schidigera-saponin A1

Details

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Internal ID 8ba5ca3f-dd3a-4fea-ad55-7f5dbff26a91
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2-[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9
SMILES (Isomeric) C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC[C@H]5[C@@]4(CC[C@@H](C5)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O[C@H]7[C@@H]([C@H]([C@@H](CO7)O)O)O)O[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)C)C)O[C@]19CCC(=C)CO9
InChI InChI=1S/C44H70O17/c1-19-7-12-44(55-17-19)20(2)30-27(61-44)14-25-23-6-5-21-13-22(8-10-42(21,3)24(23)9-11-43(25,30)4)56-41-38(60-40-36(53)34(51)32(49)28(15-45)57-40)37(33(50)29(16-46)58-41)59-39-35(52)31(48)26(47)18-54-39/h20-41,45-53H,1,5-18H2,2-4H3/t20-,21+,22-,23+,24-,25-,26+,27-,28+,29+,30-,31-,32+,33+,34-,35+,36+,37-,38+,39-,40-,41+,42-,43-,44+/m0/s1
InChI Key OKXQHXAEZMQAFY-JJUWOZROSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C44H70O17
Molecular Weight 871.00 g/mol
Exact Mass 870.46130076 g/mol
Topological Polar Surface Area (TPSA) 256.00 Ų
XlogP 1.20
Atomic LogP (AlogP) -0.17
H-Bond Acceptor 17
H-Bond Donor 9
Rotatable Bonds 8

Synonyms

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CHEMBL507469

2D Structure

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2D Structure of schidigera-saponin A1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6654 66.54%
Caco-2 - 0.8851 88.51%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6422 64.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8913 89.13%
OATP1B3 inhibitior + 0.9222 92.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.5823 58.23%
P-glycoprotein inhibitior + 0.7198 71.98%
P-glycoprotein substrate + 0.5247 52.47%
CYP3A4 substrate + 0.7491 74.91%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8216 82.16%
CYP3A4 inhibition - 0.9082 90.82%
CYP2C9 inhibition - 0.9013 90.13%
CYP2C19 inhibition - 0.8950 89.50%
CYP2D6 inhibition - 0.9360 93.60%
CYP1A2 inhibition - 0.8969 89.69%
CYP2C8 inhibition + 0.6750 67.50%
CYP inhibitory promiscuity - 0.9312 93.12%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6013 60.13%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9118 91.18%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis - 0.7132 71.32%
Human Ether-a-go-go-Related Gene inhibition + 0.7238 72.38%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.9084 90.84%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.9223 92.23%
Acute Oral Toxicity (c) I 0.7360 73.60%
Estrogen receptor binding + 0.7868 78.68%
Androgen receptor binding + 0.6852 68.52%
Thyroid receptor binding - 0.6143 61.43%
Glucocorticoid receptor binding - 0.5202 52.02%
Aromatase binding + 0.6780 67.80%
PPAR gamma + 0.6811 68.11%
Honey bee toxicity - 0.5918 59.18%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9517 95.17%

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 98.54% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.15% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 94.31% 100.00%
CHEMBL237 P41145 Kappa opioid receptor 94.19% 98.10%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.90% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.09% 97.09%
CHEMBL233 P35372 Mu opioid receptor 91.82% 97.93%
CHEMBL226 P30542 Adenosine A1 receptor 90.02% 95.93%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 88.19% 95.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.10% 92.94%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.44% 91.24%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.04% 96.77%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.53% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.32% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 82.63% 97.79%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.46% 97.50%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.74% 95.58%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 81.53% 89.05%
CHEMBL4618 P09960 Leukotriene A4 hydrolase 81.53% 97.86%
CHEMBL4581 P52732 Kinesin-like protein 1 80.26% 93.18%

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.
Atractylodes lancea
Yucca schidigera

Cross-Links

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PubChem 10700835
LOTUS LTS0064208
wikiData Q105236728