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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC43100 | ML345 |
Inhibitor of the Insulin-Degrading Enzyme (IDE)
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| DC43099 | SR-2959 |
Inhibitor of the Insulin-Degrading Enzyme (IDE)
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| DC43098 | Yunnancoronarin A |
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| DC43097 | Kaempferol tetraacetate |
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| DC43096 | Myriceric acid C |
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| DC43095 | 2,3,8-Tri-O-methylellagic acid |
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| DC43094 | Simiarenol |
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| DC43093 | PF-05274857 HCl |
Very potent inhibitor, with an IC50 of less than 10 nM for VEGFR2, MET, Kit and FLT3-ITD
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| DC43092 | ML318 |
Novel inhibitor of Pseudomonas aeruginosa PvdQ acylase, an enzyme involved in siderophore pyoverdine synthesis
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| DC43091 | Villosin C |
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| DC43090 | Villosin |
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| DC43089 | 3',5,5',7-Tetrahydroxyflavanone |
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| DC43087 | Sambutoxin |
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| DC43086 | BMS-466442 |
The first selective inhibitor of the amino acid transporter alanine serine cysteine transporter-1 (asc-1)
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| DC43085 | Cariporide Mesylate |
Selective Na+/H+ exchanger isoform 1 (NHE1) inhibitor
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| DC43084 | 3-O-(2'E ,4'Z-decadienoyl)-20-O-acetylingenol |
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| DC43083 | CMF-019 |
The first potent biased small molecule agonist at the apelin receptor, increasing cardiac contractility in vivo
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| DC43082 | Catalpalactone |
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| DC43081 | Inz-5 |
Novel Stable Fungal-Selective Inhibitor of Mitochondrial Cytochrome bc1
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| DC43079 | Nonyloxytryptamine oxalate |
Polysialic acid (PSA) mimetic as a selective 5-hydroxytryptamine receptor 1B (5-HT1B ) agonist
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| DC43077 | Harzianic acid |
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| DC43076 | CPUY192018 |
Novel potent inhibitor of the Keap1-Nrf2 PPI protein-protein interaction, showing a cytoprotective effect against DSS in both NCM460 cells and mouse colon via the activation of Nrf2 signaling
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| DC43075 | Delphinidin-3-O-rutinoside chloride |
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| DC43074 | Myricetin 3-O-galactoside |
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| DC43073 | PYD-106 |
Novel GluN2C-selective NMDA Receptor Positive Allosteric Modulator
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| DC43072 | 9,10-Dimethoxycanthin-6-one |
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| DC43071 | 4,5-Dihydroblumenol A |
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| DC43070 | 11-Deoxyalisol B |
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| DC43069 | Isatidine |
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| DC43068 | 3,5-Dihydroxy-4',7-dimethoxyflavone |
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