1-Oxacyclooctadeca-3,5-dien-2-one

Details

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Internal ID 72d70a9d-7bea-4bee-83e4-260120faa286
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 1-oxacyclooctadeca-3,5-dien-2-one
SMILES (Canonical) C1CCCCCCOC(=O)C=CC=CCCCCC1
SMILES (Isomeric) C1CCCCCCOC(=O)C=CC=CCCCCC1
InChI InChI=1S/C17H28O2/c18-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-19-17/h9,11,13,15H,1-8,10,12,14,16H2
InChI Key GILHVBYSAHCJJY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O2
Molecular Weight 264.40 g/mol
Exact Mass 264.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 6.50
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Oxacyclooctadeca-3,5-dien-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 + 0.9956 99.56%
Caco-2 + 0.6635 66.35%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4747 47.47%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9191 91.91%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.4559 45.59%
P-glycoprotein inhibitior - 0.8977 89.77%
P-glycoprotein substrate - 0.9833 98.33%
CYP3A4 substrate - 0.6523 65.23%
CYP2C9 substrate - 0.8155 81.55%
CYP2D6 substrate - 0.8775 87.75%
CYP3A4 inhibition - 0.9756 97.56%
CYP2C9 inhibition - 0.9091 90.91%
CYP2C19 inhibition - 0.8715 87.15%
CYP2D6 inhibition - 0.9602 96.02%
CYP1A2 inhibition - 0.8434 84.34%
CYP2C8 inhibition - 0.9739 97.39%
CYP inhibitory promiscuity - 0.9667 96.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.6555 65.55%
Eye corrosion + 0.9766 97.66%
Eye irritation + 0.9890 98.90%
Skin irritation - 0.5413 54.13%
Skin corrosion - 0.9892 98.92%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6985 69.85%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5928 59.28%
skin sensitisation - 0.8354 83.54%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6197 61.97%
Acute Oral Toxicity (c) II 0.7312 73.12%
Estrogen receptor binding - 0.6831 68.31%
Androgen receptor binding - 0.5659 56.59%
Thyroid receptor binding - 0.6159 61.59%
Glucocorticoid receptor binding - 0.7530 75.30%
Aromatase binding - 0.6541 65.41%
PPAR gamma - 0.5464 54.64%
Honey bee toxicity - 0.8706 87.06%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.3999 39.99%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.26% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.87% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 87.05% 89.63%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.62% 94.45%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 82.45% 87.67%
CHEMBL2581 P07339 Cathepsin D 82.37% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.16% 96.77%

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.
Angelica archangelica

Cross-Links

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PubChem 163192801
LOTUS LTS0029180
wikiData Q105009089