miller-9E-enolide

Details

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Internal ID 27033c02-e2f0-4e68-bba5-74c85aea4d2b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name [(3aR,4R,5E,11S,11aS)-6-formyl-11-hydroxy-3,10-dimethylidene-2-oxo-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl] 2-methylprop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22O6/c1-10(2)18(22)24-14-8-13(9-20)7-5-6-11(3)16(21)17-15(14)12(4)19(23)25-17/h8-9,14-17,21H,1,3-7H2,2H3/b13-8+/t14-,15-,16+,17+/m1/s1
InChI Key CCWGXWKAXMNGSZ-PBMXCAIQSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O6
Molecular Weight 346.40 g/mol
Exact Mass 346.14163842 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEMBL187789

2D Structure

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2D Structure of miller-9E-enolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9608 96.08%
Caco-2 - 0.6825 68.25%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7532 75.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8557 85.57%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior - 0.7882 78.82%
P-glycoprotein inhibitior - 0.7886 78.86%
P-glycoprotein substrate - 0.7320 73.20%
CYP3A4 substrate + 0.6248 62.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8750 87.50%
CYP3A4 inhibition - 0.9021 90.21%
CYP2C9 inhibition - 0.7820 78.20%
CYP2C19 inhibition - 0.7600 76.00%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition + 0.5320 53.20%
CYP2C8 inhibition - 0.6102 61.02%
CYP inhibitory promiscuity - 0.8648 86.48%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9343 93.43%
Carcinogenicity (trinary) Non-required 0.4736 47.36%
Eye corrosion - 0.8639 86.39%
Eye irritation - 0.8497 84.97%
Skin irritation - 0.6235 62.35%
Skin corrosion - 0.8501 85.01%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.7501 75.01%
skin sensitisation - 0.7619 76.19%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6684 66.84%
Acute Oral Toxicity (c) IV 0.3536 35.36%
Estrogen receptor binding + 0.6661 66.61%
Androgen receptor binding - 0.6441 64.41%
Thyroid receptor binding - 0.5563 55.63%
Glucocorticoid receptor binding + 0.6422 64.22%
Aromatase binding - 0.6280 62.80%
PPAR gamma + 0.6440 64.40%
Honey bee toxicity - 0.7737 77.37%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9018 90.18%

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 94.84% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.27% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.27% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 90.13% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.93% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.66% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.99% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.65% 95.50%
CHEMBL340 P08684 Cytochrome P450 3A4 82.06% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 82.00% 94.73%

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.
Milleria quinqueflora

Cross-Links

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PubChem 44398214
LOTUS LTS0154933
wikiData Q104953887