Ginsenoside Ra3 13620 InChi: InChI=1S/C13H13NO/c14-10-11-6-8-13(9-7-11)15-12-4-2-1-3-5-12/h1-9H

InChi: InChI=1S/C13H13NO/c14-10-11-6-8-13(9-7-11)15-12-4-2-1-3-5-12/h1-9H

InChiKey: USVPAMXDEQJWJM-UHFFFAOYSA-N

Smiles: CC1(C)C[C@H]2C3=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@@H]([C@@H](O[C@H]7O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]7O)[C@H](O)[C@H]6O[C@@H]6OC(CO)[C@@H](O)[C@H](O)[C@H]6O)C(O)=O)[C@](C)(CO)[C@@H]5CC[C@@]4(C)[C@]3(C)C[C@@H](O)[C@@]2(CO)[C@@H](OC(C)=O)[C@@H]1OC(=O)/C(/C)=C/C

NB598 dose-dependently inhibits insulin secretion under both basal (1 mM glucose) and glucose-stimulated (16

Psora-4 was found to be the most potent small-molecule Kv1

Ginsenoside Ra3 13620 InChi: InChI=1S/C13H13NO/c14-10-11-6-8-13(9-7-11)15-12-4-2-1-3-5-12/h1-9HGinsenoside Ra3, isolated from Panax ginseng, possesses anti cancer activity. Product information CAS Number: 90985 77 6 Molecular Weight: 1241. 41 Formula: C59H100O27 Chemical Name: 2 {[2 (7 {[4,5 dihydroxy 6 (hydroxymethyl) 3 {[3,4,5 trihydroxy 6 (hydroxymethyl)oxan 2 yl]oxy}oxan 2 yl]oxy} 11 hydroxy 3a,3b,6,6,9a pentamethyl hexadecahydro 1H cyclopenta[a]phenanthren 1 yl) 6 methylhept 5 en 2 yl]oxy} 6 ({[3,5 dihydroxy 6 (hydroxymethyl) 4 [(3,4,5