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Cat. No. Product Name Field of Application Chemical Structure
DCC5081 Tefinostat Novel monocyte/macrophage targeted histone deacetylase inhibitor
DCC5082 Teijin Compound 1 Hydrochloride Featured CCR2 antagonist 4 hydrochloride (Teijin compound 1 hydrochloride) is a potent and specific CCR2 antagonist, with IC50s of 180 nM for CCR2b. CCR2 antagonist 4 hydrochloride potently inhibits MCP-1-induced chemotaxis with an IC50 of 24 nM.
DCC5083 Teixobactin Natural antibacterial agent, being active against gram-positive bacteria.
DCC5084 Telenzepine Potent and selective M1 antimuscarinic
DCC5085 Telmesteine Mucolitic agent, inhibiting activation of nuclear factor kappa-κB (NF-κB) by blocking phosphoinositide 3-kinase/protein kinase B (PI3K/Akt)/IκB kinase (IKK) activities, showing the anti-inflammatory properties on inflammation-associated skin diseases
DCC5086 Temoporfin Photosensitizing agent used in the treatment of squamous cell carcinoma of the head and neck, also showing activity agaimst COVID-19 Mpro
DCC5087 Tenidap Sodium COX/5-LOX inhibitor and cytokine-modulating anti-inflammatory agent
DCC5088 Tertomotide Peptide vaccine, residues (611-626) of the human telomerase reverse transcriptase catalytic subunit (hTERT), for the treatment of solid cancers
DCC5089 Terutroban Sodium Selective Thromboxane_receptor>thromboxane receptor antagonist
DCC5090 Tet3.0 Mutually Orthogonal Bioorthogonal Amino Acid, Enabling Efficient Protein Dual-Labeling in Cells
DCC5091 Tetrabenazine Reversible inhibitor of vesicular monoamine transporter 2, showing anti-chorea effect and decreasing uptake of monamines into synaptic vesicles, as well as depletion of monoamine storage
DCC5092 Tetrabromobisphenol A Activator of the hepatic interferon pathway in rats
DCC5093 Tetracenomycin X Potent inhibitor of protein synthesis, inhibiting translation by binding within the ribosomal exit tunnel
DCC5094 Tetrazanbigen Inducer of S phase arrest and apoptosis in hepatocellular carcinoma QGY-7701
DCC5095 Texaline Antitubercular agent
DCC5096 Texasin Potent and selective human leukocyte 5-lipoxygenase (5-LOX) inhibitor
DCC5097 Tezosentan Novel endothelin (ET) receptor antagonist
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
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
DCC5100 Tfmo-1 Novel cell-active, selective class IIa HDAC inhibitor
DCC5101 Tfmo-12 CNS-penetrant selective class IIa histone deacetylase (HDAC) inhibitor, exploiting the >100-fold selectivity over class I/IIb HDACs
DCC5102 Tfr4oht Cyclized tamoxifen analog, selective ER modulator (SERM)
DCC5103 Tg-0054 Novel and Potent Stem Cell Mobilizer; Inhibitor of SDF-1α/CXCR4 binding
DCC5104 Tg-0205221 Novel potent SARS coronavirus (CoV) 3CL protease inhibitor (Ki = 53 nM)
DCC5105 Tg100948 Novel dual VEGFR/Src kinase inhibitor
DCC5106 Tg101114 Novel inhibitor of T315I mutant enzyme, exhibiting reasonable in vivo efficacy in a xenograft mouse model harboring T315I
DCC5107 Tg11-77 Hydrochloride Novel, Potent, Selective, Water Soluble, Brain-Permeable EP2 Receptor Antagonist
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:
DCC5109 Tg2-in-3h Highly selective, potent, cell-permeable fluorescent irreversible tissue transglutaminase (TG2) inhibitor
DCC5110 Tg3-95-1 EP2 allosteric potentiator

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