7-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one

Details

Top
Internal ID 8fa86296-c9e9-45bb-96c0-5e44d28eedd3
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 5-O-methylated flavonoids
IUPAC Name 7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O6/c1-21-14-5-9(3-4-11(14)19)13-8-12(20)17-15(22-2)6-10(18)7-16(17)23-13/h3-7,13,18-19H,8H2,1-2H3
InChI Key WRSMUTJHTHWFDH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 7-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9744 97.44%
Caco-2 + 0.7470 74.70%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.8183 81.83%
OATP2B1 inhibitior - 0.5942 59.42%
OATP1B1 inhibitior + 0.9574 95.74%
OATP1B3 inhibitior + 0.9668 96.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8445 84.45%
P-glycoprotein inhibitior - 0.7769 77.69%
P-glycoprotein substrate - 0.9192 91.92%
CYP3A4 substrate + 0.5246 52.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3531 35.31%
CYP3A4 inhibition - 0.5467 54.67%
CYP2C9 inhibition + 0.7410 74.10%
CYP2C19 inhibition + 0.8724 87.24%
CYP2D6 inhibition - 0.6703 67.03%
CYP1A2 inhibition + 0.8062 80.62%
CYP2C8 inhibition - 0.6144 61.44%
CYP inhibitory promiscuity + 0.6709 67.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6103 61.03%
Eye corrosion - 0.9826 98.26%
Eye irritation + 0.7935 79.35%
Skin irritation - 0.7095 70.95%
Skin corrosion - 0.9652 96.52%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6241 62.41%
Micronuclear + 0.8859 88.59%
Hepatotoxicity - 0.6593 65.93%
skin sensitisation - 0.9313 93.13%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.6019 60.19%
Acute Oral Toxicity (c) III 0.5861 58.61%
Estrogen receptor binding + 0.7418 74.18%
Androgen receptor binding + 0.5598 55.98%
Thyroid receptor binding + 0.6660 66.60%
Glucocorticoid receptor binding + 0.7983 79.83%
Aromatase binding - 0.5393 53.93%
PPAR gamma + 0.5865 58.65%
Honey bee toxicity - 0.8433 84.33%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7990 79.90%

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 98.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.50% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.50% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.74% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.57% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.00% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.70% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.62% 86.33%
CHEMBL4208 P20618 Proteasome component C5 89.58% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.13% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.77% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.56% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.03% 94.00%
CHEMBL2535 P11166 Glucose transporter 86.73% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.22% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.07% 95.89%
CHEMBL3194 P02766 Transthyretin 82.27% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.44% 90.71%
CHEMBL3438 Q05513 Protein kinase C zeta 81.41% 88.48%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.22% 97.14%

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.
Viscum coloratum

Cross-Links

Top
PubChem 73235351
LOTUS LTS0268590
wikiData Q105311548