2-(4'-Hydroxy-3'-methoxyphenyl)-1-methylquinolin-4-one

Details

Top
Internal ID c0ee497f-6c59-4369-9db7-cc6f1b133b02
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Phenylquinolines
IUPAC Name 2-(4-hydroxy-3-methoxyphenyl)-1-methylquinolin-4-one
SMILES (Canonical) CN1C2=CC=CC=C2C(=O)C=C1C3=CC(=C(C=C3)O)OC
SMILES (Isomeric) CN1C2=CC=CC=C2C(=O)C=C1C3=CC(=C(C=C3)O)OC
InChI InChI=1S/C17H15NO3/c1-18-13-6-4-3-5-12(13)16(20)10-14(18)11-7-8-15(19)17(9-11)21-2/h3-10,19H,1-2H3
InChI Key IPWJTTXZFDPVEQ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C17H15NO3
Molecular Weight 281.30 g/mol
Exact Mass 281.10519334 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(4'-Hydroxy-3'-methoxyphenyl)-1-methylquinolin-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9757 97.57%
Caco-2 + 0.9355 93.55%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8167 81.67%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9545 95.45%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5665 56.65%
P-glycoprotein inhibitior - 0.5885 58.85%
P-glycoprotein substrate - 0.8479 84.79%
CYP3A4 substrate + 0.5736 57.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8126 81.26%
CYP3A4 inhibition + 0.5328 53.28%
CYP2C9 inhibition - 0.7429 74.29%
CYP2C19 inhibition - 0.6826 68.26%
CYP2D6 inhibition - 0.6798 67.98%
CYP1A2 inhibition + 0.5304 53.04%
CYP2C8 inhibition - 0.5755 57.55%
CYP inhibitory promiscuity + 0.6083 60.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9710 97.10%
Carcinogenicity (trinary) Non-required 0.4105 41.05%
Eye corrosion - 0.9939 99.39%
Eye irritation + 0.5584 55.84%
Skin irritation - 0.7998 79.98%
Skin corrosion - 0.9709 97.09%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6154 61.54%
Micronuclear + 0.7959 79.59%
Hepatotoxicity + 0.5626 56.26%
skin sensitisation - 0.9374 93.74%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7650 76.50%
Acute Oral Toxicity (c) III 0.7243 72.43%
Estrogen receptor binding + 0.8995 89.95%
Androgen receptor binding + 0.7852 78.52%
Thyroid receptor binding + 0.6907 69.07%
Glucocorticoid receptor binding + 0.8446 84.46%
Aromatase binding + 0.5744 57.44%
PPAR gamma + 0.7602 76.02%
Honey bee toxicity - 0.8886 88.86%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.4445 44.45%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.68% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.88% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.03% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.83% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.63% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.56% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.37% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.41% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.38% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.55% 93.99%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 88.46% 80.78%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.94% 98.11%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 84.78% 100.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.92% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.10% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 81.05% 93.31%
CHEMBL3438 Q05513 Protein kinase C zeta 80.02% 88.48%

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.
Haplophyllum griffithianum

Cross-Links

Top
PubChem 71437555
LOTUS LTS0088558
wikiData Q105117552