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| Cat.No. | Product name | Product Description |
| R0012055 | diABZI STING agonist-1 | diABZI STING agonist-1 is a selective stimulator of interferon genes (STING) rec |
| R0012056 | STING agonist-3 | STING agonist-3, extracted from patent WO2017175147A1 (example 10), is a selecti |
| R0012057 | CC-885 | CC-885 is a cereblon (CRBN) modulator with potent anti-tumour activity. CC-885 i |
| R0012058 | NVP-DKY709 | NVP-DKY709 is a potent IKZF2 inhibitor for the research of cancers. |
| R0012059 | Migoprotafib(GDC-1971) | Migoprotafib (GDC-1971) (compound 199) is a SHP2 inhibitor. |
| R0012060 | G150 | G150 is a highly selective human cyclic GMP-AMP synthase (h-cGAS) inhibitor with |
| R0012061 | LSN3318839 | LSN3318839 is an orally efficacious positive allosteric modulator of the glucago |
| R0012062 | (S,R)-LSN3318839 | (S,R)-LSN3318839 is the stereoisomer of LSN3318839 (HY-142162). LSN3318839 is an |
| R0012063 | GLP-1受体激动剂1 | Orforglipron (LY3502970) (Compound 67) is an orally active agonist for Glucagon- |
| R0012064 | AZD0780(PCSK9-IN-12) | PCSK9-IN-12 is a heteroaryl compound. PCSK9-IN-12 has bind affinity for PCSK9 wi |
| R0012065 | Tri-GalNAc(OAc)3 TFA | Tri-GalNAc(OAc)3 TFA is a tri-GalNAc ligand that can be used for the synthesis o |
| R0012066 | 1426159-34-3 | |
| R0012067 | (3R,5S)-5-((双(4-甲氧基苯基)(苯基)甲氧基)甲基)吡咯烷-3-醇 | |
| R0016001 | DPO-1 | DPO-1 is a potent inhibitor of the voltage-gated potassium channel subtype Kv1.5 |
| 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 |
