Current Medicinal Chemistry |
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3-(Methoxymethyl)indole acid Actinomadura roseoviolacea action potential aglycone aklavinone anthracyclines Antibiotic approach atomic contributions B-Rhodomycin Bentham Science Publishers bioactivity biological biosynthetic calculated carbon cardiovascular effects carminomycin cells chemical citalopram CLOGP coeruleorubidus compounds concentration correction factors correlations coworkers Current Medicinal Chemistry cyaneus Cytorhodin cytotoxic cytotoxic properties daunorubicin derivatives descriptors developed Ditrisarubicin doxorubicin drug effects of fluoxetine enzyme experimental fluoxetine fragment galilaeus glucosinolates glycosides glycosylation group contribution methods hydrogen bonding indole-3 indole-3-methanol indoles inhibitor interactions isolated from cultures leukaemias log P0/w Medicinal Chemistry membrane metabolite methanol methyl moiety molecular molecules murine mutant strain Nogalamycin obelmycin obtained by microbial octanol OH O OH oxidation parameters paroxetine partition coefficient peucetius physicochemical predictions present purpurascens reaction reported Roa-dF Roa-dF-Rod Roa-dF=(L)CinB Roa-Rod-Rod skatole solubility solvent SSRls Streptomyces sp structures substituted surface area tricyclic antidepressants trisaccharide values violaceus violamycin vitro vivo yield