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Cat. No. Product Name Field of Application Chemical Structure
DCC5125 Thiazolidinedione-8
Novel antibiofilm agent, disturbing symbiotic balance between C. albicans and S. mutans in dual species biofilm
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DCC5124 Thiamphenicol Palmitate
Prodrug of Thiamphenicol, inhibiting the 50S subunit of the bacterial ribosome and protein translation
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DCC5123 Thdp-17
Novel glutaminase activity inhibitor, showing a partial uncompetitive inhibition in vitro and a significant reduction of ammonia and glutamate production in vivo
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DCC5122 Thalassosamide
Natural antibiotic, being active against P. aeruginosa both in vitro and in vivo.
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DCC5121 Thaigranatin T
Natural potent human carboxylesterase 2 (hCES2) inhibitor (IC50: 5.05 μM)
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DCC5120 Th1027
Novel highly potent and specific inhibitor of TLR8, targeting an unconventional pocket on the TLR8 protein-protein Interface
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DCC5119 Tgx-155
Potent and selective inhibitor of PI 3-K
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DCC5118 Tgx-115
Cell-permeable, potent, and selective inhibitor of PI 3-K isoforms p110ß/p110d
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DCC5117 Tgr5-agonist-17
Novel Potent Agonist of TGR5 Receptor
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DCC5116 Tgr5 Agonist 11d-na
Novel potent TGR5 agonist, displayind a significant glucose-lowering effect and stimulated GLP-1 and insulin secretion in TGR5H88Y mice but not in wild-type animals
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DCC5115 Tgp-200c
Novel potent and structure-specific inhibitor of pre-miR-200c, reversing a type 2 diabetes phenotype
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DCC5114 Tg4-294-2
Potent and Selective Antagonist for Human EP2 Receptors
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DCC5113 tg4-292-1
Potent and selective nociceptin opioid receptor (NOP) agonist
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DCC5112 tg4-290-1
Potent and selective nociceptin opioid receptor (NOP) agonist
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DCC5111 Tg4-166
Potent and selective nociceptin opioid receptor (NOP) agonist
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DCC5110 Tg3-95-1
EP2 allosteric potentiator
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DCC5109 Tg2-in-3h
Highly selective, potent, cell-permeable fluorescent irreversible tissue transglutaminase (TG2) inhibitor
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DCC5108 Tg-2112x
Novel inhibitor of mitochondrial calcium uptake (#333333; font-family: "Open Sans", HelveticaNeue, "Helvetica Neue", Helvetica, Arial, sans-serif; font-size: 15px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight:
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DCC5107 Tg11-77 Hydrochloride
Novel, Potent, Selective, Water Soluble, Brain-Permeable EP2 Receptor Antagonist
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DCC5106 Tg101114
Novel inhibitor of T315I mutant enzyme, exhibiting reasonable in vivo efficacy in a xenograft mouse model harboring T315I
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DCC5105 Tg100948
Novel dual VEGFR/Src kinase inhibitor
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DCC5104 Tg-0205221
Novel potent SARS coronavirus (CoV) 3CL protease inhibitor (Ki = 53 nM)
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DCC5103 Tg-0054
Novel and Potent Stem Cell Mobilizer; Inhibitor of SDF-1α/CXCR4 binding
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DCC5102 Tfr4oht
Cyclized tamoxifen analog, selective ER modulator (SERM)
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DCC5101 Tfmo-12
CNS-penetrant selective class IIa histone deacetylase (HDAC) inhibitor, exploiting the >100-fold selectivity over class I/IIb HDACs
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DCC5100 Tfmo-1
Novel cell-active, selective class IIa HDAC inhibitor
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DCC5099 Tfgf-18
Novel GSK-3β inhibitor, showing anti-neuroinflammatory effects in lipopolysaccharide (LPS) activation of spontaneously immortalized SIM-A9 microglial cells and of mouse cortical microglia, inhibiting LPS-induced production of nitric oxide and the proinfla
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DCC5098 Tfah-10n
Novel multipotent anti-Alzheimer agent, selectively inhibiting human butyrylcholinesterase (BChE), having strong antioxidant activity and good β-amyloid (Aβ) anti-aggregation properties
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DCC5097 Tezosentan
Novel endothelin (ET) receptor antagonist
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DCC5096 Texasin
Potent and selective human leukocyte 5-lipoxygenase (5-LOX) inhibitor
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