Liganolide

Details

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Internal ID 894ce895-19a3-4010-9c65-c9b79b4138b5
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name [2-[(1S,3S,4R,5S,6S)-4-acetyloxy-6-methyl-5-[(3E)-3-methylpenta-1,3-dien-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-3-yl]-1-[(2S)-3,3-dimethyloxiran-2-yl]oxyprop-2-enyl] (E)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H38O8/c1-11-14(3)17(6)30-22-21(31-18(7)28)19(13-20-27(22,10)34-20)16(5)24(32-23(29)15(4)12-2)33-25-26(8,9)35-25/h11-12,19-22,24-25H,5-6,13H2,1-4,7-10H3/b14-11+,15-12+/t19-,20-,21+,22-,24?,25+,27-/m0/s1
InChI Key SPVVYMRXVHAVJC-RTVFUSRCSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O8
Molecular Weight 490.60 g/mol
Exact Mass 490.25666817 g/mol
Topological Polar Surface Area (TPSA) 96.10 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Liganolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9713 97.13%
Caco-2 - 0.6986 69.86%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6249 62.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8873 88.73%
OATP1B3 inhibitior + 0.9236 92.36%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9281 92.81%
P-glycoprotein inhibitior + 0.7935 79.35%
P-glycoprotein substrate - 0.5535 55.35%
CYP3A4 substrate + 0.6701 67.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8899 88.99%
CYP3A4 inhibition - 0.6064 60.64%
CYP2C9 inhibition - 0.9013 90.13%
CYP2C19 inhibition - 0.7388 73.88%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.8416 84.16%
CYP2C8 inhibition - 0.6416 64.16%
CYP inhibitory promiscuity - 0.9260 92.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7943 79.43%
Carcinogenicity (trinary) Non-required 0.5723 57.23%
Eye corrosion - 0.9697 96.97%
Eye irritation - 0.8131 81.31%
Skin irritation - 0.6177 61.77%
Skin corrosion - 0.9137 91.37%
Ames mutagenesis - 0.5615 56.15%
Human Ether-a-go-go-Related Gene inhibition - 0.3816 38.16%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5864 58.64%
skin sensitisation + 0.5223 52.23%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5181 51.81%
Estrogen receptor binding + 0.7869 78.69%
Androgen receptor binding + 0.6842 68.42%
Thyroid receptor binding + 0.6621 66.21%
Glucocorticoid receptor binding + 0.8087 80.87%
Aromatase binding + 0.6615 66.15%
PPAR gamma + 0.6865 68.65%
Honey bee toxicity - 0.5918 59.18%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.9713 97.13%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.14% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 95.18% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.27% 91.11%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 92.21% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.10% 85.14%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 88.28% 85.83%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.96% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.95% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.73% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.09% 95.50%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.75% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.28% 96.95%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.85% 89.50%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 83.79% 92.95%
CHEMBL221 P23219 Cyclooxygenase-1 83.46% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.42% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.69% 97.25%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.59% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.70% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.36% 89.00%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 80.32% 90.48%

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.
Ligularia thomsonii

Cross-Links

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PubChem 13943194
LOTUS LTS0244267
wikiData Q105257625