4-(3-Hydroxy-7-phenylhept-6-enyl)phenol

Details

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Internal ID d499b296-88d2-45f9-8a29-2943f0625712
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 4-(3-hydroxy-7-phenylhept-6-enyl)phenol
SMILES (Canonical) C1=CC=C(C=C1)C=CCCC(CCC2=CC=C(C=C2)O)O
SMILES (Isomeric) C1=CC=C(C=C1)C=CCCC(CCC2=CC=C(C=C2)O)O
InChI InChI=1S/C19H22O2/c20-18(13-10-17-11-14-19(21)15-12-17)9-5-4-8-16-6-2-1-3-7-16/h1-4,6-8,11-12,14-15,18,20-21H,5,9-10,13H2
InChI Key PXPIJNMPDAFWSF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O2
Molecular Weight 282.40 g/mol
Exact Mass 282.161979940 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3-Hydroxy-7-phenylhept-6-enyl)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 - 0.5836 58.36%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.7294 72.94%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8470 84.70%
OATP1B3 inhibitior + 0.8777 87.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7402 74.02%
P-glycoprotein inhibitior - 0.8472 84.72%
P-glycoprotein substrate - 0.7252 72.52%
CYP3A4 substrate - 0.5801 58.01%
CYP2C9 substrate + 0.5799 57.99%
CYP2D6 substrate + 0.3626 36.26%
CYP3A4 inhibition - 0.6575 65.75%
CYP2C9 inhibition - 0.7442 74.42%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9073 90.73%
CYP1A2 inhibition - 0.5188 51.88%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.5787 57.87%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7239 72.39%
Carcinogenicity (trinary) Non-required 0.5624 56.24%
Eye corrosion - 0.9506 95.06%
Eye irritation + 0.5400 54.00%
Skin irritation - 0.7115 71.15%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6978 69.78%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.7407 74.07%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.8521 85.21%
Acute Oral Toxicity (c) III 0.7777 77.77%
Estrogen receptor binding + 0.8305 83.05%
Androgen receptor binding + 0.9025 90.25%
Thyroid receptor binding - 0.5913 59.13%
Glucocorticoid receptor binding - 0.5918 59.18%
Aromatase binding + 0.6463 64.63%
PPAR gamma + 0.7432 74.32%
Honey bee toxicity - 0.7594 75.94%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9500 95.00%

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 98.37% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.05% 91.11%
CHEMBL233 P35372 Mu opioid receptor 94.46% 97.93%
CHEMBL2581 P07339 Cathepsin D 94.25% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 92.49% 91.71%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 92.31% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.58% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.50% 99.17%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 90.01% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.52% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.24% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.80% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.73% 96.09%
CHEMBL242 Q92731 Estrogen receptor beta 84.75% 98.35%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 84.14% 94.23%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.94% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.00% 96.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.79% 93.81%
CHEMBL3761 Q9HCG7 Beta-glucosidase 81.39% 99.00%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.10% 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 75070115
LOTUS LTS0039009
wikiData Q105216313