3,5-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

Details

Top
Internal ID 90256840-a52a-4755-a937-a545387e5f70
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 6-prenylated flavans > 6-prenylated flavanones
IUPAC Name 3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O7/c1-11(2)5-7-13-16(28-4)10-17-18(19(13)24)20(25)21(26)22(29-17)12-6-8-15(27-3)14(23)9-12/h5-6,8-10,21-24,26H,7H2,1-4H3
InChI Key PBPNVACBMADKSI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C22H24O7
Molecular Weight 400.40 g/mol
Exact Mass 400.15220310 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3,5-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.5073 50.73%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6748 67.48%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8965 89.65%
OATP1B3 inhibitior + 0.8588 85.88%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7873 78.73%
P-glycoprotein inhibitior + 0.6687 66.87%
P-glycoprotein substrate - 0.8041 80.41%
CYP3A4 substrate + 0.5824 58.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7858 78.58%
CYP3A4 inhibition - 0.8315 83.15%
CYP2C9 inhibition + 0.9098 90.98%
CYP2C19 inhibition + 0.9329 93.29%
CYP2D6 inhibition - 0.5506 55.06%
CYP1A2 inhibition + 0.7442 74.42%
CYP2C8 inhibition + 0.5835 58.35%
CYP inhibitory promiscuity + 0.8934 89.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6702 67.02%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.6672 66.72%
Skin irritation - 0.7777 77.77%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5400 54.00%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8185 81.85%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6529 65.29%
Acute Oral Toxicity (c) III 0.6937 69.37%
Estrogen receptor binding + 0.8479 84.79%
Androgen receptor binding + 0.5763 57.63%
Thyroid receptor binding + 0.6815 68.15%
Glucocorticoid receptor binding + 0.8591 85.91%
Aromatase binding - 0.5591 55.91%
PPAR gamma + 0.8231 82.31%
Honey bee toxicity - 0.8285 82.85%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9899 98.99%

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 98.32% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.30% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 94.09% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.85% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.40% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.69% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.28% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.94% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.91% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.04% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.88% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.80% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.58% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.78% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.39% 99.23%
CHEMBL3194 P02766 Transthyretin 82.12% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.48% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.36% 95.89%

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.
Rhynchosia hirta

Cross-Links

Top
PubChem 14189050
LOTUS LTS0097400
wikiData Q105205340