7-(4-Hydroxy-3-methylbut-2-enoxy)chromen-2-one

Details

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Internal ID 801de6ed-8e13-408f-8ace-95d351f4428d
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(4-hydroxy-3-methylbut-2-enoxy)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O4/c1-10(9-15)6-7-17-12-4-2-11-3-5-14(16)18-13(11)8-12/h2-6,8,15H,7,9H2,1H3
InChI Key DJOOOTFYMSTBKM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 4
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-(4-Hydroxy-3-methylbut-2-enoxy)chromen-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 + 0.9752 97.52%
Caco-2 + 0.7816 78.16%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5903 59.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8538 85.38%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5175 51.75%
P-glycoprotein inhibitior - 0.9114 91.14%
P-glycoprotein substrate - 0.9097 90.97%
CYP3A4 substrate - 0.5384 53.84%
CYP2C9 substrate - 0.6755 67.55%
CYP2D6 substrate - 0.8357 83.57%
CYP3A4 inhibition - 0.6350 63.50%
CYP2C9 inhibition - 0.5806 58.06%
CYP2C19 inhibition + 0.7317 73.17%
CYP2D6 inhibition - 0.7563 75.63%
CYP1A2 inhibition + 0.7389 73.89%
CYP2C8 inhibition - 0.7891 78.91%
CYP inhibitory promiscuity + 0.7596 75.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.5930 59.30%
Eye corrosion - 0.9790 97.90%
Eye irritation + 0.5318 53.18%
Skin irritation - 0.7333 73.33%
Skin corrosion - 0.9654 96.54%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4831 48.31%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5175 51.75%
skin sensitisation - 0.8164 81.64%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5652 56.52%
Acute Oral Toxicity (c) III 0.5521 55.21%
Estrogen receptor binding + 0.8374 83.74%
Androgen receptor binding + 0.8049 80.49%
Thyroid receptor binding - 0.7752 77.52%
Glucocorticoid receptor binding + 0.7829 78.29%
Aromatase binding + 0.8996 89.96%
PPAR gamma + 0.7703 77.03%
Honey bee toxicity - 0.9210 92.10%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9937 99.37%

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 96.67% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 94.61% 92.51%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.81% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.33% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.96% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 92.92% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 92.75% 94.73%
CHEMBL4208 P20618 Proteasome component C5 88.31% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.09% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.02% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.13% 86.92%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 81.60% 88.00%

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.
Haplopappus multifolius

Cross-Links

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PubChem 73040280
LOTUS LTS0159178
wikiData Q104982575