7-Hydroxy-8-((3-methyl-2-butenyl)oxy)-2H-1-benzopyran-2-one

Details

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Internal ID 15bcc143-08ce-49fa-a470-73c48b59ab00
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-8-(3-methylbut-2-enoxy)chromen-2-one
SMILES (Canonical) CC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C
SMILES (Isomeric) CC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C
InChI InChI=1S/C14H14O4/c1-9(2)7-8-17-14-11(15)5-3-10-4-6-12(16)18-13(10)14/h3-7,15H,8H2,1-2H3
InChI Key RXAAPTWRRVWOCA-UHFFFAOYSA-N
Popularity 0 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 3.00
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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UNII-3U9JG90P8B
7-Hydroxy-8-((3-methyl-2-butenyl)oxy)-2H-1-benzopyran-2-one
92070-83-2
2H-1-Benzopyran-2-one, 7-hydroxy-8-((3-methyl-2-buten-1-yl)oxy)-
Q27258042

2D Structure

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2D Structure of 7-Hydroxy-8-((3-methyl-2-butenyl)oxy)-2H-1-benzopyran-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 + 0.9749 97.49%
Caco-2 + 0.8832 88.32%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7924 79.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6076 60.76%
P-glycoprotein inhibitior - 0.8115 81.15%
P-glycoprotein substrate - 0.9510 95.10%
CYP3A4 substrate - 0.5961 59.61%
CYP2C9 substrate - 0.6607 66.07%
CYP2D6 substrate - 0.8336 83.36%
CYP3A4 inhibition - 0.8028 80.28%
CYP2C9 inhibition + 0.8747 87.47%
CYP2C19 inhibition + 0.9169 91.69%
CYP2D6 inhibition + 0.5495 54.95%
CYP1A2 inhibition + 0.9117 91.17%
CYP2C8 inhibition - 0.8095 80.95%
CYP inhibitory promiscuity + 0.8495 84.95%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7432 74.32%
Eye corrosion - 0.9888 98.88%
Eye irritation + 0.9103 91.03%
Skin irritation - 0.7332 73.32%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4786 47.86%
Micronuclear - 0.5326 53.26%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation - 0.7621 76.21%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6081 60.81%
Acute Oral Toxicity (c) III 0.5504 55.04%
Estrogen receptor binding + 0.6267 62.67%
Androgen receptor binding + 0.6887 68.87%
Thyroid receptor binding + 0.6355 63.55%
Glucocorticoid receptor binding + 0.7113 71.13%
Aromatase binding + 0.6587 65.87%
PPAR gamma + 0.6971 69.71%
Honey bee toxicity - 0.9170 91.70%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9950 99.50%

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 95.62% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.56% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.04% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.74% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.70% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.60% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.36% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.90% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.81% 99.15%
CHEMBL4208 P20618 Proteasome component C5 83.05% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.30% 86.33%

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.
Melampodium divaricatum

Cross-Links

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PubChem 86254474
LOTUS LTS0027766
wikiData Q27258042