Basic Info

Common NameL-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 IDF05363
CAS Number72-18-4
PubChem CID6287
FormulaC5H11NO2
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

WikipediaL-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 DateNov 13, 2018 17:07

Chemical Taxonomy

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree NodesAmino acids and derivatives - Alpha amino acids and derivatives
Direct ParentValine and derivatives
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsValine 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
DescriptionThis 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 NameProperty Value
Molecular Weight117.148
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Complexity90.4
Monoisotopic Mass117.079
Exact Mass117.079
XLogP-2.3
Formal Charge0
Heavy Atom Count8
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

ADMET

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.5852
Human Intestinal AbsorptionHIA+0.9527
Caco-2 PermeabilityCaco2-0.8768
P-glycoprotein SubstrateNon-substrate0.7977
P-glycoprotein InhibitorNon-inhibitor0.9872
Non-inhibitor0.9955
Renal Organic Cation TransporterNon-inhibitor0.9679
Distribution
Subcellular localizationLysosome0.6892
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8395
CYP450 2D6 SubstrateNon-substrate0.8730
CYP450 3A4 SubstrateNon-substrate0.7576
CYP450 1A2 InhibitorNon-inhibitor0.8276
CYP450 2C9 InhibitorNon-inhibitor0.9523
CYP450 2D6 InhibitorNon-inhibitor0.9583
CYP450 2C19 InhibitorNon-inhibitor0.9722
CYP450 3A4 InhibitorNon-inhibitor0.9359
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9916
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9943
Non-inhibitor0.9795
AMES ToxicityNon AMES toxic0.9132
CarcinogensNon-carcinogens0.5785
Fish ToxicityLow FHMT0.5055
Tetrahymena Pyriformis ToxicityLow TPT0.9392
Honey Bee ToxicityLow HBT0.5000
BiodegradationReady biodegradable0.6460
Acute Oral ToxicityIII0.6013
Carcinogenicity (Three-class)Non-required0.7106

Model Value Unit
Absorption
Aqueous solubility0.4659LogS
Caco-2 Permeability0.4722LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.4765LD50, mol/kg
Fish Toxicity3.1930pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.1621pIGC50, ug/L

References

TitleJournalDatePubmed ID
Effectively preparing soluble ovomucin with high antiviral activity from eggwhite.Int J Biol Macromol2018 Oct 1529944939
Hemoglobin adducts of furfuryl alcohol in genetically modified mouse models: Roleof endogenous sulfotransferases 1a1 and 1d1 and transgenic humansulfotransferases 1A1/1A2.Toxicol Lett2018 Oct 129908303
Catalytic amino acid production from biomass-derived intermediates.Proc Natl Acad Sci U S A2018 May 1529712826
Serum metabolomic profile of incident diabetes.Diabetologia2018 May29556673
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 Chem2018 Mar 2829526104
Towards sustainable and multifunctional agriculture in farmland landscapes:Lessons from the integrative approach of a French LTSER platform.Sci Total Environ2018 Jun 1529426207
Comparative Metabolomic Analyses of Ipomoea lacunosa Biotypes with ContrastingGlyphosate Tolerance Captures Herbicide-Induced Differential Perturbations inCellular Physiology.J Agric Food Chem2018 Feb 2829278495
Analysis of Umami Taste Compounds in a Fermented Corn Sauce by Means ofSensory-Guided Fractionation.J Agric Food Chem2018 Feb 2829397710
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 Sci2018 Feb29248224
Alkaline pH shock enhanced production of validamycin A in fermentation ofStreptomyces hygroscopicus.Bioresour Technol2018 Feb29045927
Metabolic profiling of Garcinia mangostana (mangosteen) based on ripening stages.J Biosci Bioeng2018 Feb28970109
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 J2017 Sep28731268
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 Oct27862398
Effects of Boron Supplementation on Peripartum Dairy Cows' Health.Biol Trace Elem Res2017 Oct28229388
Quantitative 13 C-isotope labelling-based analysis to elucidate the influence of environmental parameters on the production of fermentative aromas during winefermentation.Microb Biotechnol2017 Nov28695583
Cadmium toxicity induced contrasting patterns of concentrations of freesarcosine, specific amino acids and selected microelements in two Noccaeaspecies.PLoS One2017 May 1928542385
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 Sci2017 May 127811325
Comparison on the physico-chemical and nutritional qualities of normal andabnormal colored fresh chicken liver.Anim Sci J2017 Jun27723198
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 Chem2017 Jul 2628691814
The Antagonistic Effect of Mycotoxins Deoxynivalenol and Zearalenone on Metabolic Profiling in Serum and Liver of Mice.Toxins (Basel)2017 Jan 1028075412

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
  1. 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 ]
General Function:
Propionyl-coa carboxylase activity
Gene Name:
PCCB
Uniprot ID:
P05166
Molecular Weight:
58215.13 Da
References
  1. Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. [17139284 ]
General Function:
Valine-trna ligase activity
Gene Name:
VARS
Uniprot ID:
P26640
Molecular Weight:
140474.755 Da
References
  1. Zhu B, Zhao MW, Eriani G, Wang ED: A present-day aminoacyl-tRNA synthetase with ancestral editing properties. RNA. 2007 Jan;13(1):15-21. Epub 2006 Nov 9. [17095543 ]