로60-0175번길

Ro60-0175
로60-0175번길
Ro60-0175 structure.png
식별자
  • (S)-6-클로로-5-플루오로-1H-indole-2-propaminine
CAS 번호
펍켐 CID
IUPHAR/BPS
켐스파이더
체비
ECHA InfoCard100.189.524 Edit this at Wikidata
화학 및 물리적 데이터
공식C11H12CLFN2
어금질량226.68 g·1998−1
3D 모델(JSmol)
  • C[C@@H](Cn1ccc2c1cc(c(c(2)F)Cl)Cl)n
  • InChi=1S/C11H12ClFN2/c1-7(14)6-15-3-2-8-4-10(13)9(13)9-11(8)15/h2-5,7H2,14H2,1H3/t7/m0/s1
  • 키:XJZQXUGLLXTHO-ZETCQYMHSA-N
(iii)

Ro60-0175호프만-라 로슈가 개발한 약으로 과학 연구에 응용이 가능하다.[1][2] 5-HT2B5-HT2C 세로토닌 수용체 하위유형 모두에 대해 강력하고 선택적인 작용제로 작용하며, 밀접하게 연관2A 5-HT 하위유형에 비해 선택성이 우수하며, 다른 수용체에는 친화력이 거의 또는 전혀 없다.[3][4]

참고 항목

참조

  1. ^ Quarta D, Naylor CG, Stolerman IP (August 2007). "The serotonin 2C receptor agonist Ro-60-0175 attenuates effects of nicotine in the five-choice serial reaction time task and in drug discrimination". Psychopharmacology. 193 (3): 391–402. doi:10.1007/s00213-007-0802-3. PMID 17473916. S2CID 21020653.
  2. ^ Fletcher PJ, Rizos Z, Sinyard J, Tampakeras M, Higgins GA (May 2008). "The 5-HT2C receptor agonist Ro60-0175 reduces cocaine self-administration and reinstatement induced by the stressor yohimbine, and contextual cues". Neuropsychopharmacology. 33 (6): 1402–12. doi:10.1038/sj.npp.1301509. PMID 17653111.
  3. ^ Porter RH, Benwell KR, Lamb H, Malcolm CS, Allen NH, Revell DF, et al. (September 1999). "Functional characterization of agonists at recombinant human 5-HT2A, 5-HT2B and 5-HT2C receptors in CHO-K1 cells". British Journal of Pharmacology. 128 (1): 13–20. doi:10.1038/sj.bjp.0702751. PMC 1571597. PMID 10498829.
  4. ^ Damjanoska KJ, Muma NA, Zhang Y, D'Souza DN, Garcia F, Carrasco GA, et al. (March 2003). "Neuroendocrine evidence that (S)-2-(chloro-5-fluoro-indol- l-yl)-1-methylethylamine fumarate (Ro 60-0175) is not a selective 5-hydroxytryptamine(2C) receptor agonist". The Journal of Pharmacology and Experimental Therapeutics. 304 (3): 1209–16. doi:10.1124/jpet.102.043489. PMID 12604698. S2CID 23880629.