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| Cat.No. | Product name | Product Description |
| R2304362 | BRAF inhibitor | BRAF inhibitor is a B-Raf inhibitor extracted from patent WO/2011103196 A1, Comp |
| R2304363 | TD-106 | TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein de |
| R2304364 | Argatroban | Argatroban (MD-805) is a direct, selective thrombin inhibitor. |
| R2304365 | Nilvadipine | Nilvadipine is a potent calcium channel antagonist, and the IC50 value is around |
| R2304366 | AZD7687 | AZD7687 is a potent, selective, reversible and orally active diacylglycerol acyl |
| R2304367 | L-6-Diazo-5-oxonorleucine; DON | 6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine; DON) is a glutamine anta |
| R2304368 | Azaserine | Azazerine (CI-337) is a competitive inhibitor of glutamine amidotransferase. Aza |
| R2304369 | ML418 | ML418 is a potent, selective and CNS penetrating Kir7.1 potassium channel blocke |
| R2304370 | ML289;VU0463597 | ML289 (VU0463597) is a potent, selective, and CNS-penetrant mGlu3 (IC50=0.66 μM) |
| R2304371 | MNI137 | MNI137 is a potent and selective negative allosteric modulator for group II mGlu |
| R2304372 | H3B-120 | H3B-120 is a highly selective, competitive and allosteric carbamoyl phosphate sy |
| R2304374 | FEN1-IN-4 | FEN1-IN-4 (Compound 2) is a human flap endonuclease-1 (hFEN1) inhibitor. |
| R2304375 | Ipsapirone (TVXQ7821) | Ipsapirone (TVX Q 7821) is an anxiolytic compound and a 5-HT1A receptor partial |
| R2304376 | MRS1220 | MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antag |
| R2304377 | H2L5186303 | H2L5186303 is a potent and selective LPA2 receptor (lysophosphatidic acid 2 rece |
| R2304378 | PF-543 | PF-543 (Sphingosine Kinase 1 Inhibitor II) is a potent, selective, reversible an |
| R2304379 | PF-543 hydrochloride | PF-543 hydrochloride (Sphingosine Kinase 1 Inhibitor II hydrochloride) is a pote |
| R2304380 | DAUDA | DAUDA (11-(dansylamino) undecanoic acid) is an environment-sensitive fluorescent |
| R2304381 | SR2640 | SR2640 is a potent and selective competitive leukotriene D4/leukotriene E4 antag |
| R2304382 | SR2640 hydrochloride | SR2640 (hydrochloride) is a potent and selective competitive leukotriene D4/leuk |
| R2304383 | PDE4B-IN-2;A 33 | PDE4B-IN-2 is an orally active and selective PDE4B inhibitor with an IC50 of 15 |
| R2304384 | Cediranib Maleate | Cediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR |
| R2304385 | PF-4800567 | PF-4800567 is a potent and selective inhibitor of casein kinase 1ϵ (CK1ϵ), with |
| R2304386 | WAY-658261 | |
| R2304387 | OfHex1-IN-2 | OfHex1-IN-2 (compound I-79) is a potent β-N-acetylhexosaminidase OfHex1 inhibito |
