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Home > Products
| Cat.No. | Product name | Product Description |
| R2032479 | P005672 hydrochloride;Sarecycline hydrochloride | Sarecycline, also known as WC-3035 and P005672, is a novel, tetracycline-derived |
| R2032480 | P276-00;Riviciclib hydrochloride | Riviciclib hydrochloride (P276-00) is a potent cyclin-dependent kinase (CDK) inh |
| R2032481 | PA-824 | Pretomanid (PA-824) is a small-molecule nitroimidazopyran drug candidate for the |
| R2032482 | Pacritinib(SB1518) | Pacritinib is a potent inhibitor of both wild-type JAK2 (IC50=23 nM) and JAK2V61 |
| R2032483 | PCI-24781 | Abexinostat (CRA 024781) is a novel pan-HDAC inhibitor mostly targeting HDAC1 wi |
| R2032484 | PD0325901 | PD0325901 is a selective and cell permeable MEK inhibitor with an IC50 of 0.33 n |
| R2032485 | PD151746 | PD151746 is a calpain inhibitor, shows a 20-fold selectivity for u-calpain (Ki = |
| R2032486 | PD153035 Hydrochloride(SU-5271 Hydrochloride) | PD153035 Hydrochloride (SU-5271 Hydrochloride) is a potent EGFR inhibitor with K |
| R2032487 | PD318088 | PD318088 is an allosteric MEK inhibitor. |
| R2032488 | PF03716556 | PF 03716556 is a potent, and selective H+, K+-ATPase antagonist, with a pIC50 va |
| R2032489 | PF-3758309 | PF-3758309 is a potent, orally available, and reversible ATP-competitive inhibit |
| R2032490 | PF3845 | PF-3845 is a selective fatty acid amide hydrolase (FAAH) inhibitor (Ki = 0.23 μM |
| R2032491 | PF-4708671 | PF-4708671 is a potent cell-permeable S6K1 inhibitor with a Ki of 20 nM and IC50 |
| R2032492 | PF-477736 | PF 477736 is a potent, selective ATP-competitive inhibitor of Chk1, with a Ki of |
| R2032493 | PFI-1(PF-6405761) | PFI-1 is a selective BET (bromodomain-containing protein) inhibitor for BRD4 wit |
| R2032494 | PFI-2 | PFI-2 is a a first-in-class, potent, highly selective, and cell-active inhibitor |
| R2032495 | PFI-3 | PFI-3 is a selective, potent and cell-permeable SMARCA2/4 bromodomain inhibitor |
| R2032496 | PHA-665752 | PHA-665752 is a selective, ATP-competitive, and active-site inhibitor of the cat |
| R2032497 | PHA-793887 | PHA-793887 is a potent, ATP-competitive CDK inhibitor, can inhibit Cdk2, Cdk1, C |
| R2032498 | PHA-848125;Milciclib | Milciclib (PHA-848125) is a potent, dual inhibitor of CDK and Tropomyosin recept |
| R2032499 | PI-3065;PI3065 | PI-3065 is a potent inhibitor of PI3K p110δ, with IC50 and Ki values of 5 nM and |
| R2032500 | PIK-90 | PIK-90 is a DNA-PK and PI3K inhibitor, which inhibits p110α, p110γ and DNA-PK wi |
| R2032501 | PIK93 | PIK-93 is the first potent, synthetic PI4K (PI4KIIIβ) inhibitor with IC50 of 19 |
| R2032502 | Plinabulin(NPI-2358) | Plinabulin (NPI-2358) is a vascular disrupting agen (VDA) against tubulin-depoly |
| R2032503 | PLX4720 | PLX-4720 is a potent and selective inhibitor of B-RafV600E with IC50 of 13 nM in |
