Lunatoic acid B

Details

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Internal ID 9a57813b-5722-462b-a627-43c0bbabe274
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name (E)-3-[(7R,8R)-8-[(2S,4S)-2,4-dimethylhexanoyl]oxy-7-hydroxy-7-methyl-6-oxo-8H-isochromen-3-yl]prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H26O7/c1-5-12(2)8-13(3)20(25)28-19-16-11-27-15(6-7-18(23)24)9-14(16)10-17(22)21(19,4)26/h6-7,9-13,19,26H,5,8H2,1-4H3,(H,23,24)/b7-6+/t12-,13-,19+,21-/m0/s1
InChI Key RLICWTXAOKQGIK-SNHOBTOISA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O7
Molecular Weight 390.40 g/mol
Exact Mass 390.16785316 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lunatoic acid B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5547 55.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7951 79.51%
OATP1B3 inhibitior + 0.8883 88.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7980 79.80%
P-glycoprotein inhibitior - 0.5200 52.00%
P-glycoprotein substrate - 0.5681 56.81%
CYP3A4 substrate + 0.6369 63.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9100 91.00%
CYP3A4 inhibition - 0.7697 76.97%
CYP2C9 inhibition - 0.8381 83.81%
CYP2C19 inhibition - 0.8529 85.29%
CYP2D6 inhibition - 0.9253 92.53%
CYP1A2 inhibition - 0.7872 78.72%
CYP2C8 inhibition + 0.4772 47.72%
CYP inhibitory promiscuity - 0.6719 67.19%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4578 45.78%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.8725 87.25%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9338 93.38%
Ames mutagenesis - 0.5908 59.08%
Human Ether-a-go-go-Related Gene inhibition - 0.4603 46.03%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7302 73.02%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7969 79.69%
Acute Oral Toxicity (c) III 0.6598 65.98%
Estrogen receptor binding + 0.6456 64.56%
Androgen receptor binding + 0.7795 77.95%
Thyroid receptor binding - 0.4937 49.37%
Glucocorticoid receptor binding + 0.6367 63.67%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6040 60.40%
Honey bee toxicity - 0.8167 81.67%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5605 56.05%
Fish aquatic toxicity + 0.9844 98.44%

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
CHEMBL221 P23219 Cyclooxygenase-1 97.45% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.78% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.85% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.82% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.35% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.84% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.18% 96.00%
CHEMBL2581 P07339 Cathepsin D 86.97% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.51% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.59% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.23% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 84.51% 91.19%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.10% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 83.75% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.11% 89.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.63% 96.47%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.82% 95.71%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.77% 94.08%

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 101316985
LOTUS LTS0190112
wikiData Q104397782