(S)-gamma-Octanolactone

Details

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Internal ID 191368aa-9e5d-47bf-9ed8-aa2bab7eb385
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (5S)-5-butyloxolan-2-one
SMILES (Canonical) CCCCC1CCC(=O)O1
SMILES (Isomeric) CCCC[C@H]1CCC(=O)O1
InChI InChI=1S/C8H14O2/c1-2-3-4-7-5-6-8(9)10-7/h7H,2-6H2,1H3/t7-/m0/s1
InChI Key IPBFYZQJXZJBFQ-ZETCQYMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O2
Molecular Weight 142.20 g/mol
Exact Mass 142.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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5-butyl-dihydro-furan-2-one
SCHEMBL2077469

2D Structure

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2D Structure of (S)-gamma-Octanolactone

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 + 0.8055 80.55%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Plasma membrane 0.5012 50.12%
OATP2B1 inhibitior - 0.8425 84.25%
OATP1B1 inhibitior + 0.9222 92.22%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9449 94.49%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9381 93.81%
CYP3A4 substrate - 0.6309 63.09%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.8634 86.34%
CYP3A4 inhibition - 0.9363 93.63%
CYP2C9 inhibition - 0.8382 83.82%
CYP2C19 inhibition - 0.6159 61.59%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition - 0.6366 63.66%
CYP2C8 inhibition - 0.9395 93.95%
CYP inhibitory promiscuity - 0.9058 90.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6541 65.41%
Eye corrosion + 0.7454 74.54%
Eye irritation + 0.9690 96.90%
Skin irritation + 0.7308 73.08%
Skin corrosion - 0.8572 85.72%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7002 70.02%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.5906 59.06%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.7986 79.86%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5385 53.85%
Acute Oral Toxicity (c) III 0.8612 86.12%
Estrogen receptor binding - 0.9455 94.55%
Androgen receptor binding - 0.8742 87.42%
Thyroid receptor binding - 0.8629 86.29%
Glucocorticoid receptor binding - 0.9011 90.11%
Aromatase binding - 0.8515 85.15%
PPAR gamma - 0.8457 84.57%
Honey bee toxicity - 0.9897 98.97%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.5448 54.48%
Fish aquatic toxicity + 0.8247 82.47%

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 93.76% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.75% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.33% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.69% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.96% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 82.90% 97.79%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.84% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.42% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.30% 99.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.07% 100.00%

Cross-Links

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PubChem 7057972
NPASS NPC160126
LOTUS LTS0248611
wikiData Q105117041