(E)-8-hydroxy-5-methoxy-3-(1-pentenyl)isocoumarin

Details

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Internal ID 8a16137f-a71e-4c16-9a47-06dff4b5f850
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 8-hydroxy-5-methoxy-3-[(E)-pent-1-enyl]isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O4/c1-3-4-5-6-10-9-11-13(18-2)8-7-12(16)14(11)15(17)19-10/h5-9,16H,3-4H2,1-2H3/b6-5+
InChI Key ZFVPNRFMCMVXRX-AATRIKPKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.32
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 (E)-8-hydroxy-5-methoxy-3-(1-pentenyl)isocoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9789 97.89%
Caco-2 + 0.7216 72.16%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Plasma membrane 0.5603 56.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8922 89.22%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6431 64.31%
P-glycoprotein inhibitior - 0.5717 57.17%
P-glycoprotein substrate - 0.7431 74.31%
CYP3A4 substrate + 0.5113 51.13%
CYP2C9 substrate + 0.6518 65.18%
CYP2D6 substrate - 0.8500 85.00%
CYP3A4 inhibition - 0.5549 55.49%
CYP2C9 inhibition - 0.6770 67.70%
CYP2C19 inhibition - 0.5547 55.47%
CYP2D6 inhibition - 0.8493 84.93%
CYP1A2 inhibition + 0.5509 55.09%
CYP2C8 inhibition + 0.5471 54.71%
CYP inhibitory promiscuity + 0.5845 58.45%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5626 56.26%
Eye corrosion - 0.9660 96.60%
Eye irritation + 0.5266 52.66%
Skin irritation - 0.7855 78.55%
Skin corrosion - 0.9629 96.29%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4789 47.89%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8323 83.23%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6887 68.87%
Acute Oral Toxicity (c) III 0.5390 53.90%
Estrogen receptor binding + 0.9270 92.70%
Androgen receptor binding + 0.8532 85.32%
Thyroid receptor binding - 0.5106 51.06%
Glucocorticoid receptor binding + 0.8473 84.73%
Aromatase binding + 0.8601 86.01%
PPAR gamma + 0.8183 81.83%
Honey bee toxicity - 0.9116 91.16%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9650 96.50%

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 97.86% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.77% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.71% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.36% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.62% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.11% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.67% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.56% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.32% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.86% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.38% 94.45%
CHEMBL2535 P11166 Glucose transporter 83.28% 98.75%
CHEMBL3194 P02766 Transthyretin 82.48% 90.71%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.36% 80.78%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.09% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.51% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139583882
LOTUS LTS0046362
wikiData Q75068791