Browsing Toxins By Category
Displaying toxin 1626 - 1650 of 3678 in total
| T3DB ID | Name CAS Number | Formula Weight | Structure | Type | Mechanism of Toxicity |
|---|---|---|---|---|---|
| T3D2543 | Crotoxin 9007-40-3 | Not Available 15272.965 g/mol |  |
| Crotoxin inhibits neuromuscular transmission by presynaptically blocking acetylcholine release from the nerve termini. (T170) Number of Targets: 0 |
| T3D1231 | Cupriethylenediamine 13426-91-0 | C4H14CuN4 181.727 g/mol |  |
| Excess copper is sequestered within hepatocyte lysosomes, where it is complexed with metallothionein. Copper hepatotoxicity is believed to occur when the lysosomes bec...more Number of Targets: 6 |
| T3D3816 | Cyanamide 420-04-2 | CH2N2 42.040 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: 5 |
| T3D3817 | Cyanazine 21725-46-2 | C9H13ClN6 240.693 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: 13 |
| T3D0028 | Cyanide 1957-12-05 | CN 26.018 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: 42 |
| T3D1679 | Cyanoacetamide 107-91-5 | C3H4N2O 84.077 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: 40 |
| T3D1683 | Cyanoacetic acid 372-09-8 | C3H3NO2 85.061 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 |
| T3D0673 | Cyanocobalamin 68-19-9 | C63H88CoN14O14P 1355.365 g/mol |  |
| Vitamin B12 is used in the body in two forms: Methylcobalamin and 5-deoxyadenosyl cobalamin. The enzyme methionine synthase needs methylcobalamin as a cofactor. This e...more Number of Targets: 46 |
| T3D0754 | Cyanogen 460-19-5 | C2N2 52.035 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 |
| T3D0755 | Cyanogen bromide 506-68-3 | CBrN 105.921 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: 45 |
| T3D0756 | Cyanogen chloride 506-77-4 | CClN 61.470 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 |
| T3D0758 | Cyanogen iodide 506-78-5 | CIN 152.922 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 |
| T3D3610 | Cyanoginosin-LA 96180-79-9 | C46H67N7O12 910.064 g/mol |  |
| The site of action of microcystins is the hepatocyte, the commonest cell type in the liver. They act by disrupting the cytoskeleton, the adaptable protein framework th...more Number of Targets: 23 |
| T3D4490 | Cyazofamid 120116-88-3 | C13H13ClN4O2S 324.786 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: 24 |
| T3D4491 | Cyclanilide 113136-77-9 | C11H9Cl2NO3 274.100 g/mol |  |
| Not Available Number of Targets: 21 |
| T3D0951 | Cycloate 1134-23-2 | C11H21NOS 215.356 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: 7 |
| T3D4032 | Cyclochlorotine 12663-46-6 | C24H31Cl2N5O7 572.438 g/mol |  |
| Cyclochlorotine (CC) causes hepatic necrosis and has carcinogenic properties. The in vitro application of CC on myocytes induced disruption of myofibrils and large acc...more Number of Targets: 0 |
| T3D3467 | Cyclohexane 110-82-7 | C6H12 84.160 g/mol |  |
| Petroleum distillates are central nervous system depressants and cause pulmonary damage. (A600) Number of Targets: 1 |
| T3D4763 | Cyclohexanol 108-93-0 | C6H12O 100.159 g/mol |  |
| Not Available Number of Targets: 2 |
| T3D4082 | Cyclopamine 4449-51-8 | C27H41NO2 411.620 g/mol |  |
| Cyclopamine causes usually fatal birth defects. It can prevent the fetal brain from dividing into two lobes (holoprosencephaly) and cause the development of a single e...more Number of Targets: 2 |
| T3D1398 | Cyclopentadienylcobalt dicarbonyl 12078-25-0 | C7H5CoO2 180.047 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: 35 |
| T3D3465 | Cyclopentane 287-92-3 | C5H10 70.133 g/mol |  |
| Petroleum distillates are central nervous system depressants and cause pulmonary damage. (A600) Number of Targets: 0 |
| T3D4688 | Cyclophosphamide 50-18-0 | C7H15Cl2N2O2P 261.086 g/mol |  |
| Alkylating agents work by three different mechanisms: 1) attachment of alkyl groups to DNA bases, resulting in the DNA being fragmented by repair enzymes in their atte...more Number of Targets: 2 |
| T3D3736 | Cyclopiazonic acid 18172-33-3 | C20H20N2O3 336.384 g/mol |  |
| Cyclopiazonic acid is potent and specific inhibitor of the endoplasmic and sarcoplasmic reticulum Ca+-dependent ATPases, which are essential for calcium reuptake in th...more Number of Targets: 9 |
| T3D1030 | Cycloprothrin 63935-38-6 | C24H17Cl2NO3 438.303 g/mol |  |
| Both type I and type II pyrethroids exert their effect by prolonging the open phase of the sodium channel gates when a nerve cell is excited. They appear to bind to th...more Number of Targets: 19 |