(Z)-1-(2,4,6-trihydroxyphenyl)hexadec-4-en-1-one

Details

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Internal ID 482d428f-ec53-47c3-ab8e-4edb70b0c37e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name (Z)-1-(2,4,6-trihydroxyphenyl)hexadec-4-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H34O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(24)22-20(25)16-18(23)17-21(22)26/h12-13,16-17,23,25-26H,2-11,14-15H2,1H3/b13-12-
InChI Key MUFISAIGJOKEAT-SEYXRHQNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O4
Molecular Weight 362.50 g/mol
Exact Mass 362.24570956 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 7.70
Atomic LogP (AlogP) 6.24
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-1-(2,4,6-trihydroxyphenyl)hexadec-4-en-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 + 0.9826 98.26%
Caco-2 - 0.6392 63.92%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8060 80.60%
OATP2B1 inhibitior - 0.5733 57.33%
OATP1B1 inhibitior + 0.7447 74.47%
OATP1B3 inhibitior + 0.9604 96.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8338 83.38%
BSEP inhibitior - 0.5342 53.42%
P-glycoprotein inhibitior - 0.5726 57.26%
P-glycoprotein substrate - 0.8757 87.57%
CYP3A4 substrate - 0.6016 60.16%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8310 83.10%
CYP3A4 inhibition + 0.8574 85.74%
CYP2C9 inhibition - 0.6332 63.32%
CYP2C19 inhibition + 0.6168 61.68%
CYP2D6 inhibition - 0.7407 74.07%
CYP1A2 inhibition + 0.7501 75.01%
CYP2C8 inhibition + 0.4806 48.06%
CYP inhibitory promiscuity + 0.6076 60.76%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8034 80.34%
Carcinogenicity (trinary) Non-required 0.7538 75.38%
Eye corrosion - 0.9633 96.33%
Eye irritation + 0.6342 63.42%
Skin irritation + 0.6208 62.08%
Skin corrosion - 0.8344 83.44%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7413 74.13%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5424 54.24%
skin sensitisation + 0.7031 70.31%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.5296 52.96%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6526 65.26%
Acute Oral Toxicity (c) III 0.6376 63.76%
Estrogen receptor binding + 0.7018 70.18%
Androgen receptor binding + 0.6395 63.95%
Thyroid receptor binding + 0.5208 52.08%
Glucocorticoid receptor binding + 0.5950 59.50%
Aromatase binding - 0.5390 53.90%
PPAR gamma + 0.8624 86.24%
Honey bee toxicity - 0.9826 98.26%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.8953 89.53%
Fish aquatic toxicity + 0.9962 99.62%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.98% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.25% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.05% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.15% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.17% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 86.69% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 86.13% 94.73%
CHEMBL1781 P11387 DNA topoisomerase I 85.11% 97.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.05% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.74% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.20% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.89% 86.33%

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.
Virola elongata

Cross-Links

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PubChem 14655072
LOTUS LTS0063458
wikiData Q105172279