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Cat. No. Product Name Field of Application Chemical Structure
DCC0841 Azd Cxcr2 Antagonist
Novel CXCR2 antagonist with 200 times improvement in solubility than AZD8309
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DCC0840 Aza-thip
Novel selective GABA-C antagonist
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DCC0839 Azalanstat
Inhibitor of hepatic cholesterol biosynthesis, inhibiting the cytochrome P450 enzyme lanosterol 14alpha-demethylase
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DCC0838 azadirone
Inducer of Death Receptors and Sensitizer of Human Cancer Cells to TRAIL through a p53-Independent Mechanism
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DCC0837 aza-bodipy
Near-IR probe for detecting conformational changes of Aβ1-42 soluble oligomers in vitro
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DCC0836 Aza197
Novel selective Cdc42 inhibitor, suppressing primary colon cancer growth and prolonging survival in a preclinical mouse xenograft model by downregulation of PAK1 activity
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DCC0835 Az7188
Novel weak PAR2 antagonist
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DCC0834 Az-13767370
Novel covalent ERK1/2 inhibitor
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DCC0833 Az1366
Novel tankyrase inhibitor, enhancing irinotecan activity in tumors that exhibit elevated tankyrase and irinotecan resistance
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DCC0832 Az12489875-002
Novel potent EphB4 inhibitor
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DCC0831 Az12099548
Novel transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist
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DCC0830 Az12080282 Dihydrochloride
Novel orally bioavailable inhibitor of Hedgehog signaling
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DCC0829 Az12048189
Novel transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist
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DCC0828 Az11760788
Novel transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist
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DCC0827 az1136
Second Generation
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DCC0826 ay-30068
Cyclooxygenase Inhibitor;
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DCC0825 Axt050
Novel integrin-binding peptide, inhibiting hepatocyte growth factor (HGF) signaling through Met-integrin interactions, also being an antiangiogenic agent by reducing phosphorylation of VEGR2, IGFR, and PDGFR, stabilizing vessels by disrupting α5β1 signali
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DCC0824 Axl-in-13c
Novel highly potent and orally bioavailable Axl inhibitor
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DCC0823 Ax15910
Novel potent dual ERK5 and BRD4 inhibitor
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DCC0822 Ax15892
Novel potent and selective ERK5 inhibitor
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DCC0821 Ax15839
Novel dual ERK5 and BRD4 inhibitor
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DCC0820 Ax14373
Highly specific JNK inhibitor #212121; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; word-spacing: 0
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DCC0819 Ax-10479
Zn -dependent inhibitor of human plasma Lp-PLA2
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DCC0818 Ax1/mer-in-1
Novel potent dual inhibitor of Ax1 and Mer
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DCC0817 Aws-i-169
Novel specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group
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DCC0816 Awd-12-281
Novel PDE4 inhibitor
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DCC0815 avβ5 Inhibitor 12
The first potent and selective αvβ5 integrin inhibitor
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DCC0814 avβ3 Inhibitor [351421-54-0]
Novel potent and selective αvβ3 integrin inhibitor
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DCC0813 Avx-13616
Potent broad spectrum antibacterial agent, particularly against drug-resistant Staphylococcus pathogens
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DCC0812 Avx002
Novel cytosolic phospholipase A2 group IVA (cPLA2α) inhibitor, displaying potent anti-inflammatory activity and disease-modifying properties in cellular and in vivo models
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