Taxifolin

Identification

Generic Name
Taxifolin
DrugBank Accession Number
DB02224
Background

Not Available

Type
Small Molecule
Groups
Experimental
Structure
Weight
Average: 304.2516
Monoisotopic: 304.058302738
Chemical Formula
C15H12O7
Synonyms
  • (+)-(2R,3R)-dihydroquercetin
  • (+)-dihydroquercetin
  • (+)-taxifolin
  • (2R,3R)-(+)-taxifolin
  • (2R,3R)-3,3',4',5,7-pentahydroxyflavanone
  • (2R,3R)-dihydroquercetin
  • Dihydroquercetin

Pharmacology

Indication

Not Available

Reduce drug development failure rates
Build, train, & validate machine-learning models
with evidence-based and structured datasets.
See how
Build, train, & validate predictive machine-learning models with structured datasets.
See how
Contraindications & Blackbox Warnings
Prevent Adverse Drug Events Today
Tap into our Clinical API for life-saving information on contraindications & blackbox warnings, population restrictions, harmful risks, & more.
Learn more
Avoid life-threatening adverse drug events with our Clinical API
Learn more
Pharmacodynamics

Not Available

Mechanism of action
Not Available
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
Improve decision support & research outcomes
With structured adverse effects data, including: blackbox warnings, adverse reactions, warning & precautions, & incidence rates. View sample adverse effects data in our new Data Library!
See the data
Improve decision support & research outcomes with our structured adverse effects data.
See a data sample
Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
DrugInteraction
AbciximabThe risk or severity of bleeding and hemorrhage can be increased when Taxifolin is combined with Abciximab.
AcebutololTaxifolin may decrease the antihypertensive activities of Acebutolol.
AceclofenacThe risk or severity of adverse effects can be increased when Taxifolin is combined with Aceclofenac.
AcemetacinThe risk or severity of adverse effects can be increased when Taxifolin is combined with Acemetacin.
AcenocoumarolThe risk or severity of bleeding and hemorrhage can be increased when Taxifolin is combined with Acenocoumarol.
Food Interactions
Not Available

Categories

Drug Categories
Chemical TaxonomyProvided by Classyfire
Description
This compound belongs to the class of organic compounds known as flavanonols. These are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a hydroxyl group and a ketone at the carbon C2 and C3, respectively.
Kingdom
Organic compounds
Super Class
Phenylpropanoids and polyketides
Class
Flavonoids
Sub Class
Flavans
Direct Parent
Flavanonols
Alternative Parents
3'-hydroxyflavonoids / 3-hydroxyflavonoids / 4'-hydroxyflavonoids / 5-hydroxyflavonoids / 7-hydroxyflavonoids / Chromones / Catechols / Aryl alkyl ketones / 1-hydroxy-2-unsubstituted benzenoids / 1-hydroxy-4-unsubstituted benzenoids
show 8 more
Substituents
1-benzopyran / 1-hydroxy-2-unsubstituted benzenoid / 1-hydroxy-4-unsubstituted benzenoid / 3'-hydroxyflavonoid / 3-hydroxyflavonoid / 4'-hydroxyflavonoid / 5-hydroxyflavonoid / 7-hydroxyflavonoid / Alcohol / Alkyl aryl ether
show 23 more
Molecular Framework
Aromatic heteropolycyclic compounds
External Descriptors
taxifolin (CHEBI:17948) / Dihyroflavonols (C01617)
Affected organisms
Not Available

Chemical Identifiers

UNII
9SOB9E3987
CAS number
480-18-2
InChI Key
CXQWRCVTCMQVQX-LSDHHAIUSA-N
InChI
InChI=1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H/t14-,15+/m0/s1
IUPAC Name
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-one
SMILES
O[C@@H]1[C@H](OC2=CC(O)=CC(O)=C2C1=O)C1=CC=C(O)C(O)=C1

References

General References
Not Available
KEGG Compound
C01617
PubChem Compound
439533
PubChem Substance
46508033
ChemSpider
388626
BindingDB
212435
ChEBI
17948
ChEMBL
CHEMBL66
ZINC
ZINC000100018343
PDBe Ligand
DQH
Wikipedia
Taxifolin
PDB Entries
1gp5 / 2c29 / 3tvq / 8b7u / 8b7z / 8fen / 8fev

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Solid
Experimental Properties
PropertyValueSource
logP0.95PERRISSOUD,D & TESTA,B (1986)
Predicted Properties
PropertyValueSource
Water Solubility1.16 mg/mLALOGPS
logP1.07ALOGPS
logP1.82Chemaxon
logS-2.4ALOGPS
pKa (Strongest Acidic)7.74Chemaxon
pKa (Strongest Basic)-4Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count7Chemaxon
Hydrogen Donor Count5Chemaxon
Polar Surface Area127.45 Å2Chemaxon
Rotatable Bond Count1Chemaxon
Refractivity74.61 m3·mol-1Chemaxon
Polarizability29.03 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon
Predicted ADMET Features
PropertyValueProbability
Human Intestinal Absorption+0.965
Blood Brain Barrier-0.5711
Caco-2 permeable-0.8957
P-glycoprotein substrateSubstrate0.5629
P-glycoprotein inhibitor INon-inhibitor0.9297
P-glycoprotein inhibitor IINon-inhibitor0.8382
Renal organic cation transporterNon-inhibitor0.931
CYP450 2C9 substrateNon-substrate0.7898
CYP450 2D6 substrateNon-substrate0.9116
CYP450 3A4 substrateNon-substrate0.653
CYP450 1A2 substrateInhibitor0.9106
CYP450 2C9 inhibitorNon-inhibitor0.5823
CYP450 2D6 inhibitorNon-inhibitor0.9287
CYP450 2C19 inhibitorNon-inhibitor0.9025
CYP450 3A4 inhibitorInhibitor0.6951
CYP450 inhibitory promiscuityHigh CYP Inhibitory Promiscuity0.5822
Ames testNon AMES toxic0.722
CarcinogenicityNon-carcinogens0.945
BiodegradationNot ready biodegradable0.8672
Rat acute toxicity3.0200 LD50, mol/kg Not applicable
hERG inhibition (predictor I)Weak inhibitor0.9781
hERG inhibition (predictor II)Non-inhibitor0.8161
ADMET data is predicted using admetSAR, a free tool for evaluating chemical ADMET properties. (23092397)

Spectra

Mass Spec (NIST)
Not Available
Spectra
SpectrumSpectrum TypeSplash Key
MS/MS Spectrum - ESI-TOF 25V, NegativeLC-MS/MSsplash10-00fr-0591000000-8c2bb267dbaff0ec8425
MS/MS Spectrum - ESI-TOF 20V, NegativeLC-MS/MSsplash10-0fk9-0393000000-2ad9cdbeaebe4832addf
MS/MS Spectrum - ESI-TOF , NegativeLC-MS/MSsplash10-0udi-0019000000-f4c2db21ffbf7fdec0ec
MS/MS Spectrum - ESI-TOF 25V, NegativeLC-MS/MSsplash10-00fr-0591000000-8c2bb267dbaff0ec8425
MS/MS Spectrum - ESI-TOF 20V, NegativeLC-MS/MSsplash10-0fk9-0393000000-2ad9cdbeaebe4832addf
MS/MS Spectrum - ESI-TOF , NegativeLC-MS/MSsplash10-0udi-0019000000-f4c2db21ffbf7fdec0ec
MS/MS Spectrum - DI-ESI-qTof , PositiveLC-MS/MSsplash10-0pc1-0980000000-2d1ecd15f61d12518b21
MS/MS Spectrum - DI-ESI-qTof , NegativeLC-MS/MSsplash10-004r-0960000000-22428e71371e23f8c0f1
LC-MS/MS Spectrum - LC-ESI-qTof , PositiveLC-MS/MSsplash10-0a4r-0965000000-d0ca2227f5b5c9adb509
MS/MS Spectrum - Linear Ion Trap , negativeLC-MS/MSsplash10-000i-0190000000-5cfd8e48c0ba0adace9c
MS/MS Spectrum - Linear Ion Trap , negativeLC-MS/MSsplash10-000i-0190000000-4e9899457ae22ca1e3a8
LC-MS/MS Spectrum - LC-ESI-TOF , negativeLC-MS/MSsplash10-00fr-0591000000-8c2bb267dbaff0ec8425
LC-MS/MS Spectrum - LC-ESI-TOF , negativeLC-MS/MSsplash10-0fk9-0393000000-2ad9cdbeaebe4832addf
MS/MS Spectrum - Linear Ion Trap , positiveLC-MS/MSsplash10-004i-0090000000-1c45a54959ecd51d8615
MS/MS Spectrum - , positiveLC-MS/MSsplash10-0a4r-0965000000-d0ca2227f5b5c9adb509
MS/MS Spectrum - , positiveLC-MS/MSsplash10-0ul1-0930000000-805f5b6770fe1b1ed799
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-0a4i-0059000000-9fcb8ab575ba55a6afcc
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-0f79-0096000000-43d763a8bd17f27f6089
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-0kii-0943000000-8c369bbb656cdb1fb599
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-0umi-0900000000-2d404e54d0c4becf6dea
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-009i-0920000000-76f157c881f6503a27f3
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-0v0c-1910000000-cf4c0b3988757337f82c
Predicted 1H NMR Spectrum1D NMRNot Applicable
Predicted 13C NMR Spectrum1D NMRNot Applicable
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-182.8331002
predicted
DarkChem Lite v0.1.0
[M-H]-183.2917002
predicted
DarkChem Lite v0.1.0
[M-H]-168.23116
predicted
DeepCCS 1.0 (2019)
[M+H]+183.9981002
predicted
DarkChem Lite v0.1.0
[M+H]+185.5557002
predicted
DarkChem Lite v0.1.0
[M+H]+170.58916
predicted
DeepCCS 1.0 (2019)
[M+Na]+183.1601002
predicted
DarkChem Lite v0.1.0
[M+Na]+177.32079
predicted
DeepCCS 1.0 (2019)

Drug created at June 13, 2005 13:24 / Updated at June 12, 2020 16:52