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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC43853 | Isolicoflavonol |
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| DC43852 | 7,3'-Dihydroxy-5'-methoxyisoflavone |
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| DC43851 | TG53 |
Novel inhibitor of tissue transglutaminase (TG2) and fibronectin (FN) protein-protein interaction
More description
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| DC43850 | 20-Deoxocarnosol |
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| DC43849 | TM6008 |
Novel Prolyl Hydroxylase Inhibitor Protects Against Cell Death After Hypoxia
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| DC43848 | Isomartynoside |
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| DC43847 | Sappanchalcone |
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| DC43846 | 1,5,15-Tri-O-methylmorindol |
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| 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 |
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| DC43841 | Alisol O |
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| DC43839 | Viscidulin II |
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| DC43838 | Viscidulin III |
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| DC43837 | 12-O-Tiglylphorbol-13-isobutyrate |
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| 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 |
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| 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 |
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| DC43827 | ML262 |
Potent inhibitor of lipid droplet formation
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| DC43826 | beta-Rhamnocitrin |
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| 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 |
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| DC43822 | Chamaejasmenin C |
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| DC43821 | Mogroside VI |
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| DC43820 | Chiisanoside |
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| DC43819 | UBP551 |
Selective modulator of NMDA receptors, potentiates responses at GluN1/GluN2D
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| DC43818 | IPR-803 |
Inhibitor of the uPAR·uPA protein-protein interaction, blocking cancer cell invasion
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| DC43817 | AMG-51 |
A selective inhibitor of c-Met kinase
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