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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3432 | Mmv009108 |
Novel antimalarial agent with increased efficacy against one or more pfatp4 mutated clones
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| DCC3431 | Mmv008138 |
Novel MEP pathway-targeting antimalarial agent
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| DCC3430 | Mmv007839 |
Novel potent Plasmodium lactate transporter PfFNT
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| DCC3429 | Mmv007564 |
Novel antimalarial agent against asexual stages of P. falciparum
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| DCC3428 | Mmv006764 |
The first small-molecule anti-plasmodial agent, disrupting rosetting, simultaneously restoring microcirculation and reduce parasite load
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| DCC3427 | Mmv001239 |
Novel inhibitor of lanosterol-14-alpha-demethylase (TcCyp51)
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| DCC3426 | Mms-350 |
Highly water-soluble antifibrotic agent, reducing the profibrotic phenotype induced in vitro in primary human fibroblasts and ameliorating bleomycin-induced pulmonary fibrosis in vivo
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| DCC3425 | Mmpl3-in-e11 |
Novel Mmpl3 inhibitor, indirectly blocking translocation of Trehalose Monomycolates across the IM
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| DCC3424 | M-mpep |
Negative allosteric modulator (NAM) ligand for the mGlu5 receptor
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| DCC3423 | Mmp13-in-t26c |
Novel highly potent and selective MMP13 inhibitor
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| DCC3422 | Mmh410 |
Novel potent and selective HDAC8 inhibitor
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| DCC3421 | Mmh409 |
Novel potent and selective HDAC8 inhibitor
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| DCC3420 | Mmh371 |
Novel potent and selective HDAC8 inhibitor
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| DCC3419 | Mmg-0358 |
Novel potent IDO1 inhibitor, showing low cytotoxicity and higher selectivity for IDO1 over TDO enzyme
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| DCC3418 | Mlt-695 |
Novel potent and selective MALT-1 protease inhibitor, showing improved solubility and permeability in comparison with MLT-748
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| DCC3417 | Ml-sa3 |
Potent agonist of TRPML channels specifically activating lysosomal ML1 currents
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| DCC3416 | Mls8091 |
Novel inhibitor of human cytomegalovirus (HCMV) infection
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| DCC3415 | Mls-2384 |
Novel dual JAK/Src kinase inhibitor, suppressing growth of diverse cancer cells
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| DCC3414 | Mls-2064 |
Potent inhibitor of STAT3 and Akt signaling
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| DCC3413 | Mls001158554 |
Novel Inhibitor of Human Cytomegalovirus
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| DCC3412 | Mls000733230 |
Novel potent inhibitor of EBOV infection
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| DCC3411 | Mls000545091 |
Potent and selective mixed-type inhibitor of human epithelial 15-lipoxygenase-2 (15-LOX-2)
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| DCC3410 | Mls000536924 |
Potent and selective competitive inhibitor of human epithelial 15-lipoxygenase-2 (15-LOX-2)
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| DCC3409 | Mls000099089 |
Novel selective and potent inhibitor of recombinant h12/15-LOX and cellular mouse 12/15-LOX (m12/15-LOX)
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| DCC3408 | Mln-977 |
Second generation 5-LO inhibitor, blocking the production of leukotrienes
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| DCC3407 | Mln944 |
Novel potent DNA binding agent, stabilizing topoisomerase-dependent cleavage, demonstrating exceptional efficacy against a number of murine and human tumor models
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| DCC3406 | Mln-0415 |
Novel IKK2 inhibitor, decreasing NF-κB activation and down-regulating the expression of a number of inflammatory proteins
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| DCC3405 | Mlck Inhibitor Peptide-18 |
Selective inhibitor of Myosin Light Chain Kinase (MLCK)
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| DCC3404 | ml312 |
Novel Inhibitor of Scavenger Receptor BI-mediated Lipid Uptake
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| DCC3403 | Km04794 |
Novel endoplasmic reticulum proteostasis modulator, enhancing insulin production in pancreatic β cells, inhibiting the UPR, alleviating ER stress and protein aggregation, improving intracellular insulin levels and insulin secretion
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