2-(7-Methoxy-2-oxochromen-8-yl)acetaldehyde

Details

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Internal ID 5ceee470-33c6-43f2-b242-bde7cdac9548
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 2-(7-methoxy-2-oxochromen-8-yl)acetaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H10O4/c1-15-10-4-2-8-3-5-11(14)16-12(8)9(10)6-7-13/h2-5,7H,6H2,1H3
InChI Key UIIMGHCYYQVNIS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10O4
Molecular Weight 218.20 g/mol
Exact Mass 218.05790880 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(7-Methoxy-2-oxochromen-8-yl)acetaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9770 97.70%
Caco-2 + 0.6244 62.44%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6704 67.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9906 99.06%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6912 69.12%
P-glycoprotein inhibitior - 0.9293 92.93%
P-glycoprotein substrate - 0.8168 81.68%
CYP3A4 substrate - 0.6355 63.55%
CYP2C9 substrate - 0.8186 81.86%
CYP2D6 substrate - 0.8040 80.40%
CYP3A4 inhibition - 0.7774 77.74%
CYP2C9 inhibition + 0.6847 68.47%
CYP2C19 inhibition - 0.5349 53.49%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition + 0.8396 83.96%
CYP2C8 inhibition - 0.7856 78.56%
CYP inhibitory promiscuity + 0.5877 58.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.5796 57.96%
Eye corrosion - 0.9462 94.62%
Eye irritation + 0.7698 76.98%
Skin irritation - 0.7996 79.96%
Skin corrosion - 0.9706 97.06%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5101 51.01%
Micronuclear + 0.6959 69.59%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.9265 92.65%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6615 66.15%
Acute Oral Toxicity (c) III 0.5878 58.78%
Estrogen receptor binding + 0.6194 61.94%
Androgen receptor binding + 0.6719 67.19%
Thyroid receptor binding - 0.7157 71.57%
Glucocorticoid receptor binding + 0.5647 56.47%
Aromatase binding + 0.6715 67.15%
PPAR gamma - 0.5356 53.56%
Honey bee toxicity - 0.8791 87.91%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9289 92.89%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.60% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.46% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.77% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.23% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 87.87% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.56% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.34% 94.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.10% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.05% 99.23%

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 14184382
LOTUS LTS0082344
wikiData Q104398718