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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DC43863 Momordin II
DC43859 3-MB-PP1
Highly ASKA- (analog-sensitive kinase alleles) selective inhibitor
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DC43856 Ganoderic acid C1
DC43855 Lucidenic acid A
This compound belongs to the class of chemical entities known as triterpenoids. These are terpene molecules containing six isoprene units.
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DC43854 Quercetin-3-o-rutinose
DC43853 Isolicoflavonol
DC43852 7,3'-Dihydroxy-5'-methoxyisoflavone
DC43851 TG53
Novel inhibitor of tissue transglutaminase (TG2) and fibronectin (FN) protein-protein interaction
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DC43850 20-Deoxocarnosol
DC43849 TM6008
Novel Prolyl Hydroxylase Inhibitor Protects Against Cell Death After Hypoxia
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DC43848 Isomartynoside
DC43847 Sappanchalcone
DC43846 1,5,15-Tri-O-methylmorindol
DC43845 Walsuronoid B
An inducer of mitochondrial and lysosomal dysfunction leading to apoptotic rather than autophagic cell death via ROS/p53 signaling pathways in liver cancer
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DC43843 Karavilagenin D
DC43841 Alisol O
DC43839 Viscidulin II
DC43838 Viscidulin III
DC43837 12-O-Tiglylphorbol-13-isobutyrate
DC43836 TNFalpha-IN-S10
Novel Inhibitor of TNF-α
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DC43835 SC-144 Hydrochloride
Novel orally active glycoprotein 130 (gp130) inhibitor
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DC43834 Zingiberen newsaponin
DC43833 BGT-226
A phosphatidylinositol 3-kinase (PI3K) inhibitor
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DC43832 VUF10661
Partial agonist in CXCR3-mediated chemotaxis, bound to CXCR3 in an allosteric fashion with the same efficacy as CXCL11
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DC43830 Lobelin
DC43827 ML262
Potent inhibitor of lipid droplet formation
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DC43826 beta-Rhamnocitrin
DC43825 ML170
Highly specific allosteric activator for the tumor-specific isoform of human pyruvate kinase (M2 isoform)
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DC43824 2,3,24-Trihydroxy-12-ursen-28-oic acid
DC43822 Chamaejasmenin C

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