14-Methyl-1-oxacyclotetradeca-3,5,9-trien-2-one

Details

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Internal ID ac6923dc-7152-4511-80d2-f2a95fbb9668
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 14-methyl-1-oxacyclotetradeca-3,5,9-trien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O2/c1-13-11-9-7-5-3-2-4-6-8-10-12-14(15)16-13/h3,5-6,8,10,12-13H,2,4,7,9,11H2,1H3
InChI Key SWGHGMVUPRMHSQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O2
Molecular Weight 220.31 g/mol
Exact Mass 220.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.55
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 14-Methyl-1-oxacyclotetradeca-3,5,9-trien-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 + 0.9972 99.72%
Caco-2 + 0.8407 84.07%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Plasma membrane 0.6402 64.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9122 91.22%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7772 77.72%
P-glycoprotein inhibitior - 0.9661 96.61%
P-glycoprotein substrate - 0.9306 93.06%
CYP3A4 substrate - 0.5489 54.89%
CYP2C9 substrate - 0.6339 63.39%
CYP2D6 substrate - 0.8974 89.74%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.9345 93.45%
CYP2C19 inhibition - 0.7578 75.78%
CYP2D6 inhibition - 0.9679 96.79%
CYP1A2 inhibition + 0.5875 58.75%
CYP2C8 inhibition - 0.9683 96.83%
CYP inhibitory promiscuity - 0.9558 95.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.6037 60.37%
Eye corrosion + 0.7525 75.25%
Eye irritation + 0.6054 60.54%
Skin irritation + 0.7260 72.60%
Skin corrosion - 0.9429 94.29%
Ames mutagenesis - 0.6682 66.82%
Human Ether-a-go-go-Related Gene inhibition - 0.5264 52.64%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5053 50.53%
skin sensitisation + 0.6482 64.82%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5703 57.03%
Acute Oral Toxicity (c) III 0.5566 55.66%
Estrogen receptor binding - 0.8402 84.02%
Androgen receptor binding - 0.7832 78.32%
Thyroid receptor binding - 0.7211 72.11%
Glucocorticoid receptor binding - 0.6773 67.73%
Aromatase binding - 0.7373 73.73%
PPAR gamma - 0.6234 62.34%
Honey bee toxicity - 0.9005 90.05%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8682 86.82%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 92.96% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.66% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.69% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.45% 97.25%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.73% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.29% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.29% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.93% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.89% 94.80%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.56% 92.94%

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.
Tecomella undulata

Cross-Links

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PubChem 76418365
LOTUS LTS0046601
wikiData Q105269981