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| Cat.No. | Product name | Product Description |
| R240402251 | SC-22716 | SC-22716 is a potent, competitive, reversible inhibitor of human LTA4 hydrolase, |
| R240402252 | CGS27023A | CGS 27023A is a non-peptidic, potent, and orally active stromelysin inhibitor. |
| R240402253 | DBCO-PEG4-C2-acid | DBCO-PEG4-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis |
| R240402254 | DBCO-PEG4-Val-Cit-PAB-MMAF | DBCO-PEG4-Val-Cit-PAB-MMAF consists a cleavable 4 unit PEG ADC linker (DBCO-PEG4 |
| R240402255 | Arachidonylcyclopropylamide(ACPA) | Arachidonylcyclopropylamide (ACPA) is a potent and selective CB1 receptors agoni |
| R240402256 | CAY10404 | CAY10404 is a potent and selective cyclooxygenase-2 (COX-2) inhibitor with an IC |
| R240402257 | 拟雌内酯 | Coumestrol, a phytoestrogen present in soybean products, exhibits activities aga |
| R240402258 | 氟伐他汀钠 | Fluvastatin sodium (XU 62320) is a first fully synthetic, competitive HMG-CoA re |
| R240402259 | MBCQ | MBCQ is a potent and selective cGMP-specific phosphodiesterase (PDE V; PDE5) inh |
| R240402260 | AG-1478 hydrochloride | AG-1478 hydrochloride is a selective EGFR tyrosine kinase inhibitor with IC50 of |
| R240402261 | VEGFR2-IN-2 | VEGFR2-IN-2 (compound 6e) is a potent and selective VEGFR2 inhibitor with an IC5 |
| R240402262 | Autophagy-IN-A9 | Autophagy-IN-A9 is a bioactive chemical. |
| R240402263 | 4-(2-氟-4-硝基苯氧基)-6,7-二甲氧基喹啉 | 4-(2-Fluoro-4-nitrophenoxy)-6,7-dimethoxyquinoline |
| R240402264 | 4(3H)-Quinazolinone (9CI) | QUINAZOLIN-4(3H)-ONE |
| R240402265 | EN450 | EN450 is a cysteine-reactive covalent molecular glue degrader targeting NF-κB. E |
| R240402266 | JB061 | JB061 is a nonmuscle myosin inhibitor with IC50s of 4.4 μM (Cardiac muscle myosi |
| R240402267 | DSM502 | DSM502 is a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor. DSM502 |
| R240402268 | cyt-PTPε Inhibitor-1 | cyt-PTPε Inhibitor-1 is a potent cytosolic protein tyrosine phosphatase epsilon |
| R240402270 | HT1042 | HT1042 is an inhibitor of the β5i component of the 20S proteasome complex, it is |
| R240402271 | GR-127935 | GR-127935 is a potent and selective 5-HT1B/1D receptor antagonist. |
| R240402272 | PARP/HDAC-IN-1 | PARP/HDAC-IN-1 (compound B102) is a potent dual inhibitor of PARP and HDAC. PARP |
| R240402273 | NGD94-1 | NGD94-1 is a specific dopamine D4 receptor antagonist. NGD94-1 can effectively r |
| R240402274 | 石蒜碱 | Lycorisine |
| R240402275 | 石蒜碱 | Lycorine is a natural alkaloid extracted from the Amaryllidaceae plant. It is a |
| R240402276 | 盐酸石蒜碱 | Lycorine hydrochloride (Narcissine hydrochloride) is VE-cadherin inhibitor,and h |
