Leonoside F

Details

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Internal ID b14f12b8-aceb-4809-b259-95ac433127e0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name (2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-4-yl]oxy-6-methyloxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H42O17/c1-10-16(30)19(33)22(36)27(41-10)44-24-18(32)15(9-40-25-21(35)20(34)17(31)14(8-28)42-25)43-26(23(24)37)39-6-5-11-3-4-12(29)13(7-11)38-2/h3-4,7,10,14-37H,5-6,8-9H2,1-2H3/t10-,14+,15+,16-,17+,18+,19+,20-,21+,22+,23+,24-,25+,26+,27-/m0/s1
InChI Key PSQITMLVTRISAW-DIINDGIOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H42O17
Molecular Weight 638.60 g/mol
Exact Mass 638.24219987 g/mol
Topological Polar Surface Area (TPSA) 267.00 Ų
XlogP -3.70
Atomic LogP (AlogP) -4.56
H-Bond Acceptor 17
H-Bond Donor 10
Rotatable Bonds 11

Synonyms

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RefChem:924624
(2S,3R,4R,5R,6S)-2-((2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(2-(4-hydroxy-3-methoxyphenyl)ethoxy)-6-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxymethyl)oxan-4-yl)oxy-6-methyloxane-3,4,5-triol

2D Structure

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2D Structure of Leonoside F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8789 87.89%
Caco-2 - 0.8954 89.54%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.7153 71.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8711 87.11%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6654 66.54%
P-glycoprotein inhibitior - 0.6352 63.52%
P-glycoprotein substrate - 0.5598 55.98%
CYP3A4 substrate + 0.6181 61.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7853 78.53%
CYP3A4 inhibition - 0.9548 95.48%
CYP2C9 inhibition - 0.7761 77.61%
CYP2C19 inhibition - 0.8715 87.15%
CYP2D6 inhibition - 0.9220 92.20%
CYP1A2 inhibition - 0.8845 88.45%
CYP2C8 inhibition + 0.7421 74.21%
CYP inhibitory promiscuity - 0.7935 79.35%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6889 68.89%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.9337 93.37%
Skin irritation - 0.8388 83.88%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7089 70.89%
Micronuclear - 0.7241 72.41%
Hepatotoxicity - 0.8875 88.75%
skin sensitisation - 0.8747 87.47%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.9049 90.49%
Acute Oral Toxicity (c) III 0.7868 78.68%
Estrogen receptor binding + 0.7659 76.59%
Androgen receptor binding - 0.7108 71.08%
Thyroid receptor binding + 0.5253 52.53%
Glucocorticoid receptor binding - 0.5382 53.82%
Aromatase binding + 0.6376 63.76%
PPAR gamma + 0.6852 68.52%
Honey bee toxicity - 0.7516 75.16%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.7575 75.75%

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 99.47% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.04% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.26% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.82% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.54% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.63% 94.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.94% 97.36%
CHEMBL2581 P07339 Cathepsin D 90.40% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.03% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.49% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.25% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.34% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.29% 92.94%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.72% 96.00%
CHEMBL226 P30542 Adenosine A1 receptor 82.11% 95.93%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.86% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.77% 94.45%

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.
Leonurus japonicus

Cross-Links

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PubChem 57325811
NPASS NPC204100