CAS 218934-74-8

Spirostan-2-one, 3-[(O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl)oxy]-6-hydroxy-, (3β,5α,6β,25R)-

Description:

Spirostan-2-one, 3-[(O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl)oxy]-6-hydroxy-, (3β,5α,6β,25R)- is a complex glycosylated steroid compound characterized by its spirostan structure, which features a steroid backbone with a unique arrangement of sugar moieties. This compound contains multiple glycosidic linkages, indicating its potential role in biological systems, particularly in interactions with cell membranes or as a precursor in biosynthetic pathways. The presence of hydroxyl groups contributes to its solubility and reactivity, while the specific stereochemistry (3β,5α,6β,25R) suggests particular spatial arrangements that may influence its biological activity. Such compounds are often studied for their pharmacological properties, including potential anti-inflammatory or anticancer effects, and may serve as leads for drug development. The intricate structure also highlights the importance of carbohydrate moieties in modulating the properties and functions of steroidal compounds.

Formula: C₅₆H₉₀O₂₉

InChI: InChI=1S/C56H90O29/c1-19-5-8-56(75-17-19)20(2)34-29(85-56)10-23-21-9-25(61)24-11-28(26(62)12-55(24,4)22(21)6-7-54(23,34)3)76-50-43(72)40(69)45(33(16-60)80-50)81-53-48(47(38(67)32(15-59)79-53)83-49-41(70)35(64)27(63)18-74-49)84-52-44(73)46(37(66)31(14-58)78-52)82-51-42(71)39(68)36(65)30(13-57)77-51/h19-25,27-53,57-61,63-73H,5-18H2,1-4H3/t19-,20+,21-,22+,23+,24-,25-,27-,28-,29+,30-,31-,32-,33-,34+,35+,36-,37-,38-,39+,40-,41-,42-,43-,44-,45+,46+,47+,48-,49+,50-,51+,52+,53+,54+,55-,56-/m1/s1

InChI key: InChIKey=JPQIKXKRKWQQOU-YNXBLNQZSA-N

SMILES: C[C@@]12[C@]([C@]3([C@](CC1)([C@]4(C)[C@@]([C@H](O)C3)(C[C@@H](O[C@@H]5O[C@H](CO)[C@H](O[C@H]6[C@H](O[C@H]7[C@H](O)[C@@H](O[C@@H]8O[C@H](CO)[C@@H](O)[C@H](O)[C@H]8O)[C@H](O)[C@@H](CO)O7)[C@@H](O[C@H]9[C@H](O)[C@@H](O)[C@H](O)CO9)[C@H](O)[C@@H](CO)O6)[C@H](O)[C@H]5O)C(=O)C4)[H])[H])[H])(C[C@]%10([C@@]2([C@H](C)[C@]%11(O%10)CC[C@@H](C)CO%11)[H])[H])[H]

Synonyms:

• Spirostan-2-one, 3-[(O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl)oxy]-6-hydroxy-, (3β,5α,6β,25R)-

Yayoisaponin B

CAS: 218934-74-8

Yayoisaponin B is a useful organic compound for research related to life sciences. The catalog number is T125328 and the CAS number is 218934-74-8.

Formula: C₅₀H₈₀O₂₄

Color and Shape: Solid

Molecular weight: 1065.17

Ref: TM-T125328