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Cat. No. Product Name Field of Application Chemical Structure
DCC3231 Marbotinib
Novel highly efficient dual type I/II FMS-like tyrosine kinase inhibitor, disrupting the growth of leukemic cells
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DCC3230 Maprotiline
Inhibitor of neuronal norepinephrine reuptake, reducing symptoms of anxiety associated with depression.
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DCC3229 Ma-pabc-adc-linker-18
Novel stable antibody-drug conjugate (ADC) in mouse serum
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DCC3228 Mao-b Ligand-1
Novel selective MAO-B inhibitor
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DCC3227 Mao-b Inhibitor Cc2
Novel potent and competitive inhibitor of MAO-B (IC 50 : 0.51 μM), also inhibiting BChE (IC 50 : 7.00 μM)
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DCC3226 Mao-b Inhibitor Cc1
Novel potent selective and competitive inhibitor of MAO-B (IC 50 : 0.69 μM)
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DCC3225 Mao-b Inhibitor C5
Potent and selective MAO-B inhibitor
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DCC3224 Mao-b Inhibitor C3
Novel potent and highly selective MAO-B Inhibitor
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DCC3223 Mao-b Inhibitor 58
Highly potent, selective, competitive, and reversible inhibitor of monoamine oxidase B (MAO-B).
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DCC3222 Manassantin A
Natural anticancer, anti-inflammatory, neuroleptic agent, also having human acyl-CoA:cholesterol acyltransferase (ACAT) inhibitory activities
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DCC3221 Mal-rp
Novel quantitative chemical probe for live cell labeling and imaging of proteins that are sensitive to redox modifications
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DCC3220 Malp-2s
TLR2/6 agonist, activating the MyD88 pathway, provoking natural killer (NK) cell activation, increasing co-stimulators CD80/86 and CD40
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DCC3218 Malonganenone A
Selective modulator of plasmodial Hsp70s with antimalarial activity
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DCC3217 Magreth-16a
Potent CB2 receptor inverse agonist
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DCC3216 Magnesium Oxaloacetate
Inhibitor of the amebicidal activity of activated murine macrophages, helping the parasite to survive within the mouse large intestine and increasing the survival of C. elegans exposed to H2O2
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DCC3215 Magnesium L-threonate
Inhibitor of TNF-α, preventing and restoring memory deficits associated with neuropathic pain
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DCC3214 Magl-2102
Novel reversible monoacylglycerol lipase (MAGL) inhibitor
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DCC3213 Madurmycin
Polyether ionophore antibiotic, inhibiting proliferation and induces apoptosis in myoblast cells
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DCC3212 Madtp-372
Potent and selective inhibitor of the induction of cytopathic effect by CHIKV and VEEV
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DCC3211 Macluraxanthone
Natural immunomodulator, significantly decreasing TNF-α and IL-10 cytokine production, regulating the NF-κB and MAPK signaling pathways, displaying the strongest antiproliferative effects with IC50 values of 2.84 and 0.95 μM against A431 and HeLa cancer c
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DCC3210 Mac13243
Novel inhibitor of the bacterial lipoprotein targeting chaperone, LolA
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DCC3209 Mac-0547630
Novel potent and selective inhibitor of UppS without off-target effects on membrane potential
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DCC3208 M7594_0037
Novel Peptide Deformylase (PDF) Inhibitor, having inhibitory activity against HeLa, A549 and MCF-7
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DCC3207 M-5mpep
Partial antagonist of mGlu5
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DCC3206 M4k2163
Novel CNS Penetrant ALK2 Inhibitor for the Treatment of Diffuse Intrinsic Pontine Glioma
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DCC3205 M4k2127
Novel potent and selective ALK2 inhibitor, showing high initial brain uptake, including in the region of interest (pons)
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DCC3203 M1-pam-b
Novel selective muscarinic M1 receptor positive allosteric modulator, showed both significant improvement of scopolamine-induced cognitive deficits and severe diarrhea
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DCC3202 M1-pam-a
Novel selective muscarinic M1 receptor positive allosteric modulator, significantly improved scopolamine-induced cognitive deficits without prominent signs of diarrhea at up to 1000 mg/kg in mice
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DCC3201 M-084 Hydrochloride
TRPC4/5 channel blocker, exhibiting antidepressant and anxiolytic effects
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DCC3200 Lzz-02
Novel inhibitor of the transcriptional activity of β-catenin, degrading the expression of β-catenin by stabilizing axin 2 and diminishing downstream proteins levels, including c-Myc and cyclin D1, effectively shrinking tumor xenograft derived from colonic
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