7-Hydroxy-3,5-dimethyl-1H-isochromen-1-one

Details

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Internal ID 6893e92c-7723-43b7-abc7-dc546ab047b2
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 7-hydroxy-3,5-dimethylisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O3/c1-6-3-8(12)5-10-9(6)4-7(2)14-11(10)13/h3-5,12H,1-2H3
InChI Key LAPUFWKKGOUUAN-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O3
Molecular Weight 190.19 g/mol
Exact Mass 190.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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7-hydroxy-3,5-dimethyl-isochromen-1-one
1401353-58-9
Compound NP-019606
CHEMBL3437593
AKOS027325018
7-hydroxy-3, 5-dimethyl-isochromen-1-one
NCGC00381405-01!7-hydroxy-3,5-dimethylisochromen-1-one

2D Structure

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2D Structure of 7-Hydroxy-3,5-dimethyl-1H-isochromen-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 + 0.9936 99.36%
Caco-2 + 0.8199 81.99%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6927 69.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.9693 96.93%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8590 85.90%
P-glycoprotein inhibitior - 0.9458 94.58%
P-glycoprotein substrate - 0.9490 94.90%
CYP3A4 substrate - 0.6025 60.25%
CYP2C9 substrate - 0.6106 61.06%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.8229 82.29%
CYP2C9 inhibition - 0.8511 85.11%
CYP2C19 inhibition - 0.9583 95.83%
CYP2D6 inhibition - 0.9599 95.99%
CYP1A2 inhibition + 0.7460 74.60%
CYP2C8 inhibition - 0.8739 87.39%
CYP inhibitory promiscuity - 0.9013 90.13%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5532 55.32%
Eye corrosion - 0.9542 95.42%
Eye irritation + 0.8835 88.35%
Skin irritation + 0.5736 57.36%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7206 72.06%
Micronuclear + 0.8359 83.59%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation - 0.8776 87.76%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.4783 47.83%
Acute Oral Toxicity (c) III 0.7247 72.47%
Estrogen receptor binding - 0.7700 77.00%
Androgen receptor binding + 0.5780 57.80%
Thyroid receptor binding - 0.6916 69.16%
Glucocorticoid receptor binding - 0.7318 73.18%
Aromatase binding + 0.5468 54.68%
PPAR gamma - 0.5360 53.60%
Honey bee toxicity - 0.9377 93.77%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8991 89.91%

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 95.70% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.75% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.82% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.78% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.13% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.01% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.78% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.09% 99.23%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 84.06% 95.70%
CHEMBL1951 P21397 Monoamine oxidase A 83.19% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.45% 86.33%

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 71593198
LOTUS LTS0098287
wikiData Q75069663