Ncgc00386103-01_C19H20O3_

Details

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Internal ID 9fb36ff7-61cc-4383-baa0-6c77b51a140c
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 5-hydroxy-6-(3-methylbut-2-enyl)-2-[(1E,3E)-penta-1,3-dienyl]-1-benzofuran-4-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20O3/c1-4-5-6-7-15-11-16-17(12-20)19(21)14(9-8-13(2)3)10-18(16)22-15/h4-8,10-12,21H,9H2,1-3H3/b5-4+,7-6+
InChI Key SEKUOZUOBHHCMJ-YTXTXJHMSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O3
Molecular Weight 296.40 g/mol
Exact Mass 296.14124450 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.05
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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NCGC00386103-01_C19H20O3_

2D Structure

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2D Structure of Ncgc00386103-01_C19H20O3_

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8614 86.14%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7867 78.67%
OATP2B1 inhibitior + 0.5539 55.39%
OATP1B1 inhibitior + 0.7287 72.87%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8792 87.92%
P-glycoprotein inhibitior + 0.6698 66.98%
P-glycoprotein substrate - 0.6388 63.88%
CYP3A4 substrate + 0.5369 53.69%
CYP2C9 substrate - 0.5971 59.71%
CYP2D6 substrate - 0.8242 82.42%
CYP3A4 inhibition - 0.7972 79.72%
CYP2C9 inhibition + 0.6623 66.23%
CYP2C19 inhibition + 0.7570 75.70%
CYP2D6 inhibition - 0.8905 89.05%
CYP1A2 inhibition + 0.9452 94.52%
CYP2C8 inhibition - 0.5899 58.99%
CYP inhibitory promiscuity + 0.8727 87.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5845 58.45%
Eye corrosion - 0.9784 97.84%
Eye irritation - 0.5831 58.31%
Skin irritation - 0.6293 62.93%
Skin corrosion - 0.9272 92.72%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6685 66.85%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.5071 50.71%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7673 76.73%
Acute Oral Toxicity (c) III 0.6057 60.57%
Estrogen receptor binding + 0.9607 96.07%
Androgen receptor binding + 0.7456 74.56%
Thyroid receptor binding + 0.6152 61.52%
Glucocorticoid receptor binding + 0.8554 85.54%
Aromatase binding + 0.8707 87.07%
PPAR gamma + 0.8599 85.99%
Honey bee toxicity - 0.8997 89.97%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9947 99.47%

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 98.63% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 96.22% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.59% 98.11%
CHEMBL2581 P07339 Cathepsin D 92.80% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.74% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.64% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.61% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.79% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.41% 85.14%

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 100625246
LOTUS LTS0058360
wikiData Q105251250