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Home > Products
| Cat.No. | Product name | Product Description |
| RH133222 | Darizmetinib | Darizmetinib (HRX-0215) is an orally active, potent and selective inhibitor of m |
| RH133223 | Givinostat hydrochloride | Givinostat (ITF-2357) hydrochloride is a HDAC inhibitor with an IC50 of 198 and |
| RH133225 | Braco-19 trihydrochloride | Braco-19 trihydrochloride is a potent telomerase/telomere inhibitor, preventing |
| RH133226 | CTA056 | CTA056 is an ITK (IL-2-inducible T-cell kinase) inhibitor with an IC50 of 0.1 μM |
| RH133227 | Ralometostat(TNG908) | TNG908 is a MTAP synergistic PRMT5 inhibitor. |
| RH133228 | FFN511 | FFN511 is a potent fluorescent false neurotransmitters (FFNs) that targets neuro |
| RH133229 | APG-2449 | APG-2449 is an orally active inhibitor for BCL-2 and multikinase (ALK/FAK/ROS1) |
| RH133231 | KYP-2047 | KYP-2047 is a potent and BBB-penetrating prolyl-oligopeptidase (POP) inhibitor, |
| RH133232 | MET kinase-IN-2 | MET kinase-IN-2 is a potent, selective, orally bioavailable MET kinase inhibitor |
| RH133233 | Golcadomide(CC-99282) | Golcadomide (CC-99282) is a potent and orally active CRBN E3 ligase modulator (C |
| RH133234 | HIF-2α-IN-2 | HIF-2α-IN-2 is a hypoxia-inducible factors (HIF-2α) inhibitor extracted from pat |
| RH133235 | preQ1 dihydrochloride | preQ1 dihydrochloride is a modified, guanine-derived nucleobase and a precursor |
| RH133237 | ZD 7155(hydrochloride) | ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antago |
| RH133238 | Androgen receptor antagonist 1 | Androgen receptor antagonist 1 is an orally available full androgen receptor (AR |
| RH133239 | GW-803430 | GW-803430 (GW-3430) is a potent and selective melanin-concentrating hormone rece |
| RH133243 | SB-269970 hydrochloride | SB-269970 hydrochloride is a potent, selective and brain-penetrant 5-HT7 recepto |
| RH133244 | Naporafenib(LXH254) | Naporafenib (LXH254) is a potent, selective, orally active, type II BRAF and CRA |
| RH133245 | AG-270 | AG-270 is an allosteric, noncompetitive, first-in-class, reversible and orally a |
| RH133246 | MC1742 | MC1742 is a potent HDAC inhibitor, with IC50s of 0.1 μM, 0.11 μM, 0.02 μM, 0.007 |
| RH133247 | MitoTracker Green FM | Mito-Tracker Green is a green fluorescent dye that selectively accumulates in th |
| RH133249 | PD-116948(DPCPX) | DPCPX (PD 116948), a xanthine derivative, is a highly potent and selective Adeno |
| RH133251 | GSK269962A | GSK269962A (GSK 269962) is a potent ROCK inhibitor with IC50s of 1.6 and 4 nM fo |
| RH133252 | JLK-6 | JLK-6 markedly reduce the production of amyloid β-peptide (Aβ) by amyloid-β Prec |
| RH133253 | MAT2A-IN-9 | MAT2A-IN-9 |
| RH133255 | BMS-509744 | BMS-509744 is a potent, selective and ATP competitive Itk inhibitor with an IC50 |
