β-Leucine
Names | |
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Preferred IUPAC name
3-Amino-4-methylpentanoic acid | |
Other names
DL-β-Leucine; Homovaline
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Identifiers | |
3D model (
JSmol ) |
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3DMet | |
ChEBI | |
ChemSpider | |
ECHA InfoCard
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100.200.152 |
KEGG | |
PubChem CID
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Properties | |
C6H13NO2 | |
Molar mass | 131.175 g·mol−1 |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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β-Leucine (beta-leucine) is a
Biosynthesis and metabolism in humans
A small fraction of L-leucine metabolism – less than 5% in all tissues except the
β-ketoisocaproate (β-KIC), β-ketoisocaproyl-CoA, and then acetyl-CoA by a series of uncharacterized enzymes.[1][2]
References
- ^ ISBN 978-0-12-387784-0. Archived from the original on 22 March 2018. Retrieved 6 June 2016.
Energy fuel: Eventually, most Leu is broken down, providing about 6.0kcal/g. About 60% of ingested Leu is oxidized within a few hours ... Ketogenesis: A significant proportion (40% of an ingested dose) is converted into acetyl-CoA and thereby contributes to the synthesis of ketones, steroids, fatty acids, and other compounds
Figure 8.57: Metabolism of L-leucine Archived 22 March 2018 at the Wayback Machine - ^ a b "Leucine metabolism". BRENDA. Technische Universität Braunschweig. Archived from the original on 17 August 2016. Retrieved 12 August 2016.
- ^ a b "Human Metabolome Database: Showing metabocard for Beta-Leucine (HMDB0003640)".