Relevant Data

Food Additives Approved in the United States:

Food Additives Approved by WHO:

Food Additives Approved by European Union:


General Information

Chemical nameTriethyl citrate
CAS number77-93-0
COE number11762
JECFA number629
Flavouring typesubstances
FL No.09.512
MixtureNo
Purity of the named substance at least 95% unless otherwise specified
Reference bodyJECFA

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID6506
IUPAC Nametriethyl 2-hydroxypropane-1,2,3-tricarboxylate
InChIInChI=1S/C12H20O7/c1-4-17-9(13)7-12(16,11(15)19-6-3)8-10(14)18-5-2/h16H,4-8H2,1-3H3
InChI KeyDOOTYTYQINUNNV-UHFFFAOYSA-N
Canonical SMILESCCOC(=O)CC(CC(=O)OCC)(C(=O)OCC)O
Molecular FormulaC12H20O7
Wikipediatriethyl citrate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight276.285
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count7
Rotatable Bond Count11
Complexity304.0
CACTVS Substructure Key Fingerprint A A A D c e B w O 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 D E S g g A I C C A A A B g A I A A C Q C A I A A A A A A A A A A A F A A A A B A B Y A A A A C Q A A F I A A D A A D L J g g K 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 Area99.1
Monoisotopic Mass276.121
Exact Mass276.121
XLogP3None
XLogP3-AA0.1
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count19
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
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+0.9398
Human Intestinal AbsorptionHIA+0.7254
Caco-2 PermeabilityCaco2-0.5784
P-glycoprotein SubstrateSubstrate0.5000
P-glycoprotein InhibitorNon-inhibitor0.6517
Inhibitor0.5366
Renal Organic Cation TransporterNon-inhibitor0.9266
Distribution
Subcellular localizationMitochondria0.8490
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8790
CYP450 2D6 SubstrateNon-substrate0.8970
CYP450 3A4 SubstrateNon-substrate0.5389
CYP450 1A2 InhibitorNon-inhibitor0.9126
CYP450 2C9 InhibitorNon-inhibitor0.8790
CYP450 2D6 InhibitorNon-inhibitor0.9302
CYP450 2C19 InhibitorNon-inhibitor0.8064
CYP450 3A4 InhibitorNon-inhibitor0.8369
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9263
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9892
Non-inhibitor0.8226
AMES ToxicityNon AMES toxic0.6215
CarcinogensCarcinogens 0.5000
Fish ToxicityHigh FHMT0.5917
Tetrahymena Pyriformis ToxicityHigh TPT0.9882
Honey Bee ToxicityHigh HBT0.7387
BiodegradationNot ready biodegradable0.8644
Acute Oral ToxicityIV0.6267
Carcinogenicity (Three-class)Non-required0.6687

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.0205LogS
Caco-2 Permeability0.3705LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.7021LD50, mol/kg
Fish Toxicity2.6525pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.1846pIGC50, ug/L

From admetSAR


Toxicity Profile

Route of Exposure
Mechanism of Toxicity
Metabolism
Toxicity Values
Lethal Dose
Carcinogenicity (IARC Classification)No indication of carcinogenicity to humans (not listed by IARC).
Minimum Risk Level
Health Effects
Treatment
Reference

From T3DB


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassTricarboxylic acids and derivatives
Intermediate Tree NodesNot available
Direct ParentTricarboxylic acids and derivatives
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsTricarboxylic acid or derivatives - Fatty acid ester - Fatty acyl - Tertiary alcohol - Carboxylic acid ester - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

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