CAS 158511-59-2: Eclalbasaponin I
Formula:C42H68O14
InChI:InChI=1S/C42H68O14/c1-37(2)14-15-42(36(52)56-35-33(51)31(49)29(47)23(19-44)54-35)21(16-37)20-8-9-25-39(5)12-11-27(55-34-32(50)30(48)28(46)22(18-43)53-34)38(3,4)24(39)10-13-40(25,6)41(20,7)17-26(42)45/h8,21-35,43-51H,9-19H2,1-7H3/t21-,22+,23+,24-,25+,26+,27-,28+,29+,30-,31-,32+,33+,34-,35-,39-,40+,41+,42+/m0/s1
InChI key:InChIKey=ZKMRZIYTCZLEAV-VVJIWJAZSA-N
SMILES:C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)(=O)[C@]23[C@](C=4[C@@](C)(C[C@H]2O)[C@@]5(C)[C@](CC4)([C@]6(C)[C@@](CC5)(C(C)(C)[C@@H](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)CC6)[H])[H])(CC(C)(C)CC3)[H]
Synonyms:- (+)-EclalbasaponinI
- Eclalbasaponin I
- Olean-12-en-28-oic acid, 3-(β-<span class="text-smallcaps">D</smallcap>-glucopyranosyloxy)-16-hydroxy-, β-<smallcap>D</span>-glucopyranosyl ester, (3β,16α)-
- Olean-12-en-28-oic acid, 3-(β-D-glucopyranosyloxy)-16-hydroxy-, β-D-glucopyranosyl ester, (3β,16α)-
- Eclalbasaponin C
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Found 6 products.
Eclalbasaponin I
CAS:Eclalbasaponin I: antioxidant, antitumor, protects neural cells via autophagy, inhibits hepatoma SMMC-7721 (IC50=111.1703 ug/ml).Formula:C42H68O14Purity:98.75%Color and Shape:SolidMolecular weight:796.98Eclalbasaponin i
CAS:Natural glycosideFormula:C42H68O14Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:797Eclalbasaponin I
CAS:Eclalbasaponin I is a triterpenoid saponin, which is a type of natural glycoside compound. It is derived from plants of the Euphorbia genus, known for their rich content of bioactive phytochemicals. The mode of action of Eclalbasaponin I involves modulating cellular pathways through its interactions with membrane proteins and lipid structures, influencing cellular functions and eliciting various biological activities. Research into Eclalbasaponin I has highlighted its potential therapeutic benefits, including anti-inflammatory, anti-tumor, and immunomodulatory effects. These properties make it a subject of interest in pharmacological studies focused on developing treatments for diseases characterized by inflammation and uncontrolled cell proliferation. The compound's efficacy in inhibiting specific cellular pathways offers insights into novel mechanisms of action that could be leveraged for drug development. Scientists are particularly interested in its application in cancer research and auto-immune disorders, exploring its capability to modify disease progression through biological activity modulation.Formula:C42H68O14Purity:Min. 95%Molecular weight:796.98 g/mol
