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org/wiki/Ledipasvir)
1995 Dec 5
InChi: InChI=1S/C15H16ClN3O3S/c1-19(2)13-7-5-12(6-8-13)17-15(20)18-23(21
interval 30 minutes) (10 mg/kg) in oxo-M-treated rats makes bladder capacity significantly decreased compared with oxo-M-not treated rats (intravesical instillation of vehicle)
32 microM in superoxide anion scavenging)
Pseudoginsenoside Rh2 Size:Contact [email protected] for quotation org/wiki/Ledipasvir)Pseudoginsenoside Rh2, synthesized from Ginsenoside Rh2, possesses anti cancer activitied. Product information CAS Number: 1370264 16 6 Molecular Weight: 622. 87 Formula: C36H62O8 Chemical Name: (2R,3R,4S,5S,6R) 2 {[(1S,3aR,3bR,5aR,7S,9aR,9bR,11R,11aR) 11 hydroxy 1 [(2Z) 6 hydroxy 6 methylhept 2 en 2 yl] 3a,3b,6,6,9a pentamethyl hexadecahydro 1H cyclopenta[a]phenanthren 7 yl]oxy} 6 (hydroxymethyl)oxane 3,4,5 triol Smiles: CC(C)(O)CC C=C(