CID 139590326

Details

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Internal ID f680809a-6296-4ffc-8b19-a1a2b5261450
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name [5-(4-acetyloxy-10-hydroxy-7-methoxy-3-methyl-6,9-dioxo-3,4-dihydro-1H-benzo[g]isochromen-5-yl)-7,9-dimethoxy-3-methyl-3,4-dihydro-1H-benzo[g]isochromen-4-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H34O12/c1-14-34(46-16(3)36)26-18(12-44-14)8-20-21(9-19(41-5)10-24(20)42-6)27(26)30-28-22(13-45-15(2)35(28)47-17(4)37)32(39)29-23(38)11-25(43-7)33(40)31(29)30/h8-11,14-15,34-35,39H,12-13H2,1-7H3
InChI Key MREYDAJIOFIMTM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C35H34O12
Molecular Weight 646.60 g/mol
Exact Mass 646.20502652 g/mol
Topological Polar Surface Area (TPSA) 153.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 12
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 139590326

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9800 98.00%
Caco-2 - 0.7056 70.56%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8725 87.25%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9848 98.48%
P-glycoprotein inhibitior + 0.8767 87.67%
P-glycoprotein substrate + 0.5721 57.21%
CYP3A4 substrate + 0.6696 66.96%
CYP2C9 substrate - 0.6005 60.05%
CYP2D6 substrate - 0.8709 87.09%
CYP3A4 inhibition - 0.8289 82.89%
CYP2C9 inhibition - 0.7111 71.11%
CYP2C19 inhibition - 0.5933 59.33%
CYP2D6 inhibition - 0.9578 95.78%
CYP1A2 inhibition - 0.8293 82.93%
CYP2C8 inhibition + 0.6207 62.07%
CYP inhibitory promiscuity - 0.6806 68.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6316 63.16%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8997 89.97%
Skin irritation - 0.7916 79.16%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5807 58.07%
Micronuclear + 0.6274 62.74%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation - 0.8274 82.74%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6801 68.01%
Acute Oral Toxicity (c) III 0.4337 43.37%
Estrogen receptor binding + 0.7727 77.27%
Androgen receptor binding + 0.7282 72.82%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7856 78.56%
Aromatase binding + 0.5530 55.30%
PPAR gamma + 0.6977 69.77%
Honey bee toxicity - 0.7110 71.10%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.9873 98.73%

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 99.53% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.50% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.60% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.78% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.56% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.37% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.27% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.89% 93.99%
CHEMBL2535 P11166 Glucose transporter 89.84% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.20% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 88.69% 91.49%
CHEMBL2581 P07339 Cathepsin D 88.31% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.49% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.95% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.16% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.72% 99.23%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.13% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 84.00% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.29% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.90% 95.89%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.28% 92.68%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.97% 97.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139590326
LOTUS LTS0172056
wikiData Q104171998