6-Methoxy-7-(2-methylprop-1-enoxy)chromen-2-one

Details

Top
Internal ID 10885a2d-8eac-4e45-9ae3-4d870cdb7df2
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-methoxy-7-(2-methylprop-1-enoxy)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O4/c1-9(2)8-17-13-7-11-10(6-12(13)16-3)4-5-14(15)18-11/h4-8H,1-3H3
InChI Key LDNUPHBBVMDOTA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.10
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-Methoxy-7-(2-methylprop-1-enoxy)chromen-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.9521 95.21%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6429 64.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9081 90.81%
OATP1B3 inhibitior + 0.9794 97.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5973 59.73%
P-glycoprotein inhibitior - 0.5151 51.51%
P-glycoprotein substrate - 0.8445 84.45%
CYP3A4 substrate - 0.5915 59.15%
CYP2C9 substrate - 0.7071 70.71%
CYP2D6 substrate - 0.8375 83.75%
CYP3A4 inhibition - 0.5089 50.89%
CYP2C9 inhibition - 0.7865 78.65%
CYP2C19 inhibition + 0.9261 92.61%
CYP2D6 inhibition - 0.8256 82.56%
CYP1A2 inhibition + 0.9007 90.07%
CYP2C8 inhibition - 0.7942 79.42%
CYP inhibitory promiscuity + 0.8779 87.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4999 49.99%
Eye corrosion - 0.9774 97.74%
Eye irritation + 0.8388 83.88%
Skin irritation - 0.7699 76.99%
Skin corrosion - 0.9848 98.48%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3775 37.75%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8166 81.66%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.4584 45.84%
Acute Oral Toxicity (c) III 0.4554 45.54%
Estrogen receptor binding + 0.7700 77.00%
Androgen receptor binding - 0.5323 53.23%
Thyroid receptor binding - 0.5114 51.14%
Glucocorticoid receptor binding + 0.5984 59.84%
Aromatase binding + 0.8483 84.83%
PPAR gamma - 0.5359 53.59%
Honey bee toxicity - 0.8814 88.14%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9894 98.94%

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 95.54% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.94% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.01% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.45% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.55% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.71% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.78% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.51% 94.03%
CHEMBL3401 O75469 Pregnane X receptor 82.24% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.10% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.97% 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.
Cassinia uncata

Cross-Links

Top
PubChem 14191256
LOTUS LTS0097312
wikiData Q105150288