(E)-1,7-diphenylhept-1-en-3-one

Details

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Internal ID babc5b95-8345-4c75-b4e7-2f5ac22709a6
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name (E)-1,7-diphenylhept-1-en-3-one
SMILES (Canonical) C1=CC=C(C=C1)CCCCC(=O)C=CC2=CC=CC=C2
SMILES (Isomeric) C1=CC=C(C=C1)CCCCC(=O)/C=C/C2=CC=CC=C2
InChI InChI=1S/C19H20O/c20-19(16-15-18-11-5-2-6-12-18)14-8-7-13-17-9-3-1-4-10-17/h1-6,9-12,15-16H,7-8,13-14H2/b16-15+
InChI Key XMNZHMODTJQZBP-FOCLMDBBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O
Molecular Weight 264.40 g/mol
Exact Mass 264.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-1,7-diphenylhept-1-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7843 78.43%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Plasma membrane 0.7364 73.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9170 91.70%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6770 67.70%
P-glycoprotein inhibitior - 0.8928 89.28%
P-glycoprotein substrate - 0.9117 91.17%
CYP3A4 substrate - 0.6237 62.37%
CYP2C9 substrate - 0.6145 61.45%
CYP2D6 substrate - 0.7738 77.38%
CYP3A4 inhibition - 0.8374 83.74%
CYP2C9 inhibition - 0.6327 63.27%
CYP2C19 inhibition + 0.6551 65.51%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition + 0.8674 86.74%
CYP2C8 inhibition + 0.5338 53.38%
CYP inhibitory promiscuity + 0.8426 84.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5878 58.78%
Eye corrosion - 0.5539 55.39%
Eye irritation + 0.8302 83.02%
Skin irritation + 0.5153 51.53%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8213 82.13%
Micronuclear - 0.9415 94.15%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation + 0.7277 72.77%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7807 78.07%
Acute Oral Toxicity (c) III 0.8366 83.66%
Estrogen receptor binding + 0.7816 78.16%
Androgen receptor binding + 0.5914 59.14%
Thyroid receptor binding - 0.6709 67.09%
Glucocorticoid receptor binding - 0.7846 78.46%
Aromatase binding + 0.8953 89.53%
PPAR gamma - 0.6883 68.83%
Honey bee toxicity - 0.9308 93.08%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9376 93.76%

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 95.05% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.48% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.74% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.31% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.19% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.81% 94.62%
CHEMBL5805 Q9NR97 Toll-like receptor 8 87.86% 96.25%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.72% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.62% 96.09%
CHEMBL2039 P27338 Monoamine oxidase B 87.38% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 83.84% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.86% 91.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.59% 95.50%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.32% 90.24%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 81.80% 96.67%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.33% 93.81%
CHEMBL221 P23219 Cyclooxygenase-1 80.14% 90.17%

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 101148929
LOTUS LTS0009549
wikiData Q105331248