CAS 98296-48-1
:Lanost-8-en-26-oic acid, 3,7,15-trihydroxy-11,23-dioxo-, (3β,15α)-
Description:
Lanost-8-en-26-oic acid, 3,7,15-trihydroxy-11,23-dioxo-, (3β,15α)- is a complex triterpenoid compound characterized by its multi-hydroxylated structure and specific stereochemistry. This substance features a lanostane skeleton, which is a tetracyclic structure typical of many natural products derived from fungi and plants. The presence of three hydroxyl groups at positions 3, 7, and 15 contributes to its polar nature, potentially influencing its solubility and reactivity. The dioxo functional groups at positions 11 and 23 indicate the presence of carbonyl groups, which can participate in various chemical reactions, including oxidation and reduction processes. This compound may exhibit biological activities, such as antimicrobial or anti-inflammatory properties, making it of interest in pharmaceutical research. Its specific stereochemistry, denoted by the (3β,15α) configuration, is crucial for its biological interactions and efficacy. Overall, lanost-8-en-26-oic acid is a notable example of a natural product with potential applications in medicine and biochemistry.
Formula:C30H46O7
InChI:InChI=1S/C30H46O7/c1-15(10-17(31)11-16(2)26(36)37)18-12-23(35)30(7)25-19(32)13-21-27(3,4)22(34)8-9-28(21,5)24(25)20(33)14-29(18,30)6/h15-16,18-19,21-23,32,34-35H,8-14H2,1-7H3,(H,36,37)
InChI key:InChIKey=RERVSJVGWKIGTJ-UHFFFAOYSA-N
SMILES:CC12C3=C(C4(C)C(CC3O)C(C)(C)C(O)CC4)C(=O)CC1(C)C(C(CC(CC(C(O)=O)C)=O)C)CC2O
Synonyms:- Lanost-8-en-26-oic acid, 3,7,15-trihydroxy-11,23-dioxo-, (3β,15α)-
- Ganoderic acid C2, 98%, from from Ganoderma Lucidum(Leyss. ex Fr.) Karst.
- (3beta,15alpha)-3,7,15-Trihydroxy-11,23-dioxo-lanost-8-en-26-oic acid
- GANODERIC ACID C2(SH)
- Pirlindole Impurity 1 Hydrobromide
- Lanost-8-en-26-oic acid, 3,7,15-trihydroxy-11,23-dioxo-, (3β,15α)- (9CI)
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Found 2 products.
Ganoderic acid C2
CAS:Controlled Product<p>Ganoderic acid C2 is a hepatoprotective compound that was isolated from the mushroom Ganoderma. It protects against liver damage by reducing mitochondrial membrane potential and restoring energy homeostasis in Hl-60 cells. This compound also inhibits fatty acid synthesis, which may be due to its ability to inhibit the activity of the enzyme fatty acid synthase. Ganoderic acid C2 has been shown to protect against liver damage caused by acetaminophen, carbon tetrachloride, and galactosamine. The protective effects of this compound are thought to be due in part to its ability to induce autophagy.</p>Formula:C30H46O7Purity:Min. 95%Molecular weight:518.68 g/mol
