Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • D,L-Valine [show]

General Information

MaintermDL-VALINE
Doc TypeASP
CAS Reg.No.(or other ID)516-06-3
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID1182
IUPAC Name2-amino-3-methylbutanoic acid
InChIInChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)
InChI KeyKZSNJWFQEVHDMF-UHFFFAOYSA-N
Canonical SMILESCC(C)C(C(=O)O)N
Molecular FormulaC5H11NO2
WikipediaDL-valine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight117.148
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Complexity90.4
CACTVS Substructure Key Fingerprint A A A D c c B i M A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A H g A Q C A A A D S j B g A Q C C A B A A g A I A A C Q C A A A A A A A A A A A A I G A A A A C A B A A A A A A Q A A E E A A A A A A A A A A I A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = =
Topological Polar Surface Area63.3
Monoisotopic Mass117.079
Exact Mass117.079
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count8
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

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

From admetSAR


ADMET Predicted Profile --- Regression

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

From admetSAR


Taxonomic Classification

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 - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Amine - Organic oxide - 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.

From ClassyFire