1-hydroxy-3,5,6-trimethoxy-4-[(1R)-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbut-2-enyl]-10H-acridin-9-one

Details

Top
Internal ID d63e8d84-1cfe-40a8-80ba-6e04d12e1c8f
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Acridines > Acridones
IUPAC Name 1-hydroxy-3,5,6-trimethoxy-4-[(1R)-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbut-2-enyl]-10H-acridin-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H29NO8/c1-15(2)11-19(18-12-16-7-10-25(34)40-22(16)14-23(18)37-4)26-24(38-5)13-20(33)27-29(26)32-28-17(30(27)35)8-9-21(36-3)31(28)39-6/h7-14,19,33H,1-6H3,(H,32,35)/t19-/m1/s1
InChI Key CSICEUBOWFUIAN-LJQANCHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H29NO8
Molecular Weight 543.60 g/mol
Exact Mass 543.18931688 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.63
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1-hydroxy-3,5,6-trimethoxy-4-[(1R)-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbut-2-enyl]-10H-acridin-9-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9230 92.30%
Caco-2 - 0.6173 61.73%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Nucleus 0.4462 44.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8979 89.79%
OATP1B3 inhibitior + 0.9190 91.90%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9657 96.57%
P-glycoprotein inhibitior + 0.9305 93.05%
P-glycoprotein substrate + 0.6695 66.95%
CYP3A4 substrate + 0.6282 62.82%
CYP2C9 substrate + 0.6387 63.87%
CYP2D6 substrate - 0.8662 86.62%
CYP3A4 inhibition - 0.7916 79.16%
CYP2C9 inhibition - 0.6757 67.57%
CYP2C19 inhibition + 0.5240 52.40%
CYP2D6 inhibition - 0.8286 82.86%
CYP1A2 inhibition - 0.6400 64.00%
CYP2C8 inhibition + 0.7378 73.78%
CYP inhibitory promiscuity + 0.5196 51.96%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4822 48.22%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.8546 85.46%
Skin irritation - 0.8266 82.66%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis - 0.5170 51.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7719 77.19%
Micronuclear + 0.7900 79.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8652 86.52%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7632 76.32%
Acute Oral Toxicity (c) III 0.6246 62.46%
Estrogen receptor binding + 0.8561 85.61%
Androgen receptor binding + 0.8487 84.87%
Thyroid receptor binding + 0.6602 66.02%
Glucocorticoid receptor binding + 0.8721 87.21%
Aromatase binding + 0.5801 58.01%
PPAR gamma + 0.7806 78.06%
Honey bee toxicity - 0.7981 79.81%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8719 87.19%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.77% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.52% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.99% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 95.83% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.55% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.42% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.16% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.43% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.96% 95.56%
CHEMBL2535 P11166 Glucose transporter 92.68% 98.75%
CHEMBL213 P08588 Beta-1 adrenergic receptor 91.40% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.02% 99.23%
CHEMBL1255126 O15151 Protein Mdm4 90.32% 90.20%
CHEMBL1951 P21397 Monoamine oxidase A 89.44% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.36% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.22% 90.71%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.68% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.04% 96.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.87% 89.62%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 83.84% 93.24%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.42% 80.78%
CHEMBL3194 P02766 Transthyretin 82.01% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.65% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.93% 94.73%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 80.83% 85.00%

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.
Citrus × aurantium

Cross-Links

Top
PubChem 163190064
LOTUS LTS0017305
wikiData Q104969286