Carasinaurone

Details

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Internal ID be82b13b-da6d-4d00-b9bb-d5e3736b3c7d
Taxonomy Phenylpropanoids and polyketides > Aurone flavonoids > Auronols
IUPAC Name (2S)-2,6-dihydroxy-2-[(4-hydroxyphenyl)methyl]-4-methoxy-1-benzofuran-3-one
SMILES (Canonical) COC1=CC(=CC2=C1C(=O)C(O2)(CC3=CC=C(C=C3)O)O)O
SMILES (Isomeric) COC1=CC(=CC2=C1C(=O)[C@@](O2)(CC3=CC=C(C=C3)O)O)O
InChI InChI=1S/C16H14O6/c1-21-12-6-11(18)7-13-14(12)15(19)16(20,22-13)8-9-2-4-10(17)5-3-9/h2-7,17-18,20H,8H2,1H3/t16-/m0/s1
InChI Key IQTGAKWQIFFPQX-INIZCTEOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O6
Molecular Weight 302.28 g/mol
Exact Mass 302.07903816 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.61
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Carasinaurone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9753 97.53%
Caco-2 + 0.4887 48.87%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior + 0.5586 55.86%
OATP1B1 inhibitior + 0.8787 87.87%
OATP1B3 inhibitior + 0.8896 88.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5559 55.59%
P-glycoprotein inhibitior - 0.8486 84.86%
P-glycoprotein substrate - 0.8285 82.85%
CYP3A4 substrate + 0.5493 54.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6961 69.61%
CYP3A4 inhibition - 0.7080 70.80%
CYP2C9 inhibition - 0.6558 65.58%
CYP2C19 inhibition - 0.5687 56.87%
CYP2D6 inhibition - 0.8621 86.21%
CYP1A2 inhibition - 0.6811 68.11%
CYP2C8 inhibition + 0.7506 75.06%
CYP inhibitory promiscuity - 0.5537 55.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.3762 37.62%
Eye corrosion - 0.9843 98.43%
Eye irritation + 0.7259 72.59%
Skin irritation - 0.7033 70.33%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis - 0.6254 62.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8625 86.25%
Micronuclear + 0.8077 80.77%
Hepatotoxicity - 0.6540 65.40%
skin sensitisation - 0.8530 85.30%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.7244 72.44%
Acute Oral Toxicity (c) III 0.5419 54.19%
Estrogen receptor binding + 0.7707 77.07%
Androgen receptor binding + 0.7584 75.84%
Thyroid receptor binding + 0.6438 64.38%
Glucocorticoid receptor binding + 0.7265 72.65%
Aromatase binding + 0.6800 68.00%
PPAR gamma + 0.6882 68.82%
Honey bee toxicity - 0.8486 84.86%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.8985 89.85%

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 97.24% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.41% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.78% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.62% 96.09%
CHEMBL4208 P20618 Proteasome component C5 92.72% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.48% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.23% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.64% 95.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.08% 95.17%
CHEMBL1255126 O15151 Protein Mdm4 87.53% 90.20%
CHEMBL2535 P11166 Glucose transporter 86.89% 98.75%
CHEMBL4040 P28482 MAP kinase ERK2 86.52% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.97% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.07% 96.95%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.37% 82.38%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.26% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.81% 95.89%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.51% 97.28%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.24% 85.14%

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.
Caragana sinica
Glycyrrhiza uralensis
Mitracarpus hirtus
Pterocarpus marsupium
Rheum australe
Xanthocercis zambesiaca

Cross-Links

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PubChem 101767761
NPASS NPC26774
LOTUS LTS0090434
wikiData Q105118561