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Inhibitor Report for: PMP-MeCyC

Name Class
PMP-MeCyCType (7)
Other_Name (5)
Chemical_Nomenclature7-[3,3-dimethylbutan-2-yloxy(methyl)phosphoryl]oxy-4-methyl-2-oxochromene-3-carbonitrile
FormulaC18H22NO5P
MW363.34
Paper (4)
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)
CID49795037
FamilyACHE
InChIKeyFHPKBNXJPLMRFC-UHFFFAOYSA-N
CanonicalSMILESCC1=C(C(=O)OC2=C1C=CC(=C2)OP(=O)(C)OC(C)C(C)(C)C)C#N
InChIInChI=1S/C18H22NO5P/c1-11-14-8-7-13(9-16(14)22-17(20)15(11)10-19)24-25(6,21)23-12(2)18(3,4)5/h7-9,12H,1-6H3

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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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