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N-alpha-Acetyl-L-ornithine

Names

[ CAS No. ]:
6205-08-9

[ Name ]:
N-alpha-Acetyl-L-ornithine

[Synonym ]:
N(2)-acetyl-L-ornithine
N-acetylornithine
ACETYL-L-ORNITHINE
Ornithine,N2-acetyl
AOR
(2S)-2-acetamido-5-aminopentanoic acid
N|A-Acetyl-L-ornithine
N-α-acetyl-l-ornithine
N-alpha-Acetyl-L-ornithine

Biological Activity

[Description]:

N-Acetylornithine is an intermediate in the enzymatic biosynthesis of the amino acid L-arginine from L-glutamate.

[Related Catalog]:

Natural Products >> Others
Research Areas >> Others

[Target]

Human Endogenous Metabolite


[Related Small Molecules]

3-Methyladenine | Hydrocortisone | Acetylcysteine(N-acetylcysteine) | Retinoic acid | Melatonine | Dinoprostone | Nicotinamide | Adenosine triphosphate | 4-Acetamidophenol | Prostaglandin E1 | Dehydroepiandrosterone | Corticosterone | Progesterone | Docosahexaenoic Acid | NAD+

Chemical & Physical Properties

[ Density]:
1.171g/cm3

[ Boiling Point ]:
436.2ºC at 760 mmHg

[ Molecular Formula ]:
C7H14N2O3

[ Molecular Weight ]:
174.19800

[ Flash Point ]:
217.6ºC

[ Exact Mass ]:
174.10000

[ PSA ]:
92.42000

[ LogP ]:
0.40580

[ Appearance of Characters ]:
Solid

[ Index of Refraction ]:
1.492

[ Storage condition ]:
−20°C

[ Water Solubility ]:
Freely soluble (880 g/L) (25 ºC)

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Metabolomic profiling of serum in the progression of Alzheimer's disease by capillary electrophoresis-mass spectrometry.

Electrophoresis 35(23) , 3321-30, (2014)

There is high interest in the discovery of early diagnostic biomarkers of Alzheimer's disease, for which metabolomics exhibits a great potential. In this work, a metabolomic approach based on ultrafil...

Inhibitors of N(alpha)-acetyl-L-ornithine deacetylase: synthesis, characterization and analysis of their inhibitory potency.

Amino Acids 38 , 1155-1164, (2010)

A series of N (alpha)-acyl (alkyl)- and N (alpha)-alkoxycarbonyl-derivatives of L- and D-ornithine were prepared, characterized, and analyzed for their potency toward the bacterial enzyme N (alpha)-ac...

Model-driven discovery of underground metabolic functions in Escherichia coli.

Proc. Natl. Acad. Sci. U. S. A. 112(3) , 929-34, (2015)

Enzyme promiscuity toward substrates has been discussed in evolutionary terms as providing the flexibility to adapt to novel environments. In the present work, we describe an approach toward exploring...


More Articles


Related Compounds