[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,2R,5S,8R,9S,10R,12R,16R,17S,18S,21S)-16-hydroxy-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

Details

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Internal ID 5bd7475d-ccfc-4286-ba29-523a06b3e3e2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,2R,5S,8R,9S,10R,12R,16R,17S,18S,21S)-16-hydroxy-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) CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CC7C8C(C6(CC5)C)(CCC(C8(C(CC(=O)O7)O)C)C(=C)C)C)C(=C)C)O)O)O)CO)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O)OC[C@@H]3[C@H]([C@@H]([C@H]([C@@H](O3)OC(=O)[C@]45CC[C@H]([C@H]4[C@H]6C[C@@H]7[C@H]8[C@]([C@@]6(CC5)C)(CC[C@H]([C@@]8([C@@H](CC(=O)O7)O)C)C(=C)C)C)C(=C)C)O)O)O)CO)O)O)O
InChI InChI=1S/C48H74O19/c1-19(2)22-9-12-48(14-13-45(6)24(30(22)48)15-25-40-46(45,7)11-10-23(20(3)4)47(40,8)28(50)16-29(51)63-25)44(60)67-43-37(58)34(55)32(53)27(65-43)18-61-41-38(59)35(56)39(26(17-49)64-41)66-42-36(57)33(54)31(52)21(5)62-42/h21-28,30-43,49-50,52-59H,1,3,9-18H2,2,4-8H3/t21-,22-,23-,24+,25+,26+,27+,28+,30-,31-,32+,33+,34-,35+,36+,37+,38+,39+,40-,41+,42-,43-,45+,46+,47+,48-/m0/s1
InChI Key JVLBOZIUMGNKQW-KLRHRCLXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C48H74O19
Molecular Weight 955.10 g/mol
Exact Mass 954.48243013 g/mol
Topological Polar Surface Area (TPSA) 301.00 Ų
XlogP 1.10
Atomic LogP (AlogP) -0.29
H-Bond Acceptor 19
H-Bond Donor 10
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,2R,5S,8R,9S,10R,12R,16R,17S,18S,21S)-16-hydroxy-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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6637 66.37%
Caco-2 - 0.8814 88.14%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.7297 72.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8201 82.01%
OATP1B3 inhibitior + 0.9047 90.47%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6798 67.98%
BSEP inhibitior + 0.7987 79.87%
P-glycoprotein inhibitior + 0.7453 74.53%
P-glycoprotein substrate + 0.6869 68.69%
CYP3A4 substrate + 0.7328 73.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8829 88.29%
CYP3A4 inhibition - 0.8557 85.57%
CYP2C9 inhibition - 0.8484 84.84%
CYP2C19 inhibition - 0.8895 88.95%
CYP2D6 inhibition - 0.9510 95.10%
CYP1A2 inhibition - 0.8968 89.68%
CYP2C8 inhibition + 0.7591 75.91%
CYP inhibitory promiscuity - 0.9694 96.94%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6835 68.35%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9051 90.51%
Skin irritation + 0.5069 50.69%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis - 0.7001 70.01%
Human Ether-a-go-go-Related Gene inhibition + 0.7383 73.83%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.9116 91.16%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7853 78.53%
Acute Oral Toxicity (c) I 0.4820 48.20%
Estrogen receptor binding + 0.8370 83.70%
Androgen receptor binding + 0.7506 75.06%
Thyroid receptor binding - 0.5168 51.68%
Glucocorticoid receptor binding + 0.7297 72.97%
Aromatase binding + 0.6346 63.46%
PPAR gamma + 0.8148 81.48%
Honey bee toxicity - 0.5833 58.33%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9744 97.44%

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 98.90% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.62% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.51% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 95.28% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.81% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.41% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.14% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.31% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.16% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.81% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.33% 92.94%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 88.33% 97.33%
CHEMBL2581 P07339 Cathepsin D 88.10% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.88% 93.04%
CHEMBL5255 O00206 Toll-like receptor 4 86.61% 92.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.86% 95.50%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.81% 94.80%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.19% 97.36%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.06% 92.86%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.93% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.84% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.62% 96.77%
CHEMBL1871 P10275 Androgen Receptor 83.02% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.76% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 82.18% 91.19%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.54% 91.24%
CHEMBL233 P35372 Mu opioid receptor 81.45% 97.93%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.32% 96.90%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.86% 99.23%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.61% 95.83%

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 divaricatus
Eleutherococcus senticosus

Cross-Links

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PubChem 159035775
LOTUS LTS0057627
wikiData Q105135815