53657-29-7
Chemical Structure
Sitoindoside II
- CAS No.: 53657-29-7
- Formula:C53H92O7
- Molecular Weight:841.29
IUPAC Name: ((2R,3S,4S,5R,6R)-6-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)methyl oleate
InChIKey: MEEONOMPSMYAQO-MBEOCFQISA-N
SMILES: C[C@@]12[C@]3([H])[C@](CC=C1C[C@H](CC2)O[C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)COC(CCCCCCC/C=C\CCCCCCCC)=O)([H])[C@@]5([H])[C@](CC3)([C@@](CC5)([H])[C@H](C)CC[C@@H](CC)C(C)C)C
Biological Activity: Sitoindoside II is a chemopreventive agent that induces HL-60 cell differentiation (ED50: 69 nM). Sitoindoside II can be isolated from the ethanol extract of whole plants of Munronia delavayi[1][2].
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Sitoindoside II | Sitoindoside II is a chemopreventive agent that induces HL-60 cell differentiation (ED50: 69 nM). Sitoindoside II can be isolated from the ethanol extract of whole plants of Munronia delavayi. | |||||||||||||||||||||
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References
- [1]. Rodrigues-Jesus MJ, et al. Nano-multilamellar lipid vesicles (NMVs) enhance protective antibody responses against Shiga toxin (Stx2a) produced by enterohemorrhagic Escherichia coli strains (EHEC). Braz J Microbiol. 2019 Jan;50(1):67-77. [Content Brief]
- [2]. Cai, X.-H.,et al. A New Pregnane from Munronia delavayi Franch (Meliaceae). Journal of Integrative Plant Biology, 2006. 48: 1126-1128.
