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Home > Products
| Cat.No. | Product name | Product Description |
| RH133310 | Nicotinamide riboside chloride | Nicotinamide riboside chloride, also known as NR and SRT647, is a pyridine-nucle |
| RH133311 | PSI-697 | PSI-697 is an oral P-selectin inhibitor with an IC50 of 125 μM. |
| RH1333522 | PELI1-IN-1 | PELI1-IN-1 |
| RH133315 | Lu AE51090 | Lu AE51090 is selective muscarinic M1 receptor agonist with blood-brain barrier |
| RH133314 | Olomoucine II | Olomoucine II is a potent CDK inhibitor with IC50 values of 0.06, 0.1, 0.45, 7.6 |
| RH133313 | Callocyanine | Callocyanine |
| RH133312 | Mexiletine | Mexiletine is an orally effective antiarrhythmic agent. Mexiletine exerts its ef |
| RH1333523 | ML314 | ML314 is a potent, BBB-penetrant and β-arrestin biased molecule agonist of NTR1 |
| RH133317 | Chiauranib | Chiauranib (CS2164) is an orally active multi-target inhibitor against tumor ang |
| RH133319 | β-Zearalenol | β-Zearalenol is a non-steroidal estrogenic mycotoxin synthesized by Fusarium spe |
| RH133318 | 2'3'-c-di-AM(PS)2 (Rp,Rp) disodium salt (ADU-S100 disodium salt) | 2’3’-c-di-AM(PS)2 (Rp,Rp) disodium salt (ADU-S100 disodium salt) is an activator |
| RH133320 | SB-423562 | SB-423562 is a short-acting calcium-sensing receptor (CaR) antagonist. |
| RH133321 | K-756 | K-756 is a direct and selective tankyrase (TNKS) inhibitor, which inhibits the A |
| RH133322 | XL01126 | XL01126 is a potent LRRK2 PROTAC (DC50: 14 nM (G2019S LRRK2) and 32 nM (WT LRRK2 |
| RH1333645 | SSAA09E2 | SSAA09E2 is an inhibitor of SARS-CoV (Severe acute respiratory syndrome-Coronavi |
| RH133323 | Aleniglipron | Aleniglipron is an orally active glucagon-like peptide-1 receptor (GLP-1R) agoni |
| RH133324 | AMG410 | AMG410 is a non-covalent and selective pan-KRAS inhibitor with IC50 values of 1- |
| RH133325 | YD-851 | Pyrido[2′,3′:4,5]pyrrolo[3,2-e]indazole, 8-(1,4-dimethyl-1H-1,2,3-triazol-5-yl)- |
| RH133326 | NAD 299 hydrochloride | Robalzotan hydrochloride (NAD-299 hydrochloride) is a potent and selective 5-Hy |
| RH133327 | BMS-986470 | BMS-986470, a HbF-activating CRBN E3 ligase modulator (CELMoD), is an orally act |
| RH133328 | FN-1501 | FN-1501 is a potent inhibitor of FLT3 and CDK, with IC50s of 2.47, 0.85, 1.96, a |
| RH133329 | AZD4573 | AZD4573 is a potent and highly selective CDK9 inhibitor (IC50 of <4 nM). |
| RH133330 | Hesperadin | Hesperadin is an ATP competitive indolinone inhibitor of Aurora A and B. Hespera |
| RH133331 | BET-BAY 002 | BET-BAY 002 is a potent BET inhibitor; shows efficacy in a multiple myeloma mode |
| RH133332 | PXS-4728 | PXS-4728A (BI-1467335) is a potent and orally active semicarbazide-sensitive ami |
