CAS 65247-27-0
:(2S,4R,9beta,16alpha,23E)-2-(beta-D-glucopyranosyloxy)-16,20-dihydroxy-9,10,14-trimethyl-1,11,22-trioxo-4,9-cyclo-9,10-secocholesta-5,23-dien-25-yl acetate
Description:
The chemical substance with the name "(2S,4R,9beta,16alpha,23E)-2-(beta-D-glucopyranosyloxy)-16,20-dihydroxy-9,10,14-trimethyl-1,11,22-trioxo-4,9-cyclo-9,10-secocholesta-5,23-dien-25-yl acetate" and CAS number "65247-27-0" is a complex organic compound characterized by its steroidal structure, which includes multiple hydroxyl groups and a glucopyranosyl moiety. This compound features a unique arrangement of stereocenters, contributing to its specific three-dimensional conformation and biological activity. The presence of the glucopyranosyl group suggests potential solubility in water and may influence its interaction with biological systems. The multiple keto and hydroxyl functional groups indicate that it may participate in various chemical reactions, including hydrogen bonding and redox processes. Additionally, the acetate group may enhance its lipophilicity, affecting its absorption and distribution in biological contexts. Overall, this compound's structural complexity and functional groups suggest potential applications in pharmaceuticals or biochemistry, particularly in areas related to steroid metabolism or glycosylation processes.
Formula:C38H56O13
InChI:InChI=1/C38H56O13/c1-18(40)51-33(2,3)13-12-25(42)38(9,48)30-21(41)15-35(6)24-11-10-19-20(37(24,8)26(43)16-36(30,35)7)14-22(31(47)34(19,4)5)49-32-29(46)28(45)27(44)23(17-39)50-32/h10,12-13,20-24,27-30,32,39,41,44-46,48H,11,14-17H2,1-9H3/b13-12+/t20-,21-,22+,23-,24+,27-,28+,29-,30+,32-,35+,36-,37+,38+/m1/s1
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Found 4 products.
Cucurbitacin B 2-O-β-D-glucoside
CAS:Cucurbitacin B 2-o-α2-D-glucoside has anticancer activity.Formula:C38H56O13Purity:98%Color and Shape:SolidMolecular weight:720.853Cucurbitacin B 2-o-beta-D-glucoside
CAS:<p>Cucurbitacin B 2-o-beta-D-glucoside is a glucoside derivative, which is sourced from plants within the Cucurbitaceae family. It is a secondary metabolite that acts through the inhibition of the JAK/STAT signaling pathway, crucial in cell proliferation and apoptosis. This specific mode of action gives it significant potential as a cytotoxic and anti-inflammatory agent.</p>Formula:C38H56O13Purity:Min. 95%Molecular weight:720.80 g/mol




