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CAS 74411-65-7

:

O-6-Deossi-α-L-mannopiranosil-(1→3)-O-β-D-xilopiranosil-(1→4)-O-6-deossi-α-L-mannopiranosil-(1→2)-β-D-xilopiranosil (3β,4α,16α)-3-(β-D-glucopiranosilossi)-16,23-diidrossiolean-12-en-28-oato

Descrizione:
O-6-Deossi-α-L-mannopiranosil-(1→3)-O-β-D-xilopiranosil-(1→4)-O-6-deossi-α-L-mannopiranosil-(1→2)-β-D-xilopiranosil (3β,4α,16α)-3-(β-D-glucopiranosilossi)-16,23-diidrossiolean-12-en-28-oato, con numero CAS 74411-65-7, è un composto triterpenoide glicosilato complesso. Questa sostanza presenta più unità di zucchero, tra cui α-L-mannopiranosil e β-D-xilopiranosil, che contribuiscono alla sua complessità strutturale e potenziale attività biologica. La presenza di derivati dell'acido oleanolico suggerisce che possa mostrare varie proprietà farmacologiche, inclusi effetti anti-infiammatori e antiossidanti. I suoi intricati legami glicosidici possono influenzare la sua solubilità, stabilità e interazione con i sistemi biologici. La stereochimica del composto, indicata dalle configurazioni specifiche in vari centri di carbonio, è cruciale per la sua funzione biologica e attività. In generale, questa sostanza rappresenta una classe unica di prodotti naturali che potrebbe avere applicazioni in chimica medicinale e farmacologia, giustificando ulteriori indagini sulle sue proprietà e potenziali usi terapeutici.
Formula:C58H94O26
InChI: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]
Sinonimi:
  • 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)-
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
2 prodotti.
  • Chrysanthellin B
    Extrasynthese
    + Info

    Chrysanthellin B

    CAS:
    Chrysanthellin B analytical standard provided with w/w absolute assay, to be used for quantitative titration.
    Formula:C58H94O26
    Purezza:(HPLC) ≥97%
    Colore e forma:Powder
    Peso molecolare:1207.37

    Ref: 11-0112S

    5mg
    214,00€
  • Chrysanthellin B
    Biosynth
    + Info

    Chrysanthellin B

    CAS:
    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.
    Formula:C58H94O26
    Purezza:Min. 95%
    Peso molecolare:1,207.35 g/mol

    Ref: 3D-FC65350

    1mg
    182,00€