99590-80-4
Chemical Structure
N2-Succinyl-L-ornithine
- CAS No.: 99590-80-4
- Formula:C9H16N2O5
- Molecular Weight:232.23
InChIKey: VWXQFHJBQHTHMK-LURJTMIESA-N
SMILES: NCCC[C@@H](C(O)=O)NC(CCC(O)=O)=O
Biological Activity: N2-Succinyl-L-ornithine is a metabolic intermediate and also a substrate of N2-acetylornithine 5-aminotransferase (EC 2.6.1.11). N2-Succinyl-L-ornithine acts as a precursor of Pyruvic acid (HY-Y0781) and supports the biosynthesis of α-solanine (HY-N6602) via the MEP/DOXP pathway. N2-Succinyl-L-ornithine is applicable to research related to IgA vasculitis and intestinal pathogen infections[1][2][3].
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N2-Succinyl-L-ornithine | N2-Succinyl-L-ornithine is a metabolic intermediate and also a substrate of N2-acetylornithine 5-aminotransferase (EC 2.6.1.11). N2-Succinyl-L-ornithine acts as a precursor of Pyruvic acid (HY-Y0781) and supports the biosynthesis of α-solanine (HY-N6602) via the MEP/DOXP pathway. N2-Succinyl-L-ornithine is applicable to research related to IgA vasculitis and intestinal pathogen infections. | |||||||||||||||||||||
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- [1]. Jann A, et al. N-Succinylated intermediates in an arginine catabolic pathway of Pseudomonas aeruginosa. Proceedings of the National Academy of Sciences of the United States of America. 1986 Jul;83(13):4937-41.
- [2]. Demir S, et al. Predictive biomarkers of IgA vasculitis with nephritis by metabolomic analysis. Seminars in arthritis and rheumatism. 2020 Dec;50(6):1238-1244.
- [3]. Xing SC, et al. The Combination of Lead and Bacillus coagulans R11 Increased the Concentration of Alpha-Solanine in the Cecum of Laying Hens and the Pathogens Abundance Decreased. Front Microbiol. 2020 Oct 21;11:585197.
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