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Home > Products
| Cat.No. | Product name | Product Description |
| R2103578 | DT2216 | DT2216 is a potent and selective BCL-XL degrader based on PROTAC technology. SIA |
| R2103579 | JTZ-951;Enarodustat | Enarodustat is a potent and orally active factor prolyl hydroxylase inhibitor, w |
| R2103580 | CBR-5884 | CBR-5884 is an active, selective inhibitor of phosphoglycerate dehydrogenase (PH |
| R2103581 | Homo-PROTAC cereblon degrader 1 (compound 15a) | Homo-PROTAC cereblon degrader 1 (compound 15a) is a highly potent and efficient |
| R2103582 | RU-301 | RU-301 is a pan-TAM receptor inhibitor, exerts pan-TAM inhibitory activity by bi |
| R2103583 | Desmorpholinyl Navitoclax-NH-Me | Desmorpholinyl Navitoclax-NH-Me is a Bcl-xL inhibitor. Desmorpholinyl Navitoclax |
| R2103584 | TVB-3664 | TVB-3664 is an orally available, reversible, potent, selective and highly bioava |
| R2103585 | VTP50469 | VTP50469 is a potent, highly selective and orally active Menin-MLL interaction i |
| R2103586 | G1T28;Trilaciclib | Trilaciclib is a potential first-in-class short-acting CDK4/6 inhibitor in devel |
| R2103587 | Trilaciclib hydrochloride (G1T28 hydrochloride) | Trilaciclib hydrochloride (G1T28 hydrochloride) is a CDK4/6 inhibitor with IC50s |
| R2103588 | SX682 | SX-682 is an orally bioavailable, potent allosteric inhibitor of CXCR1 and CXCR2 |
| R2103589 | Mli-2 | MLi-2 is an orally active and highly selective LRRK2 inhibitor with an IC50 of 0 |
| R2103591 | PT-2399 | PT2399 is a potent and selective HIF-2α antagonist, which directly binds to HIF- |
| R2103592 | (Rac)-PT2399 | (Rac)-PT2399 (Compound 10e), the racemate of PT2399, acts as a potent and specif |
| R2103593 | EGFR-IN-7 (compound 34) | EGFR-IN-7 (compound 34) is a selective and potent EGFR kinase inhibitor extracte |
| R2103594 | MSAB | MSAB is a potent and selective inhibitor of Wnt/β-catenin signaling. MSAB binds |
| R2103595 | Rogaratinib;BAY1163877 | Rogaratinib is a potent and selective fibroblast growth factor receptor (FGFR) i |
| R2103553 | Omadacycline hydrochloride (PTK0796 hydrochloride) | Omadacycline hydrochloride is novel, aminomethyl tetracycline antibiotic being d |
| R2103590 | MYF-01-37 | MYF-01-37 is a novel covalent inhibitor of TEAD. |
| R2061750 | TAPI-1 | TAPI-1 is a TACE (ADAM17) inhibitor and blocks the shedding of several |
| R2103596 | PQR530 | PQR530 is a potent, ATP-competitive, orally bioavailable and brain-penetrant dua |
| R2103597 | CD38 inhibitor 1 | CD38 inhibitor 1 (compound 78c) is a potent CD38 inhibitor with IC50s of 7.3 nM |
| R2103598 | Olutasidenib | Olutasidenib (FT-2102) is a highly potent, orally active, brain penetrant and se |
| R2103599 | PRN1008 | PRN1008 is a reversible covalent, selective and oral active inhibitor of Bruton’ |
| R2103600 | Allopregnanolone | Allopregnanolone, a neurosteroid synthesized from progesterone in brain, acts as |
