Cyclopentanone

Details

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Internal ID eece4f36-a082-452e-9d7e-4c720236d470
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name cyclopentanone
SMILES (Canonical) C1CCC(=O)C1
SMILES (Isomeric) C1CCC(=O)C1
InChI InChI=1S/C5H8O/c6-5-3-1-2-4-5/h1-4H2
InChI Key BGTOWKSIORTVQH-UHFFFAOYSA-N
Popularity 3,540 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O
Molecular Weight 84.12 g/mol
Exact Mass 84.057514874 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.13
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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120-92-3
Adipic ketone
Ketocyclopentane
Ketopentamethylene
Dumasin
Adipinketon
cyclopentan-1-one
oxocyclopentane
Adipin keton
NSC 4122
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclopentanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.8436 84.36%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.6539 65.39%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9842 98.42%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9392 93.92%
P-glycoprotein inhibitior - 0.9874 98.74%
P-glycoprotein substrate - 0.9976 99.76%
CYP3A4 substrate - 0.8261 82.61%
CYP2C9 substrate - 0.8484 84.84%
CYP2D6 substrate - 0.7422 74.22%
CYP3A4 inhibition - 0.9741 97.41%
CYP2C9 inhibition - 0.8830 88.30%
CYP2C19 inhibition - 0.9138 91.38%
CYP2D6 inhibition - 0.9603 96.03%
CYP1A2 inhibition - 0.8011 80.11%
CYP2C8 inhibition - 0.9980 99.80%
CYP inhibitory promiscuity - 0.9362 93.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6413 64.13%
Eye corrosion + 0.9874 98.74%
Eye irritation + 0.9951 99.51%
Skin irritation + 0.7828 78.28%
Skin corrosion - 0.5424 54.24%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7934 79.34%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation - 0.5818 58.18%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5619 56.19%
Acute Oral Toxicity (c) III 0.5772 57.72%
Estrogen receptor binding - 0.9654 96.54%
Androgen receptor binding - 0.9576 95.76%
Thyroid receptor binding - 0.9210 92.10%
Glucocorticoid receptor binding - 0.9185 91.85%
Aromatase binding - 0.8686 86.86%
PPAR gamma - 0.8934 89.34%
Honey bee toxicity - 0.9165 91.65%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.8685 86.85%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL2176772 Q9UPN9 E3 ubiquitin-protein ligase TRIM33 233.5 nM
IC50
via Super-PRED
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 135.8 nM
IC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 84.48% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.65% 91.11%

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.
Coffea arabica
Crocus sativus
Vitis rotundifolia

Cross-Links

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PubChem 8452
NPASS NPC254524
LOTUS LTS0051781
wikiData Q416065