1,2,3-trimethoxy-10H-acridin-9-one

Details

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Internal ID fd1516ac-7873-4fba-bf1b-d818de03b87d
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Acridines > Acridones
IUPAC Name 1,2,3-trimethoxy-10H-acridin-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H15NO4/c1-19-12-8-11-13(16(21-3)15(12)20-2)14(18)9-6-4-5-7-10(9)17-11/h4-8H,1-3H3,(H,17,18)
InChI Key ZUOLILKPUZXGOU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H15NO4
Molecular Weight 285.29 g/mol
Exact Mass 285.10010796 g/mol
Topological Polar Surface Area (TPSA) 56.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,2,3-trimethoxy-10H-acridin-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.7791 77.91%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5563 55.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9078 90.78%
OATP1B3 inhibitior + 0.9792 97.92%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4519 45.19%
P-glycoprotein inhibitior - 0.6349 63.49%
P-glycoprotein substrate - 0.8414 84.14%
CYP3A4 substrate + 0.5442 54.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8081 80.81%
CYP3A4 inhibition + 0.6689 66.89%
CYP2C9 inhibition - 0.9635 96.35%
CYP2C19 inhibition - 0.5273 52.73%
CYP2D6 inhibition - 0.7377 73.77%
CYP1A2 inhibition + 0.8449 84.49%
CYP2C8 inhibition - 0.5835 58.35%
CYP inhibitory promiscuity + 0.6661 66.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5572 55.72%
Eye corrosion - 0.9908 99.08%
Eye irritation + 0.8888 88.88%
Skin irritation - 0.8586 85.86%
Skin corrosion - 0.9804 98.04%
Ames mutagenesis + 0.7736 77.36%
Human Ether-a-go-go-Related Gene inhibition - 0.3788 37.88%
Micronuclear + 0.7459 74.59%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9554 95.54%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.5594 55.94%
Acute Oral Toxicity (c) II 0.4465 44.65%
Estrogen receptor binding + 0.7728 77.28%
Androgen receptor binding + 0.6613 66.13%
Thyroid receptor binding + 0.7891 78.91%
Glucocorticoid receptor binding + 0.8345 83.45%
Aromatase binding + 0.7690 76.90%
PPAR gamma + 0.6106 61.06%
Honey bee toxicity - 0.8665 86.65%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity - 0.4545 45.45%

Targets

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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
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.89% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.28% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.77% 91.11%
CHEMBL2535 P11166 Glucose transporter 93.55% 98.75%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 92.48% 98.21%
CHEMBL4302 P08183 P-glycoprotein 1 91.89% 92.98%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.67% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.23% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.19% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.25% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.01% 86.33%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.98% 92.67%
CHEMBL255 P29275 Adenosine A2b receptor 84.29% 98.59%
CHEMBL1937 Q92769 Histone deacetylase 2 84.11% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.04% 89.00%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 83.39% 81.14%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 83.32% 85.00%
CHEMBL1255126 O15151 Protein Mdm4 83.31% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.79% 96.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.37% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 81.11% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.23% 85.14%

Plants that contains it

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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.
Vepris bremekampii

Cross-Links

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PubChem 11716159
LOTUS LTS0196780
wikiData Q105383930