Pseudoginsenoside RT1 ymandelic Acid Deferitrin has the potential for

Deferitrin has the potential for beta-thalassemia major

RP 70676 is a potent inhibitor of ACAT

17-9-2-6-15-8-10-17)14-4-1-3-12-11-16-7-5-13(12)14/h1

) treatment before irradiation dramaticly increases the sensitivity to radiation therapy of mice bearing LoVo xenografts[1]

is the potent and selective small molecular inhibitor of KRAS-PDEδ interaction

Pseudoginsenoside RT1 ymandelic Acid Deferitrin has the potential forPseudoginsenoside RT1, isolated from the fruit of Randia siamensis, exhibits acute ichthyotoxic activity. Product information CAS Number: 98474 74 9 Molecular Weight: 927. 08 Formula: C47H74O18 Chemical Name: (2S,3S,4S,5R,6R) 6 {[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR) 4,4,6a,6b,11,11,14b heptamethyl 8a ({[(2S,3R,4S,5S,6R) 3,4,5 trihydroxy 6 (hydroxymethyl)oxan 2 yl]oxy}carbonyl) 1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b icosahydropicen 3