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Nω-Nitro-L-arginine methyl ester hydrochloride - 10mM in Water, high purity , CAS No.51298-62-5

    Grade & Purity:
  • 10mM in Water
In stock
Item Number
N424409
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N424409-1ml
1ml
Available within 4-8 weeks(?)
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$50.90

NOS inhibitor

View related series
Compound libraries (12325)

Basic Description

Synonyms 51298-62-5 | L-NAME hydrochloride | H-Arg(NO2)-OMe.HCl | LNAME hydrochloride | H-Arg(NO2)-Ome HCl | L-NAME HCl | Methyl N5-(imino(nitroamino)methyl)-L-ornithine monohydrochloride | NG-Nitro-L-arginine methyl ester hydrochloride | L-NAME (hydrochloride) | (S)-Methyl 2-amino
Specifications & Purity 10mM in Water
Biochemical and Physiological Mechanisms An analog of arginine that inhibits NO production. It has multiple effects on the vascular system. Inhibits relaxation induced by acetylcholine and induces an increase in arterial blood pressure. Abolishes lecithinized superoxide dismutase induced vasodil
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Nω-Nitro-L-arginine methyl ester hydrochloride has been used:

• to study the effects of brain-derived neurotrophic factor against neurotoxicity in rat cortical neurons

• to study its effect on far-infrared (FIR) enhanced microcirculation of rat skin

• to study its effect on leptin-induced regulation of myokine fibronectin type III domain containing five/irisin in murine myocytes and fat cells

• to study its effect on the levels of arginine Vasotocin and neuronal nitric oxide synthase mRNA levels in hypothalamic paraventricular nucleus and supraoptic nucleus of rat


Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Amino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent Arginine and derivatives
Alternative Parents Alpha amino acid esters  Nitroguanidines  Fatty acid esters  Nitramines  Methyl esters  Monocarboxylic acids and derivatives  Carboximidamides  Organopnictogen compounds  Organic zwitterions  Organic oxides  Monoalkylamines  Imines  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Arginine or derivatives - Alpha-amino acid ester - Nitroguanidine - Fatty acid ester - Fatty acyl - Nitramine - Methyl ester - Carboxylic acid ester - Guanidine - Organic nitro compound - Monocarboxylic acid or derivatives - Carboximidamide - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Imine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Hydrochloride - Organic zwitterion - Amine - Carbonyl group - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as arginine and derivatives. These are compounds containing arginine or a derivative thereof resulting from reaction of arginine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available

Associated Targets(Human)

NOS1 Tchem Nitric-oxide synthase, brain (1786 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NOS3 Tchem Nitric-oxide synthase, endothelial (1452 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATM Tchem Serine-protein kinase ATM (4198 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NOS1 Tchem Nitric oxide sythases; iNOS & nNOS (685 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
J774.A1 (2436 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name methyl (2S)-2-amino-5-[[amino(nitramido)methylidene]amino]pentanoate;hydrochloride
INCHI InChI=1S/C7H15N5O4.ClH/c1-16-6(13)5(8)3-2-4-10-7(9)11-12(14)15;/h5H,2-4,8H2,1H3,(H3,9,10,11);1H/t5-;/m0./s1
InChIKey QBNXAGZYLSRPJK-JEDNCBNOSA-N
Smiles COC(=O)C(CCCN=C(N)N[N+](=O)[O-])N.Cl
Isomeric SMILES COC(=O)[C@H](CCCN=C(N)N[N+](=O)[O-])N.Cl
WGK Germany 3
PubChem CID 135193
Molecular Weight 269.69
Beilstein 3744166
Reaxy-Rn 3744166

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Specific Rotation[α] 15 ° (C=3, MeOH)
Melt Point(°C) 159-161°C
Molecular Weight 269.690 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 7
Exact Mass 269.089 Da
Monoisotopic Mass 269.089 Da
Topological Polar Surface Area 149.000 Ų
Heavy Atom Count 17
Formal Charge 0
Complexity 274.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 1
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Solution Calculators

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