The title compound, C19H28O3, the fungal-transformed metabolite of the steroid methyloestrenol contains four fused rings A, B, C and D. Ring A adopts a half-chair and the transfused rings B and C adopt chair confirmations; the five-membered D ring is folded like an envelope. In the crystal, adjacent molecules are linked by O-H center dot center dot center dot O-carbonyl and O-H center dot center dot center dot O-hydroxy hydrogen bonds into a layer structure
The title compound, C31H48O6, is a polyoxygenated epoxy steroid obtained by a multi-step synthesis i...
The title compound, C22H29F3O5S [systematic name: (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluor...
The title compound, C30H48O2, contains a fused four-ring triterpenoid system. In the molecule, the t...
R factor = 0.047; wR factor = 0.119; data-to-parameter ratio = 10.6. The title compound, C19H28O3, t...
The title compound, C21H28O3, is a fungal transformed metabolite of decoxycorticosterone acetate, co...
The title compound, C22H32O4, a fungal-transformed metabolite of medroxyprogesterone, comprises one ...
The title compound, (7R,8S)-7,8-dihydroxy-3,7-dimethyl-6-oxo-7,8-dihydro-6H-isochromene-5-carbaldehy...
The steroid ring B of the title compound, C22H32O, is in a half-chair conformation. The five-membere...
The title compound, C31H48O7, a polyoxygenated steroid, was obtained by chemical oxidation of 7-dehy...
In the title compound, C20H26O2, which is the 6-methylene derivative of androstenedione and a synthe...
The steroid ring B of the title compound, C22H32O, is in a half-chair conformation. The five-membere...
(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluoromethyl-sulfonyloxy)-2,3,4,7,8,9,10,11,12,13,14,15...
R factor = 0.037; wR factor = 0.079; data-to-parameter ratio = 9.9. In the title compound, C23H34O4,...
The title steroid, C31H53NO4, was prepared from the corresponding 5α,6α-epoxycholestane. T...
The title compound, C31H48O6, is a polyoxygenated epoxy steroid obtained by a multi-step synthesis i...
The title compound, C31H48O6, is a polyoxygenated epoxy steroid obtained by a multi-step synthesis i...
The title compound, C22H29F3O5S [systematic name: (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluor...
The title compound, C30H48O2, contains a fused four-ring triterpenoid system. In the molecule, the t...
R factor = 0.047; wR factor = 0.119; data-to-parameter ratio = 10.6. The title compound, C19H28O3, t...
The title compound, C21H28O3, is a fungal transformed metabolite of decoxycorticosterone acetate, co...
The title compound, C22H32O4, a fungal-transformed metabolite of medroxyprogesterone, comprises one ...
The title compound, (7R,8S)-7,8-dihydroxy-3,7-dimethyl-6-oxo-7,8-dihydro-6H-isochromene-5-carbaldehy...
The steroid ring B of the title compound, C22H32O, is in a half-chair conformation. The five-membere...
The title compound, C31H48O7, a polyoxygenated steroid, was obtained by chemical oxidation of 7-dehy...
In the title compound, C20H26O2, which is the 6-methylene derivative of androstenedione and a synthe...
The steroid ring B of the title compound, C22H32O, is in a half-chair conformation. The five-membere...
(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluoromethyl-sulfonyloxy)-2,3,4,7,8,9,10,11,12,13,14,15...
R factor = 0.037; wR factor = 0.079; data-to-parameter ratio = 9.9. In the title compound, C23H34O4,...
The title steroid, C31H53NO4, was prepared from the corresponding 5α,6α-epoxycholestane. T...
The title compound, C31H48O6, is a polyoxygenated epoxy steroid obtained by a multi-step synthesis i...
The title compound, C31H48O6, is a polyoxygenated epoxy steroid obtained by a multi-step synthesis i...
The title compound, C22H29F3O5S [systematic name: (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluor...
The title compound, C30H48O2, contains a fused four-ring triterpenoid system. In the molecule, the t...