2-Ethylcyclopentanone

Details

Top
Internal ID e2dd8ba6-4422-4a1f-8e72-c94b8966602a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-ethylcyclopentan-1-one
SMILES (Canonical) CCC1CCCC1=O
SMILES (Isomeric) CCC1CCCC1=O
InChI InChI=1S/C7H12O/c1-2-6-4-3-5-7(6)8/h6H,2-5H2,1H3
InChI Key PPTKUTYPOKHBTL-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H12O
Molecular Weight 112.17 g/mol
Exact Mass 112.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
4971-18-0
2-Ethylcyclopentan-1-one
5-Ethylcyclopentanone
Cyclopentanone, 2-ethyl-
EINECS 225-612-7
61215-75-6
NSC105441
SCHEMBL2689519
DTXSID70976723
PPTKUTYPOKHBTL-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2-Ethylcyclopentanone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8076 80.76%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6049 60.49%
OATP2B1 inhibitior - 0.8276 82.76%
OATP1B1 inhibitior + 0.9522 95.22%
OATP1B3 inhibitior + 0.9590 95.90%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9376 93.76%
P-glycoprotein inhibitior - 0.9906 99.06%
P-glycoprotein substrate - 0.9721 97.21%
CYP3A4 substrate - 0.7283 72.83%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.8863 88.63%
CYP2C19 inhibition - 0.8991 89.91%
CYP2D6 inhibition - 0.9348 93.48%
CYP1A2 inhibition - 0.6799 67.99%
CYP2C8 inhibition - 0.9838 98.38%
CYP inhibitory promiscuity - 0.8895 88.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6938 69.38%
Eye corrosion + 0.7562 75.62%
Eye irritation + 0.9924 99.24%
Skin irritation + 0.7899 78.99%
Skin corrosion - 0.7768 77.68%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7347 73.47%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7676 76.76%
skin sensitisation + 0.7531 75.31%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5537 55.37%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6918 69.18%
Acute Oral Toxicity (c) III 0.8692 86.92%
Estrogen receptor binding - 0.9486 94.86%
Androgen receptor binding - 0.9094 90.94%
Thyroid receptor binding - 0.9415 94.15%
Glucocorticoid receptor binding - 0.9059 90.59%
Aromatase binding - 0.8985 89.85%
PPAR gamma - 0.9102 91.02%
Honey bee toxicity - 0.9797 97.97%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.7923 79.23%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.81% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.00% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.50% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.75% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.95% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 80.70% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.07% 100.00%

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.
Citrus × aurantium
Citrus trifoliata

Cross-Links

Top
PubChem 92991
NPASS NPC144855