5-Decyl-3-(2-hydroxyethyl)oxolan-2-one

Details

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Internal ID 1c0e4d7f-25ba-415d-bcbe-35d67628eb17
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 5-decyl-3-(2-hydroxyethyl)oxolan-2-one
SMILES (Canonical) CCCCCCCCCCC1CC(C(=O)O1)CCO
SMILES (Isomeric) CCCCCCCCCCC1CC(C(=O)O1)CCO
InChI InChI=1S/C16H30O3/c1-2-3-4-5-6-7-8-9-10-15-13-14(11-12-17)16(18)19-15/h14-15,17H,2-13H2,1H3
InChI Key WTYOCFGPMRJBIX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H30O3
Molecular Weight 270.41 g/mol
Exact Mass 270.21949481 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Decyl-3-(2-hydroxyethyl)oxolan-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 + 0.9882 98.82%
Caco-2 + 0.5461 54.61%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6510 65.10%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9303 93.03%
OATP1B3 inhibitior + 0.9352 93.52%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.6893 68.93%
P-glycoprotein inhibitior - 0.9080 90.80%
P-glycoprotein substrate - 0.7618 76.18%
CYP3A4 substrate - 0.5614 56.14%
CYP2C9 substrate - 0.5827 58.27%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.7899 78.99%
CYP2C9 inhibition - 0.8610 86.10%
CYP2C19 inhibition - 0.8242 82.42%
CYP2D6 inhibition - 0.9290 92.90%
CYP1A2 inhibition - 0.8293 82.93%
CYP2C8 inhibition - 0.9317 93.17%
CYP inhibitory promiscuity - 0.9353 93.53%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7324 73.24%
Eye corrosion - 0.9566 95.66%
Eye irritation + 0.7253 72.53%
Skin irritation + 0.6321 63.21%
Skin corrosion - 0.8839 88.39%
Ames mutagenesis - 0.8878 88.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4711 47.11%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5617 56.17%
skin sensitisation - 0.8579 85.79%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7653 76.53%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.7268 72.68%
Acute Oral Toxicity (c) III 0.7079 70.79%
Estrogen receptor binding - 0.6303 63.03%
Androgen receptor binding - 0.5892 58.92%
Thyroid receptor binding + 0.5871 58.71%
Glucocorticoid receptor binding - 0.5052 50.52%
Aromatase binding - 0.8006 80.06%
PPAR gamma - 0.5681 56.81%
Honey bee toxicity - 0.9779 97.79%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.6270 62.70%
Fish aquatic toxicity + 0.7929 79.29%

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
CHEMBL230 P35354 Cyclooxygenase-2 97.75% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.27% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.73% 97.29%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.78% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.43% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.29% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 88.32% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.44% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.43% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.71% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.19% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.91% 92.08%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.36% 90.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.92% 91.81%

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.
Sextonia rubra

Cross-Links

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PubChem 162927276
LOTUS LTS0143967
wikiData Q104200636