CAS 97240-03-4

O-6-Deoxy-α-L-mannopyranosyl-(1→4)-O-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl (3β,4α)-3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxyolean-12-en-28-oate

Description:

O-6-Deoxy-α-L-mannopyranosyl-(1→4)-O-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl (3β,4α)-3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxyolean-12-en-28-oate, identified by CAS number 97240-03-4, is a complex glycosylated compound characterized by its intricate structure comprising multiple sugar moieties and a triterpenoid backbone. This substance features a unique arrangement of α and β glycosidic linkages, which contribute to its solubility and biological activity. The presence of acetyl groups and hydroxyl functionalities enhances its reactivity and potential interactions with biological systems. Such compounds are often studied for their pharmacological properties, including anti-inflammatory and antimicrobial activities. The specific stereochemistry of the sugar units and the oleanolic acid derivative suggest potential applications in drug development and natural product chemistry. Overall, this compound exemplifies the complexity and diversity of glycosylated natural products, which play significant roles in various biological processes.

Formula: C₆₁H₉₈O₂₇

InChI: InChI=1S/C61H98O27/c1-25-36(65)40(69)44(73)51(81-25)86-48-32(23-78-27(3)63)84-50(47(76)43(48)72)80-22-31-39(68)42(71)46(75)53(83-31)88-55(77)61-18-16-56(4,5)20-29(61)28-10-11-34-57(6)14-13-35(58(7,24-62)33(57)12-15-60(34,9)59(28,8)17-19-61)85-54-49(38(67)30(64)21-79-54)87-52-45(74)41(70)37(66)26(2)82-52/h10,25-26,29-54,62,64-76H,11-24H2,1-9H3/t25-,26-,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-,57-,58-,59+,60+,61-/m0/s1

InChI key: InChIKey=YYMHTAGTVKFQOP-KZYQMVRLSA-N

SMILES: C(O[C@@H]1O[C@H](CO[C@@H]2O[C@H](COC(C)=O)[C@@H](O[C@H]3[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O3)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O)(=O)[C@]45[C@](C=6[C@@](C)(CC4)[C@@]7(C)[C@](CC6)([C@]8(C)[C@@](CC7)([C@@](CO)(C)[C@@H](O[C@H]9[C@H](O[C@H]%10[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O%10)[C@@H](O)[C@@H](O)CO9)CC8)[H])[H])(CC(C)(C)CC5)[H]

Synonyms:

• Olean-12-en-28-oic acid, 3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxy-, O-6-deoxy-α-L-mannopyranosyl-(1→4)-O-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, (3β,4α)-
• O-6-Deoxy-α-L-mannopyranosyl-(1→4)-O-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl (3β,4α)-3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxyolean-12-en-28-oate
• Kizuta saponin K11

Kizuta saponin K11

CAS: 97240-03-4

Kizuta saponin K11 is a saponin derived from Kalopanax pictum var. maximowiczii leaves, which is a widely used Korean medicinal plant.

Formula: C₆₁H₉₈O₂₇

Color and Shape: Solid

Molecular weight: 1263.428

Ref: TM-T41124

Kizuta saponin K11

CAS: 97240-03-4

Formula: C₆₁H₉₈O₂₇

Purity: 95%~99%

Molecular weight: 1263.43

Ref: BP-BP4878

Kizuta saponin K11

CAS: 97240-03-4

Kizuta saponin K11 is a saponin compound, which is derived from the leaves of the Hedera helix plant, commonly known as English ivy. These saponins are glycoside compounds known for their surface-active properties, due to their amphiphilic structure, which consists of a hydrophobic aglycone linked to hydrophilic sugar moieties. This unique structure allows Kizuta saponin K11 to disrupt cellular membranes, leading to its antifungal and antibacterial activities. By integrating into lipid bilayers, it increases membrane permeability, which can result in cell lysis for certain microorganisms.

Formula: C₆₁H₉₈O₂₇

Purity: Min. 95%

Molecular weight: 1,263.40 g/mol

Ref: 3D-XDA24003