1,7-Diphenyl-(6e)-6-hepten-3-one

Details

Top
Internal ID 01c00ca1-0780-4cd9-92e5-dabaf02bfae0
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name (E)-1,7-diphenylhept-6-en-3-one
SMILES (Canonical) C1=CC=C(C=C1)CCC(=O)CCC=CC2=CC=CC=C2
SMILES (Isomeric) C1=CC=C(C=C1)CCC(=O)CC/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/h1-7,9-13H,8,14-16H2/b13-7+
InChI Key VNFWNGSEJXPCSW-NTUHNPAUSA-N
Popularity 7 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H20O
Molecular Weight 264.40 g/mol
Exact Mass 264.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

Top
SCHEMBL11155173
1,7-diphenyl-(6e)-6-hepten-3-one

2D Structure

Top
2D Structure of 1,7-Diphenyl-(6e)-6-hepten-3-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.7880 78.80%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.7951 79.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8769 87.69%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6447 64.47%
P-glycoprotein inhibitior - 0.9111 91.11%
P-glycoprotein substrate - 0.9272 92.72%
CYP3A4 substrate - 0.6320 63.20%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.7149 71.49%
CYP3A4 inhibition - 0.8672 86.72%
CYP2C9 inhibition - 0.6105 61.05%
CYP2C19 inhibition + 0.5455 54.55%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition + 0.7560 75.60%
CYP2C8 inhibition - 0.6444 64.44%
CYP inhibitory promiscuity + 0.7863 78.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6577 65.77%
Eye corrosion - 0.5751 57.51%
Eye irritation + 0.8297 82.97%
Skin irritation - 0.5683 56.83%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8274 82.74%
Micronuclear - 0.9415 94.15%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.6218 62.18%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.8046 80.46%
Acute Oral Toxicity (c) III 0.8080 80.80%
Estrogen receptor binding + 0.7173 71.73%
Androgen receptor binding - 0.5273 52.73%
Thyroid receptor binding - 0.6596 65.96%
Glucocorticoid receptor binding - 0.8351 83.51%
Aromatase binding + 0.8252 82.52%
PPAR gamma - 0.6701 67.01%
Honey bee toxicity - 0.9215 92.15%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9691 96.91%

Targets

Top

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 93.86% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.31% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.17% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.77% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.28% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.87% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.20% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 83.53% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.32% 91.71%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.56% 96.25%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.02% 95.50%

Plants that contains it

Top
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.
Curcuma comosa

Cross-Links

Top
PubChem 44593373
LOTUS LTS0225826
wikiData Q76614185