4,6-Dimethoxy-7-(3-methylbut-2-enoxy)furo[2,3-b]quinoline

Details

Top
Internal ID 91fad6f5-d9d7-40d9-ae36-db1c78beece7
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Furanoquinolines
IUPAC Name 4,6-dimethoxy-7-(3-methylbut-2-enoxy)furo[2,3-b]quinoline
SMILES (Canonical) CC(=CCOC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)OC)C
SMILES (Isomeric) CC(=CCOC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)OC)C
InChI InChI=1S/C18H19NO4/c1-11(2)5-7-22-16-10-14-13(9-15(16)20-3)17(21-4)12-6-8-23-18(12)19-14/h5-6,8-10H,7H2,1-4H3
InChI Key XXXIKTRVNAFYGM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H19NO4
Molecular Weight 313.30 g/mol
Exact Mass 313.13140809 g/mol
Topological Polar Surface Area (TPSA) 53.70 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.34
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4,6-Dimethoxy-7-(3-methylbut-2-enoxy)furo[2,3-b]quinoline

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.8381 83.81%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6159 61.59%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.9434 94.34%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8918 89.18%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.7154 71.54%
CYP3A4 substrate + 0.5155 51.55%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.6999 69.99%
CYP3A4 inhibition + 0.7774 77.74%
CYP2C9 inhibition - 0.5075 50.75%
CYP2C19 inhibition + 0.5722 57.22%
CYP2D6 inhibition - 0.8374 83.74%
CYP1A2 inhibition + 0.9232 92.32%
CYP2C8 inhibition + 0.7200 72.00%
CYP inhibitory promiscuity + 0.8422 84.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5966 59.66%
Eye corrosion - 0.9875 98.75%
Eye irritation + 0.6435 64.35%
Skin irritation - 0.8142 81.42%
Skin corrosion - 0.9494 94.94%
Ames mutagenesis + 0.6646 66.46%
Human Ether-a-go-go-Related Gene inhibition + 0.9142 91.42%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7921 79.21%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7176 71.76%
Acute Oral Toxicity (c) III 0.6274 62.74%
Estrogen receptor binding + 0.8255 82.55%
Androgen receptor binding + 0.6071 60.71%
Thyroid receptor binding + 0.7490 74.90%
Glucocorticoid receptor binding + 0.9205 92.05%
Aromatase binding + 0.8501 85.01%
PPAR gamma + 0.7924 79.24%
Honey bee toxicity - 0.8960 89.60%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8840 88.40%

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
CHEMBL5747 Q92793 CREB-binding protein 94.99% 95.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.25% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.27% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.57% 91.11%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 91.18% 89.44%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.08% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 90.77% 94.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.72% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.46% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.98% 92.94%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 88.59% 92.38%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 88.41% 85.49%
CHEMBL3401 O75469 Pregnane X receptor 86.61% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.00% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.42% 89.62%
CHEMBL290 Q13370 Phosphodiesterase 3B 84.60% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.82% 94.75%
CHEMBL2535 P11166 Glucose transporter 83.68% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.14% 92.62%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.05% 95.83%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 83.02% 95.39%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.41% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.13% 96.67%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 80.82% 96.47%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.67% 95.56%

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.
Vepris nobilis

Cross-Links

Top
PubChem 13970974
LOTUS LTS0077300
wikiData Q103817993