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Home > Products
| Cat.No. | Product name | Product Description |
| R10210 | BYL719 | Alpelisib (BYL719) is a potent and selective PI3Kα inhibitor with IC50 of 5 nM i |
| R10211 | LY2886721 | LY2886721 is a BACE inhibitor used for the treatment of Alzheimer's Disease. Pha |
| R10213 | SGI1776 | SGI-1776 free base is a novel ATP competitive inhibitor of Pim1 with IC50 of 7 n |
| R10214 | LY411575; YO01027 | YO-01027 (Dibenzazepine) is a dipeptidic γ-secretase inhibitor with IC50 of 2.6 |
| R10216 | PLX4032 | Vemurafenib (PLX4032, RG7204) is a novel and potent inhibitor of B-RafV600E with |
| R10219 | AZD7762;AZD-7762 | AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell- |
| R10224 | Sirtinol | Sirtinol is a specific SIRT1 and SIRT2 inhibitor with IC50 of 131 μM and 38 μM i |
| R10225 | LY364947 | LY-364947 is a potent ATP-competitive inhibitor of TGFβR-I with IC50 of 59 nM, a |
| R10227 | TAK438; Vonoprazan Fumarate | Vonoprazan Fumarate (TAK-438) is a novel P-CAB (potassium-competitive acid block |
| R10233 | Tyrphostin A9;Tyrphostin 9; Malonoben | Tyrphostin 9 is firstly designed as an EGFR inhibitor with IC50 of 460 μM, but i |
| R10235 | GSK1838705A | GSK1838705A is a potent and reversible IGF-IR and the insulin rec |
| R10236 | Talazoparib (BMN 673) | Talazoparib (BMN 673) is a novel PARP inhibitor with IC50 of 0.58 nM in a cell-f |
| R10239 | Tubastain A | Tubastatin A is a potent and selective HDAC6 inhibitor with IC50 of 15 nM in a c |
| R10242 | AMG073 | Cinacalcet HCl represents a new class of compounds for the treatment of hyperpar |
| R10243 | Pictilisib(GDC-0941) dimethanesulfonate | Pictilisib dimethanesulfonate (GDC-0941 dimethanesulfonate) is a potent inhibito |
| R10244 | Fasiglifam (TAK-875) | TAK-875 is a selective GPR40 agonist with EC50 of 14 nM in human GPR40 expressin |
| R10245 | Ostarine; MK2866 | Andarine is a selective non-steroidal androgen receptor (AR) agonist with Ki of |
| R10246 | Semagacestat (LY450139) | Semagacestat (LY450139) is a γ-secretase blocker for Aβ42, Aβ40 and Aβ38 with IC |
| R10247 | Veliparib dihydrochloride; ABT-888 dihydrochloride | Veliparib (ABT-888) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM a |
| R10248 | NSC713200 | Bardoxolone Methyl is an IKK inhibitor, showing potent proapoptotic and anti-inf |
| R10250 | TAK632 | TAK-632 is a potent pan-Raf inhibitor with IC50 of 8.3 nM and 1.4 nM for B-Raf(w |
| R10251 | BMS232632; CGP73547; HSDB7339; | Atazanavir Sulfate is a HIV protease inhibitor with Ki of 2.66 nM in a cell-free |
| R10252 | MK1775 | MK-1775 is a potent and selective Wee1 inhibitor with IC50 of 5.2 nM in a cell-f |
| R10253 | Dacomitinib，PF299804 | Dacomitinib (PF299804, PF299) is a potent, irreversible pan-ErbB inhibitor, most |
| R10254 | AZD9291 Mesylate | AZD-9291 is a potent and selective mutated forms EGFR inhibitor(Exon 19 deletion |
