11-(2,6-Dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one

Details

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Internal ID 8e38048c-e4f8-4784-9271-3b5dd536331a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 11-(2,6-dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H30O6/c24-16-14-21(28)23(22(29)15-16)20(27)11-8-6-4-2-1-3-5-7-10-17-18(25)12-9-13-19(17)26/h9,12-15,24-26,28-29H,1-8,10-11H2
InChI Key FYQJQTJFCKNRBH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H30O6
Molecular Weight 402.50 g/mol
Exact Mass 402.20423867 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.15
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

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11-(2,6-dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one
1-Undecanone, 11-(2,6-dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-

2D Structure

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2D Structure of 11-(2,6-Dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9364 93.64%
Caco-2 - 0.7258 72.58%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.9241 92.41%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9107 91.07%
OATP1B3 inhibitior + 0.9283 92.83%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7997 79.97%
P-glycoprotein inhibitior - 0.5074 50.74%
P-glycoprotein substrate - 0.8898 88.98%
CYP3A4 substrate - 0.5534 55.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7874 78.74%
CYP3A4 inhibition + 0.6898 68.98%
CYP2C9 inhibition + 0.7096 70.96%
CYP2C19 inhibition + 0.7701 77.01%
CYP2D6 inhibition - 0.8386 83.86%
CYP1A2 inhibition + 0.6771 67.71%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.5476 54.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8334 83.34%
Carcinogenicity (trinary) Non-required 0.7340 73.40%
Eye corrosion - 0.9879 98.79%
Eye irritation + 0.5526 55.26%
Skin irritation - 0.6135 61.35%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7247 72.47%
Micronuclear - 0.7041 70.41%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7039 70.39%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6790 67.90%
Acute Oral Toxicity (c) III 0.7740 77.40%
Estrogen receptor binding + 0.7776 77.76%
Androgen receptor binding + 0.6102 61.02%
Thyroid receptor binding + 0.6579 65.79%
Glucocorticoid receptor binding + 0.7171 71.71%
Aromatase binding + 0.6472 64.72%
PPAR gamma + 0.8505 85.05%
Honey bee toxicity - 0.9739 97.39%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9819 98.19%

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 95.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.02% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.63% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.23% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.79% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.02% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.30% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.13% 86.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.82% 95.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.17% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.60% 96.95%
CHEMBL3194 P02766 Transthyretin 82.63% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 82.17% 94.75%
CHEMBL2535 P11166 Glucose transporter 81.09% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.04% 89.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.69% 96.12%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Ardisia elliptica
Ardisia humilis

Cross-Links

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PubChem 11418215
NPASS NPC276972
LOTUS LTS0005133
wikiData Q105004636