1,7-Diphenyl-1,3,5-heptratriene

Details

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Internal ID 77ef155b-f462-4aee-b922-16a3d518c9f9
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name [(1E,3E,5E)-7-phenylhepta-1,3,5-trienyl]benzene
SMILES (Canonical) C1=CC=C(C=C1)CC=CC=CC=CC2=CC=CC=C2
SMILES (Isomeric) C1=CC=C(C=C1)C/C=C/C=C/C=C/C2=CC=CC=C2
InChI InChI=1S/C19H18/c1(2-6-12-18-14-8-4-9-15-18)3-7-13-19-16-10-5-11-17-19/h1-12,14-17H,13H2/b2-1+,7-3+,12-6+
InChI Key ALZIGHRHGDHKPD-BCPZQFGSSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H18
Molecular Weight 246.30 g/mol
Exact Mass 246.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.05
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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ALZIGHRHGDHKPD-BCPZQFGSSA-N
1,7-Diphenyl-1,3,5-heptratriene

2D Structure

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2D Structure of 1,7-Diphenyl-1,3,5-heptratriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.8346 83.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.4135 41.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6383 63.83%
P-glycoprotein inhibitior - 0.9620 96.20%
P-glycoprotein substrate - 0.9368 93.68%
CYP3A4 substrate - 0.7309 73.09%
CYP2C9 substrate - 0.6406 64.06%
CYP2D6 substrate - 0.6571 65.71%
CYP3A4 inhibition - 0.8779 87.79%
CYP2C9 inhibition - 0.5555 55.55%
CYP2C19 inhibition + 0.6517 65.17%
CYP2D6 inhibition - 0.9007 90.07%
CYP1A2 inhibition + 0.7719 77.19%
CYP2C8 inhibition - 0.7000 70.00%
CYP inhibitory promiscuity + 0.8831 88.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.4204 42.04%
Eye corrosion + 0.8716 87.16%
Eye irritation + 0.9819 98.19%
Skin irritation + 0.8113 81.13%
Skin corrosion - 0.6808 68.08%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3651 36.51%
Micronuclear - 0.8772 87.72%
Hepatotoxicity - 0.5818 58.18%
skin sensitisation + 0.9738 97.38%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6299 62.99%
Acute Oral Toxicity (c) III 0.8300 83.00%
Estrogen receptor binding + 0.8727 87.27%
Androgen receptor binding - 0.6786 67.86%
Thyroid receptor binding - 0.7138 71.38%
Glucocorticoid receptor binding - 0.6498 64.98%
Aromatase binding + 0.9022 90.22%
PPAR gamma + 0.6419 64.19%
Honey bee toxicity - 0.9108 91.08%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9895 98.95%

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 92.26% 94.62%
CHEMBL2039 P27338 Monoamine oxidase B 89.87% 92.51%
CHEMBL221 P23219 Cyclooxygenase-1 89.73% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.82% 86.33%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.22% 91.71%
CHEMBL2581 P07339 Cathepsin D 86.30% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.70% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.32% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 84.06% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.57% 91.11%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.55% 96.25%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.15% 95.50%

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.
Curcuma comosa

Cross-Links

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PubChem 44560845
LOTUS LTS0001186
wikiData Q104914470