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Structure Cat No. Product Name CAS No. Product Description
MEK/PI3K-IN-2 V47224 MEK/PI3K-IN-2 2281803-33-4 MEK/PI3K-IN-2 (compound 6s) is a potent MEK/PI3K inhibitor (antagonist) with IC50s of 352 nM (MEK1), 107 nM (PI3Kα), and 137 nM (PI3Kδ).
MEK1/2-IN-2 V49622 MEK1/2-IN-2 MEK1/2-IN-2 is a potent ATP-competitive MEK1/2 inhibitor that is equally effective against wild-type MEK1/2 and a panel of MEK1/2 mutant cell lines.
Melatonin receptor agonist 1 V47308 Melatonin receptor agonist 1 2411150-76-8 Melatonin receptor agonist (activator) 1 (compound 20c) is a potent melatonin receptor (MT) agonist with Kis of 108 nM (MT2) and 1140 nM (MT1).
Melengestrol-d5 V48492 Melengestrol-d5 Melengestrol-d5 is the deuterium labelled form of Melengestrol.
Mem-C1C18 V43957 Mem-C1C18 Mem-C1C18 is a polarity-sensitive fluorescent probe with excellent plasma membrane anchorage, high brightness, and sensitive response to environmental polarity by changing fluorescence lifetime, may be utilized to quantitatively detect plasma membrane polarity changes during ferroptosis.
Meobal-d3 V46424 Meobal-d3 Meobal-d3 is a deuterium labelled form of Meobal.
MeOSuc-AAPV-AMC V42220 MeOSuc-AAPV-AMC 72252-90-5 MeOSuc-AAPV-AMC is a fluorogenic substrate for human leukocyte and porcine pancreatic elastase (Km: 362 μM, Ex=380 nm, Em=460 nm).
MeOSuc-Ala-Ala-Pro-Val-pNA V42209 MeOSuc-Ala-Ala-Pro-Val-pNA 70967-90-7 MeOSuc-Ala-Ala-Pro-Val-pNA is a sensitive fluorescent substrate for human leukocytes and porcine pancreatic elastase.
MES monohydrate V45975 MES monohydrate 145224-94-8 MES (2-Morpholinoethanesulphonic acid) monohydrate is a buffering agent used in biology and biochemistry.
MES potassium V43213 MES potassium 39946-25-3 MES (2-Morpholinoethanesulphonic acid) potassium is a buffering agent in biology and biochemistry.
Mestranol-d2 V48421 Mestranol-d2 Mestranol-d2, estrogen receptor agonist
Mestranol-d4 V48470 Mestranol-d4 Mestranol-d4, estrogen receptor agonist
MET kinase-IN-3 V47228 MET kinase-IN-3 1446324-02-2 MET kinase-IN-3 (compound 8) is an orally bioavailable MET inhibitor (antagonist) with IC50 of 9.8 nM.
Metachromins X V46026 Metachromins X 2408641-10-9 Metachromins X is a sesquiterpene quinone that blocks cell cycle progression in S/G2/M phases of HeLa/Fucci2 cells.
Metaflumizone-d4 V48611 Metaflumizone-d4 Metaflumizone-d4, sodium channel blocker
Metallo-β-lactamase-IN-2 V44478 Metallo-β-lactamase-IN-2 1501705-61-8 Metallo-β-lactamase-IN-2 is a novel andpotent metallo-β-lactamases (MBL) inhibitor with IC50 values of 0.1 μM (VIM-1), 1.3 μM (NDM-1), and 5.0 μM (IMP-7), respectively.
Metallo-β-lactamase-IN-5 V47249 Metallo-β-lactamase-IN-5 1417737-65-5 Metallo-β-lactamase-IN-5 (compound 5c) is a potent metallo-β-lactamase (MBL) inhibitor.
Metallo-β-lactamase-IN-6 V49469 Metallo-β-lactamase-IN-6 1439899-44-1 Metallo-β-lactamase-IN-6 is a novel VIM-Type metallo-β-lactamase inhibitor withantibacterial activity.
Metallo-β-lactamase-IN-7 V49472 Metallo-β-lactamase-IN-7 2752453-58-8 Metallo-β-lactamase-IN-7 is a novel VIM-Type metallo-β-lactamase inhibitor with the ability topotentiate the antibacterial activity of Meropenem against the Gram-negative bacterial strains.
Metaxalone-d6 V48462 Metaxalone-d6 1189944-95-3 Metaxalone-d6 is the deuterium labelled form of Metaxalone.
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