Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Butane-1,3-diol [show]

General Information

Mainterm1,3-BUTYLENE GLYCOL
Doc TypeASP
CAS Reg.No.(or other ID)107-88-0
Regnum 175.105
175.320
178.2010
177.1200
177.1210
177.2420
177.1680
172.712
173.220

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID7896
IUPAC Namebutane-1,3-diol
InChIInChI=1S/C4H10O2/c1-4(6)2-3-5/h4-6H,2-3H2,1H3
InChI KeyPUPZLCDOIYMWBV-UHFFFAOYSA-N
Canonical SMILESCC(CCO)O
Molecular FormulaC4H10O2
Wikipediabutylene glycol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight90.122
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Complexity28.7
CACTVS Substructure Key Fingerprint A A A D c c B g 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 G g A A C A A A C B S g g A I C A A A A A g 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 E A A A A A A A Q A A F 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 = =
Topological Polar Surface Area40.5
Monoisotopic Mass90.068
Exact Mass90.068
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count6
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


Food Additives Biosynthesis/Degradation


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9037
Human Intestinal AbsorptionHIA+0.9908
Caco-2 PermeabilityCaco2+0.5724
P-glycoprotein SubstrateNon-substrate0.6708
P-glycoprotein InhibitorNon-inhibitor0.9123
Non-inhibitor0.8958
Renal Organic Cation TransporterNon-inhibitor0.8868
Distribution
Subcellular localizationLysosome0.4672
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8073
CYP450 2D6 SubstrateNon-substrate0.8439
CYP450 3A4 SubstrateNon-substrate0.7130
CYP450 1A2 InhibitorNon-inhibitor0.5422
CYP450 2C9 InhibitorNon-inhibitor0.9170
CYP450 2D6 InhibitorNon-inhibitor0.9044
CYP450 2C19 InhibitorNon-inhibitor0.8806
CYP450 3A4 InhibitorNon-inhibitor0.9135
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9078
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8909
Non-inhibitor0.9171
AMES ToxicityNon AMES toxic0.8505
CarcinogensNon-carcinogens0.6390
Fish ToxicityLow FHMT0.9513
Tetrahymena Pyriformis ToxicityLow TPT0.9971
Honey Bee ToxicityHigh HBT0.6874
BiodegradationReady biodegradable0.9733
Acute Oral ToxicityIV0.7380
Carcinogenicity (Three-class)Non-required0.7553

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility0.7959LogS
Caco-2 Permeability1.0130LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity0.7164LD50, mol/kg
Fish Toxicity3.2619pLC50, mg/L
Tetrahymena Pyriformis Toxicity-2.1765pIGC50, ug/L

From admetSAR


Toxicity Profile

Route of ExposureNone
Mechanism of ToxicityNone
MetabolismNone
Toxicity ValuesNone
Lethal DoseNone
Carcinogenicity (IARC Classification)No indication of carcinogenicity to humans (not listed by IARC).
Minimum Risk LevelNone
Health EffectsNone
TreatmentNone
Reference

From T3DB


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassAlcohols and polyols
Intermediate Tree NodesNot available
Direct ParentSecondary alcohols
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsSecondary alcohol - Hydrocarbon derivative - Primary alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).

From ClassyFire


Targets

General Function:
Zinc ion binding
Specific Function:
Nuclear hormone receptor. The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Ligand-dependent nuclear transactivation involves either direct homodimer binding to a palindromic estrogen response element (ERE) sequence or association with other DNA-binding transcription factors, such as AP-1/c-Jun, c-Fos, ATF-2, Sp1 and Sp3, to mediate ERE-independent signaling. Ligand binding induces a conformational change allowing subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Mutual transrepression occurs between the estrogen receptor (ER) and NF-kappa-B in a cell-type specific manner. Decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter and displace RELA/p65 and associated coregulators from the promoter. Recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters and can displace CREBBP. Present with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Can also act synergistically with NF-kappa-B to activate transcription involving respective recruitment adjacent response elements; the function involves CREBBP. Can activate the transcriptional activity of TFF1. Also mediates membrane-initiated estrogen signaling involving various kinase cascades. Isoform 3 is involved in activation of NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are thought to modulate transcriptional activity by competitive ligand or DNA binding and/or heterodimerization with the full length receptor. Essential for MTA1-mediated transcriptional regulation of BRCA1 and BCAS3. Isoform 3 can bind to ERE and inhibit isoform 1.
Gene Name:
ESR1
Uniprot ID:
P03372
Molecular Weight:
66215.45 Da
References
  1. Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]

From T3DB