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Volumn 13, Issue 1, 2003, Pages 61-64

New tetrahydrobenzindoles as potent and selective 5-HT7 antagonists with increased In vitro metabolic stability

Author keywords

[No Author keywords available]

Indexed keywords

ANTIDEPRESSANT AGENT; DR 4004; DR 4485; SEROTONIN 7 RECEPTOR; SEROTONIN ANTAGONIST; UNCLASSIFIED DRUG; 2A (4 (4 PHENYL 1,2,3,6 TETRAHYDROPYRIDYL)BUTYL) 2A,3,4,5 TETRAHYDROBENZO(CD)INDOL 2(1H) ONE; 2A-(4-(4-PHENYL-1,2,3,6-TETRAHYDROPYRIDYL)BUTYL)-2A,3,4,5-TETRAHYDROBENZO(CD)INDOL-2(1H)-ONE; CYCLIC AMP; HALOGEN; INDOLE DERIVATIVE; PYRIDINE DERIVATIVE; SEROTONIN RECEPTOR;

EID: 0037421025     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(02)00842-9     Document Type: Article
Times cited : (27)

References (35)
  • 24
    • 0011962999 scopus 로고    scopus 로고
    • The oral bioavailability of compound 1 was <10% in rats.
  • 25
    • 0011987706 scopus 로고    scopus 로고
    • +).
  • 26
    • 0011931823 scopus 로고    scopus 로고
    • 2] were performed on a gently shaking platform maintained at 37 °C. Incubations were started by the addition of substrate and were stopped after 0, 10, 30 and 60 min by addition of DMF. Precipitated proteins were removed by centrifugation and supernatants were injected into the HPLC system to determine the remaining amount of each compound.
  • 27
    • 0012004262 scopus 로고    scopus 로고
    • 7 receptor, but this derivative had lower selectivity than compound 1. See ref 19.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.