Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

A3626

Sigma-Aldrich

Nα-Acetyl-L-ornithine

Synonym(s):

N2-acetyl-L-lysine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C7H14N2O3
CAS Number:
6205-08-9
Molecular Weight:
174.20
MDL number:
MFCD00065115
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
24890789
NACRES:
NA.26

Assay

≥98% (TLC)

Quality Level

200

form

powder

technique(s)

ligand binding assay: suitable

color

colorless to white

storage temp.

−20°C

SMILES string

CC(=O)N[C@@H](CCCN)C(O)=O

InChI

1S/C7H14N2O3/c1-5(10)9-6(7(11)12)3-2-4-8/h6H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t6-/m0/s1

InChI key

JRLGPAXAGHMNOL-LURJTMIESA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Biochem/physiol Actions

Nα-Acetyl-L-ornithine (AORN) is a substrate for the identification, differentiation and characterization of N(α)-acetyl-L-ornithine deacetylase(s) and of N-Acetyl-l-ornithine transcarbamylase(s) (AOTCase) found in plants, some eubacteria and some human pathogens.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Daniel Charlier et al.
Amino acids, 51(8), 1103-1127 (2019-07-04)
Already very early, the study of microbial arginine biosynthesis and its regulation contributed significantly to the development of new ideas and concepts. Hence, the term "repression" was proposed by Vogel (The chemical basis of heredity, The John Hopkins Press, Baltimore
Séverine Lemarié et al.
Plant & cell physiology, 56(11), 2158-2168 (2015-09-13)
The role of salicylic acid (SA) and jasmonic acid (JA) signaling in resistance to root pathogens has been poorly documented. We assessed the contribution of SA and JA to basal and partial resistance of Arabidopsis to the biotrophic clubroot agent
Dashuang Shi et al.
Proteins, 64(2), 532-542 (2006-06-03)
N-acetyl-L-ornithine transcarbamoylase (AOTCase) is a new member of the transcarbamoylase superfamily that is essential for arginine biosynthesis in several eubacteria. We report here crystal structures of the binary complexes of AOTCase with its substrates, carbamoyl phosphate (CP) or N-acetyl-L-ornithine (AORN)
Dashuang Shi et al.
The Journal of biological chemistry, 280(15), 14366-14369 (2005-02-26)
We have identified in Xanthomonas campestris a novel N-acetylornithine transcarbamylase that replaces ornithine transcarbamylase in the canonic arginine biosynthetic pathway of several Eubacteria. The crystal structures of the protein in the presence and absence of the reaction product, N-acetylcitrulline, were
Yongdong Li et al.
Biochemistry, 49(32), 6887-6895 (2010-08-11)
N-Acetyl-l-ornithine transcarbamylase (AOTCase), rather than ornithine transcarbamylase (OTCase), is the essential carbamylase enzyme in the arginine biosynthesis of several plant and human pathogens. The specificity of this unique enzyme provides a potential target for controlling the spread of these pathogens.
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service