1-(Meta-hydroxyphenyl)-4-hydroxy-3-isoquinolone

Details

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Internal ID 7ce98442-722f-4447-b324-8e7c541bf3d8
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Phenylpyridines
IUPAC Name 4-hydroxy-1-(3-hydroxyphenyl)-2H-isoquinolin-3-one
SMILES (Canonical) C1=CC2=C(NC(=O)C(=C2C=C1)O)C3=CC(=CC=C3)O
SMILES (Isomeric) C1=CC2=C(NC(=O)C(=C2C=C1)O)C3=CC(=CC=C3)O
InChI InChI=1S/C15H11NO3/c17-10-5-3-4-9(8-10)13-11-6-1-2-7-12(11)14(18)15(19)16-13/h1-8,17-18H,(H,16,19)
InChI Key LMAPHZXFPNPWPP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H11NO3
Molecular Weight 253.25 g/mol
Exact Mass 253.07389321 g/mol
Topological Polar Surface Area (TPSA) 69.60 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(Meta-hydroxyphenyl)-4-hydroxy-3-isoquinolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 - 0.6591 65.91%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7043 70.43%
OATP2B1 inhibitior - 0.5843 58.43%
OATP1B1 inhibitior + 0.9186 91.86%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5611 56.11%
P-glycoprotein inhibitior - 0.9111 91.11%
P-glycoprotein substrate - 0.9078 90.78%
CYP3A4 substrate - 0.5281 52.81%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8479 84.79%
CYP3A4 inhibition - 0.8782 87.82%
CYP2C9 inhibition - 0.6295 62.95%
CYP2C19 inhibition - 0.7501 75.01%
CYP2D6 inhibition - 0.8901 89.01%
CYP1A2 inhibition + 0.9066 90.66%
CYP2C8 inhibition - 0.5769 57.69%
CYP inhibitory promiscuity - 0.8159 81.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7239 72.39%
Eye corrosion - 0.9966 99.66%
Eye irritation + 0.7771 77.71%
Skin irritation - 0.7329 73.29%
Skin corrosion - 0.9750 97.50%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8789 87.89%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6597 65.97%
skin sensitisation - 0.8579 85.79%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8997 89.97%
Acute Oral Toxicity (c) II 0.3761 37.61%
Estrogen receptor binding + 0.8305 83.05%
Androgen receptor binding + 0.8233 82.33%
Thyroid receptor binding + 0.7699 76.99%
Glucocorticoid receptor binding + 0.9496 94.96%
Aromatase binding + 0.8658 86.58%
PPAR gamma + 0.9149 91.49%
Honey bee toxicity - 0.9243 92.43%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.5385 53.85%

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 96.72% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.38% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.11% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.85% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.76% 99.23%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 90.10% 83.10%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 86.74% 92.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.58% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.41% 86.33%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.75% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.26% 93.99%
CHEMBL2535 P11166 Glucose transporter 84.81% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.96% 99.15%
CHEMBL1937 Q92769 Histone deacetylase 2 82.81% 94.75%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.63% 94.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.47% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.23% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.03% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 24862111
LOTUS LTS0151912
wikiData Q77384998