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Home > Products
| Cat.No. | Product name | Product Description |
| R0016002 | EN523 | EN523 is a OTUB1 recruiter. EN523 targets a non-catalytic allosteric cysteine C2 |
| R0016003 | VX-150 | VX-150 is an orally active, highly selective NaV1.8 inhibitor. VX-150 has the po |
| R0016004 | Elexacaftor;VX-445 | Elexacaftor (VX-445, Compound 1) is a modulator of cystic fibrosis transmembrane |
| R0016007 | TPN171 | TPN171 is a potent, selective and oral bioavailable inhibitor of phosphodiestera |
| R0016008 | Puromycin dihydrochloride (CL13900 dihydrochloride) | Puromycin dihydrochloride (CL13900 dihydrochloride), an aminonucleoside antibiot |
| R0016009 | Zoledronic acid impurity A | Zoledronic acid impurity A |
| R0016010 | Bendamustine Desmethyl Impurity | N-desmethyl Bendamustine |
| R0016011 | EIDD-2749 | EIDD-2749 (4'-Fluorouridine) is an orally active RdRp inhibitor. EIDD-2749 effec |
| R0016012 | Fludarabine-Cl | Fludarabine-Cl has inhibition effect on RNA adenosine deaminase 1(ADAR1), and ca |
| R0016013 | GW274150 dihydrochloride | GW274150 (dihydrochloride) is a potent, selective, orally active and NADPH-depen |
| R0016014 | GW274150 | GW274150 is a potent, selective, orally active and NADPH-dependent inhibitor of |
| R0016015 | GW274150 phosphate | GW274150 phosphate is a potent, selective, orally active and NADPH-dependent inh |
| R0016016 | BDCRB | BDCRB is a selective Human cytomegalovirus (HCMV) inhibitor through blocking the |
| R0016017 | DL-AP5 | DL-AP5 (2-APV) is a competitive NMDA (N-methyl-D-aspartate) receptor antagonist. |
| R0016018 | DL-AP5 sodium | DL-AP5 (2-APV) sodium is a competitive NMDA (N-methyl-D-aspartate) receptor anta |
| R0016019 | 6-Hydroxy-DOPA | 6-Hydroxy-DOPA is a selective and effective allosteric inhibitor of the RAD52 ss |
| R0016020 | 5,6-Dichlorobenzimidazole riboside | 5,6-Dichlorobenzimidazole riboside (DRB) 是一种核苷类似物，可抑制几种羧基末端结构域激酶，包括酪蛋白激酶 II 和细胞周 |
| R0016022 | AJ-76 | AJ-76 ((+)-AJ 76; (1S,2R)-AJ 76) is a dopamine autoreceptor antagonist. AJ-76 ca |
| R0016023 | (+)-UH 232 | (+)-UH 232 is a partially selective agonist of the D3 receptor with an intrinsic |
| R0016024 | POMHEX | POMHEX, a racemic mixture and a cell-permeable pivaloyloxymethyl (POM) proagent |
| R0016025 | Bartsioside | Bartsioside is an anti-inflammatory agent which can be extracted from C. deserti |
| R0016026 | AZD8797 | AZD8797 (KAND567) is an allosteric non-competitive and orally active antagonist |
| R0016027 | Chelerythrine | Chelerythrine is a natural alkaloid, acts as a potent and selective Ca2+/phospho |
| R0016028 | Chelerythrine chloride | Chelerythrine chloride is a potent, cell-permeable inhibitor of protein kinase C |
| R0016029 | AMT hydrochloride | AMT hydrochloride is an iNOS inhibitor. |
