RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
| Cat.No. | Product name | Product Description |
| R2101158 | BAZ2-ICR | BAZ2-ICR is an epigenetic chemical probe and it also is a potent, selective, cel |
| R2101159 | QC6352 | QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM). |
| R2101160 | T-26c | T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibi |
| R2101161 | CDDO-2-P-Im | CDDO-2P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can |
| R2101162 | TP 235 | CDDO-Im is an activator of Nrf2 and PPAR (Kis: 232/344 nM for PPARα/PPARγ). |
| R2101163 | BAY 299 | BAY-299 is a very potent inhibitor. For BRPF2 bromodomains (BD), TAF1 BD2, TAF1L |
| R2101164 | BMS-955176;GSK3532795 | GSK3532795 is a potent, orally active, second-generation HIV-1 maturation inhib |
| R2101165 | Quarfloxin | Quarfloxin is a fluoroquinolone derivative with antineoplastic activity with IC5 |
| R2101166 | BI-3802 | BI-3802 is a highly effective BCL6 depressant, which can inhibit the BTB domain |
| R2101167 | GSK-484 | GSK484 is a potent PAD-4 inhibitor (Protein-arginine deiminase type-4). GSK484 p |
| R2101168 | BAY-850 | BAY-850 is a potent and isoform selective ATPase family AAA domain-containing pr |
| R2101169 | SB-204990 | SB 204990 is an effective and specific ATP citrate lyase enzyme inhibitor. |
| R2101170 | Quarfloxin | Quarfloxin (CX 3543) 是一种具有抗肿瘤活性的氟喹诺酮类衍生物，其靶向抑制RNA pol I的活性，在神经母细胞瘤中的IC50 值在纳摩尔级别 |
| R2101171 | CDDO-dhTFEA (RTA dh404) | CDDO-dhTFEA (RTA dh404), a synthetic oleanane triterpenoid compound, potently ac |
| R2101172 | GLPG0974 | GLPG0974 is an antagonist of free fatty acid receptor-2 (IC50: 9 nM). |
| R2101173 | Disitertide | Disitertide (P144) is an inhibitor of TGF-β1. |
| R2101174 | Alantolactone | Alantolactone(Alant camphor), a sesquiterpene lactone, has potential activity ag |
| R2101175 | Glesatinib | Glesatinib is an orally active and potent dual inhibitor of MET/SMO. Glesatinib |
| R2101176 | Halofuginone | Halofuginone，the competitive inhibitor of prolyl-tRNA synthetase（Ki=18.3 nM），cou |
| R2101177 | UK-383367 | UK-383367 (UK 383367) is a potent and selective inhibitor of BMP-1 (procollagen |
| R2101178 | TP0427736 | TP0427736 is a potent inhibitor of ALK5 kinase activity with an IC50 of 2.72 nM |
| R2101179 | LSKL | LSKL, Inhibitor of Thrombospondin TSP-1(TSP-1) is activation of TGF-β . |
| R2101180 | SMAD3;SIS3 free base | SIS3 free base is a potent and selective Smad3 phosphorylation inhibitor. SIS3 f |
| R2101181 | Oxymatrine | Oxymatrine is an alkaloid isolated from Sophora flavescens, used as the antibiot |
| R2101182 | Oroxin A | Oroxin A has antitussive and expectorant effects. |
