Lonijaposide F

Details

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Internal ID b0e75ab9-6d58-4a5c-be16-f2f57e20b720
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name 5-[(E)-2-[(2S,3R,4S)-5-carboxy-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]ethenyl]-1-ethylpyridin-1-ium-3-carboxylate
SMILES (Canonical) CC[N+]1=CC(=CC(=C1)C(=O)[O-])C=CC2C(C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)C=C
SMILES (Isomeric) CC[N+]1=CC(=CC(=C1)C(=O)[O-])/C=C/[C@H]2[C@H]([C@@H](OC=C2C(=O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C=C
InChI InChI=1S/C24H29NO11/c1-3-14-15(6-5-12-7-13(21(30)31)9-25(4-2)8-12)16(22(32)33)11-34-23(14)36-24-20(29)19(28)18(27)17(10-26)35-24/h3,5-9,11,14-15,17-20,23-24,26-29H,1,4,10H2,2H3,(H-,30,31,32,33)/b6-5+/t14-,15+,17-,18-,19+,20-,23+,24+/m1/s1
InChI Key KKLONPANWKAOPP-DFEUVTCYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H29NO11
Molecular Weight 507.50 g/mol
Exact Mass 507.17406074 g/mol
Topological Polar Surface Area (TPSA) 190.00 Ų
XlogP 0.50
Atomic LogP (AlogP) -2.07
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 9

Synonyms

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CHEBI:69644
CHEMBL1928044
Q27137985

2D Structure

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2D Structure of Lonijaposide F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9403 94.03%
Caco-2 - 0.8899 88.99%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4382 43.82%
OATP2B1 inhibitior - 0.7117 71.17%
OATP1B1 inhibitior + 0.7412 74.12%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4518 45.18%
P-glycoprotein inhibitior - 0.5721 57.21%
P-glycoprotein substrate - 0.6408 64.08%
CYP3A4 substrate + 0.6278 62.78%
CYP2C9 substrate - 0.8049 80.49%
CYP2D6 substrate - 0.8748 87.48%
CYP3A4 inhibition - 0.9377 93.77%
CYP2C9 inhibition - 0.6796 67.96%
CYP2C19 inhibition - 0.7088 70.88%
CYP2D6 inhibition - 0.8770 87.70%
CYP1A2 inhibition - 0.7091 70.91%
CYP2C8 inhibition + 0.6433 64.33%
CYP inhibitory promiscuity - 0.7814 78.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5203 52.03%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.9368 93.68%
Skin irritation - 0.7771 77.71%
Skin corrosion - 0.9299 92.99%
Ames mutagenesis + 0.5130 51.30%
Human Ether-a-go-go-Related Gene inhibition - 0.4526 45.26%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.6930 69.30%
skin sensitisation - 0.8420 84.20%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5505 55.05%
Acute Oral Toxicity (c) III 0.5760 57.60%
Estrogen receptor binding + 0.6275 62.75%
Androgen receptor binding - 0.4844 48.44%
Thyroid receptor binding + 0.5548 55.48%
Glucocorticoid receptor binding + 0.6200 62.00%
Aromatase binding + 0.6065 60.65%
PPAR gamma + 0.6007 60.07%
Honey bee toxicity - 0.7492 74.92%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.6768 67.68%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 98.27% 83.57%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.97% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.78% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 92.14% 96.95%
CHEMBL220 P22303 Acetylcholinesterase 92.04% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.46% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.34% 99.17%
CHEMBL1811 P34995 Prostanoid EP1 receptor 87.34% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.68% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.33% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 85.36% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.14% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.04% 86.92%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.79% 89.34%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.40% 97.36%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.89% 90.71%
CHEMBL5255 O00206 Toll-like receptor 4 82.68% 92.50%

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.
Lonicera japonica

Cross-Links

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PubChem 56599668
LOTUS LTS0023161
wikiData Q27137985