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Displaying toxin 1351 - 1375 of 3678 in total
T3DB ID Name
CAS Number
Formula
Weight
StructureTypeMechanism of Toxicity
T3D1354Phenylmercuric chloride
100-56-1
C6H5ClHg
313.150 g/mol
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  • Aromatic Hydrocarbon
  • Industrial/Workplace Toxin
  • Mercury Compound
  • Organic Compound
  • Organometallic
  • Pollutant
  • Synthetic Compound
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: 51
T3D1114Barium iron oxide
12047-11-9
BaFe2O4
313.015 g/mol
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  • Barium Compound
  • Industrial/Workplace Toxin
  • Inorganic Compound
  • Synthetic Compound
Barium is a competitive potassium channel antagonist that blocks the passive efflux of intracellular potassium, resulting in a shift of potassium from extracellular to...more
Number of Targets: 21
T3D0661Cobalt(II) iodide
15238-00-3
CoI2
312.742 g/mol
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  • Cobalt Compound
  • Industrial/Workplace Toxin
  • Inorganic Compound
  • Pollutant
  • Synthetic Compound
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
T3D4454Phytanic acid
14721-66-5
C20H40O2
312.530 g/mol
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  • Animal Toxin
  • Food Toxin
  • Metabolite
  • Natural Compound
  • Organic Compound
  • Plant Toxin
Not Available
Number of Targets: 4
T3D0694Nickel iodide
13462-90-3
I2Ni
312.502 g/mol
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  • Industrial/Workplace Toxin
  • Inorganic Compound
  • Nickel Compound
  • Pollutant
  • Synthetic Compound
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: 68
T3D4749Levonorgestrel
797-63-7
C21H28O2
312.446 g/mol
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  • Contraceptive Agent
  • Contraceptive Agent, Female
  • Contraceptive, Oral, Synthetic
  • Drug
  • Ester
  • Metabolite
  • Organic Compound
  • Synthetic Compound
Binds to the progesterone and estrogen receptors. Target cells include the female reproductive tract, the mammary gland, the hypothalamus, and the pituitary. Once boun...more
Number of Targets: 7
T3D2754Olanzapine
132539-06-1
C17H20N4S
312.433 g/mol
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  • Amine
  • Antiemetic
  • Antipsychotic Agent
  • Drug
  • Food Toxin
  • Metabolite
  • Organic Compound
  • Serotonin Uptake Inhibitor
  • Synthetic Compound
Olanzapine's antipsychotic activity is likely due to a combination of antagonism at D2 receptors in the mesolimbic pathway and 5HT2A receptors in the frontal cortex. A...more
Number of Targets: 36
T3D3558Cellulose nitrate
9004-70-0
C20H16N4
312.368 g/mol
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  • Explosive Agent
  • Household Toxin
  • Industrial/Workplace Toxin
  • Inorganic Compound
  • Nitrate
  • Organic Compound
  • Synthetic Compound
Nitrate's toxicity is a result of it's conversion to nitrite once in the body. Nitrite causes the autocatalytic oxidation of oxyhemoglobin to hydrogen peroxide and met...more
Number of Targets: 9
T3D0195Benzyl butyl phthalate
85-68-7
C19H20O4
312.360 g/mol
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  • Aromatic Hydrocarbon
  • Cosmetic Toxin
  • Ester
  • Ether
  • Household Toxin
  • Industrial/Workplace Toxin
  • Organic Compound
  • Phthalate
  • Plasticizer
  • Pollutant
  • Synthetic Compound
Phthalate esters are endocrine disruptors. They decrease foetal testis testosterone production and reduce the expression of steroidogenic genes by decreasing mRNA expr...more
Number of Targets: 11
T3D3674Nivalenol
23282-20-4
C15H20O7
312.315 g/mol
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  • Ester
  • Ether
  • Food Toxin
  • Fungal Toxin
  • Lachrymator
  • Metabolite
  • Mycotoxin
  • Natural Compound
  • Organic Compound
Unlike many other mycotoxins, trichothecenes do not require metabolic activation to exert their biological activity, instead directly reacting with cellular components...more
Number of Targets: 2
T3D3598Aflatoxin B1
1162-65-8
C17H12O6
312.274 g/mol
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  • Ester
  • Ether
  • Food Toxin
  • Fungal Toxin
  • Metabolite
  • Mycotoxin
  • Natural Compound
  • Organic Compound
Aflatoxin B1 requires epoxidation to aflatoxin B1 2,3-oxide for activation, which is performed by cytochome P-450 enzymes CYP1A2 and CYP3A4. It produces DNA damage, ge...more
Number of Targets: 11
T3D1818Diphenyl diselenide
1666-13-3
C12H10Se2
312.130 g/mol
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  • Aromatic Hydrocarbon
  • Industrial/Workplace Toxin
  • Organic Compound
  • Pollutant
  • Selenium Compound
  • Synthetic Compound
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
T3D19182,3-Dibromobiphenyl
115245-06-2
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19392,2'-Dibromobiphenyl
13029-09-9
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19413,5-Dibromobiphenyl
16372-96-6
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19433,3'-Dibromobiphenyl
16400-51-4
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19542,3'-Dibromobiphenyl
49602-90-6
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19552,4'-Dibromobiphenyl
49602-91-7
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19572,4-Dibromobiphenyl
53592-10-2
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19603,4'-Dibromobiphenyl
57186-90-0
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19612,5-Dibromobiphenyl
57422-77-2
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19622,6-Dibromobiphenyl
59080-32-9
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D19773,4-Dibromobiphenyl
60108-72-7
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D20194,4'-Dibromobiphenyl
92-86-4
C12H8Br2
312.000 g/mol
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  • Aromatic Hydrocarbon
  • Bromide Compound
  • Industrial/Workplace Toxin
  • Organic Compound
  • Organobromide
  • Polybrominated Biphenyl
  • Synthetic Compound
The exact mechanism of toxicty of PBBs varies depending on the specific congener. The predominant interaction is believed to involve the aryl hydrocarbon receptor (AhR...more
Number of Targets: 1
T3D1087Butachlor
23184-66-9
C17H26ClNO2
311.847 g/mol
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  • Amide
  • Amine
  • Aromatic Hydrocarbon
  • Chloroacetanilide
  • Ether
  • Organic Compound
  • Organochloride
  • Pesticide
  • Synthetic Compound
Binds to nAChRs in nervous systems. Also causes endocrine disruption in humans by binding to and inhibiting the estrogen receptor. (T10, A590)
Number of Targets: 35
Displaying toxin 1351 - 1375 of 3678 in total