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Home > Products
| Cat.No. | Product name | Product Description |
| R2032979 | ABT702 dihydrochloride | ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor (IC50=1.7 nM |
| R2032980 | BAY1436032 | BAY-1436032 is a novel pan-mutant isocitrate dehydrogenase 1 (IDH1) inhibitor. |
| R2032981 | CH-223191 | CH-223191 is a potent and specific antagonist of aryl hydrocarbon receptor (AhR) |
| R2032982 | CPI-455 | CPI-455 is a specific, pan-KDM5 inhibitor with an IC50 of 10 nM for KDM5A.CPI-45 |
| R2032983 | dasotraline | Dasotraline is a triple reuptake inhibitor that blocks dopamine, norepinephrine, |
| R2032984 | DM1-Sme | DM1-SMe is a potent maytansinoid microtubular inhibitor and an unconjugated DM1 |
| R2032985 | MDK-5220 | Orexin 2 Receptor Agonist is a potent (EC50 on OX2R is 23 nM) and OX2R-selective |
| R2032986 | Mitapivat | Mitapivat is a pyruvate kinase isoenzyme M2 (PKM2) activator. |
| R2032987 | NVP-TNKS656 | NVP-TNKS656 is a highly potent, selective, and orally active TNKS2 inhibitor wit |
| R2032988 | AZD0364 | AZD-0364 is a potent and selective ERK2 inhibitor extracted from patent WO201708 |
| R2032989 | E7820 | E7820 is an angiogenesis inhibitor by suppressing integrin a2, a cell adhesion m |
| R2032990 | EPZ031686 | EPZ031686 is an orally available SMYD3 inhibitor with an IC50 of 3 nM in cell-fr |
| R2032991 | LY3200882 | LY3200882 is a novel and highly selective inhibitor of TGF-β receptor type 1 (TG |
| R2032992 | MK8617 | MK-8617 is an orally active pan-inhibitor of hypoxia-inducible factor prolyl hyd |
| R2032993 | PF-3084014;Nirogacestat | Nirogacestat (PF-3084014) is a reversible, noncompetitive, and selective γ-secre |
| R2032994 | PF9366 | PF-9366 is a human methionine adenosyltransferase 2A (Mat2A) inhibitor, with an |
| R2032995 | Pyridostatin | Pyridostatin is a G-quadruplexe stabilizer, with a Kd of 490 nM. |
| R2032996 | Ro25-6981 | Ro 25-6981 is a potent and selective activity-dependent blocker of NMDA receptor |
| R2032997 | SC75741 | SC75741 is a broad and efficient NF-κB inhibitor with an IC50 of 200 nM for p65. |
| R2032998 | TP3654 | TP-3654 is a second-generation Pim kinase inhibitor with Ki values of 5 and 42 n |
| R2032999 | AT406 hydrochloride | AT-406 is a potent and orally bioavailable Smac mimetic and an antagonist of IAP |
| R2033000 | BS194 | BS194 is as a potent cyclin-dependent protein kinases (CDKs) inhibitor. |
| R2033001 | Cambinol | Cambinol is a SIRT1 and SIRT2 inhibitor with IC50 values of 56 and 59 μM, respec |
| R2033002 | CCT241736 | CCT241736 is a potent and orally bioavailable dual FLT3 and Aurora kinase inhibi |
| R2033003 | CFI-400437 | CFI-400437 is potent against PLK4 (IC50 = 0.6 nM) and selective against other me |
