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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H12N4O3
Molecular Weight 176.1738
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NOR-NOHA

SMILES

N[C@@H](CCNC(=N)NO)C(O)=O

InChI

InChIKey=KOBHCUDVWOTEKO-VKHMYHEASA-N
InChI=1S/C5H12N4O3/c6-3(4(10)11)1-2-8-5(7)9-12/h3,12H,1-2,6H2,(H,10,11)(H3,7,8,9)/t3-/m0/s1

HIDE SMILES / InChI

Molecular Formula C5H12N4O3
Molecular Weight 176.1738
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

N(ω)-hydroxy-nor-L-arginine (nor-NOHA), an arginase inhibitor, has therapeutic potential in the treatment of cardiovascular and obstructive airway diseases. Nor-NOHA is a reversible, competitive arginase inhibitor. The affinity of nor-NOHA for the to the arginase active site was found in the nanomolar range. Nor-NOHA has proven to be one of the strongest arginase inhibitors. Inhibition by nor-NOHA is ten times more potent on arginase II than on arginase I. The pharmacokinetics of nor-NOHA is characterized by high bioavailability, close to 100% after multiple dose and rapid elimination resulting in t1/2 of 15–30 min after intravenous and intraperitoneal administration to rats. Arginase inhibition with Nor-NOHA increased circulating arginine levels and decreased hepatic damage during liver I/R injury. Arginase blockade represents a potentially novel strategy to combat hepatic I/R injury associated with liver transplantation. Nor-NOHA is under investigation in clinical trial NCT02009527 (Arginase inhibition in ischemia-reperfusion injury).

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.5 µM [Ki]
PubMed

PubMed

TitleDatePubMed
Liver I/R injury is improved by the arginase inhibitor, N(omega)-hydroxy-nor-L-arginine (nor-NOHA).
2007 Feb
Effect of arginase inhibition on ischemia-reperfusion injury in patients with coronary artery disease with and without diabetes mellitus.
2014
Intracellular sources of ornithine for polyamine synthesis in endothelial cells.
2016 Oct
The arginase inhibitor Nω-hydroxy-nor-arginine (nor-NOHA) induces apoptosis in leukemic cells specifically under hypoxic conditions but CRISPR/Cas9 excludes arginase 2 (ARG2) as the functional target.
2018
Attenuated cutaneous microvascular function in healthy young African Americans: Role of intradermal l-arginine supplementation.
2018 Jul

Sample Use Guides

Ischemia-reperfusion Injury: 0.1 mg/ min i.a. for 20 min
Route of Administration: Intra-arterial
Nor-NOHA inhibited arginase with an IC50 value of 10 uM for intact endothelial cells (EC). Nor-NOHA (0.5 mM) alone inhibited arginase activity in EC by 98 %, increased total cellular concentrations of arginine by 14 %, and decreased total cellular concentrations of ornithine, putrescine and spermidine by 17, 65 and 74 %, respectively.
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:19:25 GMT 2023
Edited
by admin
on Sat Dec 16 10:19:25 GMT 2023
Record UNII
U0F1149OFR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NOR-NOHA
Common Name English
J842.499C
Code English
N.OMEGA.-HYDROXY-NOR-L-ARGININE
Common Name English
(2S)-2-AMINO-4-(((HYDROXYAMINO)IMINOMETHYL)AMINO)BUTANOIC ACID
Systematic Name English
N-HYDROXY-NOR-L-ARGININE
Common Name English
BUTANOIC ACID, 2-AMINO-4-(((HYDROXYAMINO)IMINOMETHYL)AMINO)-, (S)-
Systematic Name English
N-HYDROXY-NOR-ARGININE
Common Name English
Code System Code Type Description
PUBCHEM
446124
Created by admin on Sat Dec 16 10:19:25 GMT 2023 , Edited by admin on Sat Dec 16 10:19:25 GMT 2023
PRIMARY
FDA UNII
U0F1149OFR
Created by admin on Sat Dec 16 10:19:25 GMT 2023 , Edited by admin on Sat Dec 16 10:19:25 GMT 2023
PRIMARY
CAS
189302-40-7
Created by admin on Sat Dec 16 10:19:25 GMT 2023 , Edited by admin on Sat Dec 16 10:19:25 GMT 2023
PRIMARY
DRUG BANK
DB02381
Created by admin on Sat Dec 16 10:19:25 GMT 2023 , Edited by admin on Sat Dec 16 10:19:25 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY