Lobariether E

Details

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Internal ID 15ad0975-76af-42b1-af24-72a9b26af427
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid esters
IUPAC Name methyl 2-[[(3S)-5,7-dihydroxy-3-methoxy-6-methyl-1-oxo-3H-2-benzofuran-4-yl]oxy]-4-methoxy-3-[(E)-3-methoxy-3-oxoprop-1-enyl]-6-methylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H24O11/c1-10-9-13(30-3)12(7-8-14(25)31-4)20(15(10)22(28)32-5)34-21-17-16(18(26)11(2)19(21)27)23(29)35-24(17)33-6/h7-9,24,26-27H,1-6H3/b8-7+/t24-/m0/s1
InChI Key WGIXFHBMTKEIHD-UROCCOEBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H24O11
Molecular Weight 488.40 g/mol
Exact Mass 488.13186158 g/mol
Topological Polar Surface Area (TPSA) 147.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 11
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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CHEMBL4097013

2D Structure

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2D Structure of Lobariether E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9640 96.40%
Caco-2 + 0.5530 55.30%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5459 54.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8238 82.38%
OATP1B3 inhibitior - 0.2335 23.35%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6812 68.12%
P-glycoprotein inhibitior + 0.7277 72.77%
P-glycoprotein substrate - 0.6151 61.51%
CYP3A4 substrate + 0.6592 65.92%
CYP2C9 substrate - 0.6112 61.12%
CYP2D6 substrate - 0.8744 87.44%
CYP3A4 inhibition - 0.5468 54.68%
CYP2C9 inhibition - 0.5750 57.50%
CYP2C19 inhibition - 0.7403 74.03%
CYP2D6 inhibition - 0.8673 86.73%
CYP1A2 inhibition + 0.5096 50.96%
CYP2C8 inhibition + 0.7814 78.14%
CYP inhibitory promiscuity + 0.7215 72.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9743 97.43%
Carcinogenicity (trinary) Danger 0.6069 60.69%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.7045 70.45%
Skin irritation - 0.7617 76.17%
Skin corrosion - 0.9582 95.82%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.5729 57.29%
skin sensitisation - 0.8167 81.67%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7831 78.31%
Acute Oral Toxicity (c) II 0.4907 49.07%
Estrogen receptor binding + 0.8268 82.68%
Androgen receptor binding + 0.6792 67.92%
Thyroid receptor binding + 0.5547 55.47%
Glucocorticoid receptor binding + 0.8265 82.65%
Aromatase binding + 0.5601 56.01%
PPAR gamma + 0.6530 65.30%
Honey bee toxicity - 0.8306 83.06%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9897 98.97%

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 97.14% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.34% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.68% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.13% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.27% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.67% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.95% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.41% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 87.23% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.39% 91.07%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.34% 93.03%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 83.39% 98.21%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.31% 96.00%
CHEMBL4040 P28482 MAP kinase ERK2 81.24% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.02% 99.17%
CHEMBL2535 P11166 Glucose transporter 80.43% 98.75%

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 132497897
LOTUS LTS0262159
wikiData Q105304541