6-Hydroxy-3-(2-hydroxypropyl)-8-methoxy-7-methylisochromen-1-one

Details

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Internal ID c7521e44-1a18-40f7-a209-7b545f256661
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 6-hydroxy-3-(2-hydroxypropyl)-8-methoxy-7-methylisochromen-1-one
SMILES (Canonical) CC1=C(C=C2C=C(OC(=O)C2=C1OC)CC(C)O)O
SMILES (Isomeric) CC1=C(C=C2C=C(OC(=O)C2=C1OC)CC(C)O)O
InChI InChI=1S/C14H16O5/c1-7(15)4-10-5-9-6-11(16)8(2)13(18-3)12(9)14(17)19-10/h5-7,15-16H,4H2,1-3H3
InChI Key SJRQZWQQJLIKQI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O5
Molecular Weight 264.27 g/mol
Exact Mass 264.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-3-(2-hydroxypropyl)-8-methoxy-7-methylisochromen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9616 96.16%
Caco-2 + 0.8148 81.48%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6827 68.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.8550 85.50%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8801 88.01%
P-glycoprotein inhibitior - 0.8573 85.73%
P-glycoprotein substrate - 0.8793 87.93%
CYP3A4 substrate - 0.5352 53.52%
CYP2C9 substrate - 0.5537 55.37%
CYP2D6 substrate - 0.8240 82.40%
CYP3A4 inhibition - 0.9285 92.85%
CYP2C9 inhibition - 0.9223 92.23%
CYP2C19 inhibition - 0.9023 90.23%
CYP2D6 inhibition - 0.8061 80.61%
CYP1A2 inhibition + 0.5452 54.52%
CYP2C8 inhibition - 0.7920 79.20%
CYP inhibitory promiscuity - 0.7856 78.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.6109 61.09%
Eye corrosion - 0.9855 98.55%
Eye irritation + 0.6208 62.08%
Skin irritation - 0.8236 82.36%
Skin corrosion - 0.9776 97.76%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7698 76.98%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.5026 50.26%
skin sensitisation - 0.9264 92.64%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8136 81.36%
Acute Oral Toxicity (c) III 0.4319 43.19%
Estrogen receptor binding + 0.5984 59.84%
Androgen receptor binding + 0.5927 59.27%
Thyroid receptor binding - 0.5592 55.92%
Glucocorticoid receptor binding + 0.7062 70.62%
Aromatase binding + 0.6865 68.65%
PPAR gamma + 0.6998 69.98%
Honey bee toxicity - 0.9296 92.96%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9178 91.78%

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 96.14% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.95% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.70% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.53% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.71% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 90.19% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.67% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.98% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.00% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.35% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.21% 96.95%
CHEMBL2535 P11166 Glucose transporter 82.84% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.43% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.32% 93.99%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.05% 90.71%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.89% 97.21%
CHEMBL4581 P52732 Kinesin-like protein 1 80.98% 93.18%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.33% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.07% 93.65%

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 163063735
LOTUS LTS0217475
wikiData Q104197361