U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C5H11NO2
Molecular Weight 117.1463
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NORVALINE

SMILES

CCC[C@H](N)C(O)=O

InChI

InChIKey=SNDPXSYFESPGGJ-BYPYZUCNSA-N
InChI=1S/C5H11NO2/c1-2-3-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
46.0 mM [Ki]
PubMed

PubMed

TitleDatePubMed
Macrophage arginase promotes tumor cell growth and suppresses nitric oxide-mediated tumor cytotoxicity.
2001 Feb 1
Human ornithine transcarbamylase: crystallographic insights into substrate recognition and conformational changes.
2001 Mar 15
Resistance and susceptibility to Marek's disease: nitric oxide synthase/arginase activity balance.
2002 May 1
Kinetic analysis of phenylalanine dehydrogenase mutants designed for aliphatic amino acid dehydrogenase activity with guidance from homology-based modelling.
2003 Dec
Two new cyclosporin folds observed in the structures of the immunosuppressant cyclosporin G and the formyl peptide receptor antagonist cyclosporin H at ultra-high resolution.
2003 May 7
Consumption of L-arginine mediated by Entamoeba histolytica L-arginase (EhArg) inhibits amoebicidal activity and nitric oxide production by activated macrophages.
2003 Nov-Dec
Thrombin stimulates human endothelial arginase enzymatic activity via RhoA/ROCK pathway: implications for atherosclerotic endothelial dysfunction.
2004 Dec 14
High glucose augments arginase activity and nitric oxide production in the renal cortex.
2004 Jul
Enzymatic evidence for the key role of arginine in nitrogen translocation by arbuscular mycorrhizal fungi.
2007 Jun
Structural and evolutionary bioinformatics of the SPOUT superfamily of methyltransferases.
2007 Mar 5
The crystal structures of ornithine carbamoyltransferase from Mycobacterium tuberculosis and its ternary complex with carbamoyl phosphate and L-norvaline reveal the enzyme's catalytic mechanism.
2008 Jan 25
Molecular evolution of B6 enzymes: binding of pyridoxal-5'-phosphate and Lys41Arg substitution turn ribonuclease A into a model B6 protoenzyme.
2008 Jun 19
A 3(10)-helical pentapeptide in water: interplay of alpha,alpha-disubstituted amino acids and the central residue on structure formation.
2009
Kinetic and thermodynamic control in the stereoselective formation of trans- and cis-2-ferrocenyl-3-pivaloyl-4-alkyl-1,3-oxazolidin-5-ones.
2009 Feb 7
Inhibition of S6K1 accounts partially for the anti-inflammatory effects of the arginase inhibitor L-norvaline.
2009 Mar 13
Glutathione-supported arsenate reduction coupled to arsenolysis catalyzed by ornithine carbamoyl transferase.
2009 Sep 1
Specificities of olfactory receptor neuron responses to amino acids in the black bullhead catfish (Ameiurus melas).
2010 Feb
Caloric restriction reverses high-fat diet-induced endothelial dysfunction and vascular superoxide production in C57Bl/6 mice.
2010 May
Patents

Patents

Name Type Language
NORVALINE
INCI   MI   WHO-DD  
INCI  
Official Name English
Norvaline [WHO-DD]
Common Name English
(S)-2-AMINOVALERIC ACID
Systematic Name English
(S)-2-AMINOPENTANOIC ACID
Systematic Name English
(S)-(+)-2-AMINOPENTANOIC ACID
Systematic Name English
L-.ALPHA.-AMINOVALERIC ACID
Common Name English
L-NORVALINE
Systematic Name English
NORVALINE [MI]
Common Name English
NORVALINE [INCI]
Common Name English
NSC-203786
Code English
NORVALINE, L-
Systematic Name English
2S-AMINOVALERIC ACID
Common Name English
Classification Tree Code System Code
DSLD 1076 (Number of products:82)
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
DSLD 3256 (Number of products:105)
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
Code System Code Type Description
CHEBI
19475
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
ECHA (EC/EINECS)
229-543-3
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
EVMPD
SUB34283
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
MESH
C005313
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
WIKIPEDIA
NORVALINE
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
NSC
203786
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
CAS
6600-40-4
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID701018015
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
CHEBI
18314
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
MERCK INDEX
m8075
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY Merck Index
PUBCHEM
65098
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
DRUG BANK
DB04185
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
SMS_ID
100000127966
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY
FDA UNII
A70UKS48FE
Created by admin on Fri Dec 15 16:31:25 GMT 2023 , Edited by admin on Fri Dec 15 16:31:25 GMT 2023
PRIMARY