L-Valine
(right click,save link as to download,it is a temp file,please download as soon as possible, you can also use CTRL+S to save the whole html page)
Basic Info
Common Name | L-Valine(F05363) |
2D Structure | |
Description | Valine (abbreviated as Val or V) is an -amino acid with the chemical formula HO2CCH(NH2)CH(CH3)2. It is named after the plant valerian. L-Valine is one of 20 proteinogenic amino acids. Its codons are GUU, GUC, GUA, and GUG. This essential amino acid is classified as nonpolar. Along with leucine and isoleucine, valine is a branched-chain amino acid. Branched chain amino acids (BCAA) are essential amino acids whose carbon structure is marked by a branch point. These three amino acids are critical to human life and are particularly involved in stress, energy and muscle metabolism. BCAA supplementation as therapy, both oral and intravenous, in human health and disease holds great promise. BCAA denotes valine, isoleucine and leucine which are branched chain essential amino acids. Despite their structural similarities, the branched amino acids have different metabolic routes, with valine going solely to carbohydrates, leucine solely to fats and isoleucine to both. The different metabolism accounts for different requirements for these essential amino acids in humans: 12 mg/kg, 14 mg/kg and 16 mg/kg of valine, leucine and isoleucine respectively. Furthermore, these amino acids have different deficiency symptoms. Valine deficiency is marked by neurological defects in the brain, while isoleucine deficiency is marked by muscle tremors. Many types of inborn errors of BCAA metabolism exist, and are marked by various abnormalities. The most common form is the maple syrup urine disease, marked by a characteristic urinary odor. Other abnormalities are associated with a wide range of symptoms, such as mental retardation, ataxia, hypoglycemia, spinal muscle atrophy, rash, vomiting and excessive muscle movement. Most forms of BCAA metabolism errors are corrected by dietary restriction of BCAA and at least one form is correctable by supplementation with 10 mg of biotin daily. BCAA are decreased in patients with liver disease, such as hepatitis, hepatic coma, cirrhosis, extrahepatic biliary atresia or portacaval shunt; aromatic amino acids (AAA) tyrosine, tryptophan and phenylalanine, as well as methionine are increased in these conditions. Valine in particular, has been established as a useful supplemental therapy to the ailing liver. All the BCAA probably compete with AAA for absorption into the brain. Supplemental BCAA with vitamin B6 and zinc help normalize the BCAA:AAA ratio. In sickle-cell disease, valine substitutes for the hydrophilic amino acid glutamic acid in hemoglobin. Because valine is hydrophobic, the hemoglobin does not fold correctly. Valine is an essential amino acid, hence it must be ingested, usually as a component of proteins. |
FRCD ID | F05363 |
CAS Number | 72-18-4 |
PubChem CID | 6287 |
Formula | C5H11NO2 |
IUPAC Name | (2S)-2-amino-3-methylbutanoic acid |
InChI Key | KZSNJWFQEVHDMF-BYPYZUCNSA-N |
InChI | InChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/t4-/m0/s1 |
Canonical SMILES | CC(C)C(C(=O)O)N |
Isomeric SMILES | CC(C)[C@@H](C(=O)O)N |
Wikipedia | L-Valine |
Synonyms | (S)-Valine (2S)-2-amino-3-methylbutanoic acid L-valine valine 72-18-4 (S)-2-Amino-3-methylbutanoic acid 2-Amino-3-methylbutyric acid H-Val-OH (S)-2-Amino-3-methylbutyric acid L-alpha-Amino-beta-methylbutyric acid |
Classifies | Animal Toxin |
Update Date | Nov 13, 2018 17:07 |
Chemical Taxonomy
Kingdom | Organic compounds |
Superclass | Organic acids and derivatives |
Class | Carboxylic acids and derivatives |
Subclass | Amino acids, peptides, and analogues |
Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
Direct Parent | Valine and derivatives |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Valine or derivatives - Alpha-amino acid - L-alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Aliphatic acyclic compound |
Description | This compound belongs to the class of organic compounds known as valine and derivatives. These are compounds containing valine or a derivative thereof resulting from reaction of valine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
Properties
Property Name | Property Value |
---|---|
Molecular Weight | 117.148 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 2 |
Complexity | 90.4 |
Monoisotopic Mass | 117.079 |
Exact Mass | 117.079 |
XLogP | -2.3 |
Formal Charge | 0 |
Heavy Atom Count | 8 |
Defined Atom Stereocenter Count | 1 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
ADMET
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.5852 |
Human Intestinal Absorption | HIA+ | 0.9527 |
Caco-2 Permeability | Caco2- | 0.8768 |
P-glycoprotein Substrate | Non-substrate | 0.7977 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9872 |
Non-inhibitor | 0.9955 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.9679 |
Distribution | ||
Subcellular localization | Lysosome | 0.6892 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8395 |
CYP450 2D6 Substrate | Non-substrate | 0.8730 |
CYP450 3A4 Substrate | Non-substrate | 0.7576 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.8276 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9523 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9583 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9722 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9359 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9916 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9943 |
Non-inhibitor | 0.9795 | |
AMES Toxicity | Non AMES toxic | 0.9132 |
Carcinogens | Non-carcinogens | 0.5785 |
Fish Toxicity | Low FHMT | 0.5055 |
Tetrahymena Pyriformis Toxicity | Low TPT | 0.9392 |
Honey Bee Toxicity | Low HBT | 0.5000 |
Biodegradation | Ready biodegradable | 0.6460 |
Acute Oral Toxicity | III | 0.6013 |
Carcinogenicity (Three-class) | Non-required | 0.7106 |
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | 0.4659 | LogS |
Caco-2 Permeability | 0.4722 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.4765 | LD50, mol/kg |
Fish Toxicity | 3.1930 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -1.1621 | pIGC50, ug/L |
References
Title | Journal | Date | Pubmed ID |
---|---|---|---|
Effectively preparing soluble ovomucin with high antiviral activity from eggwhite. | Int J Biol Macromol | 2018 Oct 15 | 29944939 |
Hemoglobin adducts of furfuryl alcohol in genetically modified mouse models: Roleof endogenous sulfotransferases 1a1 and 1d1 and transgenic humansulfotransferases 1A1/1A2. | Toxicol Lett | 2018 Oct 1 | 29908303 |
Catalytic amino acid production from biomass-derived intermediates. | Proc Natl Acad Sci U S A | 2018 May 15 | 29712826 |
Serum metabolomic profile of incident diabetes. | Diabetologia | 2018 May | 29556673 |
Valine Supplementation in a Reduced Protein Diet Regulates Growth PerformancePartially through Modulation of Plasma Amino Acids Profile, Metabolic Responses, Endocrine, and Neural Factors in Piglets. | J Agric Food Chem | 2018 Mar 28 | 29526104 |
Towards sustainable and multifunctional agriculture in farmland landscapes:Lessons from the integrative approach of a French LTSER platform. | Sci Total Environ | 2018 Jun 15 | 29426207 |
Comparative Metabolomic Analyses of Ipomoea lacunosa Biotypes with ContrastingGlyphosate Tolerance Captures Herbicide-Induced Differential Perturbations inCellular Physiology. | J Agric Food Chem | 2018 Feb 28 | 29278495 |
Analysis of Umami Taste Compounds in a Fermented Corn Sauce by Means ofSensory-Guided Fractionation. | J Agric Food Chem | 2018 Feb 28 | 29397710 |
Varying the ratio of Lys:Met while maintaining the ratios of Thr:Phe, Lys:Thr,Lys:His, and Lys:Val alters mammary cellular metabolites, mammalian target ofrapamycin signaling, and gene transcription. | J Dairy Sci | 2018 Feb | 29248224 |
Alkaline pH shock enhanced production of validamycin A in fermentation ofStreptomyces hygroscopicus. | Bioresour Technol | 2018 Feb | 29045927 |
Metabolic profiling of Garcinia mangostana (mangosteen) based on ripening stages. | J Biosci Bioeng | 2018 Feb | 28970109 |
13 C metabolic flux profiling of Pichia pastoris grown in aerobic batch cultures on glucose revealed high relative anabolic use of TCA cycle and limitedincorporation of provided precursors of branched-chain amino acids. | FEBS J | 2017 Sep | 28731268 |
Milk protein responses to balanced amino acid and removal of Leucine and Argininesupplied from jugular-infused amino acid mixture in lactating dairy cows. | J Anim Physiol Anim Nutr (Berl) | 2017 Oct | 27862398 |
Effects of Boron Supplementation on Peripartum Dairy Cows' Health. | Biol Trace Elem Res | 2017 Oct | 28229388 |
Quantitative 13 C-isotope labelling-based analysis to elucidate the influence of environmental parameters on the production of fermentative aromas during winefermentation. | Microb Biotechnol | 2017 Nov | 28695583 |
Cadmium toxicity induced contrasting patterns of concentrations of freesarcosine, specific amino acids and selected microelements in two Noccaeaspecies. | PLoS One | 2017 May 19 | 28542385 |
Effect of elevated dietary amino acid levels in high canola meal diets onproductive traits and cecal microbiota population of broiler chickens in apair-feeding study. | Poult Sci | 2017 May 1 | 27811325 |
Comparison on the physico-chemical and nutritional qualities of normal andabnormal colored fresh chicken liver. | Anim Sci J | 2017 Jun | 27723198 |
Intervention of Dietary Dipeptide Gamma-l-Glutamyl-l-Valine (γ-EV) Ameliorates Inflammatory Response in a Mouse Model of LPS-Induced Sepsis. | J Agric Food Chem | 2017 Jul 26 | 28691814 |
The Antagonistic Effect of Mycotoxins Deoxynivalenol and Zearalenone on Metabolic Profiling in Serum and Liver of Mice. | Toxins (Basel) | 2017 Jan 10 | 28075412 |
Targets
- General Function:
- L-valine transaminase activity
- Specific Function:
- Catalyzes the first reaction in the catabolism of the essential branched chain amino acids leucine, isoleucine, and valine.
- Gene Name:
- BCAT1
- Uniprot ID:
- P54687
- Molecular Weight:
- 42965.815 Da
References
- Chen CD, Huang TF, Lin CH, Guan HH, Hsieh YC, Lin YH, Huang YC, Liu MY, Chang WC, Chen CJ: Purification, crystallization and preliminary X-ray crystallographic analysis of branched-chain aminotransferase from Deinococcus radiodurans. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Jun 1;63(Pt 6):492-4. Epub 2007 May 5. [17554170 ]