Tolclofos-methyl

General

Type : Organophosphate,Fungicide,Sulfur Compound

Chemical_Nomenclature : (2,6-dichloro-4-methylphenoxy)-dimethoxy-sulfanylidene-$l^{5}-phosphane

Canonical SMILES : CC1=CC(=C(C(=C1)Cl)OP(=S)(OC)OC)Cl

InChI : InChI=1S\/C9H11Cl2O3PS\/c1-6-4-7(10)9(8(11)5-6)14-15(16,12-2)13-3\/h4-5H,1-3H3

InChIKey : OBZIQQJJIKNWNO-UHFFFAOYSA-N

Other name(s) : Tolclofos-methyl,Tolclophos-methyl,Risolex,Rizolex,Basilex,Toclofos-methyl


MW : 301.12

Formula : C9H11Cl2O3PS

CAS_number : 57018-04-9

PubChem : 91664

UniChem : OBZIQQJJIKNWNO-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : Tolclofos-methyl ligand of proteins in family: ACHE

Stucture :

Protein :

References (3)

Title : Oxidative Activation and Degradation of Organophosphorus Pesticides Mediated by Iron Porphyrins - Fujisawa_2005_J.Pestic.Sci_30_103
Author(s) : Fujisawa T , Katagi T
Ref : Journal of Pesticide Science , 30 :103 , 2005
Abstract : Fujisawa_2005_J.Pestic.Sci_30_103
ESTHER : Fujisawa_2005_J.Pestic.Sci_30_103
PubMedSearch : Fujisawa_2005_J.Pestic.Sci_30_103
PubMedID:

Title : Evaluation of respiratory and cutaneous doses and urinary excretion of alkylphosphates by workers in greenhouses treated with omethoate, fenitrothion, and tolclofos-methyl - Aprea_2001_AIHAJ_62_87
Author(s) : Aprea C , Sciarra G , Lunghini L , Centi L , Ceccarelli F
Ref : Aihaj , 62 :87 , 2001
Abstract : Aprea_2001_AIHAJ_62_87
ESTHER : Aprea_2001_AIHAJ_62_87
PubMedSearch : Aprea_2001_AIHAJ_62_87
PubMedID: 11258873

Title : Spontaneous reactivation of mouse plasma cholinesterase after inhibition by various organophosphorus compounds - Matsubara_1984_J.Pharmacobiodyn_7_322
Author(s) : Matsubara T , Horikoshi I
Ref : J Pharmacobiodyn , 7 :322 , 1984
Abstract : Matsubara_1984_J.Pharmacobiodyn_7_322
ESTHER : Matsubara_1984_J.Pharmacobiodyn_7_322
PubMedSearch : Matsubara_1984_J.Pharmacobiodyn_7_322
PubMedID: 6470929