CAS 73793-68-7
:(5aR,5bR,7aS,8R,10aS,11aR,11bR,13aR)-8-(5-hydroxy-2-oxo-2,5-dihydrofuran-3-yl)-1,1,5a,7a,11b-pentamethyl-5b,6,7,7a,8,11b,13,13a-octahydrooxireno[4,4a]isochromeno[6,5-g][2]benzoxepine-3,10,12(1H,5aH,10aH)-trione
Description:
The chemical substance with the name "(5aR,5bR,7aS,8R,10aS,11aR,11bR,13aR)-8-(5-hydroxy-2-oxo-2,5-dihydrofuran-3-yl)-1,1,5a,7a,11b-pentamethyl-5b,6,7,7a,8,11b,13,13a-octahydrooxireno[4,4a]isochromeno[6,5-g][2]benzoxepine-3,10,12(1H,5aH,10aH)-trione" and CAS number "73793-68-7" is a complex organic compound characterized by its intricate polycyclic structure, which includes multiple fused rings and various functional groups. This compound features a pentamethyl substitution pattern, contributing to its unique stereochemistry and potentially influencing its biological activity. The presence of a hydroxy group and a diketone moiety suggests it may participate in hydrogen bonding and exhibit reactivity typical of carbonyl compounds. Its structural complexity indicates potential applications in medicinal chemistry, possibly as a lead compound for drug development. The stereochemical configuration is crucial for understanding its interactions with biological targets, which may include enzymes or receptors. Overall, this compound exemplifies the diversity of organic molecules and their potential significance in various chemical and pharmaceutical contexts.
Formula:C26H30O9
InChI:InChI=1/C26H30O9/c1-22(2)14-11-15(27)25(5)13(23(14,3)8-7-16(28)34-22)6-9-24(4)18(12-10-17(29)32-20(12)30)33-21(31)19-26(24,25)35-19/h7-8,10,13-14,17-19,29H,6,9,11H2,1-5H3/t13-,14+,17?,18+,19-,23-,24+,25+,26-/m1/s1
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Found 2 products.
Kihadanin B
CAS:Kihadanin B can repress the adipogenesis by decreasing lipid accumulation through the suppression of the Akt-FOXO1-PPARγ axis in 3T3-L1 adipocytes.Formula:C26H30O9Purity:98%Color and Shape:SolidMolecular weight:486.51Kihadanin B
CAS:<p>Kihadanin B is a bioactive natural product, which is an extract derived from the bark of the Amur cork tree, scientifically known as Phellodendron amurense. This compound exerts its effects primarily as an inhibitor of melanin synthesis. It achieves this through the modulation of the activity of tyrosinase, an enzyme crucial for the production of melanin. By interfering with this pathway, Kihadanin B effectively reduces melanin formation.</p>Formula:C26H30O9Purity:Min. 95%Molecular weight:486.50 g/mol

