7-Hydroxy-6,8-dimethoxychromen-4-one

Details

Top
Internal ID 512e7ec8-6651-4ec6-9370-07f90abc60bb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 7-hydroxy-6,8-dimethoxychromen-4-one
SMILES (Canonical) COC1=C(C(=C2C(=C1)C(=O)C=CO2)OC)O
SMILES (Isomeric) COC1=C(C(=C2C(=C1)C(=O)C=CO2)OC)O
InChI InChI=1S/C11H10O5/c1-14-8-5-6-7(12)3-4-16-10(6)11(15-2)9(8)13/h3-5,13H,1-2H3
InChI Key ANCHXLMTFNOVDK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 7-Hydroxy-6,8-dimethoxychromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 - 0.5744 57.44%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9272 92.72%
OATP1B3 inhibitior + 0.9932 99.32%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9081 90.81%
P-glycoprotein inhibitior - 0.8464 84.64%
P-glycoprotein substrate - 0.9395 93.95%
CYP3A4 substrate - 0.5068 50.68%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition + 0.5215 52.15%
CYP2C9 inhibition - 0.8938 89.38%
CYP2C19 inhibition + 0.6902 69.02%
CYP2D6 inhibition - 0.7703 77.03%
CYP1A2 inhibition + 0.9595 95.95%
CYP2C8 inhibition + 0.4471 44.71%
CYP inhibitory promiscuity + 0.5264 52.64%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6210 62.10%
Eye corrosion - 0.9551 95.51%
Eye irritation + 0.8668 86.68%
Skin irritation - 0.5807 58.07%
Skin corrosion - 0.9822 98.22%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7740 77.40%
Micronuclear + 0.8959 89.59%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9125 91.25%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7625 76.25%
Acute Oral Toxicity (c) III 0.4994 49.94%
Estrogen receptor binding + 0.6135 61.35%
Androgen receptor binding + 0.5194 51.94%
Thyroid receptor binding - 0.6375 63.75%
Glucocorticoid receptor binding - 0.5659 56.59%
Aromatase binding + 0.5239 52.39%
PPAR gamma - 0.6380 63.80%
Honey bee toxicity - 0.9421 94.21%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5402 54.02%
Fish aquatic toxicity + 0.8492 84.92%

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 99.03% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.93% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.57% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.42% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.57% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.36% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.26% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.62% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.18% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.88% 92.62%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.31% 94.03%
CHEMBL2535 P11166 Glucose transporter 81.95% 98.75%

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.
Artemisia annua
Artemisia vestita
Gelsemium elegans

Cross-Links

Top
PubChem 5318198
NPASS NPC177976