9Z-octadecadien-4R-olide

Details

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Internal ID 9abfaa3e-f831-4c3a-b5df-092a117bf66d
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (5R)-5-[(Z)-tetradec-5-enyl]oxolan-2-one
SMILES (Canonical) CCCCCCCCC=CCCCCC1CCC(=O)O1
SMILES (Isomeric) CCCCCCCC/C=C\CCCC[C@@H]1CCC(=O)O1
InChI InChI=1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-15-16-18(19)20-17/h9-10,17H,2-8,11-16H2,1H3/b10-9-/t17-/m1/s1
InChI Key MFJQEKNPFKHQHP-DOOKAGJSSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O2
Molecular Weight 280.40 g/mol
Exact Mass 280.240230259 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.56
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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CHEMBL454207
CHEBI:196513
(4r,9z)-octadec-9-en-4-olide
LMFA07040064
(5R)-5-[(Z)-tetradec-5-enyl]oxolan-2-one

2D Structure

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2D Structure of 9Z-octadecadien-4R-olide

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 + 0.8364 83.64%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Plasma membrane 0.6778 67.78%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8500 85.00%
OATP1B3 inhibitior + 0.9299 92.99%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.5622 56.22%
P-glycoprotein inhibitior - 0.7980 79.80%
P-glycoprotein substrate - 0.9101 91.01%
CYP3A4 substrate - 0.5368 53.68%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.8843 88.43%
CYP2C9 inhibition - 0.8836 88.36%
CYP2C19 inhibition - 0.5777 57.77%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.5125 51.25%
CYP2C8 inhibition - 0.8530 85.30%
CYP inhibitory promiscuity - 0.8103 81.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6308 63.08%
Eye corrosion + 0.5444 54.44%
Eye irritation + 0.9127 91.27%
Skin irritation + 0.8123 81.23%
Skin corrosion - 0.9313 93.13%
Ames mutagenesis - 0.8752 87.52%
Human Ether-a-go-go-Related Gene inhibition + 0.7456 74.56%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6299 62.99%
skin sensitisation + 0.5836 58.36%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6239 62.39%
Acute Oral Toxicity (c) III 0.5757 57.57%
Estrogen receptor binding - 0.6575 65.75%
Androgen receptor binding - 0.7545 75.45%
Thyroid receptor binding + 0.6423 64.23%
Glucocorticoid receptor binding - 0.6437 64.37%
Aromatase binding - 0.8342 83.42%
PPAR gamma + 0.6309 63.09%
Honey bee toxicity - 0.9810 98.10%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.8353 83.53%
Fish aquatic toxicity + 0.9369 93.69%

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 94.64% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.76% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.54% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.23% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.62% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.96% 97.09%
CHEMBL5255 O00206 Toll-like receptor 4 83.37% 92.50%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 82.84% 90.24%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.71% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.13% 92.08%
CHEMBL2996 Q05655 Protein kinase C delta 81.96% 97.79%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.89% 90.08%
CHEMBL4588 P22894 Matrix metalloproteinase 8 80.08% 94.66%

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.
Micromelum hirsutum

Cross-Links

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PubChem 11323473
LOTUS LTS0261608
wikiData Q105162770