DCC1265 |
Cbz-FTY720 |
FTY720 derivative |
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DCC1266 |
Cc0651 |
Novel inhibitor of the E2 ubiquitin-conjugating enzyme Cdc34A |
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DCC1267 |
Cc-3060 |
Novel Cereblon modulator, promoting ZBTB16 degradation by primarily engaging distinct structural degrons on CRBN-ZnF1 zinc finger domains |
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DCC1268 |
Cc34301 |
PqsE inhibitor, binding to the active center inhibiting PqsE's thioesterase activity in cell-based and in vitro assays |
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DCC1269 |
Cc41801 |
PqsE inhibitor, binding to the active center inhibiting PqsE's thioesterase activity in cell-based and in vitro assays |
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DCC1270 |
Cc-509 |
Novel potent orally bioavailable Syk kinase inhibitor |
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DCC1271 |
Cc-647 |
Novel Cereblon modulator, promoting ZBTB16 degradation by primarily engaging distinct structural degrons on CRBN-ZnF3 zinc finger domains |
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DCC1272 |
Ccdc919159 |
Novel Indigoid Anti-tuberculosis Agent; Antimicrobial |
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DCC1273 |
C-ceritinib Tfa Salt |
Novel coupleable ceritinib analog with a linker, also binding multiple other kinases, including FAK1, RSK1/2, ERK1/2, CAMKK2 and FER |
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DCC1274 |
Ccg-120304 |
Novel Inhibitor of TonB Function |
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DCC1275 |
Ccg-175472 |
Novel Inhibitor of TonB Function |
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DCC1276 |
ccg-206559 |
Potent photoprobe as Rho/MKL1/SRF transcription inhibitor |
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DCC1277 |
Ccg-206584 |
Novel inhibitor of G Protein-Coupled Receptor Kinase |
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DCC1278 |
Ccg-265328 |
Novel covalent selective GRK inhibitor, interacting with a nonconserved cysteine (Cys474) |
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DCC1279 |
Ccg-46842 |
Novel sialyltransferase inhibitor (IC 50 : 2 µM) |
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DCC1280 |
Cci7967 |
Novel MmpL3 inhibitor |
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DCC1281 |
(E/Z)-CCR-11
Featured
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(E/Z)-CCR-11 (Comp 12) is a selective CD38 inhibitor, with an IC50 of 20.8 μM against CD38 cyclase. (E/Z)-CCR-11 promotes increases in cellular NAD+ levels and interferon γ. |
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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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DCC1283 |
Cct245718 |
Novel dual FLT3/Aurora A inhibitor, overcoming D835Y-mediated resistance to FLT3 inhibitors in acute myeloid leukaemia cells |
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DCC1284 |
Cct245731 |
Inactive analogue of pictilisib to be used as the negative control |
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DCC1285 |
Cct245737(s) |
Highly Selective Oral Checkpoint Kinase 1 (CHK1) Inhibitor |
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DCC1286 |
Cct365386 |
Novel inhibitor of BCL6 |
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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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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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DCC1289 |
Cd08108 |
Novel MC1R agonist |
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DCC1290 |
Cd10847 |
Novel Caspase-1 inhibitor |
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DCC1291 |
cd11359 |
Novel telomerase inhibitor |
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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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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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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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