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Volumn 132, Issue 9, 2010, Pages 3063-3077

Synthesis and structure-activity correlation of natural-product inspired cyclodepsipeptides stabilizing F-actin

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL DATA; COMPOUND LIBRARIES; CYCLODEPSIPEPTIDES; CYTOTOXIC; EUKARYOTIC CELLS; F-ACTIN; FUNCTIONALIZED; FUTURE DESIGNS; HIGH RESOLUTION; HYBRID STRUCTURE; INHIBITORY EFFECT; JASPLAKINOLIDE; MACROCYLIZATION; NATURAL PRODUCTS; PHARMACOPHORES; POLYKETIDES; RESEARCH EFFORTS; RING CLOSING METATHESIS; SECONDARY METABOLITES; SMALL MOLECULES; SOLID-PHASE; STABILIZING PROPERTIES; STRUCTURAL BASIS; STRUCTURAL COMPONENT; STRUCTURAL DATA; STRUCTURE-ACTIVITY; STRUCTURE-FUNCTION STUDIES; SYNTHETIC ROUTES; TOTAL SYNTHESIS;

EID: 77949391413     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja9095126     Document Type: Article
Times cited : (85)

References (120)
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    • note
    • On cleavage of (OTBS)-or (OTIPS)-β-tyrosine-containing peptidic acids 11c-g from the polymer support (Scheme 4), varying quantities of the phenolic OH unprotected form were additionally isolated (Supporting Information). Further investigations suggested that the peptide coupling conditions (carbodiimide in combination with amino-acid and benzotriazole) were favoring undesired silyl deprotection. Fortunately, the desilylated peptides could be readily reprotected in solution using standard conditions (Supporting Information).
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    • All pictures were rendered and analyzed using PyMol, V0.99; DeLano Scientific Ltd.: Palo Alto, CA
    • All pictures were rendered and analyzed using PyMol, V0.99; DeLano Scientific Ltd.: Palo Alto, CA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.