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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1319 | Cdk-in-4.35 |
Novel potent inhibitor of cyclin-dependent kinases (CDKs) 2, 5, and 9, displaying activities across more than 60 cancer cell lines
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| DCC1318 | Cdki Hydrochloride |
Potent and selective ATP competitiive inhibitor of cycB-CDK1, cycE-CDK2, and cycD1-CDK4
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| DCC1317 | Cdk9-in-37 |
Novel inhibitor of the cyclin-dependent kinase 9 (CDK9)
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| DCC1316 | Cdk9/cyct1-in-93 |
Highly specific, ATP-competitive inhibitor of CDK9/CycT1 with antiviral activity
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| DCC1315 | Cdk9/bet-in-40 |
Novel potent dual inhibitor of CDK9 and BET proteins with balanced activities of BRD4 (IC50 = 12.7 nM) and CDK9 (IC50 = 22.4 nM), as well as good antiproliferative activities on a small cancer cell panel
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| DCC1314 | Cdk9 Degrader 45 |
Novel Potent and Selective CDK9 Degrader for Targeting Transcription Regulation in Triple-Negative Breast Cancer
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| DCC1313 | Cdk8-in-iv |
Novel CDK8 inhibitor
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| DCC1312 | Cdk8-in-iii |
Novel CDK8 inhibitor
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| DCC1311 | Cdk8-in-ii |
Novel CDK8 inhibitor
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| DCC1310 | Cdk8-in-i |
Novel potent CDK8 inhibitor
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| DCC1309 | Cdk8-in-4k |
Novel potent and highly selective CDK8 inhibitor, with no apparent potential for time-dependent CYP3A4 inhibition
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| DCC1308 | Cdk8-in-32 |
Novel highly potent, selective, permeable CDK8 inhibitor
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| DCC1307 | Cdk8-in-3 |
Novel inhibitor of CDK8
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| DCC1306 | Cdk8-in-18 |
Novel potent and selective inhibitor of CDK8, also modulating CDK19
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| DCC1305 | Cdk8/19-in-52h |
Potent dual inhibitor of CDK8/19, suppressing phosphorylated STAT1 in various cancer cells
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| DCC1304 | Cdk8/19-in-51 |
Novel potent and selective dual inhibitor of CDK8 and CDK19
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| DCC1303 | Cdk8 Inhibitor W-34 |
Novel potent CDK8 inhibitor
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| DCC1302 | Cdk6/pim1 Inhibitor 51 |
Novel potent and balanced dual CDK6/PIM1 inhibitor, showing high kinase selectivity and displaying stronger potency in reducing the burden of AML than palbociclib and SMI-4a in vivo
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| DCC1301 | Cdk6 Degrader Cp-10 |
Novel potent CDK6 degrader
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| DCC1300 | Cdk4 Inhibitor V |
Potent, ATP-binding site-targeting Cdk4/D1 inhibitor
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| DCC1299 | Cdk12-in-7 |
Novel potent and selective CDK12 inhibitor
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| DCC1298 | Cddhqd-in-1 |
Novel selective cdDHQD inhibitor
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| DCC1297 | cd4528 |
Novel agonist for the vitamin D receptor (VDR)
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| DCC1296 | cd4420 |
Novel agonist for the vitamin D receptor (VDR)
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| DCC1295 | cd4409 |
Novel agonist for the vitamin D receptor (VDR)
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| DCC1294 | Cd33 Pre-mrna Splicing Modulator 1 |
Novel CD33 pre-mRNA splicing modulator, increasing exon 2 skipping in cellular mRNA pools
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| DCC1293 | Cd22 Glycan Ligand |
Novel CD22 glycan ligand, targeting CD22-expressing B cells, uptaking and enhancing siRNA gene expression knockdown via formation of CD22 glycan ligand-conjugated siRNA
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| DCC1292 | Cd2019 |
Retinoic acid receptor beta (RARbeta) agonist, overcoming inhibition of axonal outgrowth via phosphoinositide 3-kinase signalling in the injured adult spinal cord.
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| DCC1291 | cd11359 |
Novel telomerase inhibitor
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| DCC1290 | Cd10847 |
Novel Caspase-1 inhibitor
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