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| Cat.No. | Product name | Product Description |
| R2304335 | VU0155041 | VU0155041 is a potent, selective positive allosteric modulator (PAM) of mGluR4, |
| R2304336 | SIRT2-IN-8 | SIRT2-IN-8 is a potent SIRT2 inhibitor. SIRT2-IN-8 can be used for Huntington’s |
| R2304337 | TRC051384 | TRC051384 is a heat shock protein 70 (HSP70) inducer. |
| R2304339 | IXA4 | IXA4 is a highly selective, non-toxic IRE1/XBP1s activator. IXA4 activates IRE1/ |
| R2304340 | EN106 | EN106 is a potent inhibitor of FEMIB. EN106 is a cysteine-reactive covalent liga |
| R2304341 | Inaxaplin(VX-147) | Inaxaplin (VX-147) is an orally active apolipoprotein L1 (APOL1) function inhibi |
| R2304342 | G15 | G15 is a high affinity and selective G-protein-coupled estrogen receptor (GPER/G |
| R2304343 | NCT-58 | NCT-58 is a potent inhibitor of C-terminal HSP90. NCT-58 does not induce the hea |
| R2304344 | INDY | INDY is a potent and ATP-competitive Dyrk1A and Dyrk1B inhibitor with IC50s of 0 |
| R2304345 | Pachymic acid | Pachymic acid is a lanostrane-type triterpenoid from P. cocos. Pachymic acid inh |
| R2304347 | Lys05 (Lys01 trihydrochloride) | Lys05 (Lys01 trihydrochloride) is a novel lysosomal autophagy inhibitor with IC5 |
| R2304348 | CAY10434 | CAY 10434 is a potent CYP4A hydroxylase inhibitor. CAY 10434 improves contractil |
| R2304349 | IM-54 | IM-54 is a selective inhibitor of oxidative stress-induced necrosis. IM-54 shows |
| R2304350 | ZINC05007751 | ZINC05007751 is a potent NIMA-related kinase NEK6 inhibitor with an IC50 of 3.4 |
| R2304351 | MK-8245 analog | MK-8245 is a potent, liver-targeted stearoyl-CoA desaturase (SCD) inhibitor, wit |
| R2304352 | Curcumin Glucuronide | |
| R2304353 | Elamipretide | Elamipretide (SS-31,MTP-131,Bendavia) is a small mitochondrially-targeted tetrap |
| R2304354 | AS2863619 | AS2863619 enables conversion of antigen-specific effector/memory T cells into Fo |
| R2304355 | BLU-945 | BLU-945 is a potent, highly selective, reversible and orally active epidermal gr |
| R2304356 | VH032-cyclopropane-F | VH032-cyclopropane-F is the VH032-based VHL ligand. VH032-cyclopropane-F can be |
| R2304357 | TP-064 | TP-064 is a potent and selective proteinarginine methyltransferase 4 (PRMT4; CAR |
| R2304358 | MK-212 (CPP) hydrochloride | MK-212 (CPP) monohydrochloride is a centrally acting 5-HT1C/5-HT2 agonist. MK-21 |
| R2304359 | PF07104091 | PF-07104091 inhibits CDK2, which may lead to cell cycle arrest, induce cell apop |
| R2304360 | INCB054329 | INCB054329 is a potent BET inhibitor. |
| R2304361 | ML337 | ML337 is a selective and brain-penetrant negative allosteric modulator of mGlu3, |
