Browsing Toxins By Category
Displaying toxin 3351 - 3375 of 3678 in total
T3DB ID | Name CAS Number | Formula Weight | Structure | Type | Mechanism of Toxicity |
---|---|---|---|---|---|
T3D4541 | Thidiazuron 51707-55-2 | C9H8N4OS 220.251 g/mol |
| The US EPA has found no information indicating thidiazuron shares a common mechanism of toxicity with other substances. (L2080) Number of Targets: 11 | |
T3D1011 | Thiobencarb 28249-77-6 | C12H16ClNOS 257.780 g/mol |
| Thiobencarb is a cholinesterase or acetylcholinesterase (AChE) inhibitor. Carbamates form unstable complexes with chlolinesterases by carbamoylation of the active site...more Number of Targets: 16 | |
T3D1012 | Thiocarboxime 25171-63-5 | C7H11N3O2S 201.246 g/mol |
| Thiocarboxime is a cholinesterase or acetylcholinesterase (AChE) inhibitor. Carbamates form unstable complexes with chlolinesterases by carbamoylation of the active si...more Number of Targets: 2 | |
T3D0089 | Thiocyanate 302-04-5 | CNS 58.083 g/mol |
| Thiocyanate (sulphocyanate or SCN) is believed to be a goitrogenic compound. It is a competitive inhibitor of the human thyroid sodium/iodide symporter NIS. Thus, the ...more Number of Targets: 8 | |
T3D1013 | Thiodicarb 59669-26-0 | C10H18N4O4S3 354.469 g/mol |
| Thiodicarb is a cholinesterase or acetylcholinesterase (AChE) inhibitor. Carbamates form unstable complexes with chlolinesterases by carbamoylation of the active sites...more Number of Targets: 17 | |
T3D1014 | Thiofanox 39196-18-4 | C9H18N2O2S 218.316 g/mol |
| Thiofanox is a cholinesterase or acetylcholinesterase (AChE) inhibitor. Carbamates form unstable complexes with chlolinesterases by carbamoylation of the active sites ...more Number of Targets: 2 | |
T3D1364 | Thiomersal 54-64-8 | C9H9HgNaO2S 404.810 g/mol |
| High-affinity binding of the divalent mercuric ion to thiol or sulfhydryl groups of proteins is believed to be the major mechanism for the activity of mercury. Through...more Number of Targets: 53 | |
T3D3088 | Thionin (Pyrularia pubera) Not Available | Not Available 5288.110 g/mol |
| Thionins are thought to attack the cell membrane and render it permeable. This results in the inhibition of sugar uptake and allows potassium and phosphate ions, prote...more Number of Targets: 0 | |
T3D1764 | Thionyl bromide 507-16-4 | Br2OS 207.872 g/mol |
| Bromine is a powerful oxidizing agent and is able to release oxygen free radicals from the water in mucous membranes. These free radicals are also potent oxidizers and...more Number of Targets: 6 | |
T3D2835 | Thiopental 76-75-5 | C11H18N2O2S 242.338 g/mol |
| Thiopental binds at a distinct binding site associated with a Cl- ionopore at the GABAA receptor, increasing the duration of time for which the Cl- ionopore is open. T...more Number of Targets: 12 | |
T3D3934 | Thiophanate-methyl 23564-05-8 | C12H14N4O4S2 342.394 g/mol |
| Not Available Number of Targets: 11 | |
T3D2858 | Thioridazine 50-52-2 | C21H26N2S2 370.575 g/mol |
| Thioridazine blocks postsynaptic mesolimbic dopaminergic D1 and D2 receptors in the brain; blocks alpha-adrenergic effect, depresses the release of hypothalamic and hy...more Number of Targets: 15 | |
T3D4716 | Thiotepa 52-24-4 | C6H12N3PS 189.218 g/mol |
| The alkyl group is attached to the guanine base of DNA, at the number 7 nitrogen atom of the imidazole ring. They stop tumor growth by crosslinking guanine nucleobases...more Number of Targets: 1 | |
T3D4891 | Thiourea 62-56-6 | CH4N2S 76.121 g/mol |
| Not Available Number of Targets: 1 | |
T3D4542 | Thiram 137-26-8 | C6H12N2S4 240.433 g/mol |
| Not Available Number of Targets: 33 | |
T3D1313 | Thorin 3688-92-4 | C16H11AsN2Na2O10S2 576.297 g/mol |
| Arsenic and its metabolites disrupt ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by co...more Number of Targets: 44 | |
T3D0101 | Thorium 7440-29-1 | Th 232.038 g/mol |
| The ionizing radiation produced by thorium causes cellular damage that includes DNA breakage, accurate or inaccurate repair, apoptosis, gene mutations, chromosomal cha...more Number of Targets: 1 | |
T3D0221 | Thorium-227 15623-47-9 | Th 227.028 g/mol |
| The ionizing radiation produced by thorium causes cellular damage that includes DNA breakage, accurate or inaccurate repair, apoptosis, gene mutations, chromosomal cha...more Number of Targets: 1 | |
T3D0113 | Thorium-228 14274-82-9 | Th 228.029 g/mol |
| The ionizing radiation produced by thorium causes cellular damage that includes DNA breakage, accurate or inaccurate repair, apoptosis, gene mutations, chromosomal cha...more Number of Targets: 1 | |
T3D0107 | Thorium-230 14269-63-7 | Th 230.033 g/mol |
| The ionizing radiation produced by thorium causes cellular damage that includes DNA breakage, accurate or inaccurate repair, apoptosis, gene mutations, chromosomal cha...more Number of Targets: 1 | |
T3D2926 | Tiagabine 115103-54-3 | C20H25NO2S2 375.548 g/mol |
| Though the exact mechanism by which Tiagabine exerts its effect on the human body is unknown, it does appear to operate as a selective GABA reuptake inhibitor. Number of Targets: 4 | |
T3D1015 | Tillam sulfoxide 51892-60-5 | C10H21NO2S 219.344 g/mol |
| Some thiocarbamates (EPTC, Molinate, Pebulate, and Cycloate) share a common mechanism of toxicity, i.e. the inhibition of acetylcholinesterase. An acetylcholinesterase...more Number of Targets: 2 | |
T3D0796 | Tin 7440-31-5 | Sn 118.710 g/mol |
| Organotin compounds produce neurotoxic and immunotoxic effects. Organotins may directly activate glial cells contributing to neuronal cell degeneration by local releas...more Number of Targets: 15 | |
T3D1275 | Tin chloride 7646-78-8 | Cl4Sn 260.520 g/mol |
| Inorganic and organic tin compounds are weak inhibitors of alcohol dehydrogenase. (A183) Number of Targets: 7 | |
T3D1266 | Tin selenide 1315-06-0 | SeSn 197.670 g/mol |
| Selenium readily substitutes for sulfur in biomolecules and in many biochemical reactions, especially when the concentration of selenium is high and the concentration ...more Number of Targets: 7 |