
CAS 151870-74-5: Kinsenoside
Formula:C10H16O8
InChI:InChI=1S/C10H16O8/c11-2-5-7(13)8(14)9(15)10(18-5)17-4-1-6(12)16-3-4/h4-5,7-11,13-15H,1-3H2/t4-,5-,7-,8+,9-,10-/m1/s1
InChI key:InChIKey=MQEPWBMWFIVRPS-ZGSHZZHUSA-N
SMILES:O([C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@@H]2CC(=O)OC2
Synonyms:- (+)-Kinsenoside
- (4R)-4-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)dihydro-2(3H)-furanone
- 2(3H)-Furanone, 4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)dihydro-, (4R)-
- 2(3H)-Furanone, 4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)dihydro-, (R)-
- 2(3H)-Furanone,4-(b-D-glucopyranosyloxy)dihydro-,(R)-
- 2(3H)-Furanone, 4-(β-D-glucopyranosyloxy)dihydro-, (4R)-
- (4R)-4-(β-D-Glucopyranosyloxy)dihydro-2(3H)-furanone
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Found 7 products.
Kinsenoside
CAS:Kinsenoside is a hepatoprotective agent that has been shown to have significant cytotoxicity against human cancer cells, and to inhibit the production of chemoattractant protein. Kinsenoside also has an anti-inflammatory effect, which is due to its ability to stimulate the production of IL-10, a cytokine that inhibits inflammation. Kinsenoside has been shown to have drug interactions with other drugs such as diclofenac and warfarin. This compound also interacts with Toll-like receptor 4 (TLR4), which is involved in inflammatory responses. The activity of this drug can be determined using a surface methodology on human erythrocytes.Formula:C10H16O8Purity:Min. 95%Color and Shape:SolidMolecular weight:264.23 g/molKinsenoside
CAS:Kinsenoside ((+)-Kinsenoside) shows significant antihepatotoxic, and anti-inflammatory activities.Formula:C10H16O8Purity:100% - 99.92%Color and Shape:SolidMolecular weight:264.23Kinsenoside
CAS:Kinsenoside shows significant antihepatotoxic, and anti-inflammatory activities. Kinsenoside could be useful for repairing beta cells in pancreatic islet injury as well as improving its function, it could promote the glucose tolerance of acute glucose increase in both diabetic and normal healthy rats. Kinsenoside inhibits osteoclastogenesis from macrophages by attenuating RANKL-induced NF-κB and NFATc1 activities, which in turn, prevents bone loss from OVX mice.Formula:C10H16O8Purity:95%~99%Molecular weight:264.23