Stauntoside B

Details

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Internal ID 8f7c4edc-ae70-46bb-bd1c-c46c47f6c455
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name (4E,7S,8R,11S,16R,21S)-11-[(2R,4R,5S,6R)-4-hydroxy-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-1,8-dimethyl-2,18,22-trioxapentacyclo[17.2.1.04,21.07,16.08,13]docosa-4,13-diene-3,17-dione
SMILES (Canonical) CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CC=C7C8CC(OC(=O)C6CC=C5C4)OC8(OC7=O)C)C)C)C)OC)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@@H](C[C@H](O1)O[C@@H]2[C@H](O[C@H](C[C@@H]2O)O[C@@H]3[C@H](O[C@H](C[C@H]3O)O[C@H]4CC[C@@]5([C@H]6C/C=C/7\[C@@H]8CC(OC(=O)[C@@H]6CC=C5C4)OC8(OC7=O)C)C)C)C)OC)O
InChI InChI=1S/C40H58O15/c1-18-34(43)29(46-6)17-32(47-18)52-36-20(3)49-31(16-28(36)42)51-35-19(2)48-30(15-27(35)41)50-22-11-12-39(4)21(13-22)7-8-23-25(39)10-9-24-26-14-33(53-37(23)44)54-40(26,5)55-38(24)45/h7,9,18-20,22-23,25-36,41-43H,8,10-17H2,1-6H3/b24-9+/t18-,19+,20+,22-,23+,25-,26-,27+,28-,29+,30-,31-,32+,33?,34-,35+,36+,39-,40?/m0/s1
InChI Key LLMKHWMZTMSENL-GRWKKFABSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C40H58O15
Molecular Weight 778.90 g/mol
Exact Mass 778.37757114 g/mol
Topological Polar Surface Area (TPSA) 187.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.91
H-Bond Acceptor 15
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Stauntoside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9858 98.58%
Caco-2 - 0.8696 86.96%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7972 79.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8635 86.35%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6303 63.03%
BSEP inhibitior + 0.8908 89.08%
P-glycoprotein inhibitior + 0.7489 74.89%
P-glycoprotein substrate + 0.6638 66.38%
CYP3A4 substrate + 0.7449 74.49%
CYP2C9 substrate - 0.8015 80.15%
CYP2D6 substrate - 0.8901 89.01%
CYP3A4 inhibition - 0.7453 74.53%
CYP2C9 inhibition - 0.9036 90.36%
CYP2C19 inhibition - 0.9538 95.38%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.8522 85.22%
CYP2C8 inhibition + 0.5813 58.13%
CYP inhibitory promiscuity - 0.9645 96.45%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4365 43.65%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9168 91.68%
Skin irritation + 0.5416 54.16%
Skin corrosion - 0.9078 90.78%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6453 64.53%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5658 56.58%
skin sensitisation - 0.8666 86.66%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.4522 45.22%
Acute Oral Toxicity (c) I 0.5645 56.45%
Estrogen receptor binding + 0.8420 84.20%
Androgen receptor binding + 0.7396 73.96%
Thyroid receptor binding - 0.5355 53.55%
Glucocorticoid receptor binding + 0.7556 75.56%
Aromatase binding + 0.6448 64.48%
PPAR gamma + 0.7777 77.77%
Honey bee toxicity - 0.6344 63.44%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9658 96.58%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.66% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.80% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.74% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.91% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 93.02% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.62% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.25% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.11% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.67% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.42% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.01% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.98% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.45% 100.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 86.67% 97.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.91% 92.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.39% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.20% 95.89%
CHEMBL2581 P07339 Cathepsin D 84.13% 98.95%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 82.65% 83.00%

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.
Stauntonia hexaphylla
Vincetoxicum stauntonii

Cross-Links

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PubChem 101010462
NPASS NPC161374
LOTUS LTS0018209
wikiData Q105153573