1-(3,4-Dihydroxyphenyl)-2-(4-hydroxyphenyl)ethane

Details

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Internal ID a0d4671f-9e53-48c3-b731-d20272eaa841
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[2-(4-hydroxyphenyl)ethyl]benzene-1,2-diol
SMILES (Canonical) C1=CC(=CC=C1CCC2=CC(=C(C=C2)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1CCC2=CC(=C(C=C2)O)O)O
InChI InChI=1S/C14H14O3/c15-12-6-3-10(4-7-12)1-2-11-5-8-13(16)14(17)9-11/h3-9,15-17H,1-2H2
InChI Key HPRNXGQVPZPZNM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O3
Molecular Weight 230.26 g/mol
Exact Mass 230.094294304 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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BDBM50483032
1-(3,4-dihydroxyphenyl)-2-( 4-hydroxyphenyl)ethane

2D Structure

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2D Structure of 1-(3,4-Dihydroxyphenyl)-2-(4-hydroxyphenyl)ethane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9498 94.98%
Caco-2 - 0.5487 54.87%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8898 88.98%
OATP2B1 inhibitior - 0.8448 84.48%
OATP1B1 inhibitior + 0.9396 93.96%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7952 79.52%
P-glycoprotein inhibitior - 0.9796 97.96%
P-glycoprotein substrate - 0.9252 92.52%
CYP3A4 substrate - 0.6981 69.81%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate + 0.4041 40.41%
CYP3A4 inhibition - 0.8411 84.11%
CYP2C9 inhibition + 0.7768 77.68%
CYP2C19 inhibition + 0.6466 64.66%
CYP2D6 inhibition - 0.8690 86.90%
CYP1A2 inhibition + 0.5412 54.12%
CYP2C8 inhibition + 0.5862 58.62%
CYP inhibitory promiscuity + 0.6137 61.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6923 69.23%
Carcinogenicity (trinary) Non-required 0.4987 49.87%
Eye corrosion - 0.9098 90.98%
Eye irritation + 0.9451 94.51%
Skin irritation + 0.5988 59.88%
Skin corrosion - 0.7563 75.63%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7072 70.72%
Micronuclear - 0.6141 61.41%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation + 0.8214 82.14%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5581 55.81%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7159 71.59%
Acute Oral Toxicity (c) III 0.7883 78.83%
Estrogen receptor binding + 0.8877 88.77%
Androgen receptor binding + 0.8469 84.69%
Thyroid receptor binding + 0.6846 68.46%
Glucocorticoid receptor binding + 0.7735 77.35%
Aromatase binding + 0.6741 67.41%
PPAR gamma + 0.8349 83.49%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9414 94.14%

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 97.45% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.74% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.06% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.00% 96.09%
CHEMBL3194 P02766 Transthyretin 85.98% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.14% 94.45%
CHEMBL4208 P20618 Proteasome component C5 84.23% 90.00%
CHEMBL242 Q92731 Estrogen receptor beta 83.92% 98.35%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.29% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.38% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.24% 99.15%

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.
Allium cepa

Cross-Links

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PubChem 50908655
LOTUS LTS0162196
wikiData Q105031855