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Home > Products
| Cat.No. | Product name | Product Description |
| R2032733 | UNC1079 | UNC1079 is the piperidine analog of UNC1021, as a structurally similar but signi |
| R2032734 | Uprosertib;GSK2141795 | Uprosertib (GSK2141795) is a potent and selective pan-Akt inhibitor with IC50 va |
| R2032735 | vacquinol-1 | Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma c |
| R2032736 | 10058-F4 | 10058-F4 is a c-Myc inhibitor that prevents c-Myc-Max dimerization and transacti |
| R2032737 | AAL-993 | AAL-993 is a highly potent inhibitor of VEGFR-1 (IC50 =130nM), VEGFR-2 (IC50=23n |
| R2032738 | AV412 | AV-412 free base (MP-412 free base) is an EGFR inhibitor with IC50s of 0.75, 0.5 |
| R2032739 | AZD8330 | AZD8330 (ARRY-424704) is a potent, uncompetitive MEK1/MEK2 inhibitor, with an IC |
| R2032740 | BAY80-6946(Copanlisib) | Copanlisib (BAY 80-6946) is a potent, selective and ATP-competitive pan-class I |
| R2032741 | ClozapineN-Oxide | Clozapine (N-oxide) is a pharmacologically inert metabolite of Clozapine, an ant |
| R2032742 | CP21R7 | CP21R7 is potent GSK-3β inhibitor, with an IC50 of 1.8 nM; CP21R7 also shows inh |
| R2032743 | Evatanepag;CP-533536 | Evatanepag (CP-533536) is an EP2 receptor selective prostaglandin E2 (PGE2) agon |
| R2032744 | CP-724714 | CP-724714 is a potent, selective inhibitor of HER2/ErbB2 with IC50 of 10 nM, > |
| R2032745 | DB07268 | DB07268 is a potent and selective JNK1 inhibitor with an IC50 value of 9 nM. |
| R2032746 | GDC-0879 | GDC-0879 is a potent and selective B-Raf inhibitor with an IC50 of 0.13 nM. |
| R2032747 | GSK-J1 | GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KD |
| 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 |
