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Inhibitor Report for: PMP-DDAO

Name Class
PMP-DDAOType (6)
Chemical_Nomenclaturemethylphosphonic acid pinacoyl ester 6,8-dichloro-9,9-dimethyl-7-oxo-7,9-dihydro-acridin-2-yl
FormulaC22H26Cl2NO4P
MW470.33
PaperAmitai_2006_Febs.J_273_1906
Amitai_2007_Toxicology_233_187
CommentSoman analogue. Fluorogenic organophosphate diesters that produce fluorescence emission upon hydrolysis. The first ester is ethyl (E), isopropyl (I), cyclohexyl (C) or pinacoyl (P) analogous to the structure of VX, Sarin, Cyclosarin, and Somen respectively. The fluorescent ester is 3-cyano-4-methyl-7-hydroxy coumarin (MeCyC) or 1,3-dichloro-7-hydroxy-9,9-dimethyl-9H-acridin-2-one (DDAO)
FamilyACHE
InChIKeyWFFUEFHECNYSQM-UHFFFAOYSA-N
CanonicalSMILESCC(C(C)(C)C)O[P](=O)(C)OC1=CC3=C(C=C1)N=C2C=C(C(=O)C(=C2C3(C)C)Cl)Cl
InChIInChI=1S/C22H26Cl2NO4P/c1-12(21(2,3)4)28-30(7,27)29-13-8-9-16-14(10-13)22(5,6)18-17(25-16)11-15(23)20(26)19(18)24/h8-12H,1-7H3

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Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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