N-acetylanthranilate

General

Type : Natural, Benzoate

Chemical_Nomenclature : 2-acetamidobenzoic acid

Canonical SMILES : CC(=O)NC1=CC=CC=C1C(=O)O

InChI : InChI=1S\/C9H9NO3\/c1-6(11)10-8-5-3-2-4-7(8)9(12)13\/h2-5H,1H3,(H,10,11)(H,12,13)

InChIKey : QSACCXVHEVWNMX-UHFFFAOYSA-N

Other name(s) : 2-Acetamidobenzoic acid  ||  N-ACETYLANTHRANILIC ACID  ||  2-(Acetylamino)benzoic acid  ||  2-Carboxyacetanilide  ||  Acetylanthranilic acid  ||  ZZ8  ||  2-acetamidobenzoate  ||  Acetamidobenzoate  ||  P-acetaminobenzoate  ||  2-(acetylamino)benzoate  ||  AC1NUSR8


MW : 179.17

Formula : C9H9NO3

CAS_number : 89-52-1

PubChem : 6971

UniChem : QSACCXVHEVWNMX-UHFFFAOYSA-N

References (4)

Title : Evolutionary adaptation from hydrolytic to oxygenolytic catalysis at the alpha\/beta fold - Bui_2023_Chem.Sci_14_10547
Author(s) : Bui S , Gil-Guerrero S , van der Linden P , Carpentier P , Ceccarelli M , Jambrina PG , Steiner RA
Ref : Chem Sci , 14 :10547 , 2023
Abstract :
PubMedSearch : Bui_2023_Chem.Sci_14_10547
PubMedID: 37799987
Gene_locus related to this paper: artsp-hod

Title : Structural basis for cofactor-independent dioxygenation of N-heteroaromatic compounds at the alpha\/beta-hydrolase fold - Steiner_2010_Proc.Natl.Acad.Sci.U.S.A_107_657
Author(s) : Steiner RA , Janssen HJ , Roversi P , Oakley AJ , Fetzner S
Ref : Proc Natl Acad Sci U S A , 107 :657 , 2010
Abstract :
PubMedSearch : Steiner_2010_Proc.Natl.Acad.Sci.U.S.A_107_657
PubMedID: 20080731
Gene_locus related to this paper: artsp-hod , psepu-QDO

Title : N-acetylanthranilate amidase from Arthrobacter nitroguajacolicus Ru61a, an alpha\/beta-hydrolase-fold protein active towards aryl-acylamides and -esters, and properties of its cysteine-deficient variant - Kolkenbrock_2006_J.Bacteriol_188_8430
Author(s) : Kolkenbrock S , Parschat K , Beermann B , Hinz HJ , Fetzner S
Ref : Journal of Bacteriology , 188 :8430 , 2006
Abstract :
PubMedSearch : Kolkenbrock_2006_J.Bacteriol_188_8430
PubMedID: 17041061
Gene_locus related to this paper: 9micc-q7wsq8

Title : 2,4-dioxygenases catalyzing N-heterocyclic-ring cleavage and formation of carbon monoxide. Purification and some properties of 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase from Arthrobacter sp. Ru61a and comparison with 1H-3-hydroxy-4-oxoquinoline 2,4-dioxygenase from Pseudomonas putida 33\/1 - Bauer_1996_Eur.J.Biochem_240_576
Author(s) : Bauer I , Max N , Fetzner S , Lingens F
Ref : European Journal of Biochemistry , 240 :576 , 1996
Abstract :
PubMedSearch : Bauer_1996_Eur.J.Biochem_240_576
PubMedID: 8856057
Gene_locus related to this paper: artsp-hod , psepu-QDO