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| Cat.No. | Product name | Product Description |
| R2053519 | HLM006474 | HLM006474 is a pan E2F inhibitor, which inhibits E2F4 DNA-binding with an IC50 o |
| R2053520 | Bindarit (AF2838) | Bindarit (AF2838) is a selective inhibitor of the monocyte chemotactic proteins |
| R2053521 | 9-ING-41 | 9-ING-41 is a potent glycogen synthase kinase-3 (GSK-3) inhibitor. 9-ING-41 indu |
| R2053522 | GDC-046 | GDC-046 is a potent, selective, and orally bioavailable TYK2 inhibitor with Kis |
| R2053523 | Compound Y-1 | Compound Y-1 exerts the best inhibition activity (IC50= 0.21 μM) against NA, whi |
| R2053524 | Fedratinib hydrochloride hydrate (TG-101348 hydrochloride hydrate) | Fedratinib hydrochloride hydrate (TG-101348 hydrochloride hydrate) is a potent, |
| R2053525 | (±)-BAY-1251152 | (±)-BAY-1251152 is a racemic mixture of BAY-1251152. BAY-1251152 is a potent and |
| R2053526 | EX229 | EX229, a Benzimidazole derivative, is a potent and allosteric activator of AMP-a |
| R2053527 | Autogramin-1 | Autogramin-1 potently inhibits autophagy induced by either starvation (IC50=0.17 |
| R2053528 | Encequidar mesylate (HM30181 mesylate; HM30181A mesylate) | Encequidar mesylate (HM30181 mesylate; HM30181A mesylate) is a competitive and p |
| R2053529 | Inarigivir (ORI-9020;SB-9000) | Inarigivir (ORI-9020;SB-9000) is a dinucleotide which can significantly reduce l |
| R2053530 | PF02341066 hydrochloride | Crizotinib hydrochloride (PF-02341066 hydrochloride) is an orally bioavailable, |
| R2053531 | Hydrazinium hydroxide | |
| R2053532 | Eravacycline dihydrochloride (TP-434 dihydrochloride) | Eravacycline dihydrochloride (TP-434 dihydrochloride) is a potent and broad-spec |
| R2053533 | PF-06873600 | PF-06873600 is a selective and orally bioavailable inhibitor of cyclin-dependent |
| R2053534 | Rigosertib sodium (ON-01910 sodium) | Rigosertib sodium (ON-01910 sodium) is a multi-kinase inhibitor and a selective |
| R2053535 | DO-264 | DO-264 is a selective and in vivo-active inhibitor of Abhydrolase Domain Contain |
| R2053536 | PK1-IN-4 (compound 8) | RIPK1-IN-4 (compound 8) is a potent and selective type II kinase inhibitor of re |
| R2053537 | CADD522 | CADD522 is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA |
| R2053538 | Z433927330 | Z433927330 is a potent and selective inhibitor of Aquaporin-7 (AQP7), less poten |
| R2053539 | Deferiprone | Deferiprone is the only orally active iron-chelating drug to be used therapeutic |
| R2053540 | Deferoxamine mesylate | Deferoxamine mesylate is an iron chelator that binds free iron in a stable compl |
| R2090401 | BI 894999 | BRD4 Inhibitor-10 is a potent BRD4-BD1 inhibitor extracted from patent |
| R2090901 | T-5224 | T-5224 is a transcription factor c-Fos/activator protein (AP)-1 inhibi |
| R2090921 | ML406 | ML406 is a small molecular probe that exerts anti-tb activity by inhibiting Mtbb |
