8-Methoxy-14-methyl-1-oxacyclotetradeca-6,9-diene-2,5-dione

Details

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Internal ID ebf626bb-4d3e-47e2-8d7c-84392213c916
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 8-methoxy-14-methyl-1-oxacyclotetradeca-6,9-diene-2,5-dione
SMILES (Canonical) CC1CCCC=CC(C=CC(=O)CCC(=O)O1)OC
SMILES (Isomeric) CC1CCCC=CC(C=CC(=O)CCC(=O)O1)OC
InChI InChI=1S/C15H22O4/c1-12-6-4-3-5-7-14(18-2)10-8-13(16)9-11-15(17)19-12/h5,7-8,10,12,14H,3-4,6,9,11H2,1-2H3
InChI Key ILUIRKCKSQCXHD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Methoxy-14-methyl-1-oxacyclotetradeca-6,9-diene-2,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.8804 88.04%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6681 66.81%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9015 90.15%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5781 57.81%
P-glycoprotein inhibitior - 0.8434 84.34%
P-glycoprotein substrate - 0.9013 90.13%
CYP3A4 substrate + 0.5199 51.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8965 89.65%
CYP3A4 inhibition - 0.8737 87.37%
CYP2C9 inhibition - 0.9397 93.97%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9494 94.94%
CYP1A2 inhibition - 0.6455 64.55%
CYP2C8 inhibition - 0.8818 88.18%
CYP inhibitory promiscuity - 0.9679 96.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8071 80.71%
Carcinogenicity (trinary) Non-required 0.7364 73.64%
Eye corrosion - 0.8463 84.63%
Eye irritation - 0.8397 83.97%
Skin irritation - 0.6866 68.66%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis - 0.7624 76.24%
Human Ether-a-go-go-Related Gene inhibition + 0.6436 64.36%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5447 54.47%
skin sensitisation - 0.8127 81.27%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5522 55.22%
Acute Oral Toxicity (c) III 0.6987 69.87%
Estrogen receptor binding - 0.6061 60.61%
Androgen receptor binding - 0.7514 75.14%
Thyroid receptor binding - 0.6572 65.72%
Glucocorticoid receptor binding + 0.7278 72.78%
Aromatase binding - 0.6991 69.91%
PPAR gamma - 0.6662 66.62%
Honey bee toxicity - 0.8711 87.11%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8330 83.30%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.48% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.91% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.86% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.06% 97.25%
CHEMBL2581 P07339 Cathepsin D 87.78% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.63% 92.94%
CHEMBL4208 P20618 Proteasome component C5 82.88% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.24% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.14% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.96% 99.23%
CHEMBL301 P24941 Cyclin-dependent kinase 2 80.55% 91.23%
CHEMBL5255 O00206 Toll-like receptor 4 80.46% 92.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.38% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.34% 94.80%

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 162816037
LOTUS LTS0204294
wikiData Q104168910