Grundinformationen
- Standard-SMILES
CCOP(O)(=S)OCC- InChIKey
PKUWKAXTAVNIJR-UHFFFAOYSA-N- Summenformel
- C4H11O3PS
- Durchschnittliche Molmasse
- 170,17 g/mol
- Monoisotopische Masse
- 170,01665184
Überblick
O,O-diethyl hydrogen thiophosphate is an organic thiophosphate that is the diethyl ester of phosphorothioic O,O,O-acid. It has a role as a mouse metabolite and a human xenobiotic metabolite. It is a conjugate acid of an O,O-diethyl thiophosphate.
Namen und Bezeichner
- Bevorzugter Name
- O,O-diethyl phosphorothioate
- IUPAC
- diethoxy-hydroxy-sulfanylidene-λ5-phosphane
- Englischer Name
- O,O-Diethyl thiophosphate, potassium salt
- Summenformel
- C4H11O3PS
- Molmasse
- 170.17
Namen und Synonyme
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Datenbank-Bezeichner
- CAS
2465-65-8、5871-17-0- PubChem CID
- 655
- DTXSID
DTXSID9052844- ChEMBL
CHEMBL1232328- ChEBI
CHEBI:28006- UNII
- FND2ADQ374
- Nikkaji
- J80.493B
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,4
- Polarare Oberfläche (TPSA)
- 70,8 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 4
- Schwere Atome
- 9
- Formalladung
- 0
- Komplexität
- 106
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 180 · 180-186 °C(lit.)
- Siedepunkt
- 105 · 105-106 °C(Press: 2 Torr)
- Dichte
- 1.1806 g/cm3 · 1.1806 g/cm3
- pka
- -0.1 · -0.10±0.34(Predicted)
Sicherheit und Regulatorisches
Toxikologische Informationen
Toxicity Summary
Diethylthiophosphate (DETP) induces DNA damage only in the hepatic cell lines, and this effect could be related to a secondary non-diffusible metabolite generated by the activity of P450 enzymes since P450 enzyme inhibitors also inhibited the induction of DNA damage in hepatic cells. This organophosphorous (OP) metabolite has shown some toxicity in human peripheral blood mononucleated cells (PBMC). DETP is a cytotoxic compound in human PBMC. A relationship between urinary levels of DETP and the number of sperm susceptible to chromatin alteration has been reported among rural agricultural workers. In addition, a correlation between the frequency of aneuploidy in sperm and the levels of DETP in urine was identified in a rural population exposed to OP pesticides, indicating that the potential for genotoxicity following OP exposure may depend on the type and quantity of specific metabolites produced, such as DETP. (A15411)
Sicherheitsdaten
- wgk
- 3
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26-36
Chemie und Industrie
Pharmakologische Informationen
Metabolism/Metabolites
Diethyl thiophosphate is a known human metabolite of Diazinon.
Metabolism of organophosphates occurs principally by oxidation, by hydrolysis via esterases and by reaction with glutathione. Demethylation and glucuronidation may also occur. Oxidation of organophosphorus pesticides may result in moderately toxic products. In general, phosphorothioates are not directly toxic but require oxidative metabolism to the proximal toxin. The glutathione transferase reactions produce products that are, in most cases, of low toxicity. Paraoxonase (PON1) is a key enzyme in the metabolism of organophosphates. PON1 can inactivate some organophosphates through hydrolysis. PON1 hydrolyzes the active metabolites in several organophosphates insecticides as well as, nerve agents such as soman, sarin, and VX. The presence of PON1 polymorphisms causes there to be different enzyme levels and catalytic efficiency of this esterase, which in turn suggests that different individuals may be more susceptible to the toxic effect of organophosphate exposure.
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