CAS 156967-65-6
:5bH-[1,3]Dioxino[5'',4'':2',3']oxireno[4',4'a][1]benzopyrano[5',6':6,7]indeno[1,2-b]indol-5b-ol,1,4a,4b,6,7,7a,8,13,13b,13c,14,15,15a,16a-tetradecahydro-1,1,13b,13c-tetramethyl-3-(2-methyl-1-propen-1-yl)-,(3S,4aR,4bR,5aS,5bS,7aS,13bS,13cR,15aS,16aS)-
Description:
The chemical substance known as "5bH-[1,3]Dioxino[5'',4'':2',3']oxireno[4',4'a][1]benzopyrano[5',6':6,7]indeno[1,2-b]indol-5b-ol" with the CAS number 156967-65-6 is a complex organic compound characterized by a multi-ring structure that incorporates dioxin, benzopyran, and indole moieties. This compound features a tetradecahydro framework, indicating a saturated structure with multiple chiral centers, which contributes to its stereochemical complexity. The presence of functional groups such as hydroxyl (-OH) and alkene (due to the 2-methyl-1-propen-1-yl substituent) suggests potential reactivity and biological activity. Its intricate arrangement of rings and substituents may influence its solubility, stability, and interaction with biological systems. Such compounds often exhibit interesting pharmacological properties, making them subjects of research in medicinal chemistry. However, due to the complexity of its structure, detailed studies would be necessary to fully elucidate its properties and potential applications.
Formula:C32H41NO5
Synonyms:- 5bH-[1,3]Dioxino[5'',4'':2',3']oxireno[4',4'a][1]benzopyrano[5',6':6,7]indeno[1,2-b]indol-5b-ol,1,4a,4b,6,7,7a,8,13,13b,13c,14,15,15a,16a-tetradecahydro-1,1,13b,13c-tetramethyl-3-(2-methyl-1-propenyl)-,(3S,4aR,4bR,5aS,5bS,7aS,13bS,13cR,15aS,16aS)- (9CI)
- (-)-Terpendole C
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Found 3 products.
Terpendole C
CAS:<p>Terpendole C, an indole diterpene from A. yamanashiensis, inhibits ACAT with IC50 of 2.1 μM in rats, 0.46 μM in J774 cells, non-toxic.</p>Formula:C32H41NO5Color and Shape:SolidMolecular weight:519.682Terpendole C
CAS:Formula:C32H41NO5Purity:(HPLC) ≥ 95.0%Color and Shape:White to off-white solidMolecular weight:519.7Terpendole C
CAS:<p>Terpendole C is a potent inhibitor of cholesterol acyltransferase (ACAT) and is used in the treatment of metabolic disorders. It has also been shown to decrease tremorgenic mycotoxins in perennial ryegrass, which may be due to its ability to inhibit cholesterol synthesis. Terpendole C has been found to have neovascular properties and has been shown to prevent eye disorders such as cataracts and retinopathy. It also has cancer-preventing properties, which may be due to its anti-angiogenic effects on tumor cells. This compound is a wild-type strain that inhibits the death protein, and is therefore capable of preventing apoptosis in cells.</p>Formula:C32H41NO5Purity:Min. 95%Molecular weight:519.7 g/mol


