4,5-Dihydrocanthin-6-one

Details

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Internal ID 7d5e766a-d433-4693-91aa-f5e469cb065d
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16),10,12,14-hexaen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H10N2O/c17-13-6-5-11-14-10(7-8-15-11)9-3-1-2-4-12(9)16(13)14/h1-4,7-8H,5-6H2
InChI Key KXBQYMQMSNZAKO-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10N2O
Molecular Weight 222.24 g/mol
Exact Mass 222.079312947 g/mol
Topological Polar Surface Area (TPSA) 34.90 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,5-Dihydrocanthin-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 + 0.8515 85.15%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7574 75.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9703 97.03%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior + 0.5814 58.14%
BSEP inhibitior - 0.7283 72.83%
P-glycoprotein inhibitior - 0.9218 92.18%
P-glycoprotein substrate - 0.8547 85.47%
CYP3A4 substrate + 0.5099 50.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8320 83.20%
CYP3A4 inhibition - 0.7397 73.97%
CYP2C9 inhibition - 0.8510 85.10%
CYP2C19 inhibition - 0.7521 75.21%
CYP2D6 inhibition - 0.7096 70.96%
CYP1A2 inhibition + 0.6453 64.53%
CYP2C8 inhibition - 0.7617 76.17%
CYP inhibitory promiscuity + 0.5211 52.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6195 61.95%
Eye corrosion - 0.9668 96.68%
Eye irritation - 0.7853 78.53%
Skin irritation - 0.6927 69.27%
Skin corrosion - 0.9330 93.30%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5911 59.11%
Micronuclear + 0.5859 58.59%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.8871 88.71%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6712 67.12%
Nephrotoxicity - 0.7262 72.62%
Acute Oral Toxicity (c) III 0.5442 54.42%
Estrogen receptor binding + 0.6724 67.24%
Androgen receptor binding - 0.6289 62.89%
Thyroid receptor binding + 0.6465 64.65%
Glucocorticoid receptor binding + 0.5734 57.34%
Aromatase binding + 0.6366 63.66%
PPAR gamma + 0.6727 67.27%
Honey bee toxicity - 0.9239 92.39%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.9160 91.60%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.06% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 92.70% 91.49%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 90.68% 96.47%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.41% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.95% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.63% 89.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 88.77% 92.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.89% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.91% 96.09%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 85.75% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.61% 98.95%
CHEMBL2535 P11166 Glucose transporter 85.61% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.80% 91.11%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 82.75% 95.50%
CHEMBL3384 Q16512 Protein kinase N1 82.67% 80.71%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.40% 96.67%

Cross-Links

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PubChem 76316632
NPASS NPC56233
LOTUS LTS0102173
wikiData Q105147265