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Others

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Cat. No. Product Name Field of Application Chemical Structure
DCC5137 Th-pf01
Novel orthosteric-allosteric dual inhibitor of PfHT1 as selective antimalarial agent
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DCC5136 Thk-523
Selective Tau ligand, selectively binding to neurofibrillary tangles and neuropils in people with Alzheimer's disease
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DCC5135 Thiq-20c
Steroidomimetic and Chimeric Microtubule Disruptor
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DCC5134 Thioxodihydroquinazolinone-19
Novel inducer of apoptotic cell death in platinum-resistant A2780cis human ovarian cancer cells, exhibitong a strong inhibitory effect in ovarian CSC-LCs in combination with cisplatin
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DCC5133 Thiowurtzine
Novel Potent Inhibitor of the Opioid Receptors and the Ion Channels
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DCC5132 Thiomuscimol Hydrobromide
GABAA receptor agonist
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DCC5131 Thioluciferin
Firefly luciferin analog as a key element of bioluminescent reporters for oxidation state and thiol/disulfide equilibria
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DCC5130 Thioguanine-18
Novel potent DENV2-NS2B/NS3pro inhibitor
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DCC5129 Thiocrom-31
First-in-class potent, selective, reversible, and tight binding inhibitor of human monoamine oxidase B (hMAO-B) (hMAO-B IC 50 = 1.52 ± 0.15 nM)
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DCC5128 Thiobenzanilide 63t
Novel selective anticancer agent, selectively inducing cancer cell death in a caspase independent pathway
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DCC5127 Thielocin B1
Novel protein-protein interaction inhibitor of PAC3 homodimer
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DCC5126 Thidiazuron
Highly efficient bioregulator of plant morphogenesis in the tissue culture technique, inducing diverse responses ranging from induction of callus to embryogenesis or organogenesis, acting through modulation of the endogenous plant growth regulators, modif
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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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