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 |
| R2304327 | CAY10444 (BML-241) | CAY10444 (BML-241) is a sphingosine-1-phosphate 3 (S1P3) antagonist. CAY10444 in |
| R2304328 | Saroglitazar | Saroglitazar is a novel peroxisome proliferator-activated receptor (PPAR) agonis |
| R2304329 | Ozenoxacin | Ozenoxacin is a nonfluorinated quinolone antibacterial, which shows potent activ |
| R2304330 | BI-6015 | BI-6015 is a hepatocyte nuclear factor 4α (HNF4α) antagonist that can inhibit th |
| R2304331 | FPR Agonist 43 | FPR Agonist 43 (compound 43) is a dual formyl peptide receptor 1 (FPR1) and form |
| R2304332 | GTP14564 | CAS NO.：34823-86-4Product Name：GTP14564Synonyms：GTP14564EINEC:Molecular Formula： |
| R2304333 | ML10302 hydrochloride | ML 10302 hydrochloride is a potent and selective 5-HT4 receptor agonist, with an |
| R2304334 | JNJ17203212 | JNJ-17203212 is a selective, potent and competitive TRPV1 antagonist. JNJ-172032 |
| 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 |
