Buntansin A

Details

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Internal ID 483b06e1-9a61-453d-b956-c2705dc7428e
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-methoxy-2-oxochromene-6-carboxylic acid
SMILES (Canonical) COC1=C(C=C2C=CC(=O)OC2=C1)C(=O)O
SMILES (Isomeric) COC1=C(C=C2C=CC(=O)OC2=C1)C(=O)O
InChI InChI=1S/C11H8O5/c1-15-9-5-8-6(2-3-10(12)16-8)4-7(9)11(13)14/h2-5H,1H3,(H,13,14)
InChI Key GQYZDAIERJIQDI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H8O5
Molecular Weight 220.18 g/mol
Exact Mass 220.03717335 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.50
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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7-methoxycoumarin-6-carboxylic acid
Buntansin
7-Methoxy-2-oxo-2H-1-benzopyran-6-carboxylic acid
CHEBI:178384
DTXSID001235208
52525-63-0
7-methoxy-2-oxochromene-6-carboxylic acid

2D Structure

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2D Structure of Buntansin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9729 97.29%
Caco-2 + 0.6249 62.49%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7213 72.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9343 93.43%
OATP1B3 inhibitior + 0.9943 99.43%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8305 83.05%
P-glycoprotein inhibitior - 0.9133 91.33%
P-glycoprotein substrate - 0.9369 93.69%
CYP3A4 substrate - 0.7247 72.47%
CYP2C9 substrate - 0.8303 83.03%
CYP2D6 substrate - 0.8801 88.01%
CYP3A4 inhibition - 0.8733 87.33%
CYP2C9 inhibition - 0.6892 68.92%
CYP2C19 inhibition - 0.9294 92.94%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition + 0.8604 86.04%
CYP2C8 inhibition - 0.8202 82.02%
CYP inhibitory promiscuity - 0.8223 82.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.5556 55.56%
Eye corrosion - 0.9670 96.70%
Eye irritation + 0.9030 90.30%
Skin irritation - 0.6138 61.38%
Skin corrosion - 0.9754 97.54%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9057 90.57%
Micronuclear + 0.8859 88.59%
Hepatotoxicity - 0.5716 57.16%
skin sensitisation - 0.9692 96.92%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5253 52.53%
Acute Oral Toxicity (c) III 0.5554 55.54%
Estrogen receptor binding + 0.6223 62.23%
Androgen receptor binding - 0.4903 49.03%
Thyroid receptor binding - 0.7908 79.08%
Glucocorticoid receptor binding - 0.6052 60.52%
Aromatase binding + 0.6036 60.36%
PPAR gamma + 0.7217 72.17%
Honey bee toxicity - 0.9629 96.29%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9426 94.26%

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
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.90% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 91.64% 87.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.87% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.13% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.37% 94.42%
CHEMBL2581 P07339 Cathepsin D 88.27% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.26% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.04% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.84% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.53% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.97% 96.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.62% 93.00%
CHEMBL2535 P11166 Glucose transporter 82.47% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 82.16% 90.20%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.66% 95.71%
CHEMBL4208 P20618 Proteasome component C5 80.08% 90.00%

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
Citrus maxima
Peperomia trineura

Cross-Links

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PubChem 15627934
LOTUS LTS0023831
wikiData Q105240191