7-methoxy-2-oxo-2H-chromene-8-carbaldehyde

Details

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Internal ID ce01f77a-f170-4202-96e3-4015fbf91839
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-methoxy-2-oxochromene-8-carbaldehyde
SMILES (Canonical) COC1=C(C2=C(C=C1)C=CC(=O)O2)C=O
SMILES (Isomeric) COC1=C(C2=C(C=C1)C=CC(=O)O2)C=O
InChI InChI=1S/C11H8O4/c1-14-9-4-2-7-3-5-10(13)15-11(7)8(9)6-12/h2-6H,1H3
InChI Key AOXODSXRUFTUGB-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H8O4
Molecular Weight 204.18 g/mol
Exact Mass 204.04225873 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.61
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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7-methoxy-2-oxochromene-8-carbaldehyde
Paniculal
6724-42-1
8-formyl-7-methoxycoumarin

2D Structure

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2D Structure of 7-methoxy-2-oxo-2H-chromene-8-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.7935 79.35%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6090 60.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8789 87.89%
OATP1B3 inhibitior + 1.0000 100.00%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7654 76.54%
P-glycoprotein inhibitior - 0.8979 89.79%
P-glycoprotein substrate - 0.9308 93.08%
CYP3A4 substrate - 0.6439 64.39%
CYP2C9 substrate - 0.8346 83.46%
CYP2D6 substrate - 0.8339 83.39%
CYP3A4 inhibition - 0.7865 78.65%
CYP2C9 inhibition + 0.5414 54.14%
CYP2C19 inhibition - 0.7386 73.86%
CYP2D6 inhibition - 0.9554 95.54%
CYP1A2 inhibition + 0.9785 97.85%
CYP2C8 inhibition - 0.8006 80.06%
CYP inhibitory promiscuity - 0.5527 55.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.5625 56.25%
Eye corrosion - 0.9286 92.86%
Eye irritation + 0.9514 95.14%
Skin irritation - 0.6612 66.12%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6707 67.07%
Micronuclear + 0.8159 81.59%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.9569 95.69%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6915 69.15%
Acute Oral Toxicity (c) III 0.6141 61.41%
Estrogen receptor binding - 0.4943 49.43%
Androgen receptor binding + 0.7399 73.99%
Thyroid receptor binding - 0.7367 73.67%
Glucocorticoid receptor binding - 0.5232 52.32%
Aromatase binding + 0.7705 77.05%
PPAR gamma - 0.5872 58.72%
Honey bee toxicity - 0.8898 88.98%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9596 95.96%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.52% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.92% 98.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.68% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.56% 96.00%
CHEMBL2581 P07339 Cathepsin D 84.15% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.13% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.99% 99.23%
CHEMBL1255126 O15151 Protein Mdm4 83.75% 90.20%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.59% 94.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.94% 86.33%

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.
Citrus × aurantium
Cnidium monnieri
Murraya paniculata
Prangos pabularia

Cross-Links

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PubChem 11275724
LOTUS LTS0066932
wikiData Q104394145