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| Cat.No. | Product name | Product Description |
| R2101032 | CRT5 | CRT5 (CRT0066051), a pyrazine benzamide, is a potent and selective PKD inhibitor |
| R2101033 | BMS453 | BMS-189453 (BMS189453, BMS453) is a synthetic retinoid that acts as an agonist o |
| R2101034 | Mps1-IN-3 | Mps1-IN-3 is a potent and selective MPS1 kinase inhibitor, with an IC50 of 50 nM |
| R2101035 | OS-3-106 | OS-3-106 is a novel dopamine D3 receptor-selective partial agonist. |
| R2101036 | NSC-703786 | A potent, selective antitumour agent through activation the aryl hydrocarbon rec |
| R2101037 | GW779439X | GW779439X is an inhibitor of cyclin dependent kinase. |
| R2101038 | RO2959 hydrochloride | RO2959 hydrochloride is a potent and selective CRAC channel inhibitor with an IC |
| R2101039 | Flupenthixol dihydrochloride | cis-(Z)-Flupentixol dihydrochloride is a potent and selective DA D1/D2 receptor |
| R2101040 | 4BP-TQS | 4BP-TQS is an allosteric agonist of α7 subunit-containing neuronal nicotinic ace |
| R2101041 | B355252 | B355252 is a neuroprotective agent that potentiates nerve growth factor (NGF)-in |
| R2101042 | GSK 2830371 | GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 |
| R2101043 | MONNA | MONNA is a potent TMEM16A (Anoctamin-1) blocker (IC50 = 80 nM). Exhibits >100 |
| R2101044 | TAE-1 | TAE-1 is an inhibitor of amyloid-β fibril formation and aggregation, suggesting |
| R2101045 | ML191 | ML-191 is a potent, selective GPR55 antagonist with 160 nM potency for GPR55 and |
| R2101046 | ML336 | ML-336 is an inhibitor of of the Venezuelan equine encephalitis virus (VEEV) str |
| R2101047 | GW280264X | GW280264X is an ADAM17 inhibitor. |
| R2101048 | TM5007 | TM5007 is a poent inhibitor plasminogen activator inhibitor-1 (PAI-1) with IC50 |
| R2101049 | CYM2503 | CYM2503 is a positive allosteric modulator (PAM) of the GAL2 receptor that poten |
| R2101050 | YM26734 | YM-26734 is a rabbit platelet sPLA2 inhibitor that has been used to ameliorate l |
| R2101051 | G244-LM | G244-LM is a potent and specific tankyrase 1/2 inhibitor that inhibits Wnt signa |
| R2101052 | VK-II-86 | VK-II-86 is a selective ryanodine receptor type 2 (RyR2) antagonist. |
| R2101053 | ML298 | ML298 (CID53393915) is a potent, specific inhibitor of Phospholipase D2 (PLD2) w |
| R2101054 | SW155246 | SW155246 is a potent and selective DNMT1 (DNA methyltransferase 1) inhibitor wit |
| R2101055 | ML-299 | ML299 (VU0463568) is a dual inhibitor of PLD1 and PLD2 with IC50 of 6 nM and 20 |
| R2101056 | VUF11418 | VUF11418 is a nonpeptidomimetic agonist of the G protein-coupled chemokine recep |
