3-(2,3-Dihydroxy-3-methylbutyl)-4,7-dimethoxy-1-methylquinolin-2-one

Details

Top
Internal ID 71a49363-5340-407d-b5bb-0c0df4b0abe9
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 3-(2,3-dihydroxy-3-methylbutyl)-4,7-dimethoxy-1-methylquinolin-2-one
SMILES (Canonical) CC(C)(C(CC1=C(C2=C(C=C(C=C2)OC)N(C1=O)C)OC)O)O
SMILES (Isomeric) CC(C)(C(CC1=C(C2=C(C=C(C=C2)OC)N(C1=O)C)OC)O)O
InChI InChI=1S/C17H23NO5/c1-17(2,21)14(19)9-12-15(23-5)11-7-6-10(22-4)8-13(11)18(3)16(12)20/h6-8,14,19,21H,9H2,1-5H3
InChI Key FVYSKNSDGCPVNF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C17H23NO5
Molecular Weight 321.40 g/mol
Exact Mass 321.15762283 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.23
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-(2,3-Dihydroxy-3-methylbutyl)-4,7-dimethoxy-1-methylquinolin-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8904 89.04%
Caco-2 + 0.7747 77.47%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.4095 40.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9211 92.11%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5893 58.93%
P-glycoprotein inhibitior - 0.8800 88.00%
P-glycoprotein substrate - 0.7084 70.84%
CYP3A4 substrate + 0.5624 56.24%
CYP2C9 substrate - 0.6110 61.10%
CYP2D6 substrate - 0.8153 81.53%
CYP3A4 inhibition - 0.8240 82.40%
CYP2C9 inhibition - 0.8730 87.30%
CYP2C19 inhibition - 0.8423 84.23%
CYP2D6 inhibition - 0.8911 89.11%
CYP1A2 inhibition + 0.7694 76.94%
CYP2C8 inhibition - 0.7846 78.46%
CYP inhibitory promiscuity - 0.8234 82.34%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5764 57.64%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.7086 70.86%
Skin irritation - 0.8139 81.39%
Skin corrosion - 0.9418 94.18%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7839 78.39%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.5075 50.75%
skin sensitisation - 0.8847 88.47%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.9070 90.70%
Acute Oral Toxicity (c) III 0.5827 58.27%
Estrogen receptor binding + 0.8531 85.31%
Androgen receptor binding + 0.5962 59.62%
Thyroid receptor binding + 0.7116 71.16%
Glucocorticoid receptor binding + 0.5978 59.78%
Aromatase binding + 0.5635 56.35%
PPAR gamma + 0.6862 68.62%
Honey bee toxicity - 0.8854 88.54%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.3880 38.80%

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 96.68% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.52% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.45% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 93.27% 86.92%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.74% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.21% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.09% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.65% 93.99%
CHEMBL1907 P15144 Aminopeptidase N 87.46% 93.31%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.64% 80.78%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.13% 99.15%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.69% 92.68%
CHEMBL4208 P20618 Proteasome component C5 83.76% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.34% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.98% 97.25%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.24% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.03% 89.00%
CHEMBL255 P29275 Adenosine A2b receptor 80.99% 98.59%
CHEMBL2535 P11166 Glucose transporter 80.78% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.39% 91.07%

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.
Toddalia asiatica

Cross-Links

Top
PubChem 11695457
LOTUS LTS0197511
wikiData Q105003022