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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC1248 | Cb5255829 |
Novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro
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| DCC1247 | cb3717 |
Dual thymidylate synthase and dihydrofolate reductase inhibitor
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| DCC1246 | Cb300919 |
Novel Cell_cycle>cell cycle inhibitor
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| DCC1245 | Cb28324237 |
Novel IκB kinase inhibitor
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| DCC1244 | Cb20372475 |
Novel Cyclin-dependent kinase inhibitor
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| DCC1243 | Cb17846240 |
Novel Thymidine kinase (TK) inhibitor
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| DCC1242 | Cb15143266 |
Novel IκB kinase inhibitor
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| DCC1241 | Cb14280993 |
Novel SRC kinase inhibitor
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| DCC1240 | Cb14171361 |
Novel RAF kinase inhibitor
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| DCC1239 | Caylin-2 |
Novel Mdm2 inhibitor, an analog of Nutlin-3
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| DCC1238 | Caylin-1 |
Novel Mdm2 inhibitor, an analog of Nutlin-3
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| DCC1237 | Cay10633 |
Novel potent CysLT2 receptor antagonist
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| DCC1236 | Cay10398 |
Isoform-selective inhibitor of histone deacetylase (HDAC1)
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| DCC1235 | Cay10397 |
Selective inhibitor of 15-hydroxy PGDH, significantly suppressing endogenous 11-oxo-ETE production with a corresponding increase in 11(R)-HETE
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| DCC1234 | Cavalpha2delta-1 Ligand 16rr |
Novel ligand of voltage-gated calcium channel α2δ-1 subunit (Cavα2δ-1)
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| DCC1233 | Cathepsin X Inhibitor Z9 |
Novel selective reversible inhibitor of cathepsin X
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