메뉴 건너뛰기




Volumn 6, Issue 4, 1996, Pages 385-390

Design, synthesis and X-ray crystallographic studies of [7.3.1] and [8.3.1] macrocyclic FKBP-12 ligands

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; CYCLOPHILIN; MACROCYCLIC COMPOUND; TSUKUBAENOLIDE BINDING PROTEIN; UNCLASSIFIED DRUG;

EID: 0029878149     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-894X(96)00032-7     Document Type: Article
Times cited : (8)

References (22)
  • 6
    • 84920292975 scopus 로고    scopus 로고
    • 2O, reflux, 3 hrs.)
    • 2O, reflux, 3 hrs.)
  • 10
    • 85030194837 scopus 로고    scopus 로고
    • note
    • app > 50 μM"). All data were analyzed using the software program KineTic (BioKin, Ltd., Madison, WI).
  • 14
    • 85030193749 scopus 로고    scopus 로고
    • note
    • σF) for a model containing 832 protein, 25 ligand and 90 water atoms, with root mean square deviations from ideality of 0.015Å for bond distances and 2.86° on bond angles.
  • 19
    • 85030197106 scopus 로고    scopus 로고
    • note
    • 19, plus 1% dimethyl sulfoxide as cosolvent and 100 μM FKBP. Compounds were tested for FKBP-dependent inhibition of calcineurin at their maximum solubility. Under these conditions, the apparent inhibition constant for inhibition of human recombinant calcineurin by FKBP-FK506 was 43 nM.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.