Anthracenone

Details

Top
Internal ID da7c60d4-09ae-4c39-ba95-f056505bb63b
Taxonomy Benzenoids > Anthracenes
IUPAC Name 2H-anthracen-1-one
SMILES (Canonical) C1C=CC2=CC3=CC=CC=C3C=C2C1=O
SMILES (Isomeric) C1C=CC2=CC3=CC=CC=C3C=C2C1=O
InChI InChI=1S/C14H10O/c15-14-7-3-6-12-8-10-4-1-2-5-11(10)9-13(12)14/h1-6,8-9H,7H2
InChI Key MRVNKBNZHOHVER-UHFFFAOYSA-N
Popularity 77 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H10O
Molecular Weight 194.23 g/mol
Exact Mass 194.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
101843-14-5
Anthracen-1(2H)-one
2H-anthracen-1-one;Anthrone
SCHEMBL5794930
DTXSID60595129
A843554

2D Structure

Top
2D Structure of Anthracenone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8995 89.95%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4429 44.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9628 96.28%
OATP1B3 inhibitior + 0.9719 97.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5670 56.70%
P-glycoprotein inhibitior - 0.9626 96.26%
P-glycoprotein substrate - 0.9695 96.95%
CYP3A4 substrate - 0.6029 60.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7860 78.60%
CYP3A4 inhibition - 0.8089 80.89%
CYP2C9 inhibition + 0.5819 58.19%
CYP2C19 inhibition + 0.7973 79.73%
CYP2D6 inhibition - 0.7209 72.09%
CYP1A2 inhibition + 0.9193 91.93%
CYP2C8 inhibition - 0.9640 96.40%
CYP inhibitory promiscuity + 0.6158 61.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8110 81.10%
Carcinogenicity (trinary) Non-required 0.5344 53.44%
Eye corrosion - 0.9286 92.86%
Eye irritation + 0.8679 86.79%
Skin irritation + 0.5769 57.69%
Skin corrosion - 0.9829 98.29%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6830 68.30%
Micronuclear - 0.7183 71.83%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9455 94.55%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6242 62.42%
Acute Oral Toxicity (c) II 0.5661 56.61%
Estrogen receptor binding + 0.7204 72.04%
Androgen receptor binding + 0.5636 56.36%
Thyroid receptor binding - 0.6586 65.86%
Glucocorticoid receptor binding + 0.6185 61.85%
Aromatase binding + 0.8518 85.18%
PPAR gamma + 0.6477 64.77%
Honey bee toxicity - 0.9061 90.61%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9408 94.08%

Targets

Top

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 92.63% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.32% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.06% 91.11%
CHEMBL240 Q12809 HERG 90.44% 89.76%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.00% 82.69%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.11% 96.67%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.66% 92.67%
CHEMBL2535 P11166 Glucose transporter 83.66% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.67% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.30% 99.23%
CHEMBL4208 P20618 Proteasome component C5 80.27% 90.00%

Plants that contains it

Top
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.
Karwinskia humboldtiana

Cross-Links

Top
PubChem 18614983
LOTUS LTS0234094
wikiData Q82490071