CAS 74411-65-7

O-6-Desoxy-α-L-mannopyranosyl-(1→3)-O-β-D-xylopyranosyl-(1→4)-O-6-desoxy-α-L-mannopyranosyl-(1→2)-β-D-xylopyranosyl (3β,4α,16α)-3-(β-D-glucopyranosyloxy)-16,23-dihydroxyolean-12-en-28-oat

Beschreibung:

O-6-Desoxy-α-L-mannopyranosyl-(1→3)-O-β-D-xylopyranosyl-(1→4)-O-6-desoxy-α-L-mannopyranosyl-(1→2)-β-D-xylopyranosyl (3β,4α,16α)-3-(β-D-glucopyranosyloxy)-16,23-dihydroxyolean-12-en-28-oat, mit der CAS-Nummer 74411-65-7, ist eine komplexe glykosylierte Triterpenverbindung. Diese Substanz weist mehrere Zuckeranteile auf, darunter α-L-Mannopyranosyl- und β-D-Xylopyranosyl-Einheiten, die zu ihrer strukturellen Komplexität und potenziellen biologischen Aktivität beitragen. Das Vorhandensein von Derivaten der oleanolsäure deutet darauf hin, dass sie verschiedene pharmakologische Eigenschaften aufweisen könnte, einschließlich entzündungshemmender und antioxidativer Wirkungen. Ihre komplexen glykosidischen Bindungen können ihre Löslichkeit, Stabilität und Wechselwirkungen mit biologischen Systemen beeinflussen. Die Stereochemie der Verbindung, die durch die spezifischen Konfigurationen an verschiedenen Kohlenstoffzentren angezeigt wird, ist entscheidend für ihre biologische Funktion und Aktivität. Insgesamt stellt diese Substanz eine einzigartige Klasse von Naturprodukten dar, die Anwendungen in der medizinischen Chemie und Pharmakologie haben könnte, was eine weitere Untersuchung ihrer Eigenschaften und potenziellen therapeutischen Anwendungen rechtfertigt.

Formel: C₅₈H₉₄O₂₆

InChl: InChI=1S/C58H94O26/c1-23-34(64)37(67)40(70)48(77-23)82-45-28(62)21-75-47(43(45)73)81-44-24(2)78-49(42(72)39(44)69)83-46-35(65)27(61)20-76-51(46)84-52(74)58-16-15-53(3,4)17-26(58)25-9-10-31-54(5)13-12-33(80-50-41(71)38(68)36(66)29(19-59)79-50)55(6,22-60)30(54)11-14-56(31,7)57(25,8)18-32(58)63/h9,23-24,26-51,59-73H,10-22H2,1-8H3/t23-,24-,26-,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-,54-,55-,56+,57+,58+/m0/s1

InChI Key: InChIKey=WNGIVKPPGCCJNP-XSFLSGEHSA-N

SMILES: C(O[C@H]1[C@H](O[C@H]2[C@H](O)[C@H](O)[C@@H](O[C@H]3[C@H](O)[C@@H](O[C@H]4[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O4)[C@H](O)CO3)[C@H](C)O2)[C@@H](O)[C@H](O)CO1)(=O)[C@]56[C@](C=7[C@@](C)(C[C@H]5O)[C@@]8(C)[C@](CC7)([C@]9(C)[C@@](CC8)([C@@](CO)(C)[C@@H](O[C@@H]%10O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%10O)CC9)[H])[H])(CC(C)(C)CC6)[H]

Synonyme:

• Chrysantellin B
• O-6-Deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→3)-O-β-<smallcap>D</smallcap>-xylopyranosyl-(1→4)-O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→2)-β-<smallcap>D</smallcap>-xylopyranosyl (3β,4α,16α)-3-(β-<smallcap>D</span>-glucopyranosyloxy)-16,23-dihydroxyolean-12-en-28-oate
• Olean-12-en-28-oic acid, 3-(beta-D-glucopyranosyloxy)-16,23-dihydroxy-, O-6-deoxy-alpha-l-mannopyranosyl-(1.3)-O-beta-D-xylopyranosyl-(1.4)-O-6-deoxy-alpha-l-mannopyranosyl-(1.2)-beta-D-xylopyranosyl ester, (3beta,4alpha,16alpha)-
• Olean-12-en-28-oic acid, 3-(β-<span class="text-smallcaps">D</smallcap>-glucopyranosyloxy)-16,23-dihydroxy-, O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→3)-O-β-<smallcap>D</smallcap>-xylopyranosyl-(1→4)-O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→2)-β-<smallcap>D</span>-xylopyranosyl ester, (3β,4α,16α)-
• [(2S,3R,4S,5R)-3-[(2R,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-3,4-dihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-4,5-dihydroxy-tetrahydropyran-2-yl] (4aR,5R,6aS,6aR,6bR,8aR,9R,10S,12aR,14bR)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
• O-6-Deoxy-α-L-mannopyranosyl-(1→3)-O-β-D-xylopyranosyl-(1→4)-O-6-deoxy-α-L-mannopyranosyl-(1→2)-β-D-xylopyranosyl (3β,4α,16α)-3-(β-D-glucopyranosyloxy)-16,23-dihydroxyolean-12-en-28-oate
• Olean-12-en-28-oic acid, 3-(β-D-glucopyranosyloxy)-16,23-dihydroxy-, O-6-deoxy-α-L-mannopyranosyl-(1→3)-O-β-D-xylopyranosyl-(1→4)-O-6-deoxy-α-L-mannopyranosyl-(1→2)-β-D-xylopyranosyl ester, (3β,4α,16α)-

Chrysanthellin B

CAS: 74411-65-7

Chrysanthellin B analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Formel: C₅₈H₉₄O₂₆

Reinheit: (HPLC) ≥97%

Farbe und Form: Powder

Molekulargewicht: 1207.37

Ref: 11-0112S

Chrysanthellin B

CAS: 74411-65-7

Chrysanthellin B is a bioactive compound, which is a secondary metabolite isolated from the plant Chrysanthemum indicum, known for its potential therapeutic properties. This product originates from the Asteraceae family, which is a rich source of pharmacologically active substances. The mode of action of Chrysanthellin B involves modulation of lipid metabolism and antioxidant activity, which can contribute to hepatoprotective effects. Specifically, it interacts with biochemical pathways to inhibit lipid peroxidation and promote hepatic health. Chrysanthellin B is primarily studied for its use in reducing lipid levels and protecting liver function. It has shown promise in the context of experimental models of hyperlipidemia and hepatic disorders, providing insights into potential applications in treating metabolic syndrome and related conditions. Further research is ongoing to elucidate its mechanisms and efficacy in clinical contexts.

Formel: C₅₈H₉₄O₂₆

Reinheit: Min. 95%

Molekulargewicht: 1,207.35 g/mol

Ref: 3D-FC65350