4-(2-Hydroxy-7-phenylheptyl)-2-methoxyphenol

Details

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Internal ID 6b053cd3-9b5c-4d03-bd04-3af0d693adbd
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 4-(2-hydroxy-7-phenylheptyl)-2-methoxyphenol
SMILES (Canonical) COC1=C(C=CC(=C1)CC(CCCCCC2=CC=CC=C2)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)CC(CCCCCC2=CC=CC=C2)O)O
InChI InChI=1S/C20H26O3/c1-23-20-15-17(12-13-19(20)22)14-18(21)11-7-3-6-10-16-8-4-2-5-9-16/h2,4-5,8-9,12-13,15,18,21-22H,3,6-7,10-11,14H2,1H3
InChI Key LCCOXVDJFONGRT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O3
Molecular Weight 314.40 g/mol
Exact Mass 314.18819469 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.11
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-Hydroxy-7-phenylheptyl)-2-methoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.6030 60.30%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.9469 94.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8958 89.58%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.5515 55.15%
P-glycoprotein substrate - 0.5482 54.82%
CYP3A4 substrate + 0.5787 57.87%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.5082 50.82%
CYP3A4 inhibition - 0.8658 86.58%
CYP2C9 inhibition - 0.6883 68.83%
CYP2C19 inhibition + 0.6081 60.81%
CYP2D6 inhibition - 0.8978 89.78%
CYP1A2 inhibition + 0.5462 54.62%
CYP2C8 inhibition + 0.8095 80.95%
CYP inhibitory promiscuity - 0.6158 61.58%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6098 60.98%
Eye corrosion - 0.9778 97.78%
Eye irritation - 0.8313 83.13%
Skin irritation - 0.6482 64.82%
Skin corrosion - 0.8995 89.95%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8047 80.47%
Micronuclear - 0.8041 80.41%
Hepatotoxicity - 0.7199 71.99%
skin sensitisation - 0.7724 77.24%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7627 76.27%
Acute Oral Toxicity (c) III 0.6843 68.43%
Estrogen receptor binding + 0.8395 83.95%
Androgen receptor binding + 0.7693 76.93%
Thyroid receptor binding + 0.5804 58.04%
Glucocorticoid receptor binding - 0.5518 55.18%
Aromatase binding + 0.5876 58.76%
PPAR gamma + 0.5595 55.95%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5428 54.28%
Fish aquatic toxicity + 0.9235 92.35%

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
CHEMBL2581 P07339 Cathepsin D 98.36% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.21% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.76% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.67% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 95.10% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.30% 86.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.93% 95.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.72% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.54% 94.62%
CHEMBL2535 P11166 Glucose transporter 89.83% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.77% 95.50%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.39% 92.08%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 84.67% 100.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 83.66% 94.08%
CHEMBL1907 P15144 Aminopeptidase N 82.71% 93.31%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.72% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.50% 93.99%
CHEMBL3761 Q9HCG7 Beta-glucosidase 81.09% 99.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.03% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 80.12% 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.
Actinidia polygama
Alpinia oxyphylla

Cross-Links

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PubChem 5320105
NPASS NPC7698