2-(14-Hydroxy-14,15-dimethylhexadecyl)quinoline-4(1H)-one

Details

Top
Internal ID 2414d654-bf1d-4698-8586-0dbfe5d0ca91
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 2-(14-hydroxy-14,15-dimethylhexadecyl)-1H-quinolin-4-one
SMILES (Canonical) CC(C)C(C)(CCCCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1)O
SMILES (Isomeric) CC(C)C(C)(CCCCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1)O
InChI InChI=1S/C27H43NO2/c1-22(2)27(3,30)20-16-12-10-8-6-4-5-7-9-11-13-17-23-21-26(29)24-18-14-15-19-25(24)28-23/h14-15,18-19,21-22,30H,4-13,16-17,20H2,1-3H3,(H,28,29)
InChI Key YWFRYNMHYMAQLJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C27H43NO2
Molecular Weight 413.60 g/mol
Exact Mass 413.329379614 g/mol
Topological Polar Surface Area (TPSA) 49.30 Ų
XlogP 8.70
Atomic LogP (AlogP) 7.16
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 15

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(14-Hydroxy-14,15-dimethylhexadecyl)quinoline-4(1H)-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6501 65.01%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7296 72.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9176 91.76%
P-glycoprotein inhibitior + 0.6231 62.31%
P-glycoprotein substrate - 0.6261 62.61%
CYP3A4 substrate + 0.5858 58.58%
CYP2C9 substrate + 0.6048 60.48%
CYP2D6 substrate - 0.8234 82.34%
CYP3A4 inhibition - 0.8115 81.15%
CYP2C9 inhibition - 0.8235 82.35%
CYP2C19 inhibition - 0.6287 62.87%
CYP2D6 inhibition - 0.8281 82.81%
CYP1A2 inhibition - 0.5548 55.48%
CYP2C8 inhibition - 0.7552 75.52%
CYP inhibitory promiscuity - 0.7583 75.83%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6816 68.16%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9154 91.54%
Skin irritation - 0.7863 78.63%
Skin corrosion - 0.9133 91.33%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8240 82.40%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.5823 58.23%
skin sensitisation - 0.8164 81.64%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7009 70.09%
Acute Oral Toxicity (c) III 0.6802 68.02%
Estrogen receptor binding + 0.7840 78.40%
Androgen receptor binding + 0.6113 61.13%
Thyroid receptor binding + 0.6347 63.47%
Glucocorticoid receptor binding + 0.5583 55.83%
Aromatase binding + 0.6129 61.29%
PPAR gamma + 0.6360 63.60%
Honey bee toxicity - 0.9513 95.13%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5063 50.63%
Fish aquatic toxicity + 0.8346 83.46%

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 99.42% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.47% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.82% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.78% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 94.60% 94.73%
CHEMBL2535 P11166 Glucose transporter 91.34% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.64% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 89.65% 94.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.35% 91.71%
CHEMBL2885 P07451 Carbonic anhydrase III 88.26% 87.45%
CHEMBL2179 P04062 Beta-glucocerebrosidase 88.04% 85.31%
CHEMBL255 P29275 Adenosine A2b receptor 87.49% 98.59%
CHEMBL1907 P15144 Aminopeptidase N 87.26% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.24% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.58% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.89% 85.14%
CHEMBL3524 P56524 Histone deacetylase 4 83.83% 92.97%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.02% 86.33%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 82.73% 96.37%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.05% 99.17%
CHEMBL1781 P11387 DNA topoisomerase I 80.67% 97.00%

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.
Dictyoloma vandellianum

Cross-Links

Top
PubChem 90766936
LOTUS LTS0256684
wikiData Q104202143