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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1133 | Brd7929 |
Novel multistage antimalarial inhibitor for single-dose treatment of malaria in mouse models
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| DCC1132 | Brd7539 |
Novel dihydroorotate dehydrogenase (DHODH) inhibitor
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| DCC1131 | Brd6897 |
Novel Mitochondrial Content Inducer
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| DCC1130 | Brd5384 |
Novel HDAC8 inhibitor
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| DCC1129 | Brd4097 |
Negative control in HDAC1/2/3/8 assays
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| DCC1128 | Brd4 D1 Inhibitor 26 |
Novel potent BRD4 D1 inhibitor with over 500-fold selectivity against BRD2 D1 and BRD4 D2 via ITC
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| DCC1127 | Brd4 Bd2 Inhibitor N13 |
Novel potent inhibitor of BRD4 BD2
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| DCC1126 | Brd4 Bd1-in-4 |
Novel selective BET BD1 inhibitor with preferred binding to of BRD4 BD1
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| DCC1125 | Brd3811 |
Novel non-histone nuclear substrate of histone deacetylase 8 (HDAC8)
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| DCC1124 | Brd3316 |
Novel inhibitor of parasite phenylalanyl-tRNA synthetase (PheRS)
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| DCC1123 | Brd3067 |
Negative control for tubastatin A
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| DCC1122 | brd2761 |
Positive control for HSPC toxicity; Inhibitor of STK33
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| DCC1121 | Brd2577 |
Novel HDAC inhibitor, inhibiting multiple HDAC enzymes and modulates acetylation levels in cells
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| DCC1120 | Brd20322 |
Novel potent inhibitor of spCas9, disrupting spCas9-DNA binding and exerting dose and temporal control of spCas9 in human cell lines
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| DCC1119 | Brd0761 |
Novel Inhibitor of Clostridium difficile
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| DCC1118 | Brd0026 |
Novel multistage antimalarial inhibitor
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| DCC1117 | Brazilein |
Natural small molecule isolated from dried heartwood of Caesalpinia sappan L, exhibiting multi-pharmacological activities
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| DCC1116 | Brassilexin |
Inhibitor of cyclobrassinin hydrolase, a unique enzyme from the fungal pathogen Alternaria brassicicola
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| DCC1115 | Brasofensine Maleate |
Monoamine Reuptake Inhibitor
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| DCC1113 | bractelactone |
Novel potent inhibitor of human neutrophil activations
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| DCC1112 | Bpyo-34 |
Novel apoptosis signal-regulating kinase 1 (ASK1) inhibitor with IC50 of 0.52μM in vitro in kinase assay
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| DCC1111 | Bpv(pic)k2 |
Potent and se;rctive PTEN inhibitor, activating the insulin receptor kinase, inhibiting the dephosphorylation of autophosphorylated insulin receptors and epidermal growth factor receptors of rat liver endosomes
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| DCC1110 | Bpv(phen) |
Potent direct PTEN inhibitor
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| DCC1109 | Bpr1k871 |
Novel potent and selective dual FLT3/AURKA inhibitor
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| DCC1107 | bpmetap1-in-15 |
The first potent inhibitor of Burkholderia pseudomallei methionine aminopeptidase
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| DCC1106 | Bph-652 Potassium |
Squalene synthase (SQS) inhibitor, potently inhibiting CrtM
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| DCC1105 | Bph-651 |
Novel CrtM inhibitor
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| DCC1104 | Bph-1218 |
Novel potent SQS inhibitor
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| DCC1103 | Bpc Hydroiodide |
Novel modulator of TTD-PHD histone reader module, binding to the TTD groove, competing with linker binding and promoting open TTD-PHD conformations
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| DCC1102 | Bp2-94 |
Histamine H3 receptor agonist prodrug
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