11-(Methylthiono)canthin-6-one

Details

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Internal ID 249ee0be-bbad-4857-b19e-95692228baef
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 11-methylsulfanyl-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10N2OS/c1-19-12-4-2-3-11-14(12)9-7-8-16-10-5-6-13(18)17(11)15(9)10/h2-8H,1H3
InChI Key WNKZMIHGWYGQLX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10N2OS
Molecular Weight 266.32 g/mol
Exact Mass 266.05138412 g/mol
Topological Polar Surface Area (TPSA) 60.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 11-(Methylthiono)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 + 0.9931 99.31%
Caco-2 + 0.5883 58.83%
Blood Brain Barrier + 0.9317 93.17%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7229 72.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7481 74.81%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8459 84.59%
P-glycoprotein substrate - 0.6777 67.77%
CYP3A4 substrate + 0.5325 53.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8440 84.40%
CYP3A4 inhibition + 0.7631 76.31%
CYP2C9 inhibition - 0.6758 67.58%
CYP2C19 inhibition - 0.6708 67.08%
CYP2D6 inhibition - 0.8498 84.98%
CYP1A2 inhibition + 0.9463 94.63%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.5341 53.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9323 93.23%
Carcinogenicity (trinary) Non-required 0.5282 52.82%
Eye corrosion - 0.9740 97.40%
Eye irritation - 0.6445 64.45%
Skin irritation - 0.6843 68.43%
Skin corrosion - 0.9143 91.43%
Ames mutagenesis + 0.7446 74.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6552 65.52%
Micronuclear + 0.7859 78.59%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8160 81.60%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6596 65.96%
Acute Oral Toxicity (c) III 0.5800 58.00%
Estrogen receptor binding + 0.8835 88.35%
Androgen receptor binding - 0.4914 49.14%
Thyroid receptor binding + 0.7260 72.60%
Glucocorticoid receptor binding + 0.9362 93.62%
Aromatase binding + 0.9054 90.54%
PPAR gamma + 0.5997 59.97%
Honey bee toxicity - 0.8344 83.44%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.4257 42.57%

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
CHEMBL2581 P07339 Cathepsin D 96.85% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 94.98% 89.63%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.66% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.19% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.07% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.97% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 87.83% 93.10%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.46% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.43% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.41% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.15% 93.65%
CHEMBL2535 P11166 Glucose transporter 84.04% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.45% 93.99%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.16% 100.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.68% 96.47%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.72% 96.67%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.34% 90.08%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11471113
LOTUS LTS0178462
wikiData Q77501283