Acanthosessilioside F

Details

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Internal ID 4bf6e612-e46a-4639-af4b-35b702d31a69
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,5S,6S,8R,9R,10R,12R,16R,17S,18S,21S)-6,16-dihydroxy-1,2,17-trimethyl-14-oxo-8,18-bis(prop-1-en-2-yl)-13-oxapentacyclo[10.8.1.02,10.05,9.017,21]henicosane-5-carboxylate
SMILES (Canonical) CC(=C)C1CCC2(C3C1(C(CC(=O)OC3CC4C2(CCC5(C4C(CC5O)C(=C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)C)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@@]2([C@H]3[C@]1([C@@H](CC(=O)O[C@@H]3C[C@H]4[C@]2(CC[C@@]5([C@@H]4[C@@H](C[C@@H]5O)C(=C)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)O)C)C
InChI InChI=1S/C36H54O11/c1-16(2)18-12-24(39)36(32(44)47-31-29(43)28(42)27(41)22(15-37)46-31)11-10-33(5)20(26(18)36)13-21-30-34(33,6)9-8-19(17(3)4)35(30,7)23(38)14-25(40)45-21/h18-24,26-31,37-39,41-43H,1,3,8-15H2,2,4-7H3/t18-,19-,20+,21+,22+,23+,24-,26+,27+,28-,29+,30-,31-,33+,34+,35+,36+/m0/s1
InChI Key IGMUSZZWHAZFBJ-AHTCGHMCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C36H54O11
Molecular Weight 662.80 g/mol
Exact Mass 662.36661253 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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CHEMBL2063161

2D Structure

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2D Structure of Acanthosessilioside F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7538 75.38%
Caco-2 - 0.8695 86.95%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7387 73.87%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.7937 79.37%
OATP1B3 inhibitior + 0.9066 90.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7079 70.79%
BSEP inhibitior - 0.6496 64.96%
P-glycoprotein inhibitior + 0.6890 68.90%
P-glycoprotein substrate + 0.5559 55.59%
CYP3A4 substrate + 0.7192 71.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8725 87.25%
CYP3A4 inhibition - 0.7984 79.84%
CYP2C9 inhibition - 0.8181 81.81%
CYP2C19 inhibition - 0.9028 90.28%
CYP2D6 inhibition - 0.9524 95.24%
CYP1A2 inhibition - 0.8860 88.60%
CYP2C8 inhibition + 0.6720 67.20%
CYP inhibitory promiscuity - 0.9603 96.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6940 69.40%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9134 91.34%
Skin irritation + 0.5684 56.84%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.7170 71.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6503 65.03%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6602 66.02%
skin sensitisation - 0.9158 91.58%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5209 52.09%
Acute Oral Toxicity (c) I 0.4345 43.45%
Estrogen receptor binding + 0.7010 70.10%
Androgen receptor binding + 0.7502 75.02%
Thyroid receptor binding - 0.6044 60.44%
Glucocorticoid receptor binding + 0.6290 62.90%
Aromatase binding + 0.6813 68.13%
PPAR gamma + 0.6616 66.16%
Honey bee toxicity - 0.6384 63.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9796 97.96%

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 97.74% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.29% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.38% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.48% 94.45%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.44% 96.61%
CHEMBL2996 Q05655 Protein kinase C delta 93.35% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.25% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.35% 100.00%
CHEMBL2581 P07339 Cathepsin D 88.66% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.37% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.93% 85.14%
CHEMBL5255 O00206 Toll-like receptor 4 85.65% 92.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.87% 96.95%
CHEMBL220 P22303 Acetylcholinesterase 84.10% 94.45%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.59% 93.04%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.46% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.41% 96.77%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.08% 91.24%
CHEMBL237 P41145 Kappa opioid receptor 82.08% 98.10%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.44% 95.56%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 81.10% 82.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.51% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.22% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.03% 92.62%

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.
Eleutherococcus sessiliflorus

Cross-Links

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PubChem 60155148
LOTUS LTS0235495
wikiData Q105112724