7-Hydroxy-3-methoxycoumarin

Details

Top
Internal ID 901d7f7b-cf49-4a1a-bca3-d6814e466a8a
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-3-methoxychromen-2-one
SMILES (Canonical) COC1=CC2=C(C=C(C=C2)O)OC1=O
SMILES (Isomeric) COC1=CC2=C(C=C(C=C2)O)OC1=O
InChI InChI=1S/C10H8O4/c1-13-9-4-6-2-3-7(11)5-8(6)14-10(9)12/h2-5,11H,1H3
InChI Key PGPVICRXSGQXJL-UHFFFAOYSA-N
Popularity 5 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 1.70
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
68287-05-8
Methoxy-Umbelliferon
SCHEMBL250387
A901168

2D Structure

Top
2D Structure of 7-Hydroxy-3-methoxycoumarin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9730 97.30%
Caco-2 + 0.5220 52.20%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6806 68.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8390 83.90%
OATP1B3 inhibitior + 0.9915 99.15%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7634 76.34%
P-glycoprotein inhibitior - 0.9373 93.73%
P-glycoprotein substrate - 0.7932 79.32%
CYP3A4 substrate - 0.5909 59.09%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.7933 79.33%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.7862 78.62%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition + 0.9106 91.06%
CYP2C8 inhibition - 0.6855 68.55%
CYP inhibitory promiscuity - 0.6876 68.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5260 52.60%
Eye corrosion - 0.9431 94.31%
Eye irritation + 0.9834 98.34%
Skin irritation + 0.4950 49.50%
Skin corrosion - 0.9810 98.10%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7617 76.17%
Micronuclear + 0.9059 90.59%
Hepatotoxicity - 0.5678 56.78%
skin sensitisation - 0.9369 93.69%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.4617 46.17%
Acute Oral Toxicity (c) III 0.8059 80.59%
Estrogen receptor binding + 0.6350 63.50%
Androgen receptor binding + 0.6317 63.17%
Thyroid receptor binding - 0.7572 75.72%
Glucocorticoid receptor binding - 0.5998 59.98%
Aromatase binding + 0.5729 57.29%
PPAR gamma - 0.6018 60.18%
Honey bee toxicity - 0.9321 93.21%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6349 63.49%
Fish aquatic toxicity + 0.8914 89.14%

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 94.93% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.46% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.28% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.83% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.99% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.72% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.16% 90.71%
CHEMBL2535 P11166 Glucose transporter 83.94% 98.75%
CHEMBL4208 P20618 Proteasome component C5 82.42% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 81.73% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.58% 99.23%

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.
Halocnemum strobilaceum

Cross-Links

Top
PubChem 12466112
LOTUS LTS0255555
wikiData Q105208578