4-Allyloxycoumarin

Details

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Internal ID f55bffa5-682d-4072-a1ca-a473124e527f
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 4-prop-2-enoxychromen-2-one
SMILES (Canonical) C=CCOC1=CC(=O)OC2=CC=CC=C21
SMILES (Isomeric) C=CCOC1=CC(=O)OC2=CC=CC=C21
InChI InChI=1S/C12H10O3/c1-2-7-14-11-8-12(13)15-10-6-4-3-5-9(10)11/h2-6,8H,1,7H2
InChI Key LWRKLYVFSHDLMU-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10O3
Molecular Weight 202.21 g/mol
Exact Mass 202.062994177 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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31005-07-9
4-prop-2-enoxychromen-2-one
2H-1-Benzopyran-2-one, 4-(2-propen-1-yloxy)-
ST060206
CHEMBL1957180
4-Allyloxy-cumarin
4-(Allyloxy)coumarin
4-Allyloxycoumarin, AldrichCPR
SCHEMBL8515316
DTXSID10408639
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Allyloxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.6963 69.63%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5936 59.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8972 89.72%
OATP1B3 inhibitior + 0.9639 96.39%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7750 77.50%
P-glycoprotein inhibitior - 0.8680 86.80%
P-glycoprotein substrate - 0.9610 96.10%
CYP3A4 substrate - 0.5470 54.70%
CYP2C9 substrate - 0.8346 83.46%
CYP2D6 substrate - 0.8341 83.41%
CYP3A4 inhibition - 0.5401 54.01%
CYP2C9 inhibition + 0.5178 51.78%
CYP2C19 inhibition + 0.9197 91.97%
CYP2D6 inhibition - 0.7894 78.94%
CYP1A2 inhibition + 0.8693 86.93%
CYP2C8 inhibition - 0.6262 62.62%
CYP inhibitory promiscuity + 0.8206 82.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5113 51.13%
Eye corrosion - 0.7840 78.40%
Eye irritation + 0.9536 95.36%
Skin irritation - 0.5738 57.38%
Skin corrosion - 0.9743 97.43%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5866 58.66%
Micronuclear + 0.6374 63.74%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.5986 59.86%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.4589 45.89%
Acute Oral Toxicity (c) III 0.5077 50.77%
Estrogen receptor binding + 0.6089 60.89%
Androgen receptor binding + 0.8255 82.55%
Thyroid receptor binding - 0.5597 55.97%
Glucocorticoid receptor binding - 0.6563 65.63%
Aromatase binding + 0.7773 77.73%
PPAR gamma + 0.7028 70.28%
Honey bee toxicity - 0.8106 81.06%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9833 98.33%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL261 P00915 Carbonic anhydrase I 43200 nM
43200 nM
Ki
Ki
PMID: 26688270
PMID: 22377674
CHEMBL3594 Q16790 Carbonic anhydrase IX 210 nM
210 nM
210 nM
Ki
Ki
Ki
PMID: 22377674
PMID: 26688270
via Super-PRED
CHEMBL3242 O43570 Carbonic anhydrase XII 880 nM
880 nM
880 nM
Ki
Ki
Ki
PMID: 22377674
PMID: 26688270
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.82% 91.11%
CHEMBL240 Q12809 HERG 97.80% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.30% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.08% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.21% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.47% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.70% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.76% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.15% 99.17%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.85% 94.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.60% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.01% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.09% 99.23%

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.
Derris reticulata
Eucalyptus ovata
Gentiana arisanensis
Panzerina lanata
Setaria italica
Solanum dulcamara

Cross-Links

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PubChem 5133468
NPASS NPC149545
ChEMBL CHEMBL1957180
LOTUS LTS0143292
wikiData Q82214177