(E)-1,7-diphenylhept-5-en-3-one

Details

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Internal ID 86a7b187-20c2-43f0-b804-3087a3fe407a
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name (E)-1,7-diphenylhept-5-en-3-one
SMILES (Canonical) C1=CC=C(C=C1)CCC(=O)CC=CCC2=CC=CC=C2
SMILES (Isomeric) C1=CC=C(C=C1)CCC(=O)C/C=C/CC2=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/h1-12H,13-16H2/b8-7+
InChI Key LOADXMVBIJHBTC-BQYQJAHWSA-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 4.40
Atomic LogP (AlogP) 4.38
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-5-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 + 0.7509 75.09%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Plasma membrane 0.7364 73.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9089 90.89%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6971 69.71%
P-glycoprotein inhibitior - 0.8632 86.32%
P-glycoprotein substrate - 0.9206 92.06%
CYP3A4 substrate - 0.6718 67.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6985 69.85%
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 - 0.6507 65.07%
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 + 0.8496 84.96%
Skin irritation + 0.5153 51.53%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7968 79.68%
Micronuclear - 0.9415 94.15%
Hepatotoxicity + 0.5108 51.08%
skin sensitisation + 0.7277 72.77%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7247 72.47%
Acute Oral Toxicity (c) III 0.8366 83.66%
Estrogen receptor binding + 0.8344 83.44%
Androgen receptor binding - 0.7540 75.40%
Thyroid receptor binding - 0.6978 69.78%
Glucocorticoid receptor binding - 0.8109 81.09%
Aromatase binding + 0.8913 89.13%
PPAR gamma - 0.5189 51.89%
Honey bee toxicity - 0.9145 91.45%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6300 63.00%
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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.24% 94.62%
CHEMBL2581 P07339 Cathepsin D 91.64% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.73% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.64% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.57% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.35% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 85.42% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 82.39% 94.73%

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 56973722
NPASS NPC240502
LOTUS LTS0080870
wikiData Q105154599