2-(3,4-Dihydroxy-5-methoxyphenyl)-6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one

Details

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Internal ID 688960b5-95fd-43c9-8bbf-eda0cc3e0562
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 6-prenylated flavans > 6-prenylated flavanones
IUPAC Name 2-(3,4-dihydroxy-5-methoxyphenyl)-6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H30O7/c1-14(2)6-5-7-15(3)8-9-17-18(27)12-22-24(25(17)30)19(28)13-21(33-22)16-10-20(29)26(31)23(11-16)32-4/h6,8,10-12,21,27,29-31H,5,7,9,13H2,1-4H3
InChI Key UKCODVXNYJFPIN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H30O7
Molecular Weight 454.50 g/mol
Exact Mass 454.19915329 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.46
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,4-Dihydroxy-5-methoxyphenyl)-6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9439 94.39%
Caco-2 - 0.7479 74.79%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7357 73.57%
OATP2B1 inhibitior - 0.7168 71.68%
OATP1B1 inhibitior + 0.8796 87.96%
OATP1B3 inhibitior + 0.9065 90.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9012 90.12%
P-glycoprotein inhibitior + 0.7017 70.17%
P-glycoprotein substrate - 0.7176 71.76%
CYP3A4 substrate + 0.6123 61.23%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.8017 80.17%
CYP3A4 inhibition - 0.6733 67.33%
CYP2C9 inhibition - 0.5900 59.00%
CYP2C19 inhibition + 0.5784 57.84%
CYP2D6 inhibition - 0.7429 74.29%
CYP1A2 inhibition + 0.7119 71.19%
CYP2C8 inhibition + 0.5210 52.10%
CYP inhibitory promiscuity - 0.5111 51.11%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7639 76.39%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.7868 78.68%
Skin irritation - 0.7718 77.18%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3756 37.56%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5448 54.48%
skin sensitisation - 0.8333 83.33%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7940 79.40%
Acute Oral Toxicity (c) III 0.3659 36.59%
Estrogen receptor binding + 0.8928 89.28%
Androgen receptor binding + 0.6317 63.17%
Thyroid receptor binding + 0.6058 60.58%
Glucocorticoid receptor binding + 0.7681 76.81%
Aromatase binding + 0.5607 56.07%
PPAR gamma + 0.7784 77.84%
Honey bee toxicity - 0.7460 74.60%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9960 99.60%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 60 nM
IC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.73% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.41% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.21% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.53% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.12% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.93% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.59% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.25% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.19% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.16% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.79% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.33% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.16% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.56% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.33% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.90% 92.62%
CHEMBL4208 P20618 Proteasome component C5 83.08% 90.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.74% 89.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.69% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.78% 100.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.61% 86.92%

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.
Paulownia tomentosa

Cross-Links

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PubChem 74326239
LOTUS LTS0102322
wikiData Q105274455