Phenalen-1-one

Details

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Internal ID 1bcf99fa-7e77-4054-9765-9f85bb7f07db
Taxonomy Benzenoids > Phenalenes > Phenalenones
IUPAC Name phenalen-1-one
SMILES (Canonical) C1=CC2=C3C(=C1)C=CC(=O)C3=CC=C2
SMILES (Isomeric) C1=CC2=C3C(=C1)C=CC(=O)C3=CC=C2
InChI InChI=1S/C13H8O/c14-12-8-7-10-4-1-3-9-5-2-6-11(12)13(9)10/h1-8H
InChI Key WWBGWPHHLRSTFI-UHFFFAOYSA-N
Popularity 300 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8O
Molecular Weight 180.20 g/mol
Exact Mass 180.057514874 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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PERINAPHTHENONE
1H-Phenalen-1-one
548-39-0
Phenalenone
7-Perinaphthenone
EVU6EX9G8H
NSC-150161
CCRIS 4923
EINECS 208-945-2
NSC 150161
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenalen-1-one

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 + 0.8969 89.69%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.3963 39.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9749 97.49%
OATP1B3 inhibitior + 0.9686 96.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6316 63.16%
P-glycoprotein inhibitior - 0.9647 96.47%
P-glycoprotein substrate - 0.9601 96.01%
CYP3A4 substrate - 0.6279 62.79%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8099 80.99%
CYP3A4 inhibition - 0.8706 87.06%
CYP2C9 inhibition - 0.7691 76.91%
CYP2C19 inhibition + 0.5464 54.64%
CYP2D6 inhibition - 0.8274 82.74%
CYP1A2 inhibition + 0.8825 88.25%
CYP2C8 inhibition - 0.9649 96.49%
CYP inhibitory promiscuity + 0.5790 57.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7710 77.10%
Carcinogenicity (trinary) Non-required 0.4619 46.19%
Eye corrosion - 0.8732 87.32%
Eye irritation + 0.9967 99.67%
Skin irritation + 0.6147 61.47%
Skin corrosion - 0.9864 98.64%
Ames mutagenesis + 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8150 81.50%
Micronuclear - 0.6275 62.75%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.9510 95.10%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.8669 86.69%
Acute Oral Toxicity (c) II 0.4826 48.26%
Estrogen receptor binding + 0.6964 69.64%
Androgen receptor binding + 0.6590 65.90%
Thyroid receptor binding - 0.5270 52.70%
Glucocorticoid receptor binding + 0.5619 56.19%
Aromatase binding + 0.5714 57.14%
PPAR gamma + 0.5732 57.32%
Honey bee toxicity - 0.8784 87.84%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9617 96.17%

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 94.30% 95.56%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 94.05% 96.67%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.46% 91.49%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.00% 85.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.48% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.08% 82.69%
CHEMBL2535 P11166 Glucose transporter 83.70% 98.75%
CHEMBL230 P35354 Cyclooxygenase-2 81.08% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.17% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.02% 86.33%

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.
Musa acuminata

Cross-Links

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PubChem 11050
LOTUS LTS0036770
wikiData Q72500686