Cusculine

Details

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Internal ID f593b3d1-8742-441f-86cc-090ed3f66b2a
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Acridines > Acridones
IUPAC Name 1,2,3,5,6-pentamethoxy-10H-acridin-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C(=O)C3=C(C(=C(C=C3N2)OC)OC)OC)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C(=O)C3=C(C(=C(C=C3N2)OC)OC)OC)OC
InChI InChI=1S/C18H19NO6/c1-21-11-7-6-9-14(16(11)23-3)19-10-8-12(22-2)17(24-4)18(25-5)13(10)15(9)20/h6-8H,1-5H3,(H,19,20)
InChI Key CCYFNSHESGHUKB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H19NO6
Molecular Weight 345.30 g/mol
Exact Mass 345.12123733 g/mol
Topological Polar Surface Area (TPSA) 75.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL516428

2D Structure

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2D Structure of Cusculine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.8335 83.35%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5755 57.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9510 95.10%
OATP1B3 inhibitior + 0.9768 97.68%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.6246 62.46%
P-glycoprotein substrate - 0.7116 71.16%
CYP3A4 substrate - 0.5107 51.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8081 80.81%
CYP3A4 inhibition + 0.7523 75.23%
CYP2C9 inhibition - 0.9456 94.56%
CYP2C19 inhibition - 0.6014 60.14%
CYP2D6 inhibition - 0.8422 84.22%
CYP1A2 inhibition + 0.8493 84.93%
CYP2C8 inhibition - 0.6048 60.48%
CYP inhibitory promiscuity + 0.7160 71.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6122 61.22%
Eye corrosion - 0.9924 99.24%
Eye irritation + 0.7774 77.74%
Skin irritation - 0.8675 86.75%
Skin corrosion - 0.9778 97.78%
Ames mutagenesis + 0.6436 64.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5489 54.89%
Micronuclear + 0.7359 73.59%
Hepatotoxicity + 0.6451 64.51%
skin sensitisation - 0.9529 95.29%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6130 61.30%
Acute Oral Toxicity (c) III 0.4572 45.72%
Estrogen receptor binding + 0.7476 74.76%
Androgen receptor binding + 0.6739 67.39%
Thyroid receptor binding + 0.7773 77.73%
Glucocorticoid receptor binding + 0.7733 77.33%
Aromatase binding + 0.7218 72.18%
PPAR gamma + 0.5561 55.61%
Honey bee toxicity - 0.8962 89.62%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity - 0.5418 54.18%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.39% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.56% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.48% 93.99%
CHEMBL4302 P08183 P-glycoprotein 1 93.24% 92.98%
CHEMBL255 P29275 Adenosine A2b receptor 91.33% 98.59%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.47% 94.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 89.41% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.35% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 89.17% 94.75%
CHEMBL2535 P11166 Glucose transporter 88.82% 98.75%
CHEMBL2581 P07339 Cathepsin D 86.76% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.47% 91.11%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 86.28% 93.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.46% 86.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.13% 92.68%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.71% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.53% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 82.77% 90.20%
CHEMBL1907 P15144 Aminopeptidase N 82.50% 93.31%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.47% 92.38%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 80.10% 85.00%

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.
Conchocarpus paniculatus

Cross-Links

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PubChem 44584644
LOTUS LTS0147292
wikiData Q104953950