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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC11814 | cis CM-414 |
A first-in-class, dual inhibitor of PDE5 and HDAC that inhibits HDAC1/2/3/6 (IC50=310/490/322/91 nM, respectively) and PDE5 (IC50=60 nM).
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| DC11815 | trans CM-414 |
A first-in-class, dual inhibitor of PDE5 and HDAC that inhibits HDAC1/2/3/6 (IC50=310/490/322/91 nM, respectively) and PDE5 (IC50=60 nM).
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| DC11813 | CM-414 |
A first-in-class, dual inhibitor of PDE5 and HDAC that inhibits HDAC1/2/3/6 (IC50=310/490/322/91 nM, respectively) and PDE5 (IC50=60 nM).
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| DC11653 | Ischemin |
A cell permeable CBP bromodomain inhibitor with Kd of 19 uM.
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| DC11652 | Ischemin sodium |
A cell permeable CBP bromodomain inhibitor with Kd of 19 uM.
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| DC8423 | 4SC-202 free base |
4SC-202 is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively. Also displays inhibitory activity against Lysine specific demethylase 1 (LSD1). Phase 1.
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| DCR-004 | Ellagic acid |
>98%,Standard References
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