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Ginsenoside Rh1 potently inhibits the adipogenesis
100 µM) completely blocks the proliferation of dividing NT2 cells (IC50=7 μM) and differentiated postmitotic neurons (hNT
NCC007 is a dual casein kinase Iα (CKIα) and δ (CKIδ) inhibitor with IC50s of 1
m-PEG25-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs
Proliferation of parental Ba/F3 cells was inhibited to a comparable level
Lp-PLA2-IN-1 ovalerylshikonin Ginsenoside Rh1 potently inhibits theLp PLA2 IN 1 is a potent Lipoprotein associated phospholipase A2 (Lp PLA2) inhibitor. Lp PLA2 IN 1 has the potential for atherosclerosis, Alzheimer's disease research. Product information CAS Number: 1420367 28 7 Molecular Weight: 468. 38 Formula: C21H17F5N4O3 Chemical Name: 8 [(3,5 difluoro 4 {[6 (trifluoromethyl)pyridin 3 yl]oxy}phenyl)methoxy] 1 methyl 1H,2H,3H,4H,6H [1,3]diazino[1,6 a]pyrimidin 6 one Smiles:
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