N-alpha-Acetyl-L-ornithine structure
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Common Name | N-alpha-Acetyl-L-ornithine | ||
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CAS Number | 6205-08-9 | Molecular Weight | 174.19800 | |
Density | 1.171g/cm3 | Boiling Point | 436.2ºC at 760 mmHg | |
Molecular Formula | C7H14N2O3 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 217.6ºC |
Use of N-alpha-Acetyl-L-ornithineN-Acetylornithine is an intermediate in the enzymatic biosynthesis of the amino acid L-arginine from L-glutamate. |
Name | N2-acetyl-L-ornithine |
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Synonym | More Synonyms |
Description | N-Acetylornithine is an intermediate in the enzymatic biosynthesis of the amino acid L-arginine from L-glutamate. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
Density | 1.171g/cm3 |
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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) |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2924199090 |
Precursor 0 | |
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DownStream 1 | |
HS Code | 2924199090 |
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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% |
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... |
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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... |
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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... |
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 |