13748-90-8
Chemical Structure
(S)-Leucic acid
Synonym(s): (S)-2-Hydroxy-4-methylpentanoic acid
- CAS No.: 13748-90-8
- Formula:C6H12O3
- Molecular Weight:132.16
IUPAC Name: (S)-2-hydroxy-4-methylpentanoic acid
InChIKey: LVRFTAZAXQPQHI-YFKPBYRVSA-N
SMILES: O=C(O)[C@@H](O)CC(C)C
Biological Activity: (S)-Leucic acid ((S)-2-Hydroxy-4-methylpentanoic acid) is an α-hydroxy acid found in the fermentation products of Bacillus granulobacter pectinovorum. (S)-Leucic acid is an isomer of Leucic acid (HY-30216A) and a leucine metabolite. (S)-Leucic acid acts as a D-unit subunit precursor in the biosynthesis of cryptophycins in the Nostoc cyanobacterial symbiont. (S)-Leucic acid is used in metabolism-related studies[1][2].
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(S)-Leucic acid | 99.17% | (S)-Leucic acid ((S)-2-Hydroxy-4-methylpentanoic acid) is an α-hydroxy acid found in the fermentation products of Bacillus granulobacter pectinovorum. (S)-Leucic acid is an isomer of Leucic acid (HY-30216A) and a leucine metabolite. (S)-Leucic acid acts as a D-unit subunit precursor in the biosynthesis of cryptophycins in the Nostoc cyanobacterial symbiont. (S)-Leucic acid is used in metabolism-related studies. | ||||||||||||||||||||
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(S)-Leucic acid (Standard) | 94.89% | (S)-Leucic acid (Standard) ((S)-2-Hydroxy-4-methylpentanoic acid (Standard)) is the analytical standard of (S)-Leucic acid (HY-30215). This product is intended for research and analytical applications. (S)-Leucic acid ((S)-2-Hydroxy-4-methylpentanoic acid) is an α-hydroxy acid found in the fermentation products of Bacillus granulobacter pectinovorum. (S)-Leucic acid is an isomer of Leucic acid (HY-30216A) and a leucine metabolite. (S)-Leucic acid acts as a D-unit subunit precursor in the biosynthesis of cryptophycins in the Nostoc cyanobacterial symbiont. (S)-Leucic acid is used in metabolism-related studies. | ||||||||||||||||||||
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References
- [1]. Schmidt E G, et al. THE FORMATION OF l‑LEUCIC ACID IN THE ACETONEBUTYL ALCOHOL FERMENTATION. Journal of Biological Chemistry, 1924, 61(1): 163‑175.
- [2]. Magarvey NA, et al. Biosynthetic characterization and chemoenzymatic assembly of the cryptophycins. Potent anticancer agents from cyanobionts. ACS chemical biology. 2006 Dec 15;1(12):766-79.
