6-(3,4-Dihydroxyphenyl)-4-hydroxy-3,5-hexadien-2-one

Details

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Internal ID ab56a79c-d760-450b-a304-d90a1b3c6c08
Taxonomy Benzenoids > Phenols > Benzenediols > Catechols
IUPAC Name 6-(3,4-dihydroxyphenyl)-4-hydroxyhexa-3,5-dien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O4/c1-8(13)6-10(14)4-2-9-3-5-11(15)12(16)7-9/h2-7,14-16H,1H3
InChI Key QDVIEIMMEUCFMW-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O4
Molecular Weight 220.22 g/mol
Exact Mass 220.07355886 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(3,4-Dihydroxyphenyl)-4-hydroxy-3,5-hexadien-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.7857 78.57%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8288 82.88%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9635 96.35%
OATP1B3 inhibitior + 0.9894 98.94%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5729 57.29%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9602 96.02%
CYP3A4 substrate - 0.6857 68.57%
CYP2C9 substrate - 0.8020 80.20%
CYP2D6 substrate - 0.8638 86.38%
CYP3A4 inhibition - 0.8205 82.05%
CYP2C9 inhibition - 0.6250 62.50%
CYP2C19 inhibition - 0.8369 83.69%
CYP2D6 inhibition - 0.9331 93.31%
CYP1A2 inhibition + 0.7553 75.53%
CYP2C8 inhibition - 0.7785 77.85%
CYP inhibitory promiscuity - 0.6015 60.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7434 74.34%
Carcinogenicity (trinary) Non-required 0.5731 57.31%
Eye corrosion - 0.6582 65.82%
Eye irritation + 0.9389 93.89%
Skin irritation + 0.7814 78.14%
Skin corrosion - 0.5404 54.04%
Ames mutagenesis - 0.7754 77.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7587 75.87%
Micronuclear + 0.8700 87.00%
Hepatotoxicity - 0.6101 61.01%
skin sensitisation + 0.8913 89.13%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.7221 72.21%
Acute Oral Toxicity (c) III 0.6588 65.88%
Estrogen receptor binding + 0.6763 67.63%
Androgen receptor binding + 0.8738 87.38%
Thyroid receptor binding + 0.6077 60.77%
Glucocorticoid receptor binding + 0.7523 75.23%
Aromatase binding + 0.6468 64.68%
PPAR gamma + 0.5665 56.65%
Honey bee toxicity - 0.9467 94.67%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9712 97.12%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.78% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.42% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.65% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.26% 96.00%
CHEMBL3194 P02766 Transthyretin 89.58% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.30% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.69% 89.00%
CHEMBL2581 P07339 Cathepsin D 84.70% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.59% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 81.00% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 53395354
LOTUS LTS0227110
wikiData Q15634151