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| Cat.No. | Product name | Product Description |
| R10908 | UNC-2025; UNC2025 | UNC2025 is a potent and orally bioavailable Mer/Flt3 dual inhibitor with IC50 of |
| R10911 | Motolimod;VTX-2337; VTX-378 | Motolimod (VTX-2337) is a selective and potent Toll-like receptor (TLR) 8 agonis |
| R10913 | Vipadenant; BIIB014 | Vipadenant(BIIB-014) is an adenosine A2a antagonist with Ki of 1.3 nM; less pote |
| R10914 | RGB-286638 | RGB-286638 free base is a novel CDK inhibitor with IC50s of 1 nM/2 nM/3 nM/4 nM/ |
| R10916 | SKF-86002 | SKF-86002 is a potent inhibitor of p38 MAP kinase wit IC50 of 0.5-1 uM; inhibits |
| R10919 | Defactinib;VS-6063; PF-04554878 | Defactinib (VS-6063; PF-04554878) is a novel FAK inhibitor with potential antian |
| R10926 | ZK-811752; BX 471 | BX471 (ZK-811752) is an orally active, potent and selective non-peptide CCR1 ant |
| R10931 | Calcitriol; Vitamin D3 | Calcitriol is the hormonally active form of vitamin D. |
| R10935 | AZD8186 | N/A |
| R10937 | AZD9496 | AZD9496 is a potent and selective estrogen receptor (ERα) antagonist with an IC5 |
| R10939 | BMS-911543 | BMS-911543 is a selective JAK2 inhibitor, with IC50s of 1.1 nM, less selective a |
| R10940 | PRT-060318;PRT318 | PRT-060318 (PRT318) is a novel selective inhibitor of the tyrosine kinase Syk wi |
| R10946 | Flibanserin;BIMT-17; BIMT-17BS | Flibanserin (BIMT-17) is a full agonist of the serotonin 5-HT1A receptor (Ki=1 n |
| R10948 | Lificiguat (YC-1) | Lificiguat binds to the β subunit of soluble guanylyl cyclase(sGC) with Kd of 0. |
| R10955 | RU-58841 | N/A |
| 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 |
| R10968 | FPH2; BRD-9424 | FPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-deriv |
| R10971 | NU-2058;NU2058 | NU2058 (O6-(Cyclohexylmethyl)guanine) is a potent, competitive and guanine-based |
| 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. |
| 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 |
| R10984 | ISX-9 (Synonyms: Isoxazole 9) | Isoxazole 9 (Isx-9) is a synthetic promotor of adult neurogenesis by triggering |
