L-allo-Isoleucine structure
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Common Name | L-allo-Isoleucine | ||
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CAS Number | 1509-34-8 | Molecular Weight | 131.173 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 225.8±23.0 °C at 760 mmHg | |
Molecular Formula | C6H13NO2 | Melting Point | -285ºC | |
MSDS | Chinese USA | Flash Point | 90.3±22.6 °C |
Use of L-allo-IsoleucineL-Alloisoleucine is a branched chain amino acid and is a stereo-isomer of L-isoleucine. L-Alloisoleucine is a common constituent of human plasma (albeit at low levels). |
Name | L-alloisoleucine |
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Synonym | More Synonyms |
Description | L-Alloisoleucine is a branched chain amino acid and is a stereo-isomer of L-isoleucine. L-Alloisoleucine is a common constituent of human plasma (albeit at low levels). |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 225.8±23.0 °C at 760 mmHg |
Melting Point | -285ºC |
Molecular Formula | C6H13NO2 |
Molecular Weight | 131.173 |
Flash Point | 90.3±22.6 °C |
Exact Mass | 131.094635 |
PSA | 63.32000 |
LogP | 0.73 |
Vapour Pressure | 0.0±0.9 mmHg at 25°C |
Index of Refraction | 1.463 |
Storage condition | Store at RT. |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Precursor 0 | |
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DownStream 1 | |
Interrelation between the metabolism of L-isoleucine and L-allo-isoleucine in patients with maple syrup urine disease.
Pediatr. Res. 25 , 11-14, (1989) The nonprotein amino acid L-allo-isoleucine is formed endogenously in maple syrup urine disease patients from (R)-3-methyl-2-oxo-pentanoic acid. During strict metabolic balance, the plasma L-allo-isol... |
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Functional differences in the catabolism of branched-chain L-amino acids in cultured normal and maple syrup urine disease fibroblasts.
Biochem. Med. Metab. Biol. 41 , 105-116, (1989) Possible functional differences in the catabolism of the four branched-chain L-amino acids in maple syrup urine disease were assessed using cultured human skin fibroblast stains. Transamination and ox... |
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Substrate specificity of L-delta-(alpha-aminoadipoyl)-L-cysteinyl-D-valine synthetase from Cephalosporium acremonium: demonstration of the structure of several unnatural tripeptide products.
Biochem. J. 301 , 367-372, (1994) Potential substrates for L-delta-(alpha-aminoadipoyl)-L-(cysteinyl)-D-valine (ACV) synthetase were initially identified using both the amino-acid-dependent ATP<-->pyrophosphate exchange reaction catal... |
Isoleucine, allo- |
Alloisoleucine, L- |
UNII:05T3WT3PJ1 |
L-Alloisoleucine |
alle |
Alloisoleucine |
(2S,3R)-2-Amino-3-methylpentanoic acid |
Allo-L-isoleucine |
L-Isoleucine |
l-aIle |
(+)-threo-2-Amino-3-methylpentanoic Acid |
Allo-isoleucine |
(R)-Isoleucine |
D-(-)-Isoleucine |
L(+)-Alloisoleucine |
(2S,3R)-2-Amino-3-methylpentanoic acid,L-Alloisoleucine |
a-Ile |
L-Isoleucine, allo- |
H-D-Ile-OH |
L-ALLO-ISOLEUCINE |
MFCD00066446 |
EINECS 216-142-3 |