| 词条 | Parathion S |
| 释义 |
| Name = Parathion S | ImageFile = Parathion S.svg | ImageSize = 200px | IUPACName = O,O-Diethyl S-(4-nitrophenyl) phosphorothioate | OtherNames = S-Phenyl parathion | Section1 = {{Chembox Identifiers | CASNo = 3270-86-8 | ChemSpiderID = 2297420 | PubChem = 3032440 | SMILES = CCOP(=O)(OCC)Sc1ccc(cc1)[N+](=O)[O-] | StdInChI = InChI=1S/C10H14NO5PS/c1-3-15-17(14,16-4-2)18-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3 | StdInChIKey = DSVCXDBXXBVSEB-UHFFFAOYSA-N }} | Section2 = {{Chembox Properties | C=10|H=14|N=1|O=5|P=1|S=1 | Appearance = Pale yellow crystalline solid }} | Section3 = {{Chembox Hazards | LD50 = 107 μg/kg (mice, intraperitoneal)[1] 4.41 mg/kg (rats, oral)[1] }} }}Parathion S is an organophosphate related to the organophosphate insecticide paraoxon and parathion. It's the structural isomer of parathion. Parathion S is a potent acetylcholinesterase inhibitor.[2][3] See also
References1. ^1 {{cite web |title=ChemIDplus |url=https://chem.nlm.nih.gov/chemidplus/rn/3270-86-8}} {{Acetylcholine metabolism and transport modulators}}{{Organic-compound-stub}}2. ^{{cite journal |last1=DIGGLE |first1=WM |last2=GAGE |first2=JC |title=Cholinesterase inhibition in vitro by OO-diethyl O-p-nitrophenyl thiophosphate (parathion, E 605). |journal=The Biochemical Journal |date=September 1951 |volume=49 |issue=4 |pages=491–4 |pmid=14886312 |pmc=1197537|doi=10.1042/bj0490491 }} 3. ^{{cite journal |last1=ALDRIDGE |first1=WN |last2=DAVISON |first2=AN |title=The inhibition of erythrocyte cholinesterase by tri-esters of phosphoric acid. II. Diethyl p-nitrophenyl thionphosphate (E605) and analogues. |journal=The Biochemical Journal |date=December 1952 |volume=52 |issue=4 |pages=663–71 |pmid=13018298 |pmc=1198077|doi=10.1042/bj0520663 }} 4 : Acetylcholinesterase inhibitors|Phosphorothioates|Ethyl esters|Nitrobenzenes |
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