochem. 63, 1460-1465 (1994). Benyhe et al.  Met5-enkephalin-Arg6-Phe7, an endogenous neuropeptide, binds to multiple opioid and nonopioid sites in ...</description>
		<link>http://www.izotop.hu/?p=612</link>
			</item>
	<item>
		<title>Enkephalin-Arg-Phe, [d-Ala2, d-Nle5]-, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-d-Ala-Gly-Phe-d-Nle-Arg-Phe-OH




C44H60N10O9


Descriptiond opioid agonist


Molecular weightMW 873.03 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-126



Ref.: Bozó et al.  Receptor binding and G-protein activation by new Met5-enkephalin-Arg6-Phe7 derived peptides.  Life Sci. 66, 1241-1251 (2000). </description>
		<link>http://www.izotop.hu/?p=611</link>
			</item>
	<item>
		<title>Met-Enkephalin, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Gly-Gly-Phe-Met-OH
Human b -endorphin (1-5)




C27H35N5O7S


Descriptiond opioid agonist


Molecular weightMW 573.23 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-125



Ref.: Hughes et al.  Identification of two related pentapeptides from the brain with potent opiate agonist activity.  Nature 258, 577-580 (1975). Rinne et al.  Brain methionine- and leucine-enkephalin receptors in patients with dementia. ...</description>
		<link>http://www.izotop.hu/?p=610</link>
			</item>
	<item>
		<title>Leu-Enkephalin, [d-Ala2]-, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-d-Ala-Gly-Phe-Leu-OH
DALE




C29H39N5O7


Descriptiond opioid agonist


Molecular weightMW 569.65 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-106



Ref.: Benyhe et al.  Characterisation of rat brain opioid receptors by [Tyr1-3,5-3H] d-Ala2-, Leu5-enkephalin binding.  Neurochem. Res. 10, 627-635 (1985). </description>
		<link>http://www.izotop.hu/?p=609</link>
			</item>
	<item>
		<title>Leu-Enkephalin, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Gly-Gly-Phe-Leu-OH




C28H37N5O7


DescriptionEndogenous d opioid agonist


Molecular weightMW 555.63 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-107



Ref.: Hughes et al.  Identification of two related pentapeptides from the brain with potent opiate agonist activity.  Nature 258, 577-580 (1975). Okhuto et al.  Human nasal mucosal neutral enopeptidase (NEP): location, quantitation, and secretion.  ...</description>
		<link>http://www.izotop.hu/?p=608</link>
			</item>
	<item>
		<title>Endomorphin-2, [Dmt1]-, prolyl2-3,4-3H]-</title>
		<description>H-Dmt-[3H]Pro-Phe-Phe-NH2




C34H41N5O5


DescriptionNonselective m/d opioid agonist/antagonist


Molecular weightMW 599.72 (unlabelled free peptide base)


Molar activity30-50 Ci/mmol


Product codeHS-142



Ref.: Okada et al.  Structural studies of [2 , 6 -dimethyl-l-tyrosine1]endomorphin-2 analogues: enhanced activity and cis orientation of the Dmt-Pro amide bond.  Bioorg. Med. Chem. 11, 1983-1994 (2003). Tóth et al.  New endomorphin analogs with ...</description>
		<link>http://www.izotop.hu/?p=607</link>
			</item>
	<item>
		<title>Endomorphin-2, [phenylalanyl3-4-3H]-</title>
		<description>H-Tyr-Pro-[3H]Phe-Phe-NH2




C32H37N5O5


DescriptionEndogenous m opioid agonist


Molecular weightMW 571.67 (unlabelled free peptide base)


Molar activity20-30 Ci/mmol


Product codeHS-132



Ref.: Zadina et al.  A potent and selective endogenous agonist for the mu-opiate receptor.  Nature 386, 499-502 (1997). </description>
		<link>http://www.izotop.hu/?p=606</link>
			</item>
	<item>
		<title>Endomorphin-2, [prolyl2-3,4-3H]-</title>
		<description>H-Tyr-[3H]Pro-Phe-Phe-NH2




C32H37N5O5


DescriptionEndogenous m opioid agonist


Molecular weightMW 571.67 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-124



Ref.: Zadina et al.  A potent and selective endogenous agonist for the mu-opiate receptor.  Nature 386, 499-502 (1997). </description>
		<link>http://www.izotop.hu/?p=605</link>
			</item>
	<item>
		<title>Endomorphin-2, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Pro-Phe-Phe-NH2




C32H37N5O5


DescriptionEndogenous m opioid agonist


Molecular weightMW 571.67 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-115



Ref.: Zadina et al.  A potent and selective endogenous agonist for the mu-opiate receptor.  Nature 386, 499-502 (1997). Tömböly et al.  Synthesis of tritium labelled endomorphin 2 and its stability in the radioreceptor assay.  ...</description>
		<link>http://www.izotop.hu/?p=604</link>
			</item>
	<item>
		<title>Endomorphin-1, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Pro-Trp-Phe-NH2




C34H38N6O5


DescriptionEndogenous m opioid agonist


Molecular weightMW 610.71 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-123



Ref.: Zadina et al.  A potent and selective endogenous agonist for the mu-opiate receptor.  Nature 386, 499-502 (1997). Hackler et al.  Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 from human brain cortex.  ...</description>
		<link>http://www.izotop.hu/?p=603</link>
			</item>
	<item>
		<title>Dynorphin A (1-11) amide, [d-Ala3]-, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-Gly-d-Ala-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-NH2




C64H106N22O12


Descriptionk opioid receptor agonist


Molecular weightMW 1375.68 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-122



Ref.: Lung et al.  Effect of modification of residues in position 3 of dynorphin A (1-11)-NH2 on kappa receptor selectivity and potency.  J. Med. Chem. 39, 2456-2460 (1996). </description>
		<link>http://www.izotop.hu/?p=602</link>
			</item>
	<item>
		<title>Dynorphin A (1-17), [tyrosyl1-3,5-3H]-</title>
		<description>[3H]Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-Leu-Lys-Trp-Asp-Asn-Gln-OH




C99H155N31O23


Descriptionk opioid agonist


Molecular weightMW 2147.50 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-121



Ref.: Goldstein et al.  Porcine pituitary dynorphin: complete amino acid sequence of the biologically active heptadecapeptide.  Proc. Natl. Acad. Sci. 78, 7219-7223 (1981). Yarygin et al.  Non-opioid dynorphin binding sites on secretory vesicles of a pituitary-derived ...</description>
		<link>http://www.izotop.hu/?p=601</link>
			</item>
	<item>
		<title>N,N(Me)2-Dmt-Tic-OH, [N,N,2,6-tetramethyltyrosyl1-3, 5-3H]-</title>
		<description>H-[3H]N,N(Me)2Dmt-Tic-OH




C23H28N2O4


Descriptiond opioid antagonist with extraordinary binding characteristics


Molecular weightMW 396.48 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-120



Structural formula of N,N(Me)2-Dmt-Tic-OH:



Ref.: Salvadori et al.  Evolution of the Dmt-Tic pharmacophore: N-terminal methylated derivatives with extraordinary delta opioid antagonist activity.  J. Med. Chem. 40, 3100-3108 (1997). Kertész et al.  Synthesis of ...</description>
		<link>http://www.izotop.hu/?p=600</link>
			</item>
	<item>
		<title>Dermorphin, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-d-Ala-Phe-Gly-Tyr-Pro-Ser-NH2




C40H50N8O10


DescriptionPotent and selective m opioid receptor agonist


Molecular weightMW 802.89 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-119



Ref.: Sagan et al.  Differential contribution of C-terminal regions of dermorphin and dermenkephalin to opioid-sites selection and binding potency.  Biochem. Biophys. Res. Commun. 163, 726-732 (1989). Carr et al.  Mu and delta ...</description>
		<link>http://www.izotop.hu/?p=599</link>
			</item>
	<item>
		<title>Deltorphin II, [(R)Atc3, Ile5,6]-, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-d-Ala-(R)Atc-Glu-Ile-Ile-Gly-NH2




C42H60N8O10


Descriptiond opioid agonist


Molecular weightMW 836.44 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-116



Ref.: Tóth et al.  Conformationally constrained deltorphin analogs with 2-aminotetralin-2-carboxylic acid in position 3.  J. Med. Chem. 40, 990-995 (1997). Kelly et al.  Weaning-induced development of delta opioid receptors in rat brain: differential effects of guanine ...</description>
		<link>http://www.izotop.hu/?p=598</link>
			</item>
	<item>
		<title>Deltorphin II, [Ile5,6]-, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-d-Ala-Phe-Glu-Ile-Ile-Gly-NH2




C40H58N8O10


Descriptiond opioid agonist


Molecular weightMW 810.96 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-104



Ref.: Nevin et al.  Binding characteristics of the novel highly selective delta agonist, [3H]Ile5,6deltorphin II.  Neuropeptides, 26, 261-265 (1994). </description>
		<link>http://www.izotop.hu/?p=597</link>
			</item>
	<item>
		<title>Deltorphin II, [phenylalanyl3-4-3H]-</title>
		<description>H-Tyr-d-Ala-[3H]Phe-Glu-Val-Val-Gly-NH2




C38H54N8O10


Descriptiond opioid agonist


Molecular weightMW 782.89 (unlabelled free peptide base)


Molar activity20-30 Ci/mmol


Product codeHS-103



Ref.: Búzás et al.:  Synthesis and binding characteristic of the highly delta-specific new tritiated opioid peptide, [3H]deltorphin II.  Life Sci. 50, PL75-78 (1992). </description>
		<link>http://www.izotop.hu/?p=596</link>
			</item>
	<item>
		<title>Deltorphin I, [(S)Atc3, Ile5,6]-, [tyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Tyr-d-Ala-(S)Atc-Asp-Ile-Ile-Gly-NH2




C41H58N8O10


Descriptiond opioid agonist


Molecular weightMW 822.96 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-118



Ref.: Tóth et al.  Conformationally constrained deltorphin analogs with 2-aminotetralin-2-carboxylic acid in position 3.  J. Med. Chem. 40, 990-995 (1997). Kelly et al.  Weaning-induced development of delta opioid receptors in rat brain: differential effects of guanine ...</description>
		<link>http://www.izotop.hu/?p=595</link>
			</item>
	<item>
		<title>Ac-Arg-Tyr-Tyr-Arg-Ile-Lys-ol, [3,5-3H Tyr3,3,5- 3H-Tyr4]-</title>
		<description>Ac-Arg-[3H]Tyr-[3H]Tyr-Arg-Ile-Lys-ol




C44H71N13O9


Descriptionnociceptin receptor ligand with high affinity and selectivity


Molecular weightMW 926.01 (unlabelled free base)


Molar activity60-90 Ci/mmol


Product codeHS-145



Ref.: Kocsis L. et al. Nociceptin antagonism: probing the receptor by N-acetyl oligopeptides Regul. Pept.122.199-207 (2004) Gunduz O.et al. In vitro binding and functional studies of AcRYYRIK-ol and its derivatives, novel partial agonists of the ...</description>
		<link>http://www.izotop.hu/?p=594</link>
			</item>
	<item>
		<title>Achc2-endomorphin-2, [Achc2-3,4-3H]-</title>
		<description>H-Tyr-[3H](1S,2R)Achc-Phe-Phe-NH2




C34H41N5O5


Descriptionmu opioid agonist with high affinity and high proteolytic enzyme stability


Molecular weightMW 599.67 (unlabelled free peptide base)


Molar activity30-60 Ci/mmol


Product codeHS-144



References: Tóth et al. New endomorphin analogs with m-agonist and d-antagonist properties. Pure Appl. Chem. 76, 951-957 (2004). Keresztes A. et al: New endomorphin analogues containing alicyclic beta amino acids: Influence ...</description>
		<link>http://www.izotop.hu/?p=593</link>
			</item>
	<item>
		<title>Acpc2-endomorphin-2, [3’,4’-3H-Acpc]-</title>
		<description>H-Tyr-[3H](1S,2R)Acpc-Phe-Phe-NH2




C33H39N5O5


Descriptionmu opioid agonist with high affinity and selectivity and high stability


Molecular weightMW 585.67 (unlabelled free peptide base)


Molar activity30-60 Ci/mmol


Product codeHS-143



References: Keresztes A.et al.:  Synthesis, radiolabelling and receptor binding of [3H] [(1S,2R) Acpc2] endomorphin-2 Peptides 27 (2006) 3315-3321, Keresztes A. et al: New endomorphin analogues containing alicyclic beta amino acids: ...</description>
		<link>http://www.izotop.hu/?p=592</link>
			</item>
	<item>
		<title>DALDA, [Dmt1]-, [dimethyltyrosyl1-3,5-3H]-</title>
		<description>H-[3H]Dmt-D-Arg-Phe-Lys-NH2




C32H49N9O5


Descriptionm opioid agonist


Molecular weightMW 639.80 (unlabelled free peptide base)


Molar activity40-60 Ci/mmol


Product codeHS-141



Ref.: Schiller et al.  Synthesis and in vitro opioid activity profiles of DALDA analogues.  Eur. J. Med. Chem. 35, 895-901 (2000). Zhao et al.  Profound spinal tolerance after repeated exposure to a highly selective mu-opioid peptide ...</description>
		<link>http://www.izotop.hu/?p=591</link>
			</item>
	<item>
		<title>Permethrin, [phenoxy ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Permethrin, [phenoxy ring-U-14C]

3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate


CC-386
C21H20Cl2O3
52645-53-1

 </description>
		<link>http://www.izotop.hu/?p=557</link>
			</item>
	<item>
		<title>Pentachlorophenol, [U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Pentachlorophenol, [U-14C]

pentachlorophenol


CC-274
C6Cl5OH
87-86-5

 </description>
		<link>http://www.izotop.hu/?p=556</link>
			</item>
	<item>
		<title>Parathion-methyl, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Parathion-methyl, [ring-U-14C]

O,O-dimethyl O-4-nitrophenyl phosphorothioate


CC-353
C8H10NO5PS
298-00-0

 </description>
		<link>http://www.izotop.hu/?p=555</link>
			</item>
	<item>
		<title>Parathion, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Parathion, [ring-U-14C]

O,O-diethyl O-4-nitrophenyl phosphorothioate


CC-247
C10H14NO5PS
56-38-2

 </description>
		<link>http://www.izotop.hu/?p=554</link>
			</item>
	<item>
		<title>Paraoxon, [ethyl-1-14C2 , ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Paraoxon, [ethyl-1-14C2 , ring-U-14C]

Diethyl-p-nitrophenyl phosphate


CC-385
C10H14NO6P
311-45-5

 </description>
		<link>http://www.izotop.hu/?p=553</link>
			</item>
	<item>
		<title>Oxamyl, [carbamoyl-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Oxamyl, [carbamoyl-14C]

(EZ)-N,N-dimethyl-2-methylcarbamoyloxyimino-2-(methylthio)acetamide


CC-331
C7H13N3O3S
23135-22-0

 </description>
		<link>http://www.izotop.hu/?p=552</link>
			</item>
	<item>
		<title>MSMA, [14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


MSMA, [14C]

sodium hydrogen methylarsonate


CC-271
CH4AsO3Na
2163-80-6

 </description>
		<link>http://www.izotop.hu/?p=551</link>
			</item>
	<item>
		<title>Monocrotophos, [O-methyl-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Monocrotophos, [O-methyl-14C2]

dimethyl (E)-1-methyl-2-(methylcarbamoyl)vinyl phosphate


CC-250
C7H14NO5P
6923-22-4

 </description>
		<link>http://www.izotop.hu/?p=550</link>
			</item>
	<item>
		<title>Metsulfuron-methyl,[triazinyl-2-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Metsulfuron-methyl, [triazinyl-2-14C]

2-(4-methoxy-6-methyl-1,3,5-triazin-2-ylcarbamoyl-sulfamoyl)benzoic acid


CC-360
C13H13N5O6S
79510-48-8

 </description>
		<link>http://www.izotop.hu/?p=549</link>
			</item>
	<item>
		<title>Metribuzin, [ring-6-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Metribuzin, [ring-6-14C]

4-amino-6-tert-butyl-3-methylthio-1,2,4-triazin-5(4H)-one


CC-320
C8H14N4OS
21087-64-9

 </description>
		<link>http://www.izotop.hu/?p=548</link>
			</item>
	<item>
		<title>Methoprene, [5-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Methoprene, [5-14C]

isopropyl (E,E)-(RS)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienoate


CC-420
C19H34O3
40596-69-8

 </description>
		<link>http://www.izotop.hu/?p=547</link>
			</item>
	<item>
		<title>Methomyl, [carbonyl-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Methomyl, [carbonyl-14C]

S-methyl (EZ)-N-(methylcarbamoyloxy)thioacetimidate


CC-287
C5H10N2O2S
16752-77-5

 </description>
		<link>http://www.izotop.hu/?p=546</link>
			</item>
	<item>
		<title>Methamidophos, [S-methyl-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Methamidophos, [S-methyl-14C]

(RS)-(O,S-dimethyl phosphoramidothioate)


CC-254
C2H8NO2PS
10265-92-6

 </description>
		<link>http://www.izotop.hu/?p=545</link>
			</item>
	<item>
		<title>Methabenzthiazuron, [benzene ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Methabenzthiazuron, [benzene ring-U-14C]

1-benzothiazol-2-yl-1,3-dimethylurea


CC-466
C10H11N3OS
18691-97-9

 </description>
		<link>http://www.izotop.hu/?p=544</link>
			</item>
	<item>
		<title>Metamitron, [phenyl ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Metamitron, [phenyl ring-U-14C]

4-amino-4,5-dihydro-3-methyl-6-phenyl-1,2,4-triazin-5-one


CC-409
C10H10N4O
41394-05-2

 </description>
		<link>http://www.izotop.hu/?p=543</link>
			</item>
	<item>
		<title>Metalaxyl, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Metalaxyl, [ring-U-14C]

methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate


CC-400
C15H21NO4
57837-19-1

 </description>
		<link>http://www.izotop.hu/?p=542</link>
			</item>
	<item>
		<title>Mefenacet, [aniline ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Mefenacet, [aniline ring-U-14C]

2-(1,3-benzothiazol-2-yloxy)-N-methylacetanilide


CC-383
C16H14N2O2S
73250-68-7

 </description>
		<link>http://www.izotop.hu/?p=541</link>
			</item>
	<item>
		<title>Mecoprop, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Mecoprop, [ring-U-14C]

(RS)-2-(4-chloro-o-tolyloxy)propionic acid


CC-401
C10H11ClO3
7085-19-0

 </description>
		<link>http://www.izotop.hu/?p=540</link>
			</item>
	<item>
		<title>MCPA, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


MCPA, [ring-U-14C]

(4-chloro-2-methylphenoxy)acetic acid


CC-382
C9H9ClO3
94-74-6

 </description>
		<link>http://www.izotop.hu/?p=539</link>
			</item>
	<item>
		<title>MCPA, [carboxyl-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


MCPA, [carboxyl-14C]

(4-chloro-2-methylphenoxy)acetic acid


CC-414
C9H9ClO3
94-74-6

 </description>
		<link>http://www.izotop.hu/?p=538</link>
			</item>
	<item>
		<title>Maneb, [ethylene-1,2-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Maneb, [ethylene-1,2-14C2]

manganese ethylenebis(dithiocarbamate) (polymeric) complex


CC-276
(C4H6MnN2S4)x
12427-38-2

 </description>
		<link>http://www.izotop.hu/?p=537</link>
			</item>
	<item>
		<title>Mancozeb, [ethylene-1,2-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Mancozeb, [ethylene-1,2-14C2]

manganese ethylenebis(dithiocarbamate) (polymeric) complex with zinc salt


CC-304

8018-01-7

 </description>
		<link>http://www.izotop.hu/?p=536</link>
			</item>
	<item>
		<title>Malathion, [succinyl-2,3-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Malathion, [succinyl-2,3-14C2]

diethyl (dimethoxyphosphinothioylthio)succinate


CC-246
C10H19O6PS2
121-75-5

 </description>
		<link>http://www.izotop.hu/?p=535</link>
			</item>
	<item>
		<title>Linuron, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Linuron, [ring-U-14C]

3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea


CC-310
C9H10Cl2N2O2
330-55-2

 </description>
		<link>http://www.izotop.hu/?p=534</link>
			</item>
	<item>
		<title>Linuron, [carbonyl-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Linuron, [carbonyl-14C]

3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea


CC-296
C9H10Cl2N2O2
330-55-2

 </description>
		<link>http://www.izotop.hu/?p=533</link>
			</item>
	<item>
		<title>Lindane, [ring-U-14C]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Lindane, [ring-U-14C]

1&#945;,2&#945;,3ß,4&#945;,5&#945;,6ß-hexachlorocyclohexane


CC-330
C6H6Cl6
58-89-9

 </description>
		<link>http://www.izotop.hu/?p=532</link>
			</item>
	<item>
		<title>Lenacil, [pyrimidine-4,6-14C2]</title>
		<description>


Common Name
Structure
Unlabelled IUPAC Name


Catalogue Code
*Position of Labelling
Formula
Reg. No.


Lenacil, [pyrimidine-4,6-14C2]

3-cyclohexyl-1,5,6,7-tetrahydrocyclopentapyrimidine-2,4(3H)-dione


CC-381
C13H18N2O2
2164-08-1

 </description>
		<link>http://www.izotop.hu/?p=531</link>
			</item>
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