Homo egonol beta-D-glucoside

Details

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Internal ID 99b6fa5e-1756-404d-9f0c-a6ab61afcea9
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-[3-[2-(3,4-dimethoxyphenyl)-7-methoxy-1-benzofuran-5-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H32O10/c1-31-17-7-6-15(11-19(17)32-2)18-12-16-9-14(10-20(33-3)25(16)35-18)5-4-8-34-26-24(30)23(29)22(28)21(13-27)36-26/h6-7,9-12,21-24,26-30H,4-5,8,13H2,1-3H3
InChI Key NDBXVWJEZUKCIS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H32O10
Molecular Weight 504.50 g/mol
Exact Mass 504.19954721 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 10
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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FT-0669224

2D Structure

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2D Structure of Homo egonol beta-D-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5319 53.19%
Caco-2 - 0.7868 78.68%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7187 71.87%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.8481 84.81%
OATP1B3 inhibitior + 0.9595 95.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6931 69.31%
P-glycoprotein inhibitior + 0.6281 62.81%
P-glycoprotein substrate - 0.5088 50.88%
CYP3A4 substrate + 0.6471 64.71%
CYP2C9 substrate - 0.6126 61.26%
CYP2D6 substrate - 0.7590 75.90%
CYP3A4 inhibition - 0.9402 94.02%
CYP2C9 inhibition - 0.7559 75.59%
CYP2C19 inhibition - 0.7994 79.94%
CYP2D6 inhibition - 0.9105 91.05%
CYP1A2 inhibition - 0.8264 82.64%
CYP2C8 inhibition + 0.8907 89.07%
CYP inhibitory promiscuity - 0.5221 52.21%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5700 57.00%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9507 95.07%
Skin irritation - 0.8357 83.57%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8491 84.91%
Micronuclear - 0.5341 53.41%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.9030 90.30%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.9022 90.22%
Acute Oral Toxicity (c) III 0.7055 70.55%
Estrogen receptor binding + 0.8701 87.01%
Androgen receptor binding + 0.6271 62.71%
Thyroid receptor binding + 0.6864 68.64%
Glucocorticoid receptor binding + 0.7057 70.57%
Aromatase binding + 0.6671 66.71%
PPAR gamma + 0.6959 69.59%
Honey bee toxicity - 0.7755 77.55%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.3949 39.49%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.17% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.99% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 95.05% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.47% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.26% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.22% 86.33%
CHEMBL5747 Q92793 CREB-binding protein 92.81% 95.12%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.75% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.42% 92.94%
CHEMBL4302 P08183 P-glycoprotein 1 88.84% 92.98%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.49% 85.14%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 86.37% 95.78%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.17% 96.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.29% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 83.90% 94.73%
CHEMBL2243 O00519 Anandamide amidohydrolase 83.41% 97.53%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.28% 96.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.59% 96.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.08% 95.89%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.71% 94.03%
CHEMBL5555 O00767 Acyl-CoA desaturase 80.50% 97.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.03% 90.71%

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.
Styrax ferrugineus

Cross-Links

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PubChem 78191973
LOTUS LTS0145082
wikiData Q104172331