Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
52588 | LDN-212854 | 1432597-26-6 | 98% | |
LDN-212854 is a potent and selectiveBMP receptorinhibitor with IC50 of 1.3 nM for ALK | ||||
52511 | LB-100 | 1026680-07-8 | 98% | |
LB-100 is a small-molecular protein phosphatase 2A(PP2A)inhibitor with IC50 of 0.85 M | ||||
52509 | LY-364947 | 396129-53-6 | 98% | |
LY364947 is a potent ATP-competitive inhibitor of TGFR-I with IC50 of 59 nM, exhibits | ||||
51504 | LH846 | 639052-78-1 | 98% | |
LH846 is a selective inhibitor of CK1 (IC50 values are 290 nM, 1.3 uM and 2.5 uM for | ||||
52309 | LY294002 | 154447-36-6 | 98% | |
LY294002 is the first synthetic molecule known to inhibitPI3K//withIC50of 0.5 M/0.57 | ||||
52206 | LFM-A13 | 244240-24-2 | 98% | |
Selective Bruton's tyrosine kinase (BTK) inhibitor (IC50 = 2.5 M). Also inhibits poli | ||||
51605 | LY2835219(Abemaciclib) | 1231930-82-7 | 98% | |
LY2835219 is a potent and selective inhibitor ofCDK4andCDK6withIC50of 2 nM and 10 nM, | ||||
51703 | Luminespib ( NVP-AUY922 ; VER-52296 ) | 747412-49-3 | 98% | |
NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc |
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