gitoxigenin

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; gitoxigenin
Links:	📖 PubMed
CAS RN:	[545-26-6]
Formula:	C₂₃H₃₄O₅; 390.52 ^g/_mol
InChiKey:	PVAMXWLZJKTXFW-VQMOFDJESA-N
SMILES:	C[C@]12CC[C@H](O)C[C@H]1CC[C@@H]3[C@@H]2CC[C@]4(C)[C@H]([C@@H](O)C[C@]34O)C5=CC(=O)OC5

Pharmaceutical use:	carcinostatic
Melting point:	234 °C
Log₁₀ partition octanol / water:	1.60

Isomers

Molecular structure of 4-hydroxy-7,7,10,10,13-pentamethyldecahydro-4H-1,12-methanocyclopenta[d]furo[4',3':1,8a]naphtho[2,3-e][1,3]dioxin-14(11aH)-one

alfadolone acetate

Molecular structure of alfadolone acetate

coroglaucigenin

Molecular structure of coroglaucigenin

Molecular structure of gitoxigenin

7-(hydroxymethyl)-7,10,10,13-tetramethyldecahydro-4H-1,12-methanocyclopenta[d]furo[4',3':1,8a]naphtho[2,3-e][1,3]dioxin-14(11aH)-one

Molecular structure of 7-(hydroxymethyl)-7,10,10,13-tetramethyldecahydro-4H-1,12-methanocyclopenta[d]furo[4',3':1,8a]naphtho[2,3-e][1,3]dioxin-14(11aH)-one

Molecular structure of mevastatin

3-oxoandrost-4-en-17-yl 3-hydroxy-2-(hydroxymethyl)propanoate

Molecular structure of 3-oxoandrost-4-en-17-yl 3-hydroxy-2-(hydroxymethyl)propanoate

Molecular structure of prostaglandin

Molecular structure of sarmentogenin

Molecular structure of treprostinil

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