O-Nitrophenylacetate

General

Type : Acetate || Aryl ester || 2-nitrophenyl

Chemical_Nomenclature : (2-nitrophenyl) acetate

Canonical SMILES : CC(=O)OC1=CC=CC=C1[N+](=O)[O-]

InChI : InChI=1S\/C8H7NO4\/c1-6(10)13-8-5-3-2-4-7(8)9(11)12\/h2-5H,1H3

InChIKey : MRCKRGSNLOHYRA-UHFFFAOYSA-N

Other name(s) : ONPA,     2-Nitrophenyl acetate,     O-Nitrophenyl acetate,     Acetic acid, 2-nitrophenyl ester,     2-Nitrophenol acetate,     Acetic acid, o-nitrophenyl ester


MW : 181.1

Formula : C8H7NO4

CAS_number : 610-69-5

PubChem :

UniChem :

Iuphar :

References (3)

Title : Comparison of benzil and trifluoromethyl ketone (TFK)-mediated carboxylesterase inhibition using classical and 3D-quantitative structure-activity relationship analysis - Harada_2009_Bioorg.Med.Chem_17_149
Author(s) : Harada T , Nakagawa Y , Wadkins RM , Potter PM , Wheelock CE
Ref : Bioorganic & Medicinal Chemistry , 17 :149 , 2009
Abstract : Harada_2009_Bioorg.Med.Chem_17_149
ESTHER : Harada_2009_Bioorg.Med.Chem_17_149
PubMedSearch : Harada_2009_Bioorg.Med.Chem_17_149
PubMedID: 19062296

Title : Evidence for subdomain flexibility in Drosophila melanogaster acetylcholinesterase - Stojan_2008_Biochemistry_47_5599
Author(s) : Stojan J , Ladurantie C , Siadat OR , Paquereau L , Fournier D
Ref : Biochemistry , 47 :5599 , 2008
Abstract : Stojan_2008_Biochemistry_47_5599
ESTHER : Stojan_2008_Biochemistry_47_5599
PubMedSearch : Stojan_2008_Biochemistry_47_5599
PubMedID: 18439026

Title : Inhibition of carboxylesterases by benzil (diphenylethane-1,2-dione) and heterocyclic analogues is dependent upon the aromaticity of the ring and the flexibility of the dione moiety - Hyatt_2005_J.Med.Chem_48_5543
Author(s) : Hyatt JL , Stacy V , Wadkins RM , Yoon KJ , Wierdl M , Edwards CC , Zeller M , Hunter AD , Danks MK , Crundwell G , Potter PM
Ref : Journal of Medicinal Chemistry , 48 :5543 , 2005
Abstract : Hyatt_2005_J.Med.Chem_48_5543
ESTHER : Hyatt_2005_J.Med.Chem_48_5543
PubMedSearch : Hyatt_2005_J.Med.Chem_48_5543
PubMedID: 16107154