6,7-dimethoxy-3-methyl-5-(3-methylbut-2-en-1-yl)-1H-isochromene

Details

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Internal ID 23b9060f-cd5a-49f9-982c-9c610782f91e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 6,7-dimethoxy-3-methyl-5-(3-methylbut-2-enyl)-1H-isochromene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O3/c1-11(2)6-7-14-15-8-12(3)20-10-13(15)9-16(18-4)17(14)19-5/h6,8-9H,7,10H2,1-5H3
InChI Key DMQOPCMQYIJMRB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O3
Molecular Weight 274.35 g/mol
Exact Mass 274.15689456 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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CHEBI:200531
6,7-dimethoxy-3-methyl-5-(3-methylbut-2-enyl)-1H-isochromene

2D Structure

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2D Structure of 6,7-dimethoxy-3-methyl-5-(3-methylbut-2-en-1-yl)-1H-isochromene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9421 94.21%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7307 73.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9191 91.91%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4885 48.85%
P-glycoprotein inhibitior - 0.8756 87.56%
P-glycoprotein substrate - 0.7405 74.05%
CYP3A4 substrate + 0.5174 51.74%
CYP2C9 substrate - 0.5827 58.27%
CYP2D6 substrate + 0.4034 40.34%
CYP3A4 inhibition - 0.6790 67.90%
CYP2C9 inhibition + 0.6160 61.60%
CYP2C19 inhibition + 0.8877 88.77%
CYP2D6 inhibition - 0.6430 64.30%
CYP1A2 inhibition + 0.9195 91.95%
CYP2C8 inhibition - 0.6670 66.70%
CYP inhibitory promiscuity + 0.9061 90.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7214 72.14%
Eye corrosion - 0.9822 98.22%
Eye irritation + 0.8522 85.22%
Skin irritation - 0.7831 78.31%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7287 72.87%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6602 66.02%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.8354 83.54%
Acute Oral Toxicity (c) III 0.7647 76.47%
Estrogen receptor binding + 0.7673 76.73%
Androgen receptor binding + 0.5705 57.05%
Thyroid receptor binding + 0.5482 54.82%
Glucocorticoid receptor binding + 0.5874 58.74%
Aromatase binding + 0.6996 69.96%
PPAR gamma + 0.6075 60.75%
Honey bee toxicity - 0.8401 84.01%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9768 97.68%

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 96.57% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.82% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.19% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.26% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.89% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.51% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.32% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.03% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.36% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.56% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.38% 94.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.55% 92.68%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.40% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.36% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.31% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.15% 96.95%

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 132522674
LOTUS LTS0127915
wikiData Q77279060