7-(2-Hydroxy-3-methoxy-3-methylbutoxy)-6-methoxychromen-2-one

Details

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Internal ID c569bc99-ffde-4e0f-87e5-8bd8945325a2
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(2-hydroxy-3-methoxy-3-methylbutoxy)-6-methoxychromen-2-one
SMILES (Canonical) CC(C)(C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O)OC
SMILES (Isomeric) CC(C)(C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O)OC
InChI InChI=1S/C16H20O6/c1-16(2,20-4)14(17)9-21-13-8-11-10(7-12(13)19-3)5-6-15(18)22-11/h5-8,14,17H,9H2,1-4H3
InChI Key FGRJIXKDQBFFIZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O6
Molecular Weight 308.33 g/mol
Exact Mass 308.12598835 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2-Hydroxy-3-methoxy-3-methylbutoxy)-6-methoxychromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9769 97.69%
Caco-2 + 0.8291 82.91%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6835 68.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9133 91.33%
OATP1B3 inhibitior + 0.9109 91.09%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5128 51.28%
P-glycoprotein inhibitior - 0.7833 78.33%
P-glycoprotein substrate - 0.6065 60.65%
CYP3A4 substrate - 0.5082 50.82%
CYP2C9 substrate - 0.6755 67.55%
CYP2D6 substrate - 0.8103 81.03%
CYP3A4 inhibition - 0.8543 85.43%
CYP2C9 inhibition - 0.8168 81.68%
CYP2C19 inhibition - 0.7391 73.91%
CYP2D6 inhibition - 0.8865 88.65%
CYP1A2 inhibition + 0.7014 70.14%
CYP2C8 inhibition - 0.7226 72.26%
CYP inhibitory promiscuity - 0.8805 88.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6713 67.13%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9079 90.79%
Skin irritation - 0.8041 80.41%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4177 41.77%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8343 83.43%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8764 87.64%
Acute Oral Toxicity (c) III 0.6077 60.77%
Estrogen receptor binding + 0.8444 84.44%
Androgen receptor binding + 0.5389 53.89%
Thyroid receptor binding + 0.6852 68.52%
Glucocorticoid receptor binding + 0.6441 64.41%
Aromatase binding + 0.5376 53.76%
PPAR gamma + 0.7199 71.99%
Honey bee toxicity - 0.9143 91.43%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9021 90.21%

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
CHEMBL2581 P07339 Cathepsin D 95.50% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.72% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.16% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.39% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.22% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.04% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.09% 96.09%
CHEMBL2535 P11166 Glucose transporter 87.96% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 87.53% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.87% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.57% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.17% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.87% 89.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.27% 90.71%
CHEMBL4208 P20618 Proteasome component C5 81.49% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.25% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.05% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Salvia fruticosa
Salvia virgata

Cross-Links

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PubChem 11185914
LOTUS LTS0053273
wikiData Q104396376