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产品目录

编号化学名称Cas号纯度化学结构
011801MK-80331001917-37-898% 
MK8033 is a novel and specific dual ATP competitive c-Met/Ron inhibitor (IC50=1 nM Wt
011301ML3241222800-79-498% 
ML324 is a potent JMJD2 demethylase inhibitor with demonstrated antiviral activity.
011110MK-1775955365-80-798% 
MK-1775 is a potent and selective Wee1 inhibitor with IC50 of 5.2 nM; hinders G2 DNA
010806MK-2461917879-39-198% 
MK-2461 is a novel ATP-competitive multitargeted inhibitor of activated c-Met.
010606Medetomidine hydrochloride86347-15-198% 
Medetomidine Hydrochloride is an agonist of adrenergic alpha-2 receptor, which is use
010424MK-2048870005-19-998% 
MK-2048 is a second generation integrase inhibitor, intended to be used against HIV i
51627MK76221227923-29-698% by HPLC 
MK-7622isused as adjunctive therapy to acetylcholinesterase inhibitors (AChEIs) for t
123007MK-48271038915-60-498% 
MK-4827 is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 nM/2.1 nM; with grea
122949MK-0752471905-41-698% 
MK-0752 is a moderately potent -secretase inhibitor, which reduces A40 production wit
122819MK8745885325-71-398% 
MK-8745 is a novel Aurora-A specific inhibitor. MK8745 induced apoptotic cell death i
122217MK 886118414-82-798% 
MK 886 is a leukotriene antagonist. It may perform this by blocking the 5-lipoxygenas
122101ML2161430213-30-198% 
ML216 is a potent inhibitor of the DNA unwinding activity of BLM helicase; showing si
121508Masitinib790299-79-598% 
Masitinib is a novel inhibitor for Kit and PDGFR/ with IC50 of 200 nM and 540 nM/800
121504MK-51081010085-13-898% 
MK-5108 is a highly selective Aurora A inhibitor with IC50 of 0.064 nM; 220- and 190-
121502Mandyphos SL-M004-1494227-37-197% 
Coming soon!
121425Marbofloxacin115550-35-198% 
Marbofloxacin is a potent antibiotic of which depends upon its inhibition of DNA-gyra
120712Micafungin sodium208538-73-298% 
Micafungin is an antifungal drug that belongs to the antifungal class of compounds kn
120703Memantine hydrochloride41100-52-198% 
Coming soon!
51128031-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol924909-16-098% by HPLC at 254nm 
1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol
111305MCB-6131162656-22-598% 
Coming soon!
111303MG-132133407-82-698% 
MG-132 is an inhibitor of proteasome with IC50 of 100 nM, and also inhibits calpain w
111015Mocetinostat(MGCD0103)726169-73-998% by HPLC/HNMR 
Mocetinostat is an orally-bioavailable, spectrum-selective HDAC inhibitor. Mocetinost
111013MGCD-265-analog875337-44-3≧98.0%
MGCD-265-analogis a tyrosine kinase inhibitor that selectively targets MET and Axl.MG
102610MDL 2817088191-84-898% 
MDL 28170 is a potent, cell-permeable, and selective inhibitor of calpain and catheps
102207MI-7731303607-60-498% 
MI-773 is an orally available spiro-oxindole HDM2 (human double minute 2) antagonist
101915MK-0822603139-19-198% 
MK-0822 is an inhibitor of cathepsin K with potential anti-osteoporotic activity. It
101204ML2045465-86-198% 
ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 ion cha
92215methyl 2-formyl-1,3-thiazole-4-carboxylate921927-88-098% 
Coming soon!
922135-(methoxycarbonyl)-1-tosyl-1Hpyrrol-3-yl-3-boronic acid916177-00-998% 
Coming soon!
922032-Methyl-1-benzofuran-6-ol54584-24-698% 
Coming soon!