1-(2,4,6-Trihydroxyphenyl)-11-(2-hydroxyphenyl)undecan-1-one

Details

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Internal ID 2032f14e-6865-413b-ab9b-5554a64cae17
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 11-(2-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H30O5/c24-18-15-21(27)23(22(28)16-18)20(26)14-8-6-4-2-1-3-5-7-11-17-12-9-10-13-19(17)25/h9-10,12-13,15-16,24-25,27-28H,1-8,11,14H2
InChI Key KRAWWRGYJVWEDK-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H30O5
Molecular Weight 386.50 g/mol
Exact Mass 386.20932405 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.45
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,4,6-Trihydroxyphenyl)-11-(2-hydroxyphenyl)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 - 0.6720 67.20%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.9241 92.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9426 94.26%
OATP1B3 inhibitior + 0.9283 92.83%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7004 70.04%
P-glycoprotein inhibitior - 0.5364 53.64%
P-glycoprotein substrate - 0.8621 86.21%
CYP3A4 substrate - 0.5594 55.94%
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 + 0.5153 51.53%
CYP inhibitory promiscuity - 0.5476 54.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8334 83.34%
Carcinogenicity (trinary) Non-required 0.7340 73.40%
Eye corrosion - 0.9879 98.79%
Eye irritation + 0.5892 58.92%
Skin irritation - 0.6135 61.35%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7389 73.89%
Micronuclear - 0.7041 70.41%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7039 70.39%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5703 57.03%
Acute Oral Toxicity (c) III 0.7740 77.40%
Estrogen receptor binding + 0.7943 79.43%
Androgen receptor binding + 0.7331 73.31%
Thyroid receptor binding + 0.6573 65.73%
Glucocorticoid receptor binding + 0.6977 69.77%
Aromatase binding + 0.5960 59.60%
PPAR gamma + 0.8183 81.83%
Honey bee toxicity - 0.9361 93.61%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5500 55.00%
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 98.98% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.87% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.05% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.46% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.44% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.98% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.53% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 85.78% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.64% 86.33%
CHEMBL4208 P20618 Proteasome component C5 82.79% 90.00%

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 11234557
NPASS NPC20782
LOTUS LTS0176047
wikiData Q105144905