GR-89696
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(IUPAC) ime | |||
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methyl 4-[2-(3,4-dichlorophenyl)acetyl]-3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate | |||
Klinički podaci | |||
Identifikatori | |||
CAS broj | 126766-32-3 | ||
ATC kod | ? | ||
PubChem[1][2] | 3505 | ||
Hemijski podaci | |||
Formula | C19H25Cl2N3O3 | ||
Mol. masa | 414.325 g/mol | ||
SMILES | eMolekuli & PubHem | ||
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Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
GR-89696 je lek koji deluje kao visoko selektivni κ-opioidni agonist.[3] On pokazuje selektivno dejstvo u različitim životinjskim modelima, i smatra se da je on selektivan za κ2 tip receptora.[4][5][6] Nedavne studije indiciraju da su GR-89696 i srodni κ2-selektivni agonisti korisni u sprečavanju svrabeža koji je uobičajena nuspojava konvencionalnih opioidnih analgetika, bez dodatnih nuspojava ne-selektivnih kapa agonista.[7]
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Naylor A, Judd DB, Lloyd JE, Scopes DI, Hayes AG, Birch PJ (July 1993). „A potent new class of kappa-receptor agonist: 4-substituted 1-(arylacetyl)-2-[(dialkylamino)methyl]piperazines”. Journal of Medicinal Chemistry 36 (15): 2075–83. PMID 8393489.
- ↑ Herrero JF, Headley PM (September 1993). „Functional evidence for multiple receptor activation by kappa-ligands in the inhibition of spinal nociceptive reflexes in the rat”. British Journal of Pharmacology 110 (1): 303–9. PMC 2176008. PMID 8220893.
- ↑ Ho J, Mannes AJ, Dubner R, Caudle RM (April 1997). „Putative kappa-2 opioid agonists are antihyperalgesic in a rat model of inflammation”. The Journal of Pharmacology and Experimental Therapeutics 281 (1): 136–41. PMID 9103490.
- ↑ Butelman ER, Ko MC, Traynor JR, Vivian JA, Kreek MJ, Woods JH (September 2001). „GR89,696: a potent kappa-opioid agonist with subtype selectivity in rhesus monkeys”. The Journal of Pharmacology and Experimental Therapeutics 298 (3): 1049–59. PMID 11504802.
- ↑ Ko MC, Husbands SM (January 2009). „Effects of atypical kappa-opioid receptor agonists on intrathecal morphine-induced itch and analgesia in primates”. The Journal of Pharmacology and Experimental Therapeutics 328 (1): 193–200. DOI:10.1124/jpet.108.143925. PMC 2719014. PMID 18842704.