Browsing Toxins By Category
Displaying toxin 451 - 475 of 3678 in total
| T3DB ID | Name CAS Number | Formula Weight | Structure | Type | Mechanism of Toxicity |
|---|---|---|---|---|---|
| T3D1842 | m-Cresol 108-39-4 | C7H8O 108.138 g/mol |  |
| m-Cresol is a cholinesterase or acetylcholinesterase (AChE) inhibitor. A cholinesterase inhibitor (or 'anticholinesterase') suppresses the action of acetylcholinestera...more Number of Targets: 5 |
| T3D1689 | Adiponitrile 111-69-3 | C6H8N2 108.141 g/mol |  |
| Organic nitriles decompose into cyanide ions both in vivo and in vitro. Consequently the primary mechanism of toxicity for organic nitriles is their production of toxi...more Number of Targets: 39 |
| T3D1574 | Palladium hydride 12648-42-9 | H2Pd 108.440 g/mol |  |
| Due to their ability to form strong complexes with both inorganic and organic ligands, palladium ions can disturb cellular equilibria, replace other essential ions, an...more Number of Targets: 6 |
| T3D1784 | Bromoethane 74-96-4 | C2H5Br 108.965 g/mol |  |
| Organobromide compounds, especially alkylbromides are strong alkylating agents. Consequently they can randomly modify the surfaces of proteins and lipids, leading to ...more Number of Targets: 3 |
| T3D1441 | Chromium(III) fluoride 7788-97-8 | CrF3 108.991 g/mol |  |
| Trivalent chromium may also form complexes with peptides, proteins, and DNA, resulting in DNA-protein crosslinks, DNA strand breaks, DNA-DNA interstrand crosslinks, ch...more Number of Targets: 5 |
| T3D3599 | 2-Aminophenol 95-55-6 | C6H7NO 109.126 g/mol |  |
| 2-Aminophenol interacts with both adult and fetal hemoglobin, forming methemoglobin. In comparison to its isomers, 3-aminophenol and 4-aminophenol, 2-aminophenol is th...more Number of Targets: 9 |
| T3D3600 | 4-Aminophenol 123-30-8 | C6H7NO 109.126 g/mol |  |
| 4-Aminobiphenyl requires metabolic activation in order to exert its toxicity. This is catalyzed by N-hydroxylation via cytochrome P450 1A2, then followed by O-sulfatio...more Number of Targets: 6 |
| T3D3601 | 3-Aminophenol 591-27-5 | C6H7NO 109.126 g/mol |  |
| 3-Aminophenol interacts with both adult and fetal hemoglobin, forming methemoglobin. In comparison to its isomers, 2-aminophenol and 4-aminophenol, 3-aminophenol is th...more Number of Targets: 15 |
| T3D1375 | Beryllium silicate 13598-00-0 | Be2O4Si 110.108 g/mol |  |
| Once in the body, beryllium acts as a hapten and interacts with human leucocyte antigen (HLA) DP presenting cells in the lungs, becoming physically associated with a m...more Number of Targets: 3 |
| T3D4575 | Pyrocatechol 120-80-9 | C6H6O2 110.111 g/mol |  |
| Not Available Number of Targets: 1 |
| T3D4577 | Hydroquinone 123-31-9 | C6H6O2 110.111 g/mol |  |
| Not Available Number of Targets: 11 |
| T3D4580 | 1,3-Benzenediol 108-46-3 | C6H6O2 110.111 g/mol |  |
| Not Available Number of Targets: 12 |
| T3D0689 | Nickel cyanide 557-19-7 | C2N2Ni 110.728 g/mol |  |
| Nickel is known to substitute for other essential elements in certain enzmes, such as calcineurin. It is genotoxic, and some nickel compounds have been shown to promot...more Number of Targets: 110 |
| T3D1819 | Selenium dioxide 7446-08-4 | O2Se 110.960 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: 0 |
| T3D1395 | Cobalt(II) cyanide 542-84-7 | C2CoN2 110.968 g/mol |  |
| Cobalt is believed to exhibit its toxicity through a oxidant-based and free radical-based processes. It produces oxygen radicals and may be oxidized to ionic cobalt, c...more Number of Targets: 77 |
| T3D1906 | cis-1,3-Dichloropropene 10061-01-5 | C3H4Cl2 110.970 g/mol |  |
| The primary toxic effects of cis-1,3-dichloropropene are portal-of-entry effects resulting from the chemical reactivity of the compound and its physicochemical propert...more Number of Targets: 3 |
| T3D1907 | trans-1,3-Dichloropropene 10061-02-6 | C3H4Cl2 110.970 g/mol |  |
| The primary toxic effects of trans-1,3-dichloropropene are portal-of-entry effects resulting from the chemical reactivity of the compound and its physicochemical prope...more Number of Targets: 3 |
| T3D1908 | 1,1-Dichloropropene 563-58-6 | C3H4Cl2 110.970 g/mol |  |
| The primary toxic effects of 1,1-dichloropropene are portal-of-entry effects resulting from the chemical reactivity of the compound and its physicochemical properties....more Number of Targets: 3 |
| T3D1909 | 1,2-Dichloropropene 563-54-2 | C3H4Cl2 110.970 g/mol |  |
| Metabolism of 1,2-D in the rat results in the formation of a mercapturic acid conjugate excreted largely in the urine. Proposed reactive intermediates include 1,2-epox...more Number of Targets: 3 |
| T3D1910 | 2,3-Dichloropropene 78-88-6 | C3H4Cl2 110.970 g/mol |  |
| The primary toxic effects of 2,3-dichloropropene are portal-of-entry effects resulting from the chemical reactivity of the compound and its physicochemical properties....more Number of Targets: 3 |
| T3D1911 | 3,3-Dichloropropene 563-57-5 | C3H4Cl2 110.970 g/mol |  |
| The primary toxic effects of 3,3-dichloropropene are portal-of-entry effects resulting from the chemical reactivity of the compound and its physicochemical properties....more Number of Targets: 3 |
| T3D1820 | Selenium Sulfide 7446-34-6 | SSe 111.030 g/mol |  |
| Selenium sulfide can be decomposed to selenium ions. Selenium readily substitutes for sulfur in biomolecules and in many biochemical reactions, especially when the con...more Number of Targets: 0 |
| T3D1823 | Selenium hexasulfide 75926-26-0 | SSe 111.030 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: 0 |
| T3D1705 | Methyl cyanoacrylate 137-05-3 | C5H5NO2 111.099 g/mol |  |
| Organic nitriles decompose into cyanide ions both in vivo and in vitro. Consequently the primary mechanism of toxicity for organic nitriles is their production of toxi...more Number of Targets: 39 |
| T3D1810 | Bromine dioxide 21255-83-4 | BrO2 111.903 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 |