(6e)-1,7-Diphenylhept-6-en-3-ol

Details

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Internal ID 585f740c-250b-4082-8e07-5fbf517d2c28
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name (E)-1,7-diphenylhept-6-en-3-ol
SMILES (Canonical) C1=CC=C(C=C1)CCC(CCC=CC2=CC=CC=C2)O
SMILES (Isomeric) C1=CC=C(C=C1)CCC(CC/C=C/C2=CC=CC=C2)O
InChI InChI=1S/C19H22O/c20-19(16-15-18-11-5-2-6-12-18)14-8-7-13-17-9-3-1-4-10-17/h1-7,9-13,19-20H,8,14-16H2/b13-7+
InChI Key DPRCKWANIKZGTF-NTUHNPAUSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O
Molecular Weight 266.40 g/mol
Exact Mass 266.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.47
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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(6e)-1,7-diphenylhept-6-en-3-ol

2D Structure

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2D Structure of (6e)-1,7-Diphenylhept-6-en-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.8270 82.70%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.5705 57.05%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9274 92.74%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7493 74.93%
P-glycoprotein inhibitior - 0.8815 88.15%
P-glycoprotein substrate - 0.8099 80.99%
CYP3A4 substrate - 0.6420 64.20%
CYP2C9 substrate + 0.5764 57.64%
CYP2D6 substrate + 0.3767 37.67%
CYP3A4 inhibition - 0.8982 89.82%
CYP2C9 inhibition - 0.7387 73.87%
CYP2C19 inhibition - 0.5808 58.08%
CYP2D6 inhibition - 0.8889 88.89%
CYP1A2 inhibition + 0.7256 72.56%
CYP2C8 inhibition - 0.8644 86.44%
CYP inhibitory promiscuity - 0.5102 51.02%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7039 70.39%
Carcinogenicity (trinary) Non-required 0.6447 64.47%
Eye corrosion - 0.8666 86.66%
Eye irritation - 0.5000 50.00%
Skin irritation + 0.5501 55.01%
Skin corrosion - 0.9286 92.86%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8156 81.56%
Micronuclear - 0.8915 89.15%
Hepatotoxicity - 0.5908 59.08%
skin sensitisation + 0.7152 71.52%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.8672 86.72%
Acute Oral Toxicity (c) III 0.7159 71.59%
Estrogen receptor binding + 0.7103 71.03%
Androgen receptor binding + 0.6528 65.28%
Thyroid receptor binding - 0.6947 69.47%
Glucocorticoid receptor binding - 0.6836 68.36%
Aromatase binding + 0.5411 54.11%
PPAR gamma - 0.5216 52.16%
Honey bee toxicity - 0.8310 83.10%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9437 94.37%

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 96.23% 94.62%
CHEMBL2581 P07339 Cathepsin D 93.14% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.54% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.17% 86.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.97% 94.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.19% 96.09%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 87.49% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.99% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.38% 99.17%
CHEMBL233 P35372 Mu opioid receptor 86.11% 97.93%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.89% 93.99%
CHEMBL3902 P09211 Glutathione S-transferase Pi 85.42% 93.81%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.84% 96.00%
CHEMBL2039 P27338 Monoamine oxidase B 84.31% 92.51%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.00% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 83.87% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.32% 95.50%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.46% 96.25%

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 5316931
LOTUS LTS0012596
wikiData Q104986670