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| Cat.No. | Product name | Product Description |
| R11037 | FPS-ZM1 | FPS-ZM1 is a high-affinity RAGE inhibitor with a Ki of 25 nM. |
| R11039 | SW044248;SW-044248 | SW044248 is a non-canonical topoisomerase I inhibitor, and selectively toxic for |
| R11041 | LLY 507 | LLY-507 is a potent and selective inhibitor of protein-lysine methyltransferase |
| R10894 | Elacridar (Synonyms: GF120918; GW0918; GG918; GW120918) | Elacridar (GF120918; GW0918) is a P-glycoprotein inhibitor, and has been used b |
| R10932 | BAY 11-7082 | BAY 11-7082 is a NF-κB inhibitor, inhibits TNFα-induced IκBα phosphorylation wit |
| R10966 | PS-1145 | PS-1145 is a specific IKK inhibitor with IC50 of 88 nM. |
| R10972 | SB202190 ; FHPI | SB202190 (FHPI) is a potent p38 MAPK inhibitor targeting p38α/β with IC50 of 50 |
| R10999 | Taladegib;LY2940680 | Taladegib (LY2940680) binds to the Smoothened (Smo) receptor and potently inhibi |
| R11027 | G-749 | G-749 is a novel and potent FLT3 inhibitor with IC50 of 0.4 nM, 0.6 nM and 1 nM |
| R11044 | ARRY-380 analog | ARRY-380 analog, an inhibitor of EGFR (ErbB1), is extracted from patent WO201515 |
| R11045 | Danusertib;PHA-739358 | Danusertib is a pyrrolo-pyrazole and aurora kinase inhibitor with IC50 of 13, 79 |
| R11046 | PHA-680632 | N/A |
| R11047 | BMS-3 | BMS-3 is a potent LIMK inhibitor with IC50s of 5 nM and 6 nM for LIMK1 and LIMK2 |
| R11048 | BMS-5 (Synonyms: LIMKi 3) | BMS-5 (LIMKi 3) is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 |
| R11049 | PCI34051;PCI-34051 | PCI-34051 is a potent and selective HDAC8 inhibitor with IC50 of 10 nM, with > |
| R11050 | SCR7 | SCR7 is a DNA Ligase IV inhibitor with anticancer activity and is also a CRISPR |
| R11051 | SB-3CT | SB-3CT is a potent and competitive matrix metalloproteinase MMP-2 and MMP-9 inhi |
| R11052 | PF-2545920 | PF-2545920 is a potent and selective PDE10A inhibitor with IC50&n |
| R11053 | FIIN-2 | FIIN-2 is an irreversible inhibitor of FGFR with an IC50 of 3.1, 4.3, 27, and 45 |
| R11054 | AP26113 | ALK-IN-1 (Brigatinib analog) is a potent and selective active inhibitor of anapl |
| R11055 | E7080 Mesylate;lenvatinib Mesylate | Lenvatinib mesylate (E7080 mesylate), an oral, multi-targeted tyrosine kinase in |
| R11056 | Vandetanib | N/A |
| R11057 | Eliglustat hemitartrate (Synonyms: Genz-112638; Eliglustat tartrate) | Eliglustat tartrate (Genz-112638), a specific inhibitor of glucosylceramide synt |
| R11058 | Elagolix (NBI-56418) | Elagolix is a highly potent, selective, orally-active, short-duration, non-pepti |
| R11063 | Genz-123346 free base | Genz-123346 (free base) is an inhibitor of GL1 synthase that blocks the conversi |
