2-(3,4-dihydroxyphenyl)-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene-3,5,7-triol

Details

Top
Internal ID 0ecbf6a7-6205-4b34-a941-f90823e26724
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Catechins
IUPAC Name 2-(3,4-dihydroxyphenyl)-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene-3,5,7-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22O6/c1-10(2)3-5-12-15(22)9-18-13(19(12)25)8-17(24)20(26-18)11-4-6-14(21)16(23)7-11/h3-4,6-7,9,17,20-25H,5,8H2,1-2H3
InChI Key IQDFKWMQHFUYNY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H22O6
Molecular Weight 358.40 g/mol
Exact Mass 358.14163842 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(3,4-dihydroxyphenyl)-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene-3,5,7-triol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9747 97.47%
Caco-2 - 0.8120 81.20%
Blood Brain Barrier - 0.5379 53.79%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.5935 59.35%
OATP2B1 inhibitior - 0.5694 56.94%
OATP1B1 inhibitior + 0.8920 89.20%
OATP1B3 inhibitior + 0.9740 97.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4608 46.08%
P-glycoprotein inhibitior - 0.6426 64.26%
P-glycoprotein substrate - 0.8295 82.95%
CYP3A4 substrate + 0.5139 51.39%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate + 0.4552 45.52%
CYP3A4 inhibition - 0.7813 78.13%
CYP2C9 inhibition - 0.5250 52.50%
CYP2C19 inhibition + 0.5319 53.19%
CYP2D6 inhibition - 0.7636 76.36%
CYP1A2 inhibition - 0.6097 60.97%
CYP2C8 inhibition - 0.6076 60.76%
CYP inhibitory promiscuity + 0.5675 56.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6968 69.68%
Eye corrosion - 0.9897 98.97%
Eye irritation + 0.5664 56.64%
Skin irritation - 0.7569 75.69%
Skin corrosion - 0.9076 90.76%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6762 67.62%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.7249 72.49%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8873 88.73%
Acute Oral Toxicity (c) III 0.4815 48.15%
Estrogen receptor binding + 0.8064 80.64%
Androgen receptor binding + 0.7403 74.03%
Thyroid receptor binding + 0.7526 75.26%
Glucocorticoid receptor binding + 0.8380 83.80%
Aromatase binding + 0.7496 74.96%
PPAR gamma + 0.8629 86.29%
Honey bee toxicity - 0.8707 87.07%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9852 98.52%

Targets

Top

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 99.71% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.64% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 93.79% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.64% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.73% 85.14%
CHEMBL2581 P07339 Cathepsin D 90.16% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.53% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.47% 94.45%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 89.17% 96.37%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.02% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.34% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.15% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.72% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.69% 100.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 73813322
LOTUS LTS0008305
wikiData Q105117711