Metabolites

5-Aminovaleric acid View larger

5-Aminovaleric acid

AT5089

CAS 660-88-8

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Data sheet

Molecular FormulaC5H11NO2
Molecular Weight117.15
CAS Numbers660-88-8
Storage Condition0C Short Term, -20C Long Term
SolubilityDMSO
Purity98% by HPLC
SMILES CodeNCCCCC(O)=O
ReferencesSantos A , Zanetta S , Cresteil T , et al. Metabolism of irinotecan [CPT-11] by CYP3A4 and CYP3A5 in humans[J]. Clinical Cancer Research, 2000, 6[5] 2012-2020.

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5-aminovalerate (or 5-aminopentanoic acid) is a lysine degradation product. It can be produced both endogenously or through bacterial catabolism of lysine. 5-aminovalerate is formed via the following multi-step reaction: L-lysine leads to cadverine leads to L-piperideine leads 5-aminovalerate . In other words it is a metabolite of cadaverine which is formed via the intermediate, 1-piperideine. Cadaverine is a foul-smelling diamine compound produced by protein hydrolysis during putrefaction of animal tissue. High levels of 5-aminovalerate in biofluids may indicate bacterial overgrowth or endogenous tissue necrosis. In most cases endogenous 5-aminovalerate is thought to be primarily a microbial metabolite produced by the gut or oral microflora, although it can be produced endogenously. 5-aminopentanoic acid is an in vivo substrate of 4-aminobutyrate:2-oxoglutarate aminotransferase .