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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC0811 | Avoenin |
Natural potent antienterovirus D68 (anti-EV-D68) agent
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| DCC0810 | Avicenol A |
Cancer chemoprevebtive agent
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| DCC0809 | Ave6971 |
Novel antistaphyloccocal agent, attenuating inhibition of hERG potassium channel current
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| DCC0808 | Ave-0991 Sodium Salt |
Novel angiotensin-(1-7) Mas receptor agonist
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| DCC0807 | Ave0991 |
Novel non-peptide Ang-(1-7) mimetic, inhibiting perivascular inflammation, through the reduction of chemokine expression in pVAT, as well as through direct actions on monocytes/macrophages inhibiting their activation
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