SB-228357

SB-228357
SB-228357
SB-228357 structure.png
식별자
  • N-(3-플루오로-5-피리딘-3-ylphenyl)-5-메톡시-6-(트리플루오로메틸)-2,3-디하이드로인돌-1-카복사미드
CAS 번호
펍켐 CID
켐스파이더
유니
케그
체비
켐벨
CompTox 대시보드 (EPA)
화학 및 물리적 데이터
공식C22H17F4N3O2
어금질량431.391 g·1911−1
3D 모델(JSmol)
  • COC1=C(C=C2C(=C1)CCN2C(=O)NC3=CC(=CC(=C3)C4=CN=CC=C4)C(F)(F)f
  • InChI=1S/C22H17F4N3O2/c1-31-20-9-13-4-6-29(19(13)11-18(20)22(24,25)26)21(30)28-17-8-15(7-16(23)10-17)14-3-2-5-27-12-14/h2-3,5,7-12H,4,6H2,1H3,(H,28,30)
  • 키:RRJLJKRFFRZRAF-UHFFFAOYSA-N

SB-2283575HT2B 수용체5HT2C 수용체의 길항제 역할을 하는 약물이다. 동물 모델에서 항우울제항불안제 효과가 있으며,[1][2] 심장 섬유블라스트의 5-HT2B 매개 증식을 억제한다.[3]

참고 항목

참조

  1. ^ Reavill C, Kettle A, Holland V, Riley G, Blackburn TP (February 1999). "Attenuation of haloperidol-induced catalepsy by a 5-HT2C receptor antagonist". British Journal of Pharmacology. 126 (3): 572–4. doi:10.1038/sj.bjp.0702350. PMC 1565856. PMID 10188965.
  2. ^ Bromidge SM, Dabbs S, Davies DT, Davies S, Duckworth DM, Forbes IT, et al. (March 2000). "Biarylcarbamoylindolines are novel and selective 5-HT(2C) receptor inverse agonists: identification of 5-methyl-1-[[2-[(2-methyl-3-pyridyl)oxy]- 5-pyridyl]carbamoyl]-6-trifluoromethylindoline (SB-243213) as a potential antidepressant/anxiolytic agent". Journal of Medicinal Chemistry. 43 (6): 1123–34. doi:10.1021/jm990388c. PMID 10737744.
  3. ^ Hutcheson JD, Ryzhova LM, Setola V, Merryman WD (November 2012). "5-HT(2B) antagonism arrests non-canonical TGF-β1-induced valvular myofibroblast differentiation". Journal of Molecular and Cellular Cardiology. 53 (5): 707–14. doi:10.1016/j.yjmcc.2012.08.012. PMC 3472096. PMID 22940605.