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| Cat.No. | Product name | Product Description |
| R2032696 | PF-04457845 | PF-04457845 is a highly efficacious and selective FAAH inhibitor with IC50 value |
| R2032697 | PF-4989216 | PF-4989216 is a potent and selective PI3Kα inhibitor with a Ki of 0.6 nM. |
| R2032698 | Pyridone6 | Pyridone 6 is a pan-JAK inhibitor, which potently inhibits the JAK kinase family |
| R2032699 | R1530 | R1530 is the multikinase inhibitor with potential antiangiogenesis and antineopl |
| R2032700 | RO4987655(CH-4987655) | RO4987655 is an orally active and highly selective MEK inhibitor with an IC50 of |
| R2032701 | Selinexor(KPT-330) | Selinexor (KPT-330), analog of KPT-185, is an orally bioavailable selective CRM1 |
| R2032702 | SU5614 | SU5614 is a potent and selective FLT3 inhibitor.SU5614 has inhibitory activity f |
| R2032703 | TRAM-34 | TRAM-34 is a highly selective blocker of intermediate-conductance calcium-activa |
| R2032704 | A-1210477 | A-1210477 is a potent and selective inhibitor of MCL-1 with a Ki of 0.45 nM. |
| R2032705 | TAK-063;Balipodect | Balipodect (TAK-063) is a highly potent, selective and orally active PDE10A inhi |
| R2032706 | UNC0646 | UNC0646 is a potent and selective G9a inhibitor with IC50 of 6 nM.IC50 value: 6 |
| R2032707 | HO-3867 | HO-3867 is a selective and potent STAT3 inhibitor and shows good antitumor activ |
| R2032708 | PFI-4 | PFI-4 is a potent and selective and cell permeable BRPF1 bromodomain inhibitor ( |
| R2032709 | TCS359 | TCS 359, a 2-acylaminothiophene-3-carboxamide, is a potent inhibitor of FLT3 wit |
| R2032710 | LJH685 | LJH685 is a potent, specific and selective RSK inhibitor, inhibits RSK1, 2, and |
| R2032711 | LJI308 | LJI308 is a new and potent pan-RSK inhibitor, with IC50 of 6 nM, 4 nM, and 13 nM |
| R2032712 | AS703026;Pimasertib | Pimasertib (AS703026) is a highly selective, potent, ATP non-competitive alloste |
| R2032713 | Solcitinib;GSK-2586184;GLPG-0778) | Solcitinib is an orally active, competitive, potent, selective JAK1 inhibitor, w |
| R2032714 | A-366 | A-366 is a potent histone methyltransferase G9a inhibitor with an IC50 of 3.3 nM |
| R2032715 | AZ6102 | AZ6102 is a potent dual TNKS1 and TNKS2 inhibitor, with IC50s of 3 nM and 1 nM, |
| R2032716 | BI-7273 | BI-7273 is a selective, and cell-permeable BRD9 inhibitor, with an IC50 and a Kd |
| R2032717 | FIIN-3 | FIIN-3 is an irreversible inhibitor of FGFR with an IC50 of 13.1, 21, 31.4, and |
| R2032718 | Glutaminase C-IN-1(968) | Glutaminase C-IN-1 (Compound 968) is an allosteric inhibitor of Glutaminase C th |
| R2032719 | GSK-2881078 | GSK 2881078 is a selective androgen receptor modulator potentially for the treat |
| R2032720 | I-BRD9 | I-BRD9 is the first selective cellular chemical probe for BRD9 (pIC50=7.3).IC50 |
