(2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6,14-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID e10bfecd-228e-46b5-a89e-b9b27d675c9c
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name (2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6,14-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4([C@@H](C[C@@H](C5)O[C@H]6[C@@H]([C@H]([C@H]([C@H](O6)CO)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)O)O)O)C)C)O[C@]1(CC[C@H](C)CO[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)O
InChI InChI=1S/C45H74O20/c1-18(17-59-40-36(55)33(52)31(50)26(14-46)61-40)7-10-45(58)19(2)30-25(65-45)13-24-22-6-5-20-11-21(12-29(49)44(20,4)23(22)8-9-43(24,30)3)60-41-38(57)35(54)39(28(16-48)63-41)64-42-37(56)34(53)32(51)27(15-47)62-42/h5,18-19,21-42,46-58H,6-17H2,1-4H3/t18-,19-,21+,22+,23-,24-,25-,26+,27+,28+,29+,30-,31+,32+,33-,34-,35+,36+,37+,38+,39-,40+,41+,42-,43-,44-,45-/m0/s1
InChI Key ITELQBHECKPJMK-IOSULQPQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C45H74O20
Molecular Weight 935.10 g/mol
Exact Mass 934.47734475 g/mol
Topological Polar Surface Area (TPSA) 328.00 Ų
XlogP -1.60
Atomic LogP (AlogP) -2.89
H-Bond Acceptor 20
H-Bond Donor 13
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4S,5S,6R)-2-[(2S)-4-[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6,14-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7571 75.71%
Caco-2 - 0.8876 88.76%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7376 73.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8747 87.47%
OATP1B3 inhibitior + 0.8994 89.94%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.7193 71.93%
P-glycoprotein inhibitior + 0.7374 73.74%
P-glycoprotein substrate + 0.6353 63.53%
CYP3A4 substrate + 0.7486 74.86%
CYP2C9 substrate - 0.8020 80.20%
CYP2D6 substrate - 0.8336 83.36%
CYP3A4 inhibition - 0.9268 92.68%
CYP2C9 inhibition - 0.9182 91.82%
CYP2C19 inhibition - 0.9234 92.34%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.9102 91.02%
CYP2C8 inhibition + 0.6854 68.54%
CYP inhibitory promiscuity - 0.9302 93.02%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5116 51.16%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9080 90.80%
Skin irritation + 0.4929 49.29%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.8937 89.37%
Human Ether-a-go-go-Related Gene inhibition + 0.8043 80.43%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.8158 81.58%
skin sensitisation - 0.9214 92.14%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8430 84.30%
Acute Oral Toxicity (c) I 0.5904 59.04%
Estrogen receptor binding + 0.8456 84.56%
Androgen receptor binding + 0.7178 71.78%
Thyroid receptor binding - 0.5183 51.83%
Glucocorticoid receptor binding + 0.6197 61.97%
Aromatase binding + 0.7051 70.51%
PPAR gamma + 0.7756 77.56%
Honey bee toxicity - 0.6122 61.22%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9176 91.76%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.44% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 97.29% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.86% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.46% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.29% 97.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.51% 92.86%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.02% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.33% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.63% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.85% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.44% 95.89%
CHEMBL2094135 Q96BI3 Gamma-secretase 85.56% 98.05%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.42% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 84.63% 94.75%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.57% 97.29%
CHEMBL1914 P06276 Butyrylcholinesterase 83.96% 95.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.15% 97.25%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 82.98% 98.46%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.57% 100.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.47% 96.21%
CHEMBL2360 P00492 Hypoxanthine-guanine phosphoribosyltransferase 82.27% 87.38%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.20% 97.33%
CHEMBL3401 O75469 Pregnane X receptor 82.08% 94.73%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 81.96% 89.05%
CHEMBL1871 P10275 Androgen Receptor 81.92% 96.43%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.28% 100.00%
CHEMBL5028 O14672 ADAM10 80.57% 97.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.55% 94.00%
CHEMBL242 Q92731 Estrogen receptor beta 80.53% 98.35%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.30% 96.90%
CHEMBL5255 O00206 Toll-like receptor 4 80.11% 92.50%
CHEMBL2581 P07339 Cathepsin D 80.02% 98.95%

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.
Polygonatum kingianum

Cross-Links

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PubChem 163194319
LOTUS LTS0096489
wikiData Q105119991