Negundin A

Details

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Internal ID 3b726cdc-fd34-4d79-8e62-8890e0d03d3c
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name 6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3H-benzo[f][1]benzofuran-2-one
SMILES (Canonical) COC1=CC2=CC3=C(CC(=O)O3)C(=C2C=C1O)C4=CC(=C(C=C4)O)OC
SMILES (Isomeric) COC1=CC2=CC3=C(CC(=O)O3)C(=C2C=C1O)C4=CC(=C(C=C4)O)OC
InChI InChI=1S/C20H16O6/c1-24-17-5-10(3-4-14(17)21)20-12-8-15(22)18(25-2)7-11(12)6-16-13(20)9-19(23)26-16/h3-8,21-22H,9H2,1-2H3
InChI Key SJEMORVRSMFGIP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H16O6
Molecular Weight 352.30 g/mol
Exact Mass 352.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Negundin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.7831 78.31%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8166 81.66%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior - 0.2565 25.65%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6822 68.22%
P-glycoprotein inhibitior - 0.6404 64.04%
P-glycoprotein substrate - 0.8555 85.55%
CYP3A4 substrate + 0.5294 52.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6710 67.10%
CYP3A4 inhibition - 0.5311 53.11%
CYP2C9 inhibition + 0.8905 89.05%
CYP2C19 inhibition + 0.7506 75.06%
CYP2D6 inhibition - 0.7237 72.37%
CYP1A2 inhibition + 0.6120 61.20%
CYP2C8 inhibition + 0.7697 76.97%
CYP inhibitory promiscuity + 0.7356 73.56%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Warning 0.3566 35.66%
Eye corrosion - 0.9888 98.88%
Eye irritation + 0.7345 73.45%
Skin irritation - 0.7606 76.06%
Skin corrosion - 0.9719 97.19%
Ames mutagenesis + 0.5446 54.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6620 66.20%
Micronuclear + 0.8759 87.59%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9057 90.57%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6638 66.38%
Acute Oral Toxicity (c) III 0.5349 53.49%
Estrogen receptor binding + 0.8786 87.86%
Androgen receptor binding + 0.6280 62.80%
Thyroid receptor binding + 0.6841 68.41%
Glucocorticoid receptor binding + 0.9410 94.10%
Aromatase binding - 0.5344 53.44%
PPAR gamma + 0.7929 79.29%
Honey bee toxicity - 0.8725 87.25%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.9591 95.91%

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 98.86% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.93% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.76% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.96% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.34% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.53% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 89.76% 93.31%
CHEMBL2581 P07339 Cathepsin D 89.36% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.81% 96.09%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 87.48% 95.53%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.33% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.03% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.98% 85.14%
CHEMBL2535 P11166 Glucose transporter 85.36% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.81% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.11% 92.94%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.42% 92.38%
CHEMBL4208 P20618 Proteasome component C5 81.27% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.88% 90.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.29% 98.11%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 80.24% 85.00%

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.
Vitex negundo

Cross-Links

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PubChem 10043572
NPASS NPC28248
LOTUS LTS0071047
wikiData Q104399076