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Cat. No.	Product Name	Field of Application
DC3160	Montelukast Sodium Featured	Montelukast belongs to a group of medications known as leukotriene receptor antagonists.
DC8931	Mosapride	Mosapride is a gastroprokinetic agent that acts as a selective 5HT4 agonist.
DC12485	Mosedipimod	Mosedipimod (EC-18, 1-palmitoyl-2-linoleoyl-3-acetylglycerol) is a synthetic monoacetyldiaglyceride that stimulates T cell production of IL-2, IL-4, IL-12, IFN-γ, and GM-CSF in vitro.
DC7200	Motesanib Diphosphate (AMG-706) Featured	Motesanib (AMG-706) is a potent ATP-competitive inhibitor of VEGFR1/2/3 with IC50 of 2 nM/3 nM/6 nM, respectively; similar activity against Kit, ~10-fold more selective for VEGFR than PDGFR and Ret.
DC10284	Motesanib Featured	Motesanib is a potent ATP-competitive inhibitor of VEGFR1/2/3 with IC50s of 2 nM/3 nM/6 nM, respectively, and has similar activity against Kit, and is appr 10-fold more selective for VEGFR than PDGFR and Ret.
DC8815	Motolimod (VTX-2337) Featured	Motolimod (VTX-2337) is a novel TLR8 agonist that activates NK cells and augments ADCC.
DC4226	Moxifloxacin hydrochloride Featured	Moxifloxacin(Avelox, Avalox) is a fourth generation synthetic fluoroquinolone antibacterial agent.
DCAPI1331	Moxonidine	Moxonidine
DCAPI1572	Moxonidine hydrochloride	Moxonidine hydrochloride
DC10326	Mozavaptan	Mozavaptan (OPC31260) is a orally effective, nonpeptide vasopressin V2 receptor antagonist with an IC50 of 14 nM.
DC22554	MP-A08	MP-A08 is a first-in-class, highly selective, ATP competitive sphingosine kinase (SphK) inhibitor (Ki of 6.9/27 uM for SK2/SK1).
DC11856	MPC-0767	MPC-0767 (MPC0767, MPC3100 mesylate hydrate) is an L-alanine ester prodrug of MPC-3100, which is a potent, selective, orally bioavailable Hsp90 inhibitor with IC50 of 0.14 uM.
DC22290	Aranidipine (MPC1304) Featured	MPC1304 is a Ca2+ channel antagonist with potent and long-lasting antihypertensive effects. IC50 & Target: Ca2+ Channel.
DC7202	MPC-3100	MPC-3100 is an orally bioavailable, synthetic, second-generation small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity.
DC8339	MPEP hydrochloride Featured	MPEP is a potent, highly selective non-competitive antagonist at the mGlu5a receptor subtype (IC50 = 36 nM) while having no agonist or antagonist activities at the mGlu1b receptor at concentrations up to 30 μM.
DC1015	MPEP Featured	MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM.
DC20464	mPGES1-IN-16	mPGES1-IN-16 is a potent and selective mPGES-1 inhibitor with IC50 of 1 nM.
DC20465	mPGES1-IN-17d	mPGES1-IN-17d is a potent, selective mPGES-1 inhibitor with enzyme IC50 of 8 nM, A549 cell IC50 of 16.24 nM, human whole blood IC50 of 249.9 nM.
DC11241	MP-HJ-1b	MP-HJ-1b is a novel potent inhibitor of microtubule and tumor cell growth, binds the colchicine pocket at the intra-dimer interface, depolymerizes microtubules and affects spindle formation.
DC10063	MPI-5a Featured	MPI_5a is a potent selective inhibitor of HDAC6, and poorly blocks other HDAC enzymes.
DC7470	MPI-0479605 Featured	MPI-0479605 is an ATP competitive and selective inhibitor of mitotic kinase Mps1 with IC50 of 1.8 nM, >40-fold selectivity over other kinases.
DC8119	Mps1-IN-2 Featured	Mps1-IN-2 is a potent Mps1 kianse inhibitor with IC50 value of 145 nM.
DC23974	Mps1-IN-3 Featured	Mps1-IN-3 is a selective and highly potent Mps1 kinase inhibitor with IC50 of 50 nM.
DC10951	MPT0E028	MPT0E028 is a potent HDAC inhibitor that inhibits nuclear HDAC activity with IC50 of 11.1 nM in HeLa cells, 9-30 times more potent than SAHA.
DC10938	MPT0G211	MPT0G211 is a novel potent, selective HDAC6 inhibitor with IC50 of 0.291 nM, displays >1,000-fold selectivity over other HDAC isoforms.
DC9542	MPTP (hydrochloride) Featured	MPTP HCl induced reduction in the DOPAC HVA/dopamine (DA) ratio and increase in striatal ascorbate (AS) oxidation in rats
DC10437	MRE-269 Featured	MRE-269 is an active metabolite of selexipag, and acts as a selective IP receptor agonist.
DC3122	MRK003	MRK003 is a γ-secretase inhibitor exhibits promising in vitro pre-clinical activity in multiple myeloma and non-Hodgkin's lymphoma.
DC23877	MRK-560	MRK-560 is a potent, brain-penetrant and orally bioavailable γ-secretase inhibitor that inhibits proteolytic cleavage of APP over the Notch pathway.
DC23655	MRK-623	MRK-623 is a potent, α2/α3 subunit functionally selectiviie GABAA receptor agonist..

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