3,8-dihydroxy-6-methoxy-3,4,5-trimethyl-4H-isochromen-1-one

Details

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Internal ID 81079ae4-031c-4978-a5cb-d471aaee485e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 3,8-dihydroxy-6-methoxy-3,4,5-trimethyl-4H-isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O5/c1-6-9(17-4)5-8(14)11-10(6)7(2)13(3,16)18-12(11)15/h5,7,14,16H,1-4H3
InChI Key XLJAJFLQTGWNES-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8-dihydroxy-6-methoxy-3,4,5-trimethyl-4H-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 + 0.9304 93.04%
Caco-2 + 0.5236 52.36%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7629 76.29%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.9097 90.97%
OATP1B3 inhibitior + 0.9572 95.72%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9449 94.49%
P-glycoprotein inhibitior - 0.8855 88.55%
P-glycoprotein substrate - 0.8731 87.31%
CYP3A4 substrate + 0.5910 59.10%
CYP2C9 substrate + 0.6245 62.45%
CYP2D6 substrate - 0.8534 85.34%
CYP3A4 inhibition - 0.8543 85.43%
CYP2C9 inhibition - 0.9293 92.93%
CYP2C19 inhibition - 0.8546 85.46%
CYP2D6 inhibition - 0.9063 90.63%
CYP1A2 inhibition + 0.6669 66.69%
CYP2C8 inhibition - 0.6973 69.73%
CYP inhibitory promiscuity - 0.6700 67.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5736 57.36%
Eye corrosion - 0.9581 95.81%
Eye irritation - 0.6901 69.01%
Skin irritation - 0.6557 65.57%
Skin corrosion - 0.9770 97.70%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6704 67.04%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9397 93.97%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6047 60.47%
Acute Oral Toxicity (c) II 0.5036 50.36%
Estrogen receptor binding - 0.4792 47.92%
Androgen receptor binding - 0.5318 53.18%
Thyroid receptor binding + 0.5185 51.85%
Glucocorticoid receptor binding - 0.4737 47.37%
Aromatase binding - 0.4927 49.27%
PPAR gamma + 0.6319 63.19%
Honey bee toxicity - 0.8470 84.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5404 54.04%
Fish aquatic toxicity + 0.8862 88.62%

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 98.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.16% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.00% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.03% 92.94%
CHEMBL4208 P20618 Proteasome component C5 87.85% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.89% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.43% 85.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.90% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.84% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.83% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.32% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.99% 97.14%
CHEMBL2581 P07339 Cathepsin D 84.92% 98.95%
CHEMBL2535 P11166 Glucose transporter 81.01% 98.75%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.07% 82.38%

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 162978788
LOTUS LTS0025689
wikiData Q104201100