Leptodactylone

Details

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Internal ID a113b6c7-89fa-49cd-806d-ae4b90961f6e
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 8-hydroxy-5,7-dimethoxychromen-2-one
SMILES (Canonical) COC1=CC(=C(C2=C1C=CC(=O)O2)O)OC
SMILES (Isomeric) COC1=CC(=C(C2=C1C=CC(=O)O2)O)OC
InChI InChI=1S/C11H10O5/c1-14-7-5-8(15-2)10(13)11-6(7)3-4-9(12)16-11/h3-5,13H,1-2H3
InChI Key TUFLVKBJDSZLAW-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEBI:6411
CHEMBL595334
61899-44-3
C09271
AC1L9CAZ
8-hydroxy-5,7-dimethoxychromen-2-one
5,7-dimethoxy-8-hydroxycoumarin
DTXSID80331748
8-hydroxy-5,7-dimethoxy-chromen-2-one
Q27107198

2D Structure

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2D Structure of Leptodactylone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9643 96.43%
Caco-2 + 0.5814 58.14%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6686 66.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8993 89.93%
OATP1B3 inhibitior + 0.9746 97.46%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8296 82.96%
P-glycoprotein inhibitior - 0.8425 84.25%
P-glycoprotein substrate - 0.8521 85.21%
CYP3A4 substrate - 0.6157 61.57%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.7395 73.95%
CYP2C9 inhibition - 0.9291 92.91%
CYP2C19 inhibition - 0.7830 78.30%
CYP2D6 inhibition - 0.8714 87.14%
CYP1A2 inhibition + 0.8253 82.53%
CYP2C8 inhibition - 0.6694 66.94%
CYP inhibitory promiscuity - 0.6635 66.35%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6010 60.10%
Eye corrosion - 0.9585 95.85%
Eye irritation + 0.8836 88.36%
Skin irritation - 0.6008 60.08%
Skin corrosion - 0.9837 98.37%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8150 81.50%
Micronuclear + 0.9059 90.59%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7907 79.07%
Acute Oral Toxicity (c) II 0.6201 62.01%
Estrogen receptor binding + 0.7035 70.35%
Androgen receptor binding + 0.6781 67.81%
Thyroid receptor binding - 0.6768 67.68%
Glucocorticoid receptor binding + 0.6693 66.93%
Aromatase binding + 0.7789 77.89%
PPAR gamma + 0.6638 66.38%
Honey bee toxicity - 0.9130 91.30%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5849 58.49%
Fish aquatic toxicity + 0.9128 91.28%

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 98.27% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.42% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.84% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.45% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.81% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.49% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.32% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.00% 98.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.31% 89.62%
CHEMBL2535 P11166 Glucose transporter 81.22% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.10% 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.
Artemisia capillaris
Citrus medica
Lobelia chinensis

Cross-Links

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PubChem 442134
NPASS NPC82271
LOTUS LTS0222392
wikiData Q27107198