2-Heptyl-6-methoxybenzene-1,4-diol

Details

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Internal ID dcacadbe-6a3b-408b-b04d-f424eb83ebbd
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2-heptyl-6-methoxybenzene-1,4-diol
SMILES (Canonical) CCCCCCCC1=C(C(=CC(=C1)O)OC)O
SMILES (Isomeric) CCCCCCCC1=C(C(=CC(=C1)O)OC)O
InChI InChI=1S/C14H22O3/c1-3-4-5-6-7-8-11-9-12(15)10-13(17-2)14(11)16/h9-10,15-16H,3-8H2,1-2H3
InChI Key QKNKJZPSRUAQDS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H22O3
Molecular Weight 238.32 g/mol
Exact Mass 238.15689456 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 3
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 2-Heptyl-6-methoxybenzene-1,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.7885 78.85%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8956 89.56%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.8357 83.57%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7475 74.75%
P-glycoprotein inhibitior - 0.9333 93.33%
P-glycoprotein substrate - 0.6419 64.19%
CYP3A4 substrate - 0.5369 53.69%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate + 0.4683 46.83%
CYP3A4 inhibition - 0.7553 75.53%
CYP2C9 inhibition - 0.7083 70.83%
CYP2C19 inhibition - 0.5404 54.04%
CYP2D6 inhibition - 0.7531 75.31%
CYP1A2 inhibition + 0.6755 67.55%
CYP2C8 inhibition + 0.8212 82.12%
CYP inhibitory promiscuity - 0.5957 59.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7643 76.43%
Carcinogenicity (trinary) Non-required 0.6386 63.86%
Eye corrosion - 0.8906 89.06%
Eye irritation + 0.8493 84.93%
Skin irritation - 0.5922 59.22%
Skin corrosion - 0.6910 69.10%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7458 74.58%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5433 54.33%
skin sensitisation + 0.6044 60.44%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5497 54.97%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6118 61.18%
Acute Oral Toxicity (c) III 0.7697 76.97%
Estrogen receptor binding + 0.7946 79.46%
Androgen receptor binding + 0.6168 61.68%
Thyroid receptor binding + 0.5546 55.46%
Glucocorticoid receptor binding + 0.5675 56.75%
Aromatase binding - 0.6667 66.67%
PPAR gamma + 0.7269 72.69%
Honey bee toxicity - 0.9788 97.88%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.8291 82.91%
Fish aquatic toxicity + 0.9891 98.91%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.97% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.82% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.61% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.89% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 94.17% 89.63%
CHEMBL2581 P07339 Cathepsin D 93.53% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.83% 86.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.70% 95.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.37% 89.62%
CHEMBL2885 P07451 Carbonic anhydrase III 85.24% 87.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.22% 92.62%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.56% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.39% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 82.31% 94.73%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.87% 91.81%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.77% 92.68%
CHEMBL1907 P15144 Aminopeptidase N 80.89% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.57% 96.00%

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.
Primula obconica

Cross-Links

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PubChem 163194545
LOTUS LTS0013450
wikiData Q105223220