94492-22-5
Chemical Structure
Cistanoside C
- CAS No.: 94492-22-5
- Formula:C30H38O15
- Molecular Weight:638.61
InChIKey: SUNMCVVGOLDIKD-CPPDSBOHSA-N
SMILES: OC(C=C1/C=C/C(O[C@H]([C@H](O[C@H]([C@@H]2O)OCCC3=CC(OC)=C(C=C3)O)CO)[C@@H]2O[C@H]4[C@@H]([C@@H]([C@H]([C@@H](O4)C)O)O)O)=O)=C(C=C1)O
Biological Activity: Cistanoside C is a phenylpropanoid glycoside with free radical scavenging, DNA repair and DNA minor groove binding activities. Cistanoside C scavenges hydrated electrons and hydroxyl radicals. Cistanoside C inhibits the proliferation of cancer cells. Cistanoside C can be used in research related to leukemia, liver cancer, lung adenocarcinoma and gastric adenocarcinoma[1][2][3].
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Cistanoside C | Cistanoside C is a phenylpropanoid glycoside with free radical scavenging, DNA repair and DNA minor groove binding activities. Cistanoside C scavenges hydrated electrons and hydroxyl radicals. Cistanoside C inhibits the proliferation of cancer cells. Cistanoside C can be used in research related to leukemia, liver cancer, lung adenocarcinoma and gastric adenocarcinoma. | |||||||||||||||||||||
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References
- [1]. Delalande O, et al. Docking study of cistanoside C to telomeric DNA fragment. SAR QSAR Environ Res. 2002 Dec;13(7-8):675-88. [Content Brief]
- [2]. Shi Y, et al. Dietary phytophenols act as scavengers of reducing radicals. Food chemistry. 2011 Feb 15;124(4):1322-7.
- [3]. Sperandio O, et al. Theoretical study of fast repair of DNA damage by cistanoside C and analogs: mechanism and docking. SAR QSAR Environ Res. 2002 Mar;13(2):243-60. [Content Brief]
