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Volumn 13, Issue 5, 2005, Pages 1487-1496

Optimization of a coagulation factor VIIa inhibitor found in factor Xa inhibitor library

Author keywords

Factor VIIa; Inhibitor

Indexed keywords

3 [4 AMIDINO 2 [2 (2 AMINOBENZOTHIAZOLE 6 CARBONYL)AMINOETHOXY]PHENYL] 2 OXOPROPIONIC ACID BISTRIFLUOROACETATE; 3 [4 AMIDINO 2 [2 (2 AMINOQUINOLINE 6 CARBONYL)AMINOETHOXY]PHENYL] 2 OXOPROPIONIC ACID BISTRIFLUOROACETATE; 3 [4 AMIDINO 2 [2 (4 AMIDINOBENZOYLAMINO)ETHOXY]PHENYL] 2 OXOPROPIONIC ACID BISTRIFLUOROACETATE; 4 BENZOYLAMINO 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID TRIFLUOROACETATE; 4 [(2 AMINOBENZIMIDAZOLE 5 CARBONYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [(2 AMINOBENZOTHIAZOLE 6 CARBONYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [(2 AMINOQUINOLINE 6 CARBONYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [(2 METHYLBENZIMIDAZOLE 5 CARBONYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [(4 GUANIDINO 3 METHYLBENZOYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [(4 GUANIDINOBENZOYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [(BENZIMIDAZOLE 5 CARBONYL)AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; 4 [[4 (1 METHYLGUANIDINO)BENZOYL]AMINO] 5 [5 AMIDINO 2 (2 CARBOXY 2 OXOETHYL)PHENOXY]PENTANOIC ACID BISTRIFLUOROACETATE; BLOOD CLOTTING FACTOR 10A INHIBITOR; BLOOD CLOTTING FACTOR 7A INHIBITOR; THROMBOPLASTIN; UNCLASSIFIED DRUG;

EID: 13444256329     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2004.12.033     Document Type: Article
Times cited : (18)

References (23)
  • 3
    • 0035021780 scopus 로고    scopus 로고
    • Much effort has been focused on thrombin or fXa inhibitors: C.A. Coburn Exp. Opin. Ther. Pat. 11 5 2001 721 738
    • (2001) Exp. Opin. Ther. Pat. , vol.11 , Issue.5 , pp. 721-738
    • Coburn, C.A.1
  • 16
    • 85030820729 scopus 로고    scopus 로고
    • Düsseldorf, August
    • In our study on fXa inhibitors, the crystal structure of an 2-substituted APPA-trypsin complex shows that although the bonding linkage is formed between the pyruvic acid moiety and the Ser 195, the overall docking mode including the pyruvic acid is still similar to that of the calculated noncovalent 2-substituted APPA-fXa complex. Therefore we consider the overall docking mode of 1a will be similar to the noncovalently calculated binding mode: Takahashi, M.; Sagi, K.; Yamanashi, M.; Makino, S.; Suzuki, N.; Takayanagi, M.; Nakagawa, T.; Ishikawa, K.; Shoji, M. 13th European Symposium on Quantitative Structure-Activity Relationships, Düsseldorf, August 2000
    • (2000) 13th European Symposium on Quantitative Structure-Activity Relationships
    • Takahashi, M.1    Sagi, K.2    Yamanashi, M.3    Makino, S.4    Suzuki, N.5    Takayanagi, M.6    Nakagawa, T.7    Ishikawa, K.8    Shoji, M.9
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.