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Home > Products
| Cat.No. | Product name | Product Description |
| R2101020 | CRT0066101 dihydrochloride | CRT0066101 is a specific inhibitor of all Protein kinase D (PKD) isoforms. |
| R2101021 | AA92593 | AA92593 (Opn4 Antagonist) is a potent antagonist of melanopsin-mediated phototra |
| R2101022 | ML335 | ML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1 |
| R2101023 | VK-II-36 | VK-II-36 is a carvedilol analog that suppresses sarcoplasmic reticulum (SR) Ca(2 |
| R2101024 | YMU1 | ML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1 |
| R2101025 | ML254 | ML254 is shown to competitively interact with the MPEP allosteric binding site. |
| R2101026 | PU-H54 | A potent, selective Grp94 inhibitor. |
| R2101027 | ML303 | ML303 is a pyrazolopyridine influenza virus nonstructural protein 1 (NS1) antago |
| R2101028 | Nisoxetine hydrochloride | Nisoxetine hydrochloride is a potent and selective inhibitor of noradrenaline tr |
| R2101029 | ASN03576800 | ASN03576800 is an inhibitor of the VP40 matrix protein. |
| R2101030 | HA-155 | HA155 (Autotaxin Inhibitor IV), a boronic acid-based compound, inhibits autotaxi |
| R2101031 | CYM5520 | noncompetitive allosteric agonist of S1P2 |
| R2101032 | CRT5 | CRT5 (CRT0066051), a pyrazine benzamide, is a potent and selective PKD inhibitor |
| R2101033 | BMS453 | BMS-189453 (BMS189453, BMS453) is a synthetic retinoid that acts as an agonist o |
| R2101034 | Mps1-IN-3 | Mps1-IN-3 is a potent and selective MPS1 kinase inhibitor, with an IC50 of 50 nM |
| R2101035 | OS-3-106 | OS-3-106 is a novel dopamine D3 receptor-selective partial agonist. |
| R2101036 | NSC-703786 | A potent, selective antitumour agent through activation the aryl hydrocarbon rec |
| R2101037 | GW779439X | GW779439X is an inhibitor of cyclin dependent kinase. |
| R2101038 | RO2959 hydrochloride | RO2959 hydrochloride is a potent and selective CRAC channel inhibitor with an IC |
| R2101039 | Flupenthixol dihydrochloride | cis-(Z)-Flupentixol dihydrochloride is a potent and selective DA D1/D2 receptor |
| R2101040 | 4BP-TQS | 4BP-TQS is an allosteric agonist of α7 subunit-containing neuronal nicotinic ace |
| R2101041 | B355252 | B355252 is a neuroprotective agent that potentiates nerve growth factor (NGF)-in |
| R2101042 | GSK 2830371 | GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 |
| R2101043 | MONNA | MONNA is a potent TMEM16A (Anoctamin-1) blocker (IC50 = 80 nM). Exhibits >100 |
| R2101044 | TAE-1 | TAE-1 is an inhibitor of amyloid-β fibril formation and aggregation, suggesting |
