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Home > Products
| Cat.No. | Product name | Product Description |
| 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 |
| R2304388 | Trequinsin hydrochloride | Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of platelet C |
| R2304389 | CLP257 | CLP257 is a selective K+-Cl− cotransporter KCC2 activator with an EC50 of 616 nM |
| R2304390 | TC-MCH 7c | TC-MCH 7c, a phenylpyridone derivative, is an orally available, selective and br |
| R2304391 | FTIDC | FTIDC is an orally active, noncompetitive, selective allosteric metabotropic glu |
| R2304393 | FMF-04-159-2 | FMF-04-159-2 is a covalent CDK14 inhibitor. FMF-04-159-2 inhibits CDK14 and CDK2 |
| R2304394 | Pedunculoside | Pedunculoside exerts lipid-lowering effects partly through the regulation of lip |
| R2304395 | PF-06465469 | PF-06465469 is a covalent inhibitor of ITK with an IC50 of 2 nM. |
| R2304396 | CATPB | CATPB is a potent, selective free fatty acid receptor 2 (FFA2R/GPR43) antagonist |
| R2304397 | NTRC-824 | NTRC-824 (Compound 5) is a potent, selective and neurotensin-like nonpeptide neu |
| R2304398 | CGP-53353 (DAPH-7) | CGP-53353 (DAPH-7) is an potent PKC inhibitor with IC50s of 0.41 mM and 3.8 mM f |
| R2304401 | Elacestrant dihydrochloride | Elacestrant (RAD1901) dihydrochloride is an orally available and selective estro |
| R2304402 | Elacestrant | Elacestrant (RAD1901) is an orally available and selective estrogen receptor deg |
| R2304403 | Almonertinib;HS-10296 | Almonertinib (HS-10296) is an orally available, irreversible, third-generation E |
| R2304404 | CAY10603 | CAY10603 (BML-281) is a potent and selective HDAC6 inhibitor, with an IC50 of 2 |
