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| Cat.No. | Product name | Product Description |
| R2101132 | RG7834 | RG7834 (RO 7020322) is a highly selective and orally bioavailable HBV inhibitor, |
| R2101133 | OSMI-1 | OSMI-1 is an inhibitor of O-GlcNAc transferase (OGT). |
| R2101134 | SEMBL | SEMBL is a potent NF-κB inhibitor that inhibits DNA binding of NF-κB component p |
| R2101135 | Bleomycin sulfate | Bleomycin Sulfate, a glycopeptide antibiotic, is an anticancer agent for squamou |
| R2101136 | Bleomycin hydrochloride | Bleomycin hydrochloride is an antitumor antibiotic which induces apoptosis. |
| R2101137 | Orelabrutinib | Orelabrutinib is an orally active and irreversible inhibitor of Bruton's tyrosin |
| R2101138 | NRC-2694 | NRC-2694 is an antagonist of the epidermal growth factor receptor (EGFR). It has |
| R2101139 | GSK366 | GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor (IC50s: 0.7 nM an |
| R2101140 | AMG 232 | AMG 232 is a potent, selective and orally available inhibitor of p53-MDM2 intera |
| R2101141 | Indirubin | Indirubin is a potent cyclin-dependent kinases and GSK-3β inhibitor with IC50 of |
| R2101143 | RepSox | RepSox is a potent and selective of the TGFβR-1/ALK5 inhibitor. |
| R2101144 | Voxtalisib (XL765, SAR245409) | Voxtalisib (SAR245409, XL765) is a dual inhibitor of mTOR/PI3K, mostly for p110γ |
| R2101145 | Aliskiren | Aliskiren is the first in a class of drugs called direct renin inhibitors. |
| R2101146 | SAR-020106 | SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an I |
| R2101147 | A-893 | A-893 is a cell-active inhibitor of Methyltransferase SMYD2, with an IC50 of 2.8 |
| R2101148 | Mirogabalin besylate | Mirogabalin besylate is a selective and orally available ligand for the α2δ subu |
| R2101149 | Px-104 | (-)-PX20606 trans isomer is an agonist of FXR (EC50s: 18 and 29 nM for FXR in FR |
| R2101150 | RUC-4 | RUC-4 (RUC4;RUC 4) is a potent, selective, non-RGD-mimetic αIIbβ3 integrin recep |
| R2101151 | GDC-0077 | GDC-0077 (RG6114) is a potent, orally available, and selective inhibitor of PI3K |
| R2101152 | CYC065;CDK259 | CYC065 is an orally available, second-generation ATP-competitive inhibitor of CD |
| R2101153 | LX-2761 | LX2761 is a chemically stable and effective inhibitor against sodium-dependent g |
| R2101154 | Baloxavir | Baloxavir is a first-in-class cap-dependent endonuclease inhibitor of the influe |
| R2101155 | ARS-1323 | ARS-1323 (the racemate of ARS-1620) is a mutant K-ras G12C inhibitor extracted f |
| R2101156 | CDDO-2-P-Im | CDDO-3P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can |
| R2101157 | R-268712 | R-268712 is an effective and selective inhibitor of ALK5 IC50: 2.5 nM). |
