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Cat. No. Product Name Field of Application Chemical Structure
DCC1265 Cbz-FTY720 FTY720 derivative
DCC1266 Cc0651 Novel inhibitor of the E2 ubiquitin-conjugating enzyme Cdc34A
DCC1267 Cc-3060 Novel Cereblon modulator, promoting ZBTB16 degradation by primarily engaging distinct structural degrons on CRBN-ZnF1 zinc finger domains
DCC1268 Cc34301 PqsE inhibitor, binding to the active center inhibiting PqsE's thioesterase activity in cell-based and in vitro assays
DCC1269 Cc41801 PqsE inhibitor, binding to the active center inhibiting PqsE's thioesterase activity in cell-based and in vitro assays
DCC1270 Cc-509 Novel potent orally bioavailable Syk kinase inhibitor
DCC1271 Cc-647 Novel Cereblon modulator, promoting ZBTB16 degradation by primarily engaging distinct structural degrons on CRBN-ZnF3 zinc finger domains
DCC1272 Ccdc919159 Novel Indigoid Anti-tuberculosis Agent; Antimicrobial
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
DCC1274 Ccg-120304 Novel Inhibitor of TonB Function
DCC1275 Ccg-175472 Novel Inhibitor of TonB Function
DCC1276 ccg-206559 Potent photoprobe as Rho/MKL1/SRF transcription inhibitor
DCC1277 Ccg-206584 Novel inhibitor of G Protein-Coupled Receptor Kinase
DCC1278 Ccg-265328 Novel covalent selective GRK inhibitor, interacting with a nonconserved cysteine (Cys474)
DCC1279 Ccg-46842 Novel sialyltransferase inhibitor (IC 50 : 2 µM)
DCC1280 Cci7967 Novel MmpL3 inhibitor
DCC1281 (E/Z)-CCR-11 Featured (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.
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
DCC1283 Cct245718 Novel dual FLT3/Aurora A inhibitor, overcoming D835Y-mediated resistance to FLT3 inhibitors in acute myeloid leukaemia cells
DCC1284 Cct245731 Inactive analogue of pictilisib to be used as the negative control
DCC1285 Cct245737(s) Highly Selective Oral Checkpoint Kinase 1 (CHK1) Inhibitor
DCC1286 Cct365386 Novel inhibitor of BCL6
DCC1287 Ccta-1523 Novel inhibitor of the efflux function of ABCG2, selectively reversing ABCG2-mediated MDR in cancer cells in vitro and in vivo
DCC1288 Ccw 28-3 Novel potent covalent BRD4 degrader, degrading BRD4 in a proteasome- and RNF4-dependent manner without inhibiting RNF4 autoubiquitination activity
DCC1289 Cd08108 Novel MC1R agonist
DCC1290 Cd10847 Novel Caspase-1 inhibitor
DCC1291 cd11359 Novel telomerase inhibitor
DCC1292 Cd2019 Retinoic acid receptor beta (RARbeta) agonist, overcoming inhibition of axonal outgrowth via phosphoinositide 3-kinase signalling in the injured adult spinal cord.
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
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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