5-Methoxycanthin-6-one

Details

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Internal ID c6e1a64f-1056-45cc-b843-6df1f35e54eb
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 3-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one
SMILES (Canonical) COC1=CC2=NC=CC3=C2N(C1=O)C4=CC=CC=C34
SMILES (Isomeric) COC1=CC2=NC=CC3=C2N(C1=O)C4=CC=CC=C34
InChI InChI=1S/C15H10N2O2/c1-19-13-8-11-14-10(6-7-16-11)9-4-2-3-5-12(9)17(14)15(13)18/h2-8H,1H3
InChI Key TXEFUSAHPIYZHD-UHFFFAOYSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10N2O2
Molecular Weight 250.25 g/mol
Exact Mass 250.074227566 g/mol
Topological Polar Surface Area (TPSA) 44.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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15071-56-4
5-Methoxy-Canthin-6-one
UNII-VVM1A8LM35
VVM1A8LM35
5-Methoxycanthinone
METHOXYCANTHIN-6-ONE,5-
NSC88929
Canthin-6-one, 5-methoxy-
5-Methoxy-6H-indolo(3,2,1-de)(1,5)naphthyridin-6-one
5-Methoxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Methoxycanthin-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.7310 73.10%
Blood Brain Barrier + 0.9696 96.96%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8280 82.80%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9656 96.56%
OATP1B3 inhibitior + 0.9606 96.06%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8348 83.48%
BSEP inhibitior + 0.6068 60.68%
P-glycoprotein inhibitior - 0.7486 74.86%
P-glycoprotein substrate - 0.6597 65.97%
CYP3A4 substrate + 0.5715 57.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8321 83.21%
CYP3A4 inhibition - 0.5725 57.25%
CYP2C9 inhibition - 0.8144 81.44%
CYP2C19 inhibition + 0.7056 70.56%
CYP2D6 inhibition - 0.8490 84.90%
CYP1A2 inhibition + 0.9735 97.35%
CYP2C8 inhibition + 0.5853 58.53%
CYP inhibitory promiscuity + 0.7302 73.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5312 53.12%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.4814 48.14%
Skin irritation - 0.8429 84.29%
Skin corrosion - 0.9650 96.50%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6267 62.67%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5823 58.23%
skin sensitisation - 0.9079 90.79%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5837 58.37%
Acute Oral Toxicity (c) III 0.5468 54.68%
Estrogen receptor binding + 0.6605 66.05%
Androgen receptor binding + 0.5830 58.30%
Thyroid receptor binding + 0.6632 66.32%
Glucocorticoid receptor binding + 0.8635 86.35%
Aromatase binding + 0.8157 81.57%
PPAR gamma - 0.6284 62.84%
Honey bee toxicity - 0.9143 91.43%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.6918 69.18%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 20300 nM
IC50
PMID: 25819098

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.16% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.74% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.15% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.49% 86.33%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 92.72% 96.47%
CHEMBL2535 P11166 Glucose transporter 91.89% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.49% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.20% 93.99%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 89.17% 92.67%
CHEMBL255 P29275 Adenosine A2b receptor 84.93% 98.59%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.87% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.60% 99.23%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 83.12% 85.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.93% 91.11%
CHEMBL3524 P56524 Histone deacetylase 4 81.45% 92.97%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.96% 96.67%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.81% 100.00%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 80.71% 95.50%

Cross-Links

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PubChem 259218
NPASS NPC12649
ChEMBL CHEMBL508649
LOTUS LTS0119214
wikiData Q27292037