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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| 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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