Detetrahydroconidendrin

Details

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Internal ID b8c1f3ed-76d0-4ef1-9cd4-953f045af29c
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 7-hydroxy-9-(4-hydroxy-3-methoxyphenyl)-6-methoxy-1H-benzo[f][2]benzofuran-3-one
SMILES (Canonical) COC1=CC2=CC3=C(COC3=O)C(=C2C=C1O)C4=CC(=C(C=C4)O)OC
SMILES (Isomeric) COC1=CC2=CC3=C(COC3=O)C(=C2C=C1O)C4=CC(=C(C=C4)O)OC
InChI InChI=1S/C20H16O6/c1-24-17-6-10(3-4-15(17)21)19-12-8-16(22)18(25-2)7-11(12)5-13-14(19)9-26-20(13)23/h3-8,21-22H,9H2,1-2H3
InChI Key JJVJBPKUTANWEW-UHFFFAOYSA-N
Popularity 6 references 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) 3.61
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL486411

2D Structure

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2D Structure of Detetrahydroconidendrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.7841 78.41%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8573 85.73%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9460 94.60%
OATP1B3 inhibitior - 0.2243 22.43%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6280 62.80%
P-glycoprotein inhibitior - 0.6709 67.09%
P-glycoprotein substrate - 0.8431 84.31%
CYP3A4 substrate + 0.5637 56.37%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8050 80.50%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition + 0.9714 97.14%
CYP2C19 inhibition + 0.8161 81.61%
CYP2D6 inhibition - 0.7173 71.73%
CYP1A2 inhibition + 0.6651 66.51%
CYP2C8 inhibition + 0.6470 64.70%
CYP inhibitory promiscuity + 0.8517 85.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9310 93.10%
Carcinogenicity (trinary) Non-required 0.4764 47.64%
Eye corrosion - 0.9867 98.67%
Eye irritation + 0.7217 72.17%
Skin irritation - 0.7801 78.01%
Skin corrosion - 0.9730 97.30%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7501 75.01%
Micronuclear + 0.8474 84.74%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8902 89.02%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.5656 56.56%
Acute Oral Toxicity (c) III 0.6459 64.59%
Estrogen receptor binding + 0.9104 91.04%
Androgen receptor binding + 0.7388 73.88%
Thyroid receptor binding + 0.7134 71.34%
Glucocorticoid receptor binding + 0.9260 92.60%
Aromatase binding - 0.5359 53.59%
PPAR gamma + 0.7015 70.15%
Honey bee toxicity - 0.8859 88.59%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.9758 97.58%

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 96.78% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.80% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 95.77% 91.49%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 95.42% 98.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.36% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.24% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.16% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.64% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 90.43% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.53% 85.14%
CHEMBL3438 Q05513 Protein kinase C zeta 88.54% 88.48%
CHEMBL2535 P11166 Glucose transporter 88.31% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.10% 92.62%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 88.00% 95.53%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.16% 99.23%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.95% 80.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.41% 96.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.89% 96.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.86% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.52% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.77% 92.94%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.45% 92.38%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.30% 96.00%

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.
Juniperus formosana
Vitex negundo
Vitex trifolia subsp. litoralis

Cross-Links

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PubChem 10617963
NPASS NPC261322
LOTUS LTS0057908
wikiData Q105129970