6-Hexadecanolactone

Details

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Internal ID 3a9f88bc-3ef7-4f21-93eb-2aa9d3866d95
Taxonomy Organoheterocyclic compounds > Lactones
IUPAC Name 7-decyloxepan-2-one
SMILES (Canonical) CCCCCCCCCCC1CCCCC(=O)O1
SMILES (Isomeric) CCCCCCCCCCC1CCCCC(=O)O1
InChI InChI=1S/C16H30O2/c1-2-3-4-5-6-7-8-9-12-15-13-10-11-14-16(17)18-15/h15H,2-14H2,1H3
InChI Key JDBCCUBGERLOBZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H30O2
Molecular Weight 254.41 g/mol
Exact Mass 254.224580195 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.00
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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6-hexadecanolactone
SCHEMBL2959263
JDBCCUBGERLOBZ-UHFFFAOYSA-N

2D Structure

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2D Structure of 6-Hexadecanolactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.7552 75.52%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Plasma membrane 0.4705 47.05%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.4732 47.32%
P-glycoprotein inhibitior - 0.8771 87.71%
P-glycoprotein substrate - 0.8817 88.17%
CYP3A4 substrate - 0.5565 55.65%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.8634 86.34%
CYP3A4 inhibition - 0.9349 93.49%
CYP2C9 inhibition - 0.8769 87.69%
CYP2C19 inhibition - 0.7651 76.51%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.5810 58.10%
CYP2C8 inhibition - 0.8953 89.53%
CYP inhibitory promiscuity - 0.9517 95.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6622 66.22%
Eye corrosion + 0.7520 75.20%
Eye irritation + 0.9610 96.10%
Skin irritation + 0.7278 72.78%
Skin corrosion - 0.8392 83.92%
Ames mutagenesis - 0.8315 83.15%
Human Ether-a-go-go-Related Gene inhibition - 0.4427 44.27%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5693 56.93%
skin sensitisation - 0.5387 53.87%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8650 86.50%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.5915 59.15%
Acute Oral Toxicity (c) III 0.6911 69.11%
Estrogen receptor binding - 0.8241 82.41%
Androgen receptor binding - 0.8696 86.96%
Thyroid receptor binding - 0.4904 49.04%
Glucocorticoid receptor binding - 0.7097 70.97%
Aromatase binding - 0.8134 81.34%
PPAR gamma - 0.5246 52.46%
Honey bee toxicity - 0.9855 98.55%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.8082 80.82%
Fish aquatic toxicity + 0.8292 82.92%

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
CHEMBL2581 P07339 Cathepsin D 97.39% 98.95%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 92.81% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.57% 97.25%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.78% 100.00%
CHEMBL230 P35354 Cyclooxygenase-2 88.51% 89.63%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.72% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 87.39% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.06% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 85.77% 92.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.45% 90.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.54% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.24% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.14% 93.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.64% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.83% 92.62%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.11% 91.81%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.08% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.71% 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.
Ageratina viscosa

Cross-Links

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PubChem 17949562
LOTUS LTS0177175
wikiData Q105125322