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Volumn 38, Issue 4, 2010, Pages 149-158

Synthesis and tubulin-binding properties of new allocolchicinoids

Author keywords

Allocolchicinoids; Diels Alder reaction; Enyne; Metathesis; Tubulin inhibitors

Indexed keywords

ALKALOID DERIVATIVE; ALLOCOLCHICINE; ALLOCOLCHICINOID B; ALLOCOLCHICINOID C; ALLOCOLCHICINOID DERIVATIVE; BIPHENYL DERIVATIVE; COLCHICINE; ESTER DERIVATIVE; METHYL GROUP; TUBULIN; UNCLASSIFIED DRUG;

EID: 77954214072     PISSN: 00452068     EISSN: 10902120     Source Type: Journal    
DOI: 10.1016/j.bioorg.2010.03.003     Document Type: Article
Times cited : (28)

References (59)
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    • To our knowledge, while compound 9, 13, 15 are unknown, only one report has hitherto been published describing 11 by transformation of colchicine: B.P. Vaterlaus, and G. Muller Bull. Soc. Chim. Fr. 1957 1329
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    • The colchicine numbering has been used throughout this paper
    • The colchicine numbering has been used throughout this paper.
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    • See Supporting Information: Figure 1; computed three-dimensional structures of compounds 9, 11, 13
    • See Supporting Information: Figure 1; computed three-dimensional structures of compounds 9, 11, 13.
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    • Allocolchicine (2) itself occurs as an approximate 3:1 mixture of aR/aS atropoisomers and has a biaryl dihedral angle of 49°, see: M.F. Mackay, E. Lacey, and P. Burden Acta Crystallogr. Sect. C 45 1989 799
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    • Computed three-dimensional structures of compounds 14, 15, 40, 43 have been generated. See Supporting Information
    • Computed three-dimensional structures of compounds 14, 15, 40, 43 have been generated. See Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.