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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1280 | Cci7967 |
Novel MmpL3 inhibitor
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| DCC1279 | Ccg-46842 |
Novel sialyltransferase inhibitor (IC 50 : 2 µM)
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| DCC1278 | Ccg-265328 |
Novel covalent selective GRK inhibitor, interacting with a nonconserved cysteine (Cys474)
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| DCC1277 | Ccg-206584 |
Novel inhibitor of G Protein-Coupled Receptor Kinase
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| DCC1276 | ccg-206559 |
Potent photoprobe as Rho/MKL1/SRF transcription inhibitor
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| DCC1274 | Ccg-120304 |
Novel Inhibitor of TonB Function
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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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| DCC1272 | Ccdc919159 |
Novel Indigoid Anti-tuberculosis Agent; Antimicrobial
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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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| DCC1270 | Cc-509 |
Novel potent orally bioavailable Syk kinase inhibitor
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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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| 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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| 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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| DCC1266 | Cc0651 |
Novel inhibitor of the E2 ubiquitin-conjugating enzyme Cdc34A
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| DCC1265 | Cbz-FTY720 |
FTY720 derivative
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| DCC1264 | Cbtf-ee |
The first Gatekeeper RXR antagonist that does not show allosteric inhibition in permissive RXR heterodimers, binding domain (LBD) at the entrance of the ligand binding pocket (LBP), blocking access to the LBP and thus serving as a gatekeeper
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| DCC1263 | Cbs-3595 |
Novel Dual p38α MAPK/PDE-4 Inhibitor with Activity against TNFα -related Diseases
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| DCC1262 | Cbn209350 |
Novel KDM4 inhibitor, inhibiting equally all members of the KDM4 family and exhibiting modest selectivity over other JmjC-KDMs including KDM2A and PHF8
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| DCC1261 | Cbn207192 |
Novel selective inhibitor of KDM4s, inhibiting all members of the KDM4(A-E) subfamily
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| DCC1259 | Cbl0100 |
Novel inhibitor of viral transcriptional elongation, blocking both HIV-1 replication and reactivation
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| DCC1258 | Cbb1007 |
Novel cell-permeable, potent, reversible, and substrate competitive LSD1 inhibitor, promoting the adipogenic differentiation of hESCs
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| DCC1257 | Cbap-bpyne |
The first clickable, photoreactive probe that inhibits both γ-secretase and PSase activities and specifically labels PS1-NTF and signal peptide peptidase (SPP)
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| DCC1256 | Cb97929926 |
Novel Protein kinase A and B inhibitor
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| DCC1255 | Cb9125618 |
Novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro
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| DCC1254 | Cb9029936 |
Novel potent inhibitor of filamentation and biofilm formation by the Candida albicans SC5314 strain
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| DCC1253 | Cb-892 |
Novel inhibitor of HIV-1 gene expression
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| DCC1252 | Cb7833407 |
Selective inhibitor of Adenylyl Cyclase isoform-2 (AC2)
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| DCC1251 | Cb6513745 |
Novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro
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| DCC1250 | Cb5660386 |
Novel inhibitor of HIV-1 entry
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| DCC1249 | cb5468139 |
Selective sphingosine kinase 1 (SK1) inhibitor
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