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| Cat.No. | Product name | Product Description |
| R2032281 | TAK-285 | TAK-285 is a potent, selective, ATP-competitive and orally active HER2 and EGFR( |
| R2032282 | SC1(Pluripotin) | Pluripotin is a dual inhibitor of ERK1 and RasGAP with KDs of 98 nM and 212 nM, |
| R2032283 | AZD8186 | AZD8186 is a PI3K inhibitor, which potently inhibits PI3Kβ (IC50=4 nM) and PI3Kδ |
| R2032284 | SRT3109 | SRT3109 is an antagonist of CXCR2, with a pIC50 of 8.2, and used in the research |
| R2032285 | TG101209 | TG101209 is a selective JAK2 inhibitor with IC50 of 6 nM, less potent to Flt3 an |
| R2032286 | CC-223 | CC-223 is a potent, selective, and orally bioavailable inhibitor of mTOR kinase, |
| R2032287 | Bexagliflozin;EGT1442;EGT0001442;THR-1442 | Bexagliflozin is a potent and selective SGLT2 inhibitor with IC50 value of 5.6 μ |
| R2032288 | MK-886 (L 663536) | MK-886 (L 663536) is a potent, cell-permeable and orally active FLAP (IC50 of 30 |
| R2032289 | ABT639;ABT-639 | ABT-639 is a novel, peripherally acting, selective T-type Ca2+ channel blocker. |
| R2032290 | CHIR-090;CHIR090 | CHIR-090 is a potent, slow, tight-binding inhibitor of the LpxC deacetylase.It b |
| R2032291 | FLT3-IN-2 | FLT3-IN-2 is a FLT3 inhibitor with IC50 of ＜ 1 μM, detailed information refer to |
| R2032292 | GDC0084 | GDC-0084 is a brain penetrant inhibitor of PI3K and mTOR, with Kis of 2 nM, 46 n |
| R2032293 | AC710 | AC710 is a potent PDGFR inhibitor with Kds of 0.6, 1.57, 1, 1.3, 1.0 nM for FLT3 |
| R2032294 | P7C3-A20 | P7C3-A20 is a derivative of P7C3 with potent neuroprotective activity. |
| R2032295 | NSC23766;NSC-23766 | NSC 23766 is a specific inhibitor of the binding and activation of Rac GTPase, u |
| R2032296 | GSK484 hydrochloride(GTPL8577) | GSK484 hydrochloride (GTPL8577) is a selective and reversible peptidylarginine d |
| R2032297 | GDC-0810;Lifirafenib(BGB-283) | Lifirafenib (BGB-283) is a novel and potent Raf Kinase and EGFR inhibitor with I |
| R2032298 | A 769662 | A-769662 is a potent, reversible AMPK activator with EC50 of 0.8 μM. |
| R2032299 | MT-1303;Amiselimod | Amiselimod is a novel sphingosine 1-phosphate receptor-1 (S1P1) modulator, desig |
| R2032301 | SB415286 | SB 415286 is a potent and selective cell permeable inhibitor of GSK-3α, with an |
| R2032302 | Tomivosertib(eFT508) | Tomivosertib (eFT508) is a potent, highly selective, and orally bioavailable MNK |
| R2032303 | AG-1478;Tyrphostin AG-1478;NSC 693255 | AG-1478 is a selective EGFR tyrosine kinase inhibitor with IC50 of 3 nM. |
| R2032304 | KPT9274 | KPT-9274 is an orally bioavailable, dual PAK4/Nicotinamide phosphoribosyltransfe |
| R2032305 | Lanabecestat;AZD3293;LY3314814 | Lanabecestat (AZD3293) is a potent, highly permeable, orally active and blood-br |
| R2032306 | RX-518 | EGFR-IN-3 is an epidermal growth factor receptor (EGFR) inhibitor. |
