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| Cat.No. | Product name | Product Description |
| R21082279 | THIACETAZONE | Thioacetazone is a thiosemicarbazone that thioacetazone treatment of pulmonary t |
| R21082280 | R547 | R547 is a potent ATP-competitive inhibitor of CDK1/2/4 with Ki of 2 nM/3 nM/1 nM |
| R21082281 | YS-49 | YS-49 is an activator of PI3K/Akt (a downstream target of RhoA). |
| R21082282 | YM-90K hydrochloride | YM90K hydrochloride is an antagonist of AMPA receptor. |
| R21082283 | AG-490 | (E/Z)-AG490 ((E/Z)-Tyrphostin AG490) is a racemate of (E) -Ag490 and (Z) -Ag490. |
| R21082284 | D-6413 | D-64131 is a tubulin polymerization inhibitor that competitively binds to αβ -tu |
| R21082285 | KU14R | KU14R is an insulin receptor antagonist, which can selectively block insulin sec |
| R21082286 | Amsilarotene;TAC-101 | Amsilarotene inhibits the phosphorylation of retinoblastoma gene product (RB) an |
| R21082287 | GW7647 | |
| R21082288 | LY2623091 | LY2623091 (LY-2623091) is an oral halocorticoid receptor antagonist for the trea |
| R21082289 | SMI-4a | Tcs-pim-1-4a is a PIM inhibitor that blocks mTORC1 activity through AMPK activat |
| R21082290 | LY500307 | Erteberel (LY500307) is a potent, selective estrogen receptor β (ERβ) inhibitor |
| R21082291 | NVP-QAV-572 | Nav1.7-in-2 is a potent PI3K inhibitor with IC50 of 10 nM. For details, see Exam |
| R21082292 | LX1606 | Telotristat ethyl (LX1606) is an oral tryptophan hydroxylase inhibitor that redu |
| R21082293 | Asunaprevir(BMS-650032) | |
| R21082294 | AS-252424 | As252424 is a potent selective PI3Kγ inhibitor with IC50 of 30±10 nM. |
| R21082296 | tomeglovir | Tomeglovir is an anti-CMV agent that inhibits the progression of viral DNA in mu |
| R21082297 | OTSSP167 hydrochloride | OTSSP167 is a potent MELK inhibitor with IC50 value of 0.41 nM. |
| R21082298 | K145 hydrochloride | K145 hydrochloride was a selective inhibitor of SphK2 with IC50 of 4.3μM, and sh |
| R21082299 | TH-237A | Th-237a (MESO-GS 164) is a neuroprotective agent with good blood-brain barrier p |
| R21082300 | Deferitrin | Deferitrin (GT-56-252) is a deferric sulfide (DFT) analogue, which is a trident |
| R21082301 | MX1013 | MX1013 is a dipeptide pan-caspase inhibitor that inhibits caspase-1 |
| R21082302 | Pardoprunox | Pardoprunox(SLV-308) is an agonist of dopamine receptors D2, D3, and 5-HT1A, an |
| R21082303 | CP465022 hydrochloride | CP 465022 hydrochloride is a selective GluR (AMPA) antagonist which is non-compe |
| R21082304 | JZL-195 | JZL195 is a highly effective and selective dual inhibitor of FAAH/MAGL, with IC5 |