2-(13-Acetyloxytridecyl)-4-methylidene-5-oxooxolane-3-carboxylic acid

Details

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Internal ID a55ef0b6-5283-46c1-a9bb-8cf7919ad8db
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 2-(13-acetyloxytridecyl)-4-methylidene-5-oxooxolane-3-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H34O6/c1-16-19(20(23)24)18(27-21(16)25)14-12-10-8-6-4-3-5-7-9-11-13-15-26-17(2)22/h18-19H,1,3-15H2,2H3,(H,23,24)
InChI Key UJAPYEXSFLHVPF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H34O6
Molecular Weight 382.50 g/mol
Exact Mass 382.23553880 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(13-Acetyloxytridecyl)-4-methylidene-5-oxooxolane-3-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9449 94.49%
Caco-2 - 0.7586 75.86%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8482 84.82%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9067 90.67%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7775 77.75%
P-glycoprotein inhibitior - 0.5959 59.59%
P-glycoprotein substrate - 0.9355 93.55%
CYP3A4 substrate + 0.5633 56.33%
CYP2C9 substrate + 0.5894 58.94%
CYP2D6 substrate - 0.9079 90.79%
CYP3A4 inhibition - 0.8218 82.18%
CYP2C9 inhibition - 0.8243 82.43%
CYP2C19 inhibition - 0.7896 78.96%
CYP2D6 inhibition - 0.9079 90.79%
CYP1A2 inhibition - 0.5925 59.25%
CYP2C8 inhibition - 0.8604 86.04%
CYP inhibitory promiscuity - 0.8605 86.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.7315 73.15%
Eye corrosion - 0.9539 95.39%
Eye irritation - 0.5859 58.59%
Skin irritation + 0.5188 51.88%
Skin corrosion - 0.9234 92.34%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4506 45.06%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8605 86.05%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.7803 78.03%
Acute Oral Toxicity (c) III 0.6872 68.72%
Estrogen receptor binding + 0.6336 63.36%
Androgen receptor binding + 0.5557 55.57%
Thyroid receptor binding - 0.5402 54.02%
Glucocorticoid receptor binding + 0.6052 60.52%
Aromatase binding - 0.5967 59.67%
PPAR gamma - 0.5273 52.73%
Honey bee toxicity - 0.8874 88.74%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5274 52.74%
Fish aquatic toxicity + 0.9793 97.93%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.62% 94.62%
CHEMBL4040 P28482 MAP kinase ERK2 93.90% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.13% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.02% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.32% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.05% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.32% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.22% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.79% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162909664
LOTUS LTS0141737
wikiData Q105273826