219827
L-α-羟基异己酸
98%
别名:
2-羟基-4-甲基戊酸, L-2-羟基-4-甲基戊酸, L-白氨酸
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关于此项目
线性分子式:
(CH3)2CHCH2CH(OH)CO2H
化学文摘社编号:
分子量:
132.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
51113400
EC Number:
237-329-6
MDL number:
产品名称
L-α-羟基异己酸, 98%
InChI key
LVRFTAZAXQPQHI-YFKPBYRVSA-N
InChI
1S/C6H12O3/c1-4(2)3-5(7)6(8)9/h4-5,7H,3H2,1-2H3,(H,8,9)/t5-/m0/s1
SMILES string
CC(C)C[C@H](O)C(O)=O
assay
98%
form
powder
optical activity
[α]22/D −26.3°, c = 1 in 1 M NaOH
mp
78-80 °C (lit.)
functional group
carboxylic acid
hydroxyl
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Fernanda U Fontella et al.
Metabolic brain disease, 17(1), 47-54 (2002-03-16)
In this study we investigated the in vitro effects of the metabolites accumulating in maple syrup urine disease on lipid peroxidation in brain of young rats. Chemiluminescence and thiobarbituric acid-reactive substances were measured in brain homogenates from 7- and 30-day-old
Takayoshi Awakawa et al.
Nature communications, 9(1), 3534-3534 (2018-09-01)
Reprogramming of the NRPS/PKS assembly line is an attractive method for the production of new bioactive molecules. However, it is usually hampered by the loss of intimate domain/module interactions required for the precise control of chain transfer and elongation reactions.
Charles H Lang et al.
American journal of physiology. Endocrinology and metabolism, 305(3), E416-E428 (2013-06-13)
Muscle disuse atrophy is observed routinely in patients recovering from traumatic injury and can be either generalized resulting from extended bed rest or localized resulting from single-limb immobilization. The present study addressed the hypothesis that a diet containing 5% α-hydroxyisocaproic
Antti A Mero et al.
Journal of the International Society of Sports Nutrition, 7, 1-1 (2010-01-07)
Alfa-Hydroxy-isocaproic acid (HICA) is an end product of leucine metabolism in human tissues such as muscle and connective tissue. According to the clinical and experimental studies, HICA can be considered as an anti-catabolic substance. The present study investigated the effects
L J Spaapen et al.
Journal of inherited metabolic disease, 10(4), 383-390 (1987-01-01)
Analysis of urinary organic acids in patients admitted for screening for inborn errors of metabolism incidentally revealed the presence of abnormal amounts of 4-hydroxyphenyllactate (4-HPLA) and phenyllactate (PLA). These compounds are found in tyrosinaemia and phenylketonuria but in our patients
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