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| Cat.No. | Product name | Product Description |
| R2101183 | UNC2541 | UNC2541 is a potent and Mer tyrosine kinase (MerTK)-specific inhibitor. It also |
| R2101184 | Inolitazone | Inolitazone a novel high-affinity agonist of PPARγ. It is dependent upon PPARγ f |
| R2101185 | AMR69 D5 | Pirfenidone D5 is a deuterium labeled Pirfenidone. Pirfenidone is an antifibroti |
| R2101186 | BIBF0775 | BIBF0775 is a selective TGFβ type I receptor (Alk5) inhibitor (IC50: 34 nM). |
| R2101187 | MRTX1257 | MRTX-1257 is a selective, irreversible, and covalent inhibitor of KRAS G12C. It |
| R2101188 | MLT-747 | MLT-747 is an effective and allosteric inhibitor of MALT1. It binds MALT1 in the |
| R2101189 | Asiaticoside | Asiaticoside (Madecassol) is the active chemical component of the plant Centella |
| R2101190 | NPS-1034 | NPS-1034 is a dual Met/Axl inhibitor with IC50 of 48 nM and 10.3 nM, respectivel |
| R2101191 | LLY-283 | LLY-283 is an effective and selective inhibitor of protein arginine methyltransf |
| R2101192 | SJ000291942 | SJ000291942 is an activator of the canonical bone morphogenetic proteins (BMP) s |
| R2101193 | SB-505124 hydrochloride | SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5 with IC50 of 129 nM an |
| R2101194 | MLT-748 | MLT-748 is an effective, selective, and allosteric MALT1 inhibitor. It binds MAL |
| R2101195 | SHP394 | SHP394 is an orally efficacious inhibitor of protein tyrosine phosphatase SHP2 ( |
| R2101196 | KRAS G12C inhibitor 13 | KRAS G12C inhibitor 13 is a KRAS G12C inhibitor . |
| R2101197 | GW6604 | GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity |
| R2101198 | Gypenoside XLIX | Extracted from whole herb of Gynostemsma pentaphyllum(Thunb.)Mak.;Store the prod |
| R2101199 | Fenofibric acid | Fenofibric Acid is the active form of fenofibrate, a synthetic phenoxy-isobutyri |
| R2101200 | R916562 | R916562 is an orally active and selective Axl/VEGF-R2 inhibitor with IC50s of 13 |
| R2101201 | RU-302 | RU-302 is a pan inhibitor of TAM. RU-302 potently blocks Gas6-inducible Axl rece |
| R2101202 | BAY-677 | BAY-677 is an inactive control for BAY-678. BAY-678 is an orally bioavailable, h |
| R2101203 | RU-19110(HBr) | Halofuginone specifically inhibits collagen type I gene expression and matrix me |
| R2101204 | Chebulinic acid | Chebulinic acid is a potent inhibitor of M. tuberculosis DNA gyrase. It also can |
| R2101205 | Gemfibrozil | Gemfibrozil (CI-719) is an activator of peroxisome proliferator-activated recept |
| R2101206 | Pioglitazone | Pioglitazone is an insulin sensitizing agent and thiazolidinedione that is indic |
| R2101207 | EMT inhibitor-1 | EMT inhibitor -1 is an inhibitor of Hippo, Wnt signaling and TGF- macrophages (T |
