5,7-Dihydroxy-2-(4-hydroxy-3-methylphenyl)-6-methoxychromen-4-one

Details

Top
Internal ID 91a704c3-fd7d-4a07-8fa5-41085cd3c7c1
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name 5,7-dihydroxy-2-(4-hydroxy-3-methylphenyl)-6-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O6/c1-8-5-9(3-4-10(8)18)13-6-11(19)15-14(23-13)7-12(20)17(22-2)16(15)21/h3-7,18,20-21H,1-2H3
InChI Key AOAPCDXPLWGVGI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H14O6
Molecular Weight 314.29 g/mol
Exact Mass 314.07903816 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5,7-Dihydroxy-2-(4-hydroxy-3-methylphenyl)-6-methoxychromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9440 94.40%
Caco-2 + 0.8511 85.11%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6642 66.42%
OATP2B1 inhibitior + 0.5663 56.63%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9261 92.61%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6539 65.39%
P-glycoprotein inhibitior - 0.5724 57.24%
P-glycoprotein substrate - 0.8953 89.53%
CYP3A4 substrate + 0.5326 53.26%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition + 0.7817 78.17%
CYP2C9 inhibition + 0.6258 62.58%
CYP2C19 inhibition + 0.8187 81.87%
CYP2D6 inhibition - 0.6249 62.49%
CYP1A2 inhibition + 0.8668 86.68%
CYP2C8 inhibition + 0.7027 70.27%
CYP inhibitory promiscuity + 0.8459 84.59%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6581 65.81%
Eye corrosion - 0.9779 97.79%
Eye irritation + 0.7399 73.99%
Skin irritation - 0.6522 65.22%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7471 74.71%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9222 92.22%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8672 86.72%
Acute Oral Toxicity (c) III 0.5920 59.20%
Estrogen receptor binding + 0.9101 91.01%
Androgen receptor binding + 0.8584 85.84%
Thyroid receptor binding + 0.6754 67.54%
Glucocorticoid receptor binding + 0.8729 87.29%
Aromatase binding + 0.7709 77.09%
PPAR gamma + 0.8483 84.83%
Honey bee toxicity - 0.8639 86.39%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8636 86.36%

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 99.01% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.80% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.66% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.19% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.11% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.27% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.55% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.76% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.22% 94.73%
CHEMBL3194 P02766 Transthyretin 87.91% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.84% 94.45%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.74% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.99% 99.23%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.95% 83.57%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.40% 98.11%

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.
Arnica acaulis
Balsamorhiza deltoidea

Cross-Links

Top
PubChem 162970547
LOTUS LTS0194847
wikiData Q104915515