Cuspanine

Details

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Internal ID dede93f5-6c56-4a8c-9f40-a7c6a6dde575
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Acridines > Acridones
IUPAC Name 1-hydroxy-2,3,5,6-tetramethoxy-10H-acridin-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C(=O)C3=C(C(=C(C=C3N2)OC)OC)O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C(=O)C3=C(C(=C(C=C3N2)OC)OC)O)OC
InChI InChI=1S/C17H17NO6/c1-21-10-6-5-8-13(16(10)23-3)18-9-7-11(22-2)17(24-4)15(20)12(9)14(8)19/h5-7,20H,1-4H3,(H,18,19)
InChI Key AJRHMDUHBMQVJL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H17NO6
Molecular Weight 331.32 g/mol
Exact Mass 331.10558726 g/mol
Topological Polar Surface Area (TPSA) 86.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL478767

2D Structure

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2D Structure of Cuspanine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9536 95.36%
Caco-2 + 0.8270 82.70%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4515 45.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9300 93.00%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5519 55.19%
P-glycoprotein inhibitior - 0.7156 71.56%
P-glycoprotein substrate - 0.7079 70.79%
CYP3A4 substrate + 0.5190 51.90%
CYP2C9 substrate - 0.8026 80.26%
CYP2D6 substrate - 0.8257 82.57%
CYP3A4 inhibition + 0.5298 52.98%
CYP2C9 inhibition - 0.8764 87.64%
CYP2C19 inhibition - 0.5526 55.26%
CYP2D6 inhibition - 0.6516 65.16%
CYP1A2 inhibition + 0.5767 57.67%
CYP2C8 inhibition + 0.5693 56.93%
CYP inhibitory promiscuity + 0.5903 59.03%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6525 65.25%
Eye corrosion - 0.9937 99.37%
Eye irritation + 0.8649 86.49%
Skin irritation - 0.8555 85.55%
Skin corrosion - 0.9607 96.07%
Ames mutagenesis + 0.5936 59.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6612 66.12%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5701 57.01%
skin sensitisation - 0.9340 93.40%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7871 78.71%
Acute Oral Toxicity (c) III 0.5816 58.16%
Estrogen receptor binding + 0.7924 79.24%
Androgen receptor binding + 0.6078 60.78%
Thyroid receptor binding + 0.8049 80.49%
Glucocorticoid receptor binding + 0.8383 83.83%
Aromatase binding + 0.7934 79.34%
PPAR gamma + 0.6693 66.93%
Honey bee toxicity - 0.9401 94.01%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity - 0.6500 65.00%

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 98.32% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.68% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.98% 95.56%
CHEMBL213 P08588 Beta-1 adrenergic receptor 93.53% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.70% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.68% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 92.38% 94.75%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 91.00% 92.68%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.53% 96.09%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 90.51% 93.24%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.77% 89.00%
CHEMBL2581 P07339 Cathepsin D 88.58% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.12% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.84% 86.33%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 86.60% 98.21%
CHEMBL255 P29275 Adenosine A2b receptor 84.76% 98.59%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.09% 99.17%
CHEMBL4302 P08183 P-glycoprotein 1 83.73% 92.98%
CHEMBL1951 P21397 Monoamine oxidase A 83.13% 91.49%
CHEMBL1255126 O15151 Protein Mdm4 82.45% 90.20%
CHEMBL4208 P20618 Proteasome component C5 80.99% 90.00%

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 44584643
LOTUS LTS0246400
wikiData Q104913343