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| Cat.No. | Product name | Product Description |
| R2032155 | MK-0524;Laropiprant | Laropiprant is a potent, selective DP receptor antagonist with Ki values of 0.57 |
| R2032156 | Mubritinib(TAK 165) | Mubritinib (TAK-165) is a potent and selective EGFR2/HER2 inhibitor with an IC50 |
| R2032157 | Nolatrexed dihydrochloride(AG-337 dihydrochloride) | Nolatrexed dihydrochloride (AG 337) is a non-competitive lipophilic inhibitor of |
| R2032158 | GS9620;Vesatolimod(GS-9620) | Vesatolimod (GS-9620) is a potent, selective and orally active agonist of Toll-L |
| R2032159 | Ribociclib;LEE011 | Ribociclib (LEE01) is a highly specific CDK4/6 inhibitor with IC50 values of 10 |
| R2032160 | Everolimus;RAD001;SDZ-RAD | Everolimus (RAD001) is a potent mTOR inhibitor that binds to FKBP-12 to generate |
| R2032162 | PF-04971729(Ertugliflozin) | Ertugliflozin (PF-04971729) is a potent, selective and orally active inhibitor o |
| R2032163 | OligoMycin A | Oligomycin A, created by Streptomyces, acts as a mitochondrial F0F1-ATPase inhib |
| R2032164 | 吡美莫司;匹美克莫司;PiMecroliMus | Pimecrolimus is an immunophilin ligand, which binds specifically to the cytosoli |
| R2032165 | pirodavir | Pirodavir is a potent, broad-spectrum picornavirus inhibitor, and is highly acti |
| R2032166 | Raltegravir(MK0518) | Raltegravir is a potent integrase (IN) inhibitor, used to treat HIV infection. |
| R2032167 | Regadenoson | Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator |
| R2032168 | Apabetalone;RVX-208 | Apabetalone (RVX-208) is an inhibitor of BET transcriptional regulators with sel |
| R2032169 | Saracatinib(AZD0530) | Saracatinib (AZD0530) is a potent Src family inhibitor with IC50s of 2.7 to 11 n |
| R2032170 | Preladenant | Preladenant is a potent and competitive antagonist of the human adenosine A2A re |
| R2032171 | Telatinib | Telatinib (Bay 57-9352) is an orally active, small molecule inhibitor of VEGFR2, |
| R2032172 | Triciribine | Triciribine is a DNA synthesis inhibitor, also inhibits Akt and HIV-1/2 with IC5 |
| R2032173 | Vilanterol(GW642444 | Vilanterol (GW642444) is a long-acting β2-adrenoceptor (β2-AR) agonist with 24 h |
| R2032174 | VisModegib(GDC0449) | Vismodegib (GDC-0449) is an orally active hedgehog pathway inhibitor with an IC5 |
| R2032175 | Zosuquidar(LY3359793HCl | Zosuquidar trihydrochloride is an inhibitor of P-glycoprotein with a Ki value of |
| R2032176 | BAF312(SiponiMod) | Siponimod (BAF-312) is a potent and selective sphingosine-1-phosphate (S1P) rece |
| R2032177 | ZotaroliMus(ABT-578) | Zotarolimus is a tetrazole-containing Rapamycin analog which is used as animmuno |
| R2032178 | Deforolimus(AP23573;MK-8669) | Deforolimus (AP23573; MK-8669) is a potent and selective mTOR inhibitor; inhibit |
| R2032179 | XiMelagatran | Ximelagatran (H 376/95) is an orally active thrombin inhibitor that selectively |
| R2032180 | PF-03394197(Oclacitinib) | Oclacitinib is a novel JAK inhibitor.Oclacitinib is most potent at inhibiting JA |
