1-Cyclopentylhexacosan-4-one

Details

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Internal ID 8322eb05-3a0c-4b89-a15d-c9e285797930
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 1-cyclopentylhexacosan-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H60O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-28-31(32)29-24-27-30-25-22-23-26-30/h30H,2-29H2,1H3
InChI Key JDCUYANHWUVPEM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H60O
Molecular Weight 448.80 g/mol
Exact Mass 448.464416533 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 14.10
Atomic LogP (AlogP) 11.13
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Cyclopentylhexacosan-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 - 0.6324 63.24%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.3582 35.82%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9330 93.30%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4529 45.29%
P-glycoprotein inhibitior - 0.7119 71.19%
P-glycoprotein substrate - 0.8614 86.14%
CYP3A4 substrate - 0.5777 57.77%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9840 98.40%
CYP2C9 inhibition - 0.9154 91.54%
CYP2C19 inhibition - 0.9192 91.92%
CYP2D6 inhibition - 0.9537 95.37%
CYP1A2 inhibition + 0.6512 65.12%
CYP2C8 inhibition - 0.8170 81.70%
CYP inhibitory promiscuity - 0.8455 84.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6853 68.53%
Eye corrosion + 0.9531 95.31%
Eye irritation + 0.9261 92.61%
Skin irritation + 0.8291 82.91%
Skin corrosion - 0.8935 89.35%
Ames mutagenesis - 0.9337 93.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4646 46.46%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5602 56.02%
skin sensitisation + 0.7916 79.16%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7073 70.73%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.7742 77.42%
Acute Oral Toxicity (c) III 0.7607 76.07%
Estrogen receptor binding - 0.7648 76.48%
Androgen receptor binding - 0.8830 88.30%
Thyroid receptor binding + 0.5809 58.09%
Glucocorticoid receptor binding + 0.5870 58.70%
Aromatase binding - 0.6523 65.23%
PPAR gamma - 0.5354 53.54%
Honey bee toxicity - 0.9915 99.15%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8223 82.23%
Fish aquatic toxicity + 0.8562 85.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.73% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.54% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 96.23% 89.63%
CHEMBL2581 P07339 Cathepsin D 95.53% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.15% 95.17%
CHEMBL220 P22303 Acetylcholinesterase 92.64% 94.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 92.29% 100.00%
CHEMBL240 Q12809 HERG 91.92% 89.76%
CHEMBL5255 O00206 Toll-like receptor 4 91.83% 92.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.46% 99.17%
CHEMBL1968 P07099 Epoxide hydrolase 1 90.57% 98.57%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.06% 93.56%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 90.04% 90.24%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.45% 85.94%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 87.93% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.79% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.18% 82.69%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.87% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.22% 97.29%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.09% 98.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.69% 91.11%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.01% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.87% 93.04%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.86% 95.27%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.36% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 81.76% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.01% 96.61%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.90% 96.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.66% 93.03%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.54% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.34% 92.86%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.11% 97.50%

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.
Ligularia macrophylla

Cross-Links

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PubChem 14132245
LOTUS LTS0043563
wikiData Q105125374