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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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DCC1289 Cd08108
Novel MC1R agonist
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DCC1288 Ccw 28-3
Novel potent covalent BRD4 degrader, degrading BRD4 in a proteasome- and RNF4-dependent manner without inhibiting RNF4 autoubiquitination activity
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DCC1287 Ccta-1523
Novel inhibitor of the efflux function of ABCG2, selectively reversing ABCG2-mediated MDR in cancer cells in vitro and in vivo
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DCC1286 Cct365386
Novel inhibitor of BCL6
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DCC1285 Cct245737(s)
Highly Selective Oral Checkpoint Kinase 1 (CHK1) Inhibitor
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DCC1284 Cct245731
Inactive analogue of pictilisib to be used as the negative control
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DCC1283 Cct245718
Novel dual FLT3/Aurora A inhibitor, overcoming D835Y-mediated resistance to FLT3 inhibitors in acute myeloid leukaemia cells
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DCC1282 Ccr4-in-22
Novel CCR4 antagonist, enhancing DC activation and homing to the regional lymph node and showing potent vaccine adjuvant activity through the inhibition of regulatory T-cell recruitment
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