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Ezlopitant
Clinical data
Other namesCJ-11,974; (2S,3S)-2-Diphenylmethyl-3-[(5-isopropyl-2-methoxybenzyl)amino]quinuclidine [1]
Routes of
administration		 By mouth
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Pharmacokinetic data
Excretion Urine (32%), Feces (51%)
Identifiers
  • (2S,3S)-2-Benzhydryl-N-[(5-isopropyl-2-methoxy-phenyl)methyl]quinuclidin-3-amine
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC31H38N2O
Molar mass454.658 g·mol−1
3D model ( JSmol)
  • COc1ccc(cc1CN[C@H]2C3CCN(CC3)[C@H]2C(c4ccccc4)c5ccccc5)C(C)C
  • InChI=1S/C31H38N2O/c1-22(2)26-14-15-28(34-3)27(20-26)21-32-30-25-16-18-33(19-17-25)31(30)29(23-10-6-4-7-11-23)24-12-8-5-9-13-24/h4-15,20,22,25,29-32H,16-19,21H2,1-3H3/t30-,31-/m0/s1
  • Key:XPNMCDYOYIKVGB-CONSDPRKSA-N

Ezlopitant ( INN, [1] code name CJ-11,974) is an NK1 receptor antagonist. [2] [3] [4] It has antiemetic and antinociceptive effects. [5] [6] Pfizer was developing ezlopitant for the treatment of irritable bowel syndrome but it appears to have been discontinued. [2]

See also

References

  1. ^ a b "International Nonproprietary Names for Pharmaceutical Substances (INN). Recommended International Nonproprietary Names: List 44" (PDF). World Health Organization. pp. 194–5. Retrieved 17 November 2016.
  2. ^ a b Evangelista S (October 2001). "Eziopitant. Pfizer". Current Opinion in Investigational Drugs. 2 (10): 1441–3. PMID  11890362.
  3. ^ Diemunsch P, Grélot L (September 2000). "Potential of substance P antagonists as antiemetics". Drugs. 60 (3): 533–46. doi: 10.2165/00003495-200060030-00002. PMID  11030465. S2CID  25136161.
  4. ^ Giardina GA, Gagliardi S, Martinelli M (August 2003). "Antagonists at the neurokinin receptors--recent patent literature". IDrugs: The Investigational Drugs Journal. 6 (8): 758–72. PMID  12917772.
  5. ^ Tsuchiya M, Fujiwara Y, Kanai Y, et al. (November 2002). "Anti-emetic activity of the novel nonpeptide tachykinin NK1 receptor antagonist ezlopitant (CJ-11,974) against acute and delayed cisplatin-induced emesis in the ferret". Pharmacology. 66 (3): 144–52. doi: 10.1159/000063796. PMID  12372904. S2CID  37936941.
  6. ^ Tsuchiya M, Sakakibara A, Yamamoto M (January 2005). "A tachykinin NK1 receptor antagonist attenuates the 4 beta-phorbol-12-myristate-13-acetate-induced nociceptive behaviour in the rat". European Journal of Pharmacology. 507 (1–3): 29–34. doi: 10.1016/j.ejphar.2004.11.028. PMID  15659291.


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