Vedaklidin

Из Википедије, слободне енциклопедије
Vedaklidin
(IUPAC) ime
(3-(3-1-butiltio)-1,2,5-tiadiazol-4-il)-1-azabiciklo-2.2.2-oktan
Klinički podaci
Identifikatori
CAS broj 141575-52-2
ATC kod nije dodeljen
PubChem[1][2] 60868
ChemSpider[3] 54852
UNII 98IW5HAV1N YesY
Hemijski podaci
Formula C13H21N3S2 
Mol. masa 283,455 g/mol
SMILES eMolekuli & PubHem
Farmakoinformacioni podaci
Trudnoća  ?
Pravni status

Vedaklidin (LY-297,802, NNC 11-1053) je analgetski lek koji deluje kao mešoviti agonist-antagonist na muscarinskim acetilholinskim receptorima. On je potentan i selektivan agonist na M1 i M4 podtipovima, a antagonist na M2, M3 i M5 podtipovima.[4][5] Vedaklidin je oralno aktivan i efektivan analgetik, koji je više od tri puta potentniji od morfina. Njegove nuspojave su salivacija i tremor, koje se javljaju pri dozama koje su nekoliko puta veće od efektivne.[6][7][8] Klinička ispitivanja su pokazala da on ima neznatan potencijal za razvoj zavisnosti ili zloupotrebu.[9] Dalja ispitivanja s ciljem utvđivanja moguće kliničke primene u tretiranju neuropatičkog bola i olakšavanja bola uzrokovanog kancerom su u toku.[10]

Reference[уреди]

  1. ^ 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.  edit
  2. ^ 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. 
  3. ^ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining“. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.  edit
  4. ^ Shannon HE, Womer DE, Bymaster FP, Calligaro DO, DeLapp NC, Mitch CH, Ward JS, Whitesitt CA, Swedberg MD, Sheardown MJ, Fink-Jensen A, Olesen PH, Rimvall K, Sauerberg P. In vivo pharmacology of butylthio[2.2.2] (LY297802 / NNC11-1053), an orally acting antinociceptive muscarinic agonist. Life Sciences. 1997;60(13-14):969-76. PMID 9121363
  5. ^ Womer DE, Shannon HE (2000). „Reversal of pertussis toxin-induced thermal allodynia by muscarinic cholinergic agonists in mice“. Neuropharmacology 39 (12): 2499–504. DOI:10.1016/S0028-3908(00)00068-X. PMID 10974334. 
  6. ^ Swedberg MD, Sheardown MJ, Sauerberg P, Olesen PH, Suzdak PD, Hansen KT, Bymaster FP, Ward JS, Mitch CH, Calligaro DO, Delapp NW, Shannon HE. Butylthio[2.2.2] (NNC 11-1053/LY297802): an orally active muscarinic agonist analgesic. Journal Pharmacology and Experimental Therapeutics. 1997 May;281(2):876-83. PMID 9152397
  7. ^ Shannon HE, Sheardown MJ, Bymaster FP, Calligaro DO, Delapp NW, Gidda J, Mitch CH, Sawyer BD, Stengel PW, Ward JS, Wong DT, Olesen PH, Suzdak PD, Sauerberg P, Swedberg MD. Pharmacology of butylthio[2.2.2] (LY297802/NNC11-1053): a novel analgesic with mixed muscarinic receptor agonist and antagonist activity. Journal of Pharmacology and Experimental Therapeutics. 1997 May;281(2):884-94. PMID 9152398
  8. ^ Shannon HE, Jones CK, Li DL, Peters SC, Simmons RM, Iyengar S (2001). „Antihyperalgesic effects of the muscarinic receptor ligand vedaclidine in models involving central sensitization in rats“. Pain 93 (3): 221–7. DOI:10.1016/S0304-3959(01)00319-0. PMID 11514081. 
  9. ^ Petry NM, Bickel WK, Huddleston J, Tzanis E, Badger GJ (1998). „A comparison of subjective, psychomotor and physiological effects of a novel muscarinic analgesic, LY297802 tartrate, and oral morphine in occasional drug users“. Drug and alcohol dependence 50 (2): 129–36. DOI:10.1016/S0376-8716(98)00026-X. PMID 9649964. 
  10. ^ Tata AM (2008). „Muscarinic acetylcholine receptors: new potential therapeutic targets in antinociception and in cancer therapy“. Recent patents on CNS drug discovery 3 (2): 94–103. DOI:10.2174/157488908784534621. PMID 18537768. 

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