RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
Home > Products
| Cat.No. | Product name | Product Description |
| 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 |
| R2032721 | LDC000067 | LDC000067 is a highly specific CDK9 inhibitor with an IC50 value of 44±10 nM in |
| R2032722 | MI-136 | MI-136 inhibits DHT-induced expression of androgen receptor (AR) target genes.Ta |
| R2032723 | Naloxegol oxalate;NKTR-118 oxalate;AZ-13337019 oxalate) | Naloxegol oxalate (NKTR-118 oxalate; AZ-13337019 oxalate) is an opioid-receptor |
| R2032724 | ns11021 | NS 11021 is a potent and specific Ca2-activated big-conductance K＋ Channels (KCa |
| R2032725 | NSC348884 | NSC348884 is a nucleophosmin inhibitor disrupts oligomer formation and induces a |
| R2032726 | Obatoclax Mesylate(GX15-070 Mesylate) | Obatoclax Mesylate (GX15-070 Mesylate) is an inhibitor of the BCL-2 family prote |
| R2032727 | PF-04929113(SNX-5422) | SNX-5422 (PF-04929113), a prodrug of SNX-2112, is an orally active Hsp90 inhibit |
| R2032728 | PH797804 | PH-797804 is a ATP-competitive, selective p38α/p38β inhibitor (IC50=26 nM and Ki |
