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Home > Products
| Cat.No. | Product name | Product Description |
| R10952 | Cobimetinib;GDC-0973; XL518 | Cobimetinib (GDC-0973, RG7420) is a potent and highly selective MEK1 inhibitor w |
| R10953 | ABC294640 | ABC294640 is an orally bioavailable and selective sphingosine kinase-2 (SphK2) i |
| R10954 | LY3039478;Crenigacestat | LY3039478 is an orally bioavailable Notch inhibitor with an IC50 of ~1 nM in mos |
| R10955 | RU-58841 | N/A |
| R10957 | PI103 | PI-103 is a multi-targeted PI3K inhibitor for p110α/β/δ/γ with IC50 of 2 nM/3 nM |
| R10958 | AS605240 | AS-605240 selectively inhibits PI3Kγ with IC50 of 8 nM, over 30-fold and 7.5-fol |
| R10959 | Cobimetinib R-enantiomer;GDC-0973 R-enantiomer; XL-518 R-enantiomer | Cobimetinib R-enantiomer is the less active R-enantiomer of Cobimetinib. Cobimet |
| R10961 | SAR407899 hydrochloride | SAR407899 hydrochloride is a selective, potent and ATP-competitive ROCK inhibito |
| R10962 | Tenofovir alafenamide hemifumarate (Synonyms: GS-7340 (hemifumarate)) | GS-7340 (Tenofovir alafenamide) hemifumarate is an investigational oral prodrug |
| R10963 | GS7340 impurity1 | Tenofovir alafenamide (GS-7340) is an investigational oral prodrug of Tenofovir. |
| R10967 | PF-431396 | PF-431396 is a dual PYK2/FAK inhibitor with IC50 of 11 nM and 2 nM, respectively |
| R10968 | FPH2; BRD-9424 | FPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-deriv |
| R10969 | HS-173 | HS-173 is a potent PI3Kα inhibitor with IC50 of 0.8 nM. |
| R10970 | BMS-833923 | BMS-833923 is an orally bioavailable Smoothened antagonist. Phase 2. |
| R10971 | NU-2058;NU2058 | NU2058 (O6-(Cyclohexylmethyl)guanine) is a potent, competitive and guanine-based |
| R10973 | CB-5083 | CB-5083 is a potent, selective, and orally bioavailable p97 AAA ATPase inhibitor |
| R10974 | AZ7371 | TBA-7371 is a potent, noncovalent DprE1 inhibitor. TBA-7371 has potent antituber |
| R10976 | STF31 | STF-31 is a selective glucose transporter GLUT1 inhibitor. |
| R10977 | PIK-294 | PIK-294 is a highly selective p110δ inhibitor with IC50 of 10 nM, 1000-, 49- and |
| R10978 | BIX-01294 | BIX01294 is an inhibitor of G9a histone methyltransferase with IC50 of 2.7 μM in |
| R10979 | ML204 | ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 io |
| R10980 | 3-Cyano-7-ethoxycoumarin | 3-Cyano-7-ethoxycoumarin is a fluorogenic cytochrome P-450 substrate that genera |
| R10981 | UNC0379 | UNC0379 is a selective, substrate competitive inhibitor of N-lysine methyltransf |
| R10983 | MPI-0479605 | MPI-0479605 is an ATP competitive and selective inhibitor of mitotic kinase Mps1 |
| R10984 | ISX-9 (Synonyms: Isoxazole 9) | Isoxazole 9 (Isx-9) is a synthetic promotor of adult neurogenesis by triggering |
