RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
Home > Products
| Cat.No. | Product name | Product Description |
| R2032303 | AG-1478;Tyrphostin AG-1478;NSC 693255 | AG-1478 is a selective EGFR tyrosine kinase inhibitor with IC50 of 3 nM. |
| R2032304 | KPT9274 | KPT-9274 is an orally bioavailable, dual PAK4/Nicotinamide phosphoribosyltransfe |
| R2032305 | Lanabecestat;AZD3293;LY3314814 | Lanabecestat (AZD3293) is a potent, highly permeable, orally active and blood-br |
| R2032306 | RX-518 | EGFR-IN-3 is an epidermal growth factor receptor (EGFR) inhibitor. |
| R2032307 | LY3214996 | LY3214996 is a highly selective inhibitor of ERK1 and ERK2, with IC50 of 5 nM fo |
| R2032308 | TMP195 | TMP195 is a selective class IIa histone deacetylase (HDAC) inhibitor with an IC5 |
| R2032309 | AM966 | AM966 is a high affinity, selective, oral LPA1-antagonist, inhibits LPA-stimulat |
| R2032310 | 6-OAU;GTPL5846 | 6-OAU(GTPL5846; 6-n-octylaminouracil) is a surrogate agonist of GPR84; activates |
| R2032311 | AB-423 | AB-423 is an inhibitor of HBV capsid assembly, and potent inhibits HBV replicati |
| R2032312 | ALW-II-41-27 | ALW-II-41-27 is a Eph family tyrosine kinase inhibitor with an IC50 of 11 nM for |
| R2032313 | Linrodostat;BMS-986205;ONO-7701 | Linrodostat (BMS-986205) is a selective and irreversible indoleamine 2,3-dioxyge |
| R2032314 | dBET1 | dBET1 is a potent BRD4 protein degrader based on PROTAC technology with an EC50 |
| R2032315 | AZD5582 | AZD5582 is an antagonist of the inhibitor of apoptosis proteins (IAPs), which bi |
| R2032316 | Cilofexor(GS-9674) | Cilofexor (GS-9674) is a farnesoid X receptor (FXR) agonist. |
| R2032317 | AG-1557 | AG1557 is a specific and ATP competitive inhibitor of epidermal growth factor re |
| R2032318 | CPI-1205 | CPI-1205, a highly potent and selective EZH2 inhibitor (biochemical IC50=2 nM, c |
| R2032320 | L-701324 | L-701324 is an orally active and long acting anticonvulsant with high affinity a |
| R2032321 | Tanzisertib(CC-930) | Tanzisertib (CC-930) is a potent JNK1/2/3 inhibitor with IC50s of 61/7/6 nM, res |
| R2032322 | 1-NM-PP1 | 1-NM-PP1, a cell-permeable PP1 analog, is a potent Src family kinases inhibitor |
| R2032323 | MK-8353(SCH900353) | MK-8353 (SCH900353) is a potent, selective and orally available ERK1/2 inhibitor |
| R2032324 | IWP-O1 | IWP-O1 is a highly potent Porcupine (Porcn) inhibitor, with an EC50 of 80 pM in |
| R2032325 | (-)-Blebbistatin | (-)-Blebbistatin is an S enantiomer of blebbistatin.Blebbistatin is a potent and |
| R2032326 | 4EGI-1 | 4EGI-1 is an inhibitor of eIF4E/eIF4G interaction, with a Kd of 25 μM against eI |
| R2032327 | 6H05 | 6H05 is a selective, and allosteric inhibitor of oncogenic mutant K-Ras(G12C).IC |
| R2032328 | A-205804 | A-205804 is a potent and selective inhibitor of E-selectin and ICAM-1 expression |
