Anthrone

Details

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Internal ID 242a76f3-7fdb-438e-aea8-f98f861c745d
Taxonomy Benzenoids > Anthracenes
IUPAC Name 10H-anthracen-9-one
SMILES (Canonical) C1C2=CC=CC=C2C(=O)C3=CC=CC=C31
SMILES (Isomeric) C1C2=CC=CC=C2C(=O)C3=CC=CC=C31
InChI InChI=1S/C14H10O/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-8H,9H2
InChI Key RJGDLRCDCYRQOQ-UHFFFAOYSA-N
Popularity 7,035 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O
Molecular Weight 194.23 g/mol
Exact Mass 194.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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90-44-8
9(10H)-Anthracenone
Carbothrone
Anthranone
9-Oxoanthracene
anthracen-9(10H)-one
10H-anthracen-9-one
9,10-Dihydro-9-oxoanthracene
Az-O
Anthracene, 9,10-dihydro-9-oxo-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Anthrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8823 88.23%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.5687 56.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9703 97.03%
OATP1B3 inhibitior + 0.9690 96.90%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9216 92.16%
P-glycoprotein substrate - 0.9853 98.53%
CYP3A4 substrate - 0.7150 71.50%
CYP2C9 substrate - 0.8297 82.97%
CYP2D6 substrate - 0.7137 71.37%
CYP3A4 inhibition - 0.9201 92.01%
CYP2C9 inhibition - 0.6074 60.74%
CYP2C19 inhibition - 0.5183 51.83%
CYP2D6 inhibition - 0.7892 78.92%
CYP1A2 inhibition + 0.9478 94.78%
CYP2C8 inhibition - 0.9941 99.41%
CYP inhibitory promiscuity - 0.5602 56.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7810 78.10%
Carcinogenicity (trinary) Non-required 0.5600 56.00%
Eye corrosion - 0.9131 91.31%
Eye irritation + 0.9629 96.29%
Skin irritation + 0.7041 70.41%
Skin corrosion - 0.9812 98.12%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7657 76.57%
Micronuclear - 0.7076 70.76%
Hepatotoxicity + 0.7694 76.94%
skin sensitisation + 0.9122 91.22%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6265 62.65%
Acute Oral Toxicity (c) III 0.6585 65.85%
Estrogen receptor binding + 0.9016 90.16%
Androgen receptor binding - 0.7555 75.55%
Thyroid receptor binding + 0.5475 54.75%
Glucocorticoid receptor binding + 0.6209 62.09%
Aromatase binding + 0.8274 82.74%
PPAR gamma + 0.6387 63.87%
Honey bee toxicity - 0.8516 85.16%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9267 92.67%

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 94.72% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.43% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.67% 82.69%
CHEMBL1951 P21397 Monoamine oxidase A 87.70% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.79% 91.11%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 85.03% 92.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.35% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.43% 96.67%

Plants that contains it

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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.
Rheum officinale
Rheum palmatum
Rheum tanguticum

Cross-Links

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PubChem 7018
NPASS NPC267262
ChEMBL CHEMBL124440