6-Methoxy-7-hydroxychromone

Details

Top
Internal ID b496daf8-b12d-4c56-a14e-3f6aaba67acf
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 7-hydroxy-6-methoxychromen-4-one
SMILES (Canonical) COC1=C(C=C2C(=C1)C(=O)C=CO2)O
SMILES (Isomeric) COC1=C(C=C2C(=C1)C(=O)C=CO2)O
InChI InChI=1S/C10H8O4/c1-13-10-4-6-7(11)2-3-14-9(6)5-8(10)12/h2-5,12H,1H3
InChI Key ZRNARVWAJZIBTH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H8O4
Molecular Weight 192.17 g/mol
Exact Mass 192.04225873 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
6-Methoxy-7-hydroxychromone

2D Structure

Top
2D Structure of 6-Methoxy-7-hydroxychromone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9836 98.36%
Caco-2 + 0.7754 77.54%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7146 71.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9620 96.20%
OATP1B3 inhibitior + 0.9973 99.73%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9141 91.41%
P-glycoprotein inhibitior - 0.9166 91.66%
P-glycoprotein substrate - 0.9665 96.65%
CYP3A4 substrate - 0.5408 54.08%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition - 0.5835 58.35%
CYP2C9 inhibition - 0.8319 83.19%
CYP2C19 inhibition + 0.7001 70.01%
CYP2D6 inhibition - 0.8533 85.33%
CYP1A2 inhibition + 0.9798 97.98%
CYP2C8 inhibition - 0.6663 66.63%
CYP inhibitory promiscuity + 0.5273 52.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5441 54.41%
Eye corrosion - 0.9412 94.12%
Eye irritation + 0.9897 98.97%
Skin irritation + 0.5142 51.42%
Skin corrosion - 0.9802 98.02%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7333 73.33%
Micronuclear + 0.8959 89.59%
Hepatotoxicity - 0.5855 58.55%
skin sensitisation - 0.9229 92.29%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.5797 57.97%
Acute Oral Toxicity (c) III 0.8366 83.66%
Estrogen receptor binding + 0.6128 61.28%
Androgen receptor binding - 0.5987 59.87%
Thyroid receptor binding - 0.7182 71.82%
Glucocorticoid receptor binding - 0.4699 46.99%
Aromatase binding - 0.5149 51.49%
PPAR gamma - 0.6693 66.93%
Honey bee toxicity - 0.9251 92.51%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5902 59.02%
Fish aquatic toxicity + 0.8149 81.49%

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 98.80% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.14% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.92% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 92.09% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.06% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.37% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.39% 89.00%
CHEMBL2581 P07339 Cathepsin D 86.11% 98.95%
CHEMBL2535 P11166 Glucose transporter 83.20% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 81.30% 94.73%

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.
Acicarpha tribuloides
Hedysarum polybotrys
Salicornia maritima

Cross-Links

Top
PubChem 91011769
NPASS NPC195774
LOTUS LTS0168335
wikiData Q105382089