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Cat.No. | Product name | Product Description |
R21122006 | C-170 | STING-IN-2 (C-170) is a potent and covalent STING inhibitor. STING-IN-2 efficien |
R21122007 | DPI-201-106;SDZ-201106 | DPI-201-106 is a cardioselective inhibitor of the TTX-resistant h1 Na channel in |
R21122008 | LASV inhibitor 3.3 | LASV inhibitor 3.3 (LAMP1 inhibitor 3.3) is a specific inhibitor of Lassa fever |
R21122009 | GSK3987 | GSK3987 is a potent and specific liver X receptor (LXR) dual agonist of LXRalpha |
R21122010 | L82-G17 | |
R21122011 | Arimoclomol;BRX-220 | Arimoclomol (BRX-220 Free Base) is a coinducer of heat shock protein (HSP). |
R21122012 | AGI-001;Espindolol | Espindolol is a β-adrenoceptor antagonist potentially for the treatment of cache |
R21122013 | PDZ1i | PDZ1i (113B7) is a specific inhibitor of MDA-9/Syntenin activity, which inhibits |
R21122014 | ARN-21934 | Arn-21934 is a novel and highly selective human topoisomerase IIα inhibitor with |
R21122015 | SID 26681509 | SID 26681509 is a potent, reversible, competitive and selective inhibitor of hum |
R21122016 | FFN246 | FFN246 is a novel fluorescent substrate of 5-hydroxytryptamine transporter and v |
R21122017 | superstat | Novel selective histone deacetylase 6 (HDAC6) inhibitors enhance immunotherapy i |
R21122018 | VU-29 | Vu-29 is a positive allosteric regulator of metabolic glutamate 5 (mGlu5) recept |
R21122019 | Phevamine A | Novel plant immune response inhibitors. |
R21122020 | ML202 | |
R21122021 | Adaphostin | Adaphostin is a novel activator of Fas-mediated death pathway in Bcr/Abl-positiv |
R21122022 | BRD0418 | Novel upregulation factors expressed by TRIB1 lead to reprogramming of hepatic l |
R21122023 | BTA-EG4 hydrate | |
R21122024 | BRD-K98645985 | Brd-k98645985 is a class of 12 yuan macrocyclic lactam and is also an inhibitor |
R21122025 | GSK778 | GSK778 (iBET-BD1) is a potent and selective BD1 bromodomain inhibitor of the BET |
R21122026 | Synucleozid | Synucleozid (NSC 377363) is a potent inhibitor of the SNCA mRNA that encodes α-s |
R21122027 | APS6-45 | APS6-45 is an orally active tumor-calibrated inhibitor (TCI). APS6-45 inhibits R |
R21122028 | SW-100 | SW-100, a selective histone deacetylase 6 (HDAC6) inhibitor with an IC50 of 2.3 |
R21122029 | SB-224289 hydrochloride | SB-224289 hydrochloride is a selective 5-HT1B receptor antagonist, with anxiolyt |
R21122030 | SKI-178 | SKI-178 is a potent sphingosine kinase-1 (SphK1) and SphK2 inhibitor. SKI-178 is |