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Volumn 8, Issue 12, 1998, Pages 1531-1536

Design and synthesis of an orally active GPIIb/IIIa antagonist based on a phenylpiperazine scaffold

Author keywords

Antagonists; Anticoagulants; Isosteres; Molecular modelling mechanics

Indexed keywords

4 [4 [4 (AMINOIMINOMETHYL)PHENYL] 1 PIPERAZINYL] 1 PIPERIDINEACETIC ACID; ANTICOAGULANT AGENT; FIBRINOGEN RECEPTOR; FIBRINOGEN RECEPTOR ANTAGONIST; PIPERAZINE DERIVATIVE; RO 43 8857; UNCLASSIFIED DRUG;

EID: 0032537620     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(98)00257-1     Document Type: Article
Times cited : (7)

References (14)
  • 7
    • 0010436814 scopus 로고    scopus 로고
    • note
    • 2)=NH method. After protection of the amidine moiety with a Boc group and catalytic removal of the Z protective group 17 was obtained.
  • 8
    • 0010435995 scopus 로고    scopus 로고
    • note
    • 7 The phenylpiperazines 19-20 were synthesized by heating of methyl-m-aminophenylacetate and ethyl-p-amino phenylacetate, respectively, with bis-2-chloroethylamine hydrochloride in chlorobenzene at reflux for 14h. The phenylpiperazines 18, 22 and 23 are commercially available. 24 was obtained after heating of 3-(4-aminophenyl)-propionic acid tert-butyl ester (obtained after catalytic hydrogenation of E-3-(4-nitrophenyl)-propenoic acid tert-butyl ester) with bis-2-chloroethylamine hydrochloride in chlorobenzene at reflux for 14h.
  • 10
    • 0010481417 scopus 로고    scopus 로고
    • note
    • +), found: 354,4028.
  • 13


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.