4,8,12-Trimethyl-1-oxacyclotrideca-3,7,11-trien-2-one

Details

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Internal ID d675964d-470d-4a74-bcb1-16b814e885dd
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 4,8,12-trimethyl-1-oxacyclotrideca-3,7,11-trien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-12-6-4-8-13(2)10-15(16)17-11-14(3)9-5-7-12/h6,9-10H,4-5,7-8,11H2,1-3H3
InChI Key NMEKMYDKPCWTTQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.94
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 4,8,12-Trimethyl-1-oxacyclotrideca-3,7,11-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 + 0.9968 99.68%
Caco-2 + 0.9612 96.12%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.4355 43.55%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9752 97.52%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6476 64.76%
P-glycoprotein inhibitior - 0.9321 93.21%
P-glycoprotein substrate - 0.9440 94.40%
CYP3A4 substrate - 0.6250 62.50%
CYP2C9 substrate + 0.5814 58.14%
CYP2D6 substrate - 0.9053 90.53%
CYP3A4 inhibition - 0.8908 89.08%
CYP2C9 inhibition - 0.8413 84.13%
CYP2C19 inhibition - 0.7050 70.50%
CYP2D6 inhibition - 0.9072 90.72%
CYP1A2 inhibition + 0.5552 55.52%
CYP2C8 inhibition - 0.9679 96.79%
CYP inhibitory promiscuity - 0.9072 90.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.5947 59.47%
Eye corrosion - 0.6990 69.90%
Eye irritation + 0.7226 72.26%
Skin irritation + 0.5077 50.77%
Skin corrosion - 0.9813 98.13%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7151 71.51%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.5855 58.55%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7541 75.41%
Acute Oral Toxicity (c) III 0.6342 63.42%
Estrogen receptor binding - 0.7382 73.82%
Androgen receptor binding - 0.6315 63.15%
Thyroid receptor binding - 0.7317 73.17%
Glucocorticoid receptor binding - 0.5093 50.93%
Aromatase binding - 0.6941 69.41%
PPAR gamma - 0.5083 50.83%
Honey bee toxicity - 0.9217 92.17%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9771 97.71%

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 93.08% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.93% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 85.92% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.52% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.43% 93.40%
CHEMBL3401 O75469 Pregnane X receptor 83.48% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.81% 100.00%

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 85312537
LOTUS LTS0058952
wikiData Q105181725