7-(2-Hydroxy-3,3-dimethylbutoxy)-6-methoxychromen-2-one

Details

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Internal ID 16c02efb-36f5-4e25-a392-bdb30e3b6a15
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(2-hydroxy-3,3-dimethylbutoxy)-6-methoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O5/c1-16(2,3)14(17)9-20-13-8-11-10(7-12(13)19-4)5-6-15(18)21-11/h5-8,14,17H,9H2,1-4H3
InChI Key HWUGSZDCJZLGDI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O5
Molecular Weight 292.33 g/mol
Exact Mass 292.13107373 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2-Hydroxy-3,3-dimethylbutoxy)-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 + 0.9810 98.10%
Caco-2 + 0.8605 86.05%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9140 91.40%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5143 51.43%
P-glycoprotein inhibitior - 0.8691 86.91%
P-glycoprotein substrate - 0.6242 62.42%
CYP3A4 substrate - 0.5426 54.26%
CYP2C9 substrate - 0.8377 83.77%
CYP2D6 substrate - 0.8158 81.58%
CYP3A4 inhibition - 0.8810 88.10%
CYP2C9 inhibition - 0.8755 87.55%
CYP2C19 inhibition - 0.7509 75.09%
CYP2D6 inhibition - 0.8312 83.12%
CYP1A2 inhibition + 0.6589 65.89%
CYP2C8 inhibition - 0.7743 77.43%
CYP inhibitory promiscuity - 0.8762 87.62%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6754 67.54%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.8767 87.67%
Skin irritation - 0.8022 80.22%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7000 70.00%
Micronuclear - 0.5467 54.67%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8447 84.47%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8192 81.92%
Acute Oral Toxicity (c) III 0.6414 64.14%
Estrogen receptor binding + 0.8371 83.71%
Androgen receptor binding - 0.4862 48.62%
Thyroid receptor binding + 0.6174 61.74%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6712 67.12%
PPAR gamma + 0.7710 77.10%
Honey bee toxicity - 0.9129 91.29%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8999 89.99%

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 95.97% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.87% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.83% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.64% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.20% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.78% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.40% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.35% 96.00%
CHEMBL2535 P11166 Glucose transporter 86.16% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.04% 95.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.70% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.39% 90.71%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.67% 89.62%
CHEMBL3401 O75469 Pregnane X receptor 83.61% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.04% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.22% 89.00%
CHEMBL4208 P20618 Proteasome component C5 81.84% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.07% 97.25%
CHEMBL4581 P52732 Kinesin-like protein 1 80.59% 93.18%

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.
Daphne oleoides

Cross-Links

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PubChem 101101558
LOTUS LTS0026367
wikiData Q104667841