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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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DCC3199 Lyso-7
Inhibitor of cyclooxygenase (COX); Pan partial agonist of PPARγ, PPARα and PPARβ/δ
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DCC3198 Lysine Orotate
Inhibitor of viral replication, especially useful in the treatment of the Herpes family of viruses which includes Herpes Simplex 1 and 2 , EBV , CMV and Varicella.
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DCC3197 Lyngbyastatin 7
Natural Potent Marine-Derived Elastase Inhibitor
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DCC3196 Ly-hn2am
Nove fluorescent probe for highly sensitive monitoring drug induced lysosomal pH value changes, exhibiting good biological compatibility, low cytotoxicity and high resistance to photobleaching
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DCC3195 Lyc-31138
Novel F1F0-ATPase modulator, significantly decreasing M2 glutamate and increasing M4 glutamate
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DCC3194 Ly-580276
Novel inhibitor of the type I transforming growth factor beta receptor (TβRI)
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DCC3193 Ly544344
Prodrug of LY354740, highly selective and potent agonist of group II mGlu receptors (mGluR2)
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DCC3192 Ly-466195
Novel competitive GLUK5 receptor antagonist
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