SB-357134

SB-357134
SB-357134
SB357134.png
식별자
  • N-(2,5-디브로모-3-플루오페닐)-4-메톡시-3-(1-피페라지닐)벤젠설폰아미드
펍켐 CID
IUPHAR/BPS
켐스파이더
켐벨
화학 및 물리적 데이터
공식C17H18BR2FN3O3S
어금질량523.22 g·190−1
3D 모델(JSmol)
  • C3CN3c1cc(ccc1OC)S(=O)NC2cc(Br)cc(F)c2Br
  • InChI=1S/C17H18Br2FN3O3S/c1-26-16-3-2-12(10-15(16)23-6-4-21-5-7-23)27(24,25)22-14-9-11(18)8-13(20)17(14)19/h2-3,8-10,21-22H,4-7H2,1H3 ☒N
  • 키:BLWAZZXRTFJE-UHFFFAOYSA-N ☒N
☒NcheckY (이게 뭐야?) (iii)

SB-357134는 과학 연구에 사용되는 약물이다. 그것은 강력하고 선택적이며 구두로 활성화된 5-HT6 수용체 길항제 역할을 한다.[1] SB-357134와 다른 5-HT6 길항제들은 동물 연구에서 비등방성 효과를 보이며,[2][3][4] 조현병, 알츠하이머병 등 인지장애에 대한 잠재적인 새로운 치료법으로 제안되어 왔다.

참조

  1. ^ Bromidge SM, Clarke SE, Gager T, Griffith K, Jeffrey P, Jennings AJ, et al. (January 2001). "Phenyl benzenesulfonamides are novel and selective 5-HT6 antagonists: identification of N-(2,5-dibromo-3-fluorophenyl)-4-methoxy-3-piperazin-1-ylbenzenesulfonamide (SB-357134)". Bioorganic & Medicinal Chemistry Letters. 11 (1): 55–8. doi:10.1016/S0960-894X(00)00597-7. PMID 11140733.
  2. ^ Rogers DC, Hagan JJ (November 2001). "5-HT6 receptor antagonists enhance retention of a water maze task in the rat". Psychopharmacology. 158 (2): 114–9. doi:10.1007/s002130100840. PMID 11702084. S2CID 29472459.
  3. ^ Stean TO, Hirst WD, Thomas DR, Price GW, Rogers D, Riley G, et al. (April 2002). "Pharmacological profile of SB-357134: a potent, selective, brain penetrant, and orally active 5-HT(6) receptor antagonist". Pharmacology, Biochemistry, and Behavior. 71 (4): 645–54. doi:10.1016/S0091-3057(01)00742-0. PMID 11888556. S2CID 34925312.
  4. ^ Perez-García G, Meneses A (July 2005). "Oral administration of the 5-HT6 receptor antagonists SB-357134 and SB-399885 improves memory formation in an autoshaping learning task". Pharmacology, Biochemistry, and Behavior. 81 (3): 673–82. doi:10.1016/j.pbb.2005.05.005. PMID 15964617. S2CID 19789219.