메뉴 건너뛰기




Volumn 55, Issue 3, 2007, Pages 393-402

Indoline derivatives II: Synthesis and factor Xa (FXa) inhibitory activities

Author keywords

Anticoagulant; Factor Xa (FXa) inhibitory activity; Indoline derivative

Indexed keywords

5 [1 (ACETYMIDOYL)PIPERIDIN 4 YLOXY] 2 (7 AMIDINONAPHTHALEN 2 YL) 1 (ETHANESULFONYL)INDOLINE; [(5 [1 (ACETIMIDOYL)PIPERIDIN 4 YLOXY] 2 (7 AMIDINONAPHTHALEN 2 YL) INDOLIN 1 YL)SULFONYL]ACETIC ACID DIHYDROCHLORIDE; [5 [1 (ACETYMIDOYL)PIPERIDIN 4 YLOXY] 2 (7 AMIDINONAPHTHALEN 2 YL)INDOLIN 1 YL]SULFONYL ACETIC ACID; BLOOD CLOTTING FACTOR 10A; BLOOD CLOTTING FACTOR 10A INHIBITOR; ETHANESULFOYL; UNCLASSIFIED DRUG;

EID: 34047126829     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.393     Document Type: Article
Times cited : (14)

References (24)
  • 11
    • 34047124612 scopus 로고    scopus 로고
    • 1H-NMR spectra.
    • 1H-NMR spectra.
  • 18
    • 34047126725 scopus 로고    scopus 로고
    • At first, we tried to adopt aryl amino reaction against trifluoromethanesulfonate 24 to prepare methylaminoindoline derivative 33.24,25 In spite of many efforts, the reaction was result in recovery of compound 24
    • 24,25) In spite of many efforts, the reaction was result in recovery of compound 24.
  • 20
    • 34047128489 scopus 로고    scopus 로고
    • In the previous report, S-3 was obtained from separation of (RS)-3 by preparative chiral HPLC, S)-3 was converted to compound (R)-35, then we determined the stereochemistry of (R)-35 and (S)-3 (the starting material of (R)-35) by X-ray crystallographic analysis of (R)-35. This time, each retention time of (S)-3 and (R)-3 was already in hand, so we determined their stereochemistry by comparison of its retention time, Chemical Equation Presented
    • In the previous report, (S)-3 was obtained from separation of (RS)-3 by preparative chiral HPLC. (S)-3 was converted to compound (R)-35, then we determined the stereochemistry of (R)-35 and (S)-3 (the starting material of (R)-35) by X-ray crystallographic analysis of (R)-35. This time, each retention time of (S)-3 and (R)-3 was already in hand, so we determined their stereochemistry by comparison of its retention time. (Chemical Equation Presented)
  • 22
    • 34047102764 scopus 로고    scopus 로고
    • max (10 min) was 7.0 mg/ml. As a result, no significant difference was observed in plasma concentration of both compounds. This result indicates that the difference of toxicity between (RS)-1 and 11d isn't induced by the plasma concentration but these compounds themselves (unpublished data).
    • max (10 min) was 7.0 mg/ml. As a result, no significant difference was observed in plasma concentration of both compounds. This result indicates that the difference of toxicity between (RS)-1 and 11d isn't induced by the plasma concentration but these compounds themselves (unpublished data).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.