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Demonstration of a pronounced effect of noncovalent binding selectivity on the (+)-CC-1065 DNA alkylation and identification of the pharmacophore of the alkylation subunit.

Studies on the structural origin of the DNA alkylation selectivity of the antitumor antibiotic (+)-CC-1065 are detailed. The sites of alkylation of double-stranded DNA were examined for simple derivatives of 7-methyl-1,2,8,8a-tetrahydrocycloprop[1,2-c]pyrrolo[3,2-e]indol- 4(5H)-one (CPI), (+)-CC-106...

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Detaylı Bibliyografya
Asıl Yazarlar: Boger, D L, Zarrinmayeh, H, Munk, S A, Kitos, P A, Suntornwat, O
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1991
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC51032/
https://ncbi.nlm.nih.gov/pubmed/1847523
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