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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| DCC1101 | Bp13944 |
Novel, Potential Dengue Virus NS2B/NS3 Protease Inhibitor
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| DCC1100 | Bp-1-108 |
Potent and selective STAT5 inhibitor
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| DCC1099 | Bp1.4160 |
Novel and highly potent histamine H3 receptor ligand
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| DCC1098 | Bot-64 |
Novel IKK-2 inhibitor, targeting the Ser177 and/or Ser181 residues in the kinase's activation loop domain.
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| DCC1097 | Bos-6-2-2-6-crbn |
Proteolysis targeting chimeras (PROTAC), acting as a degrader of oncogenic BCR-ABL
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| DCC1096 | Bos-318 |
Novel. highly potent, selective, cell-permeable furin inhibitor, rescuing key features of cystic fibrosis airway disease
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| DCC1095 | Bop-jf549 |
Novel BOP-conjufated fluorescent dual α9β1/α4β1 integrin inhibitor
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| DCC1094 | Bont-in-33 |
Novel potent inhibitor of Botulinum neurotoxin/A light chain (BoNT/A LC)
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| DCC1093 | Bont/a Lc Inhibitor 33 |
Potent Botulinum Neurotoxin A Light-Chain Inhibitor
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