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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3243 | Mbp-c12 |
Novel detergent, showing enhanced stability to all tested proteins compared to a gold standard detergent (DDM)
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| DCC3242 | Mbls-in-5 |
Novel non-hemolytic and low toxic inhibitor of metallo-β-lactamases (MBLs), restoring the activity of meropenem against Escherichia coli, Citrobacter freundii, Proteus mirabilis and Klebsiella pneumonia, which carried resistance genes of blaNDM-1
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| DCC3241 | Mb-211 |
Novel inhibitor of dengue and West Nile virus NS2B-NS3 protease
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| DCC3240 | Mb16695 |
Novel Inhibitor of Mycobacterium tuberculosis α-1,4-Glucan Branching Enzyme (GlgB)
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| DCC3239 | Mb06322 |
Prodrug of MB05032, acting as potent and selective inhibitor of fructose 1,6-bisphosphatase for controlling gluconeogenesis in type 2 diabetes
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| DCC3238 | Mb-001 |
Novel potent inhibitor of the membrane-bound retinoid isomerase RPE65
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| DCC3237 | Maysin |
Natural Anti-inflammation Agent, Attenuating Amyloid Plaques by Inducing Humoral Immune Response with Th2 Skewed Cytokine Response in the Tg (APPswe, PS1dE9) Alzheimer's Mouse Model
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| DCC3236 | May1-in-13a |
Novel potent inhibitor of May1 with Ki = 12 ± 1 nM, also inhibiting wild-type HIV-1 protease with Ki = 32 ± 5 pM and three drug resistance-associated mutants with Ki values ranging from 24 to 320 pM
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| DCC3235 | Massiliamide |
Novel potent tyrosinase inhibitor from the Gram-negative bacterium Massilia albidiflava DSM 17472T
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| DCC3233 | Maritinone |
Novel, active, and less toxic anti-tuberculosis (anti-TB) agent
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| DCC3232 | Margatoxin |
Inhibitor of voltage-gated K(+) (Kv) channels Kv1.3 and Kv1.5
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| 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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