2-(2'-Hydroxy-4'-methoxyphenyl)-5,8-dimethoxy-3-propyl-1h-quinolin-4-one

Details

Top
Internal ID 9f48660e-fb28-4980-a247-5fe7eeee0f83
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Phenylquinolines
IUPAC Name 2-(2-hydroxy-4-methoxyphenyl)-5,8-dimethoxy-3-propyl-1H-quinolin-4-one
SMILES (Canonical) CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=C(C=C(C=C3)OC)O
SMILES (Isomeric) CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=C(C=C(C=C3)OC)O
InChI InChI=1S/C21H23NO5/c1-5-6-14-19(13-8-7-12(25-2)11-15(13)23)22-20-17(27-4)10-9-16(26-3)18(20)21(14)24/h7-11,23H,5-6H2,1-4H3,(H,22,24)
InChI Key KRDLFYZITUNBOK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C21H23NO5
Molecular Weight 369.40 g/mol
Exact Mass 369.15762283 g/mol
Topological Polar Surface Area (TPSA) 77.00 Ų
XlogP 4.10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(2'-Hydroxy-4'-methoxyphenyl)-5,8-dimethoxy-3-propyl-1h-quinolin-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
No predicted properties yet!

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
CHEMBL2581 P07339 Cathepsin D 97.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.42% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.90% 91.11%
CHEMBL4208 P20618 Proteasome component C5 94.07% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.06% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.95% 86.33%
CHEMBL255 P29275 Adenosine A2b receptor 93.42% 98.59%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.33% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.30% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 93.16% 93.31%
CHEMBL2535 P11166 Glucose transporter 92.31% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.60% 91.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.77% 86.92%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.02% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 83.91% 90.20%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 83.49% 93.24%
CHEMBL3194 P02766 Transthyretin 82.90% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 81.67% 94.75%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.05% 94.80%

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.
Alpinia officinarum
Casimiroa edulis
Espeletiopsis purpurascens
Helianthus californicus
Hornstedtia reticulata
Imperata cylindrica
Phlebodium aureum
Plectranthus hereroensis
Spiraea prunifolia
Ursinia anthemoides

Cross-Links

Top
PubChem 24766568
NPASS NPC118418
LOTUS LTS0171597
wikiData Q105144939