Canthin-6-One

Details

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Internal ID a27061ff-3f4c-4cfb-a27f-d305c5c9073c
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one
SMILES (Canonical) C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3
SMILES (Isomeric) C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3
InChI InChI=1S/C14H8N2O/c17-13-6-5-11-14-10(7-8-15-11)9-3-1-2-4-12(9)16(13)14/h1-8H
InChI Key ZERVJPYNQLONEK-UHFFFAOYSA-N
Popularity 144 references in papers

Physical and Chemical Properties

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Molecular Formula C14H8N2O
Molecular Weight 220.23 g/mol
Exact Mass 220.063662883 g/mol
Topological Polar Surface Area (TPSA) 34.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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479-43-6
6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one
NSC 103003
NSC-103003
6H-Indolo(3,2,1-de)(1,5)naphthyridin-6-one
UNII-3FK17S759N
CHEBI:3363
Indolo[3,2,1-de][1,5]naphthyridin-6-one
3FK17S759N
1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-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 Canthin-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 + 0.9961 99.61%
Caco-2 + 0.7895 78.95%
Blood Brain Barrier + 0.8567 85.67%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7974 79.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9676 96.76%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8364 83.64%
BSEP inhibitior - 0.5271 52.71%
P-glycoprotein inhibitior - 0.9121 91.21%
P-glycoprotein substrate - 0.8909 89.09%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.8539 85.39%
CYP3A4 inhibition + 0.5412 54.12%
CYP2C9 inhibition - 0.9053 90.53%
CYP2C19 inhibition - 0.8515 85.15%
CYP2D6 inhibition - 0.7147 71.47%
CYP1A2 inhibition + 0.9339 93.39%
CYP2C8 inhibition - 0.6783 67.83%
CYP inhibitory promiscuity - 0.5364 53.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9423 94.23%
Carcinogenicity (trinary) Non-required 0.5753 57.53%
Eye corrosion - 0.9522 95.22%
Eye irritation + 0.8291 82.91%
Skin irritation - 0.6670 66.70%
Skin corrosion - 0.9546 95.46%
Ames mutagenesis + 0.7230 72.30%
Human Ether-a-go-go-Related Gene inhibition - 0.7207 72.07%
Micronuclear + 0.7459 74.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8233 82.33%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4710 47.10%
Acute Oral Toxicity (c) III 0.4674 46.74%
Estrogen receptor binding + 0.7012 70.12%
Androgen receptor binding - 0.5278 52.78%
Thyroid receptor binding + 0.7518 75.18%
Glucocorticoid receptor binding + 0.8513 85.13%
Aromatase binding + 0.7796 77.96%
PPAR gamma + 0.6340 63.40%
Honey bee toxicity - 0.8926 89.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.5679 56.79%

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
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.21% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.72% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.96% 98.95%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 91.47% 96.47%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.65% 85.14%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 87.99% 92.67%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.82% 94.62%
CHEMBL3524 P56524 Histone deacetylase 4 86.88% 92.97%
CHEMBL2535 P11166 Glucose transporter 86.38% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.13% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.96% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.68% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.72% 93.99%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 81.64% 95.83%
CHEMBL2954 P25774 Cathepsin S 81.41% 95.60%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 80.93% 85.49%
CHEMBL1781 P11387 DNA topoisomerase I 80.10% 97.00%

Cross-Links

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PubChem 97176
NPASS NPC293487
ChEMBL CHEMBL156897
LOTUS LTS0216343
wikiData Q27106045