Cat. No. | Product Name | Field of Application | Chemical Structure |
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DCC5245 | Trpa1-in-2 |
Novel potent and selective TRPA1 inhibitor, interacting with the N-terminal ankyrin repeat (ankyrinR) domain
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DCC5244 | Trpa1 Agonist 2c |
Novel Photosensitive and Photoswitchable TRPA1 Agonist, Optically Control Pain through Channel Desensitization
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DCC5243 | Trovafloxacin |
Fluroquinolone antibiotic, suppressing c-Myc transcription and myeloma growth, inhibiting pannexin-1 channels through which ATP is released as find-me signals in apoptotic Jurkat cells
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DCC5242 | Tropisetron |
Serotonin 5-HT3 receptor antagonist
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DCC5241 | Tropanserin |
Potent and selective 5-HT3 receptor antagonist
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DCC5240 | trmd-in-51 |
First-in-class highly potent and selective inhibitor of TrmD (bacterial t-RNA-(N1G37) methyltransferase)
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DCC5239 | Trka-in-1 |
Novel potent and selective inhibitor of Tropomyosin-related kinase A (TrkA)
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DCC5238 | Trk-130 |
Novel opioid ligand for treatment of overactive bladder, acting as a μ-opioid receptor partial agonist
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DCC5237 | Trk Inhibitor 7d |
First Highly Selective and Broadly Effective Macrocycle-Based Type II TRK Inhibitor that Overcome Clinically Acquired Resistance
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DCC5236 | Tritiozine |
Novel anti-secretory and antiulcer agent for treatment of peptic ulcer disease and hypersecretory disorders
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DCC5235 | Triplin |
Copper ion chelator, causing the triple response phenotype by affecting copper ion transport in ethylene signaling from ATX1 to RAN1
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DCC5234 | Tripartin |
Specific inhibitor of the histone H3 lysine 9 demethylase KDM4 in HeLa cells.
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DCC5233 | Trimipramine |
Antipsychotic and sedative agent as a potent antagonist of H1, 5-HT2A, and alpha1-adrenergic receptors
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DCC5232 | Trigonellinamide |
Metabolite of nicotinamide; Specific and potent inhibitor of NNMT, increasing histone methylation at H3K4 and methylated H3K4 occupancy at gene promoters
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DCC5231 | Trifluoroacetyl Lysine |
Novel Bromodomain Binding Mimic of Lysine Acetylation
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DCC5230 | Trifluoperazine N-glucuronide |
Metabolite of Trifluoperazine; Antidepressant and antipsychotic
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DCC5229 | Tridecyl 2-aminoacetate Hydrochloride |
Potent NAE-hydrolyzing acid amidase (NAAA) inhibitor
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DCC5228 | Triciribine Phosphate |
AKT Inhibitor, Enhancing Gemcitabine Activity in Pancreatic Cancer Cells
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DCC5227 | Triazophos |
EC 3.1.1.7 (Acetylcholinesterase) inhibitor, acting as an insecticide, an acaricide, an agrochemical, and a nematicide
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DCC5226 | Trenbolone Enanthate |
Potent and long-acting derivative of the hormone Trenbolone
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DCC5225 | Trehalose-6-phosphate |
Central sugar signal in plants, regulating sucrose use and allocation, underpinning crop growth and development
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DCC5224 | Trc210258 |
Novel TGR5 agonist, reducing glycemic and dyslipidemic cardiovascular risk in animal models of diabesity
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DCC5223 | trapoxin B |
Inhibitor of histone deacetylases
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DCC5222 | Trantinterol |
Novel Highly Selective β2-Adrenoceptor Agonist as an Oral Antiasthmatic Agent
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DCC5221 | trans-resveratrol-4'-o-glucuronide |
Metabolite of Resveratrol
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DCC5220 | trans-resveratrol-3-o-glucuronide |
Metabolite of Resveratrol
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DCC5219 | Trans-ocma |
Natural specific inhibitor of γ-secretase, decreasing amyloid-beta levels without influencing cleavage of Notch, showing strong growth inhibitory effects on cancer cell lines and significant anti-complement activity, also acting as a PTP1B inhibitor
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DCC5218 | Trans-miyabenol C |
Natural resveratrol trimer, acting as a protein kinase C inhibitor
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DCC5217 | Trans-cbtbp |
Novel KGA allosteric inhibitor
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DCC5216 | Trans-bopc1 |
Novel HuR binder, modulating HuR-RNA interactions
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