BMY-14802

BMY-14802
BMY-14802
BMY-14802 Structure.svg
임상자료
기타 이름BMS-181100; MJ-14802
ATC 코드
  • 없음
식별자
  • 1-(4-148페닐)-4-[4-(5-16-피리미딘-2-yl)piperazin-1-yl]부탄-1-올
CAS 번호
펍켐 CID
IUPHAR/BPS
켐스파이더
유니
켐벨
CompTox 대시보드 (EPA)
화학 및 물리적 데이터
공식C18H22F2N4O
어금질량348.398 g·1998−1 g·1998
3D 모델(JSmol)
  • c1cc(F)cc1C(O)CCN2CCN(CC2)c3ncc(F)cn3
  • InChI=1S/C18H22F2N4O/c19-15-5-3-14(4-6-15)17(25)2-1-7-23-8-10-24(11-9-23)18-21-12-16(20)13-22-18/h3-6,12-13,17,25H,1-2,7-11H2 ☒N
  • 키:ZXUYYYZPJUGQHLQ-UHFFFAOYSA-N ☒N
☒NcheckY (이게 뭐야?) (iii)

BMY-14802BMS-181100으로도 알려져 있으며, 시그마 수용체 길항제 5-HT 수용체1A 작용제 역할을 하는 항정신병 효과를 가진 약이다.[1][2][3][4] 또한 5-HT2 수용체와 D 수용체에도4 친화력을 가지고 있다.[5] 그 약은 정신 질환 치료를 위한 임상 3상에 도달했지만 결코 시판되지 않았다.[6]

참조

  1. ^ Taylor DP, Eison MS, Moon SL, Schlemmer RF, Shukla UA, VanderMaelen CP, Yocca FD, Gallant DJ, Behling SH, Boissard CG (1993). "A role for sigma binding in the antipsychotic profile of BMY 14802?". NIDA Research Monograph. 133: 125–57. PMID 8232511.
  2. ^ Vanecek SA, Essman WD, Taylor DP, Woods JH (January 1998). "Discriminative stimulus characteristics of BMY 14802 in the pigeon". The Journal of Pharmacology and Experimental Therapeutics. 284 (1): 1–9. PMID 9435153.
  3. ^ Kitanaka J, Kitanaka N, Tatsuta T, Hall FS, Uhl GR, Tanaka K, Nishiyama N, Morita Y, Takemura M (May 2009). "Sigma1 receptor antagonists determine the behavioral pattern of the methamphetamine-induced stereotypy in mice". Psychopharmacology. 203 (4): 781–92. doi:10.1007/s00213-008-1425-z. PMC 3157915. PMID 19052726.
  4. ^ Paquette MA, Foley K, Brudney EG, Meshul CK, Johnson SW, Berger SP (July 2009). "The sigma-1 antagonist BMY-14802 inhibits L-DOPA-induced abnormal involuntary movements by a WAY-100635-sensitive mechanism". Psychopharmacology. 204 (4): 743–54. doi:10.1007/s00213-009-1505-8. PMC 2845289. PMID 19283364.
  5. ^ Luis M. Botana; Mabel Loza (20 April 2012). Therapeutic Targets: Modulation, Inhibition, and Activation. John Wiley & Sons. pp. 248–. ISBN 978-1-118-18552-0.
  6. ^ "BMS 181100 - AdisInsight".