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| Cat.No. | Product name | Product Description |
| R2032748 | MK-2461 | MK-2461 is a novel ATP-competitive multitargeted inhibitor of activated c-Met wi |
| R2032749 | PF8380 | PF-8380 is a potent autotaxin inhibitor with an IC50 of 2.8 nM in isolated enzym |
| R2032750 | PRX08066 | PRX-08066 Maleic acid is a selective 5-HT2B receptor antagonist with IC50 of 3.4 |
| R2032751 | RO41-1049 HCL | Ro 41-1049 hydrochloride is a reversible and selective inhibitor of monoamine ox |
| R2032752 | Ro41-1049 hydrochloride | Ro 41-1049 hydrochloride is a reversible and selective inhibitor of monoamine ox |
| R2032753 | Tetrabenazine | Tetrabenazine (Racemate) is a selective and reversible inhibitor of vesicular mo |
| R2032754 | Vadimezan(DMXAA;ASA-404) | Vadimezan (DMXAA; ASA-404), the tumor vascular disrupting agent (tumor-VDA), is |
| R2032755 | ms023 | MS023 is a potent, selective, and cell-active inhibitor of human type I protein |
| R2032756 | Brincidofovir(CMX001) | Brincidofovir (CMX001; HDP-CDV) is an orally active, lipophilic form of cidofovi |
| R2032757 | FRAX1036 | FRAX1036 is a PAK inhibitor with Kis of 23.3 nM, 72.4 nM, and 2.4 μM for PAK1, P |
| R2032758 | Itacitinib | Itacitinib is an orally bioavailable and selective inhibitor of JAK1, with >2 |
| R2032759 | JI-101 | JI-101 is an orally available multi-kinase inhibitor of VEGFR2，PDGFRβ and EphB4 |
| R2032760 | PF2545920;Mardepodect(PF-2545920) | Mardepodect (PF-2545920) is a potent, orally active and selective PDE10A inhibit |
| R2032761 | RPI-1 | RPI-1 is a competitive, potent ATP-dependent Ret kinase inhibitor. |
| R2032762 | SNX-2112(PF-04928473) | SNX-2112 (PF 04928473) is an orally active Hsp90 inhibitor, with a Kd of 16 nM f |
| R2032763 | AG14361 | AG14361 is a potent PARP-1 inhibitor, with a Ki of < 5 nM, and in permeabiliz |
| R2032764 | AGK2 | AGK2 is a selective SIRT2 inhibitor with IC50 of 3.5 μM.AGK2 can also inhibit SI |
| R2032765 | AM2394 | AM-2394 is a structurally distinct glucokinase activator (GKA).AM-2394 activates |
| R2032766 | Bevirimat | Bevirimat (PA-457; MPC-4326; YK FH312) is an anti-HIV drug derived from a betuli |
| R2032767 | BMS707035 | BMS-707035 is an HIV-1 integrase (IN) inhibitor with an IC50 value of 15 nM.IC50 |
| R2032768 | CDKI-73 | CDKI-73 is a potent CDK9 inhibitor with Ki of 4 nM; shows selective toxicity to |
| R2032769 | cpi-637 | CPI-637 is a selective and potent CBP/EP300 bromodomain inhibitor with IC50 valu |
| R2032770 | EHT1864 | EHT 1864 is an inhibitor of Rac family small GTPases.EHT 1864 directly binds and |
| R2032771 | EPZ020411 | EPZ020411 is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has ＞ |
| R2032772 | Fenebrutinib(GDC-0853) | Fenebrutinib (GDC-0853) is a potent, selective, and noncovalent bruton's tyrosin |
