(5S)-5-hexyloxolan-2-one

Details

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Internal ID c47408cd-1f47-455c-b4ed-af8fbfa96ec2
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (5S)-5-hexyloxolan-2-one
SMILES (Canonical) CCCCCCC1CCC(=O)O1
SMILES (Isomeric) CCCCCC[C@H]1CCC(=O)O1
InChI InChI=1S/C10H18O2/c1-2-3-4-5-6-9-7-8-10(11)12-9/h9H,2-8H2,1H3/t9-/m0/s1
InChI Key IFYYFLINQYPWGJ-VIFPVBQESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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(S)-gamma-Decalactone
107797-27-3
(R)-.gamma.-decalactone
(5S)-5-hexyl-2-oxolanone
SCHEMBL9392299
IFYYFLINQYPWGJ-VIFPVBQESA-N
A836936

2D Structure

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2D Structure of (5S)-5-hexyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8269 82.69%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.4605 46.05%
OATP2B1 inhibitior - 0.8431 84.31%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8899 88.99%
P-glycoprotein inhibitior - 0.9735 97.35%
P-glycoprotein substrate - 0.9127 91.27%
CYP3A4 substrate - 0.5958 59.58%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.8634 86.34%
CYP3A4 inhibition - 0.9096 90.96%
CYP2C9 inhibition - 0.8493 84.93%
CYP2C19 inhibition - 0.6249 62.49%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition - 0.6255 62.55%
CYP2C8 inhibition - 0.9182 91.82%
CYP inhibitory promiscuity - 0.9030 90.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6560 65.60%
Eye corrosion + 0.6594 65.94%
Eye irritation + 0.9611 96.11%
Skin irritation + 0.8099 80.99%
Skin corrosion - 0.8543 85.43%
Ames mutagenesis - 0.9152 91.52%
Human Ether-a-go-go-Related Gene inhibition - 0.6408 64.08%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5701 57.01%
skin sensitisation - 0.5935 59.35%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8542 85.42%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5224 52.24%
Acute Oral Toxicity (c) III 0.6100 61.00%
Estrogen receptor binding - 0.8560 85.60%
Androgen receptor binding - 0.8511 85.11%
Thyroid receptor binding - 0.8620 86.20%
Glucocorticoid receptor binding - 0.7931 79.31%
Aromatase binding - 0.8286 82.86%
PPAR gamma - 0.6706 67.06%
Honey bee toxicity - 0.9885 98.85%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.7904 79.04%
Fish aquatic toxicity + 0.8534 85.34%

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 94.02% 98.95%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 91.53% 90.24%
CHEMBL230 P35354 Cyclooxygenase-2 90.16% 89.63%
CHEMBL2996 Q05655 Protein kinase C delta 89.55% 97.79%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.88% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.33% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.72% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.47% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.27% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.15% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 82.54% 92.50%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.52% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.03% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.82% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.07% 100.00%

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.
Akebia quinata
Akebia trifoliata
Angelica acutiloba
Angelica gigas
Angelica sinensis
Daucus carota
Glehnia littoralis

Cross-Links

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PubChem 7057904
NPASS NPC52309
LOTUS LTS0132445
wikiData Q105112487