DCC5081 |
Tefinostat |
Novel monocyte/macrophage targeted histone deacetylase inhibitor |
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DCC5082 |
Teijin Compound 1 Hydrochloride
Featured
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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. |
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DCC5083 |
Teixobactin |
Natural antibacterial agent, being active against gram-positive bacteria. |
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DCC5084 |
Telenzepine |
Potent and selective M1 antimuscarinic |
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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 |
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DCC5086 |
Temoporfin |
Photosensitizing agent used in the treatment of squamous cell carcinoma of the head and neck, also showing activity agaimst COVID-19 Mpro |
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DCC5087 |
Tenidap Sodium |
COX/5-LOX inhibitor and cytokine-modulating anti-inflammatory agent |
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DCC5088 |
Tertomotide |
Peptide vaccine, residues (611-626) of the human telomerase reverse transcriptase catalytic subunit (hTERT), for the treatment of solid cancers |
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DCC5089 |
Terutroban Sodium |
Selective Thromboxane_receptor>thromboxane receptor antagonist |
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DCC5090 |
Tet3.0 |
Mutually Orthogonal Bioorthogonal Amino Acid, Enabling Efficient Protein Dual-Labeling in Cells |
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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 |
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DCC5092 |
Tetrabromobisphenol A |
Activator of the hepatic interferon pathway in rats |
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DCC5093 |
Tetracenomycin X |
Potent inhibitor of protein synthesis, inhibiting translation by binding within the ribosomal exit tunnel |
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DCC5094 |
Tetrazanbigen |
Inducer of S phase arrest and apoptosis in hepatocellular carcinoma QGY-7701 |
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DCC5095 |
Texaline |
Antitubercular agent |
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DCC5096 |
Texasin |
Potent and selective human leukocyte 5-lipoxygenase (5-LOX) inhibitor |
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DCC5097 |
Tezosentan |
Novel endothelin (ET) receptor antagonist |
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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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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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DCC5100 |
Tfmo-1 |
Novel cell-active, selective class IIa HDAC inhibitor |
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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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DCC5102 |
Tfr4oht |
Cyclized tamoxifen analog, selective ER modulator (SERM) |
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DCC5103 |
Tg-0054 |
Novel and Potent Stem Cell Mobilizer; Inhibitor of SDF-1α/CXCR4 binding |
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DCC5104 |
Tg-0205221 |
Novel potent SARS coronavirus (CoV) 3CL protease inhibitor (Ki = 53 nM) |
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DCC5105 |
Tg100948 |
Novel dual VEGFR/Src kinase inhibitor |
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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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DCC5107 |
Tg11-77 Hydrochloride |
Novel, Potent, Selective, Water Soluble, Brain-Permeable EP2 Receptor Antagonist |
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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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DCC5109 |
Tg2-in-3h |
Highly selective, potent, cell-permeable fluorescent irreversible tissue transglutaminase (TG2) inhibitor |
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DCC5110 |
Tg3-95-1 |
EP2 allosteric potentiator |
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