N-(4-nitrophenyl)-butyramide

General

Type : Amidase substrate, pNP

Chemical_Nomenclature : N-(4-nitrophenyl)butanamide

Canonical SMILES : CCCC(=O)NC1=CC=C(C=C1)[N+](=O)[O-]

InChI : InChI=1S\/C10H12N2O3\/c1-2-3-10(13)11-8-4-6-9(7-5-8)12(14)15\/h4-7H,2-3H2,1H3,(H,11,13)

InChIKey : YATAVUWVWRFIRI-UHFFFAOYSA-N

Other name(s) : N-(4-nitrophenyl)butanamide  ||  p-nitrobutyranilide  ||  NSC404442  ||  Oprea1_433813


MW : 208.21

Formula : C10H12N2O3

CAS_number : 54191-12-7

PubChem : 346259

UniChem : YATAVUWVWRFIRI-UHFFFAOYSA-N

Target

Structures : No structure

Families : Canar_LipB, Carb_B_Bacteria

References (2)

Title : Combined Theoretical and Experimental Study to Unravel the Differences in Promiscuous Amidase Activity of Two Nonhomologous Enzymes - Galmes_2021_ACS.Catal_11_8635
Author(s) : Galmes M , Nodling AR , Luk L , Swiderek K , Moliner V
Ref : ACS Catal , 11 :8635 , 2021
Abstract :
PubMedSearch : Galmes_2021_ACS.Catal_11_8635
PubMedID: 35875595
Gene_locus related to this paper: bacsu-pnbae , canar-LipB

Title : Exploring the Origin of Amidase Substrate Promiscuity in CALB by a Computational Approach - Galmes_2020_ACS.Catal_10_1938
Author(s) : Galmes MA , Garcia-Junceda E , Swiderek K , Moliner V
Ref : ACS Catal , 10 :1938 , 2020
Abstract :
PubMedSearch : Galmes_2020_ACS.Catal_10_1938
PubMedID:
Gene_locus related to this paper: canar-LipB