منابع مشابه
Synthetic cardenolides and related products.
ABSTRACT Since the publication in 1785 of one of the great classics of clinical medicine, 'An Account of the Foxglove and Some of its Medical Uses' by William Withering', the steroidal glycosides of digitalis have maintained a unique position among drugs. Their usefulness as life saving products is unchallenged and yet very few drugs are known to possess a narrower margin of safety. Their toxic...
متن کاملThe incubation of 13α,17-dihydroxystemodane with Cephalosporium aphidicola.
The biotransformation of 13α,17-dihydroxystemodane (3) with the fungus Cephalosporium aphidicola afforded 13α,17,18-trihydroxystemodane (4), 3β,13α,17-tri-hydroxystemodane (5), 13α,17-dihydroxy-stemodan-18-oic acid (6), 3β,11β,13α,17-tetra-hydroxystemodane (7), 11β,13α,17,18-tetrahydroxystemodane (8) and 3β,13α,17,18-tetra-hydroxystemodane (9). The hydroxylation at C-18 of the substrate points ...
متن کامل6-Hydroxyimino-5α-cholestane
The title compound, C(27)H(47)NO, is a steroid derivative composed of a saturated carbon fused-ring framework with an alkyl side chain. Ring bond lengths have normal values with an average of 1.533 (2) Å, while the cholestane side chain shows an average bond length of 1.533 (2) Å. The three cyclohexane rings adopt chair conformations or close to chair conformations while the cyclopentane ring i...
متن کاملSynthesis and Biological Evaluation of Triazolyl 13α-Estrone-Nucleoside Bioconjugates.
2'-Deoxynucleoside conjugates of 13α-estrone were synthesized by applying the copper-catalyzed alkyne-azide click reaction (CuAAC). For the introduction of the azido group the 5'-position of the nucleosides and a propargyl ether functional group on the 3-hydroxy group of 13α-estrone were chosen. The best yields were realized in our hands when the 3'-hydroxy groups of the nucleosides were protec...
متن کامل5α-Dihydrovespertilin acetate
In the title compound, C(24)H(36)O(4) [systematic name: (20S)-3β-acet-oxy-16α-hydr-oxy-22,23-bis-nor-5α,17β-cholano(22-16)lac-tone], the three six-membered rings adopt classical chair conformations, while the five-membered rings are in envelope conformations. The ester group attached to ring A is in an equatorial position. Rings A/B, B/C and C/D are trans-fused, whereas rings D/E are cis-fused....
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ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1973
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.21.2209