4-Hepten-3-one, 7-(4-hydroxyphenyl)-1-phenyl-, (E)-

Details

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Internal ID d38613de-a8dc-42e8-a228-31a4b959316a
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 7-(4-hydroxyphenyl)-1-phenylhept-4-en-3-one
SMILES (Canonical) C1=CC=C(C=C1)CCC(=O)C=CCCC2=CC=C(C=C2)O
SMILES (Isomeric) C1=CC=C(C=C1)CCC(=O)C=CCCC2=CC=C(C=C2)O
InChI InChI=1S/C19H20O2/c20-18(13-10-16-6-2-1-3-7-16)9-5-4-8-17-11-14-19(21)15-12-17/h1-3,5-7,9,11-12,14-15,21H,4,8,10,13H2
InChI Key VPCHZECKYCDVSA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H20O2
Molecular Weight 280.40 g/mol
Exact Mass 280.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.08
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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7-(4-HYDROXYPHENYL)-1-PHENYLHEPT-4-EN-3-ONE
SCHEMBL6373438

2D Structure

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2D Structure of 4-Hepten-3-one, 7-(4-hydroxyphenyl)-1-phenyl-, (E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5752 57.52%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.5353 53.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8990 89.90%
OATP1B3 inhibitior + 0.9184 91.84%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8853 88.53%
P-glycoprotein inhibitior - 0.8133 81.33%
P-glycoprotein substrate - 0.9241 92.41%
CYP3A4 substrate - 0.5792 57.92%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8105 81.05%
CYP3A4 inhibition - 0.6390 63.90%
CYP2C9 inhibition - 0.7163 71.63%
CYP2C19 inhibition + 0.6358 63.58%
CYP2D6 inhibition - 0.9449 94.49%
CYP1A2 inhibition + 0.6012 60.12%
CYP2C8 inhibition + 0.7399 73.99%
CYP inhibitory promiscuity - 0.5379 53.79%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7168 71.68%
Carcinogenicity (trinary) Non-required 0.6170 61.70%
Eye corrosion - 0.9339 93.39%
Eye irritation + 0.9018 90.18%
Skin irritation - 0.6334 63.34%
Skin corrosion - 0.9804 98.04%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5723 57.23%
Micronuclear - 0.8256 82.56%
Hepatotoxicity - 0.6592 65.92%
skin sensitisation + 0.7760 77.60%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6806 68.06%
Acute Oral Toxicity (c) III 0.5968 59.68%
Estrogen receptor binding + 0.8871 88.71%
Androgen receptor binding + 0.7015 70.15%
Thyroid receptor binding - 0.5488 54.88%
Glucocorticoid receptor binding + 0.6213 62.13%
Aromatase binding + 0.8784 87.84%
PPAR gamma + 0.6818 68.18%
Honey bee toxicity - 0.9149 91.49%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9290 92.90%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.10% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.89% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.62% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.64% 95.50%
CHEMBL2581 P07339 Cathepsin D 89.09% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.91% 86.33%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 84.95% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.99% 96.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.23% 91.71%

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.
Alpinia officinarum

Cross-Links

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PubChem 69757384
LOTUS LTS0228143
wikiData Q105290643