soyasaponin I(1-)

Details

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Internal ID ea2c5453-c6d2-409e-81d9-e0422772076d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)[O-])O)O)CO)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@H]([C@H](O[C@H]2O[C@@H]3[C@H]([C@@H]([C@H](O[C@H]3O[C@H]4CC[C@]5([C@H]([C@@]4(C)CO)CC[C@@]6([C@@H]5CC=C7[C@]6(CC[C@@]8([C@H]7CC(C[C@H]8O)(C)C)C)C)C)C)C(=O)[O-])O)O)CO)O)O)O)O)O
InChI InChI=1S/C48H78O18/c1-21-29(52)31(54)35(58)40(61-21)65-37-32(55)30(53)24(19-49)62-41(37)66-38-34(57)33(56)36(39(59)60)64-42(38)63-28-12-13-45(5)25(46(28,6)20-50)11-14-48(8)26(45)10-9-22-23-17-43(2,3)18-27(51)44(23,4)15-16-47(22,48)7/h9,21,23-38,40-42,49-58H,10-20H2,1-8H3,(H,59,60)/p-1/t21-,23-,24+,25+,26+,27+,28-,29-,30-,31+,32-,33-,34-,35+,36-,37+,38+,40-,41-,42+,44+,45-,46+,47+,48+/m0/s1
InChI Key PTDAHAWQAGSZDD-IOVCITQVSA-M
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C48H77O18-
Molecular Weight 942.10 g/mol
Exact Mass 941.51099060 g/mol
Topological Polar Surface Area (TPSA) 298.00 Ų
XlogP 3.00
Atomic LogP (AlogP) -0.63
H-Bond Acceptor 18
H-Bond Donor 10
Rotatable Bonds 9

Synonyms

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CHEBI:62916
Q27132277

2D Structure

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2D Structure of soyasaponin I(1-)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4610 46.10%
Caco-2 - 0.9373 93.73%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.8191 81.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8410 84.10%
OATP1B3 inhibitior - 0.4818 48.18%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6276 62.76%
BSEP inhibitior + 0.7841 78.41%
P-glycoprotein inhibitior + 0.7526 75.26%
P-glycoprotein substrate - 0.6388 63.88%
CYP3A4 substrate + 0.7264 72.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8757 87.57%
CYP3A4 inhibition - 0.9437 94.37%
CYP2C9 inhibition - 0.8709 87.09%
CYP2C19 inhibition - 0.8928 89.28%
CYP2D6 inhibition - 0.9338 93.38%
CYP1A2 inhibition - 0.8767 87.67%
CYP2C8 inhibition + 0.7330 73.30%
CYP inhibitory promiscuity - 0.9697 96.97%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6159 61.59%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9081 90.81%
Skin irritation - 0.6283 62.83%
Skin corrosion - 0.9435 94.35%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7702 77.02%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.8899 88.99%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.7918 79.18%
Acute Oral Toxicity (c) III 0.7689 76.89%
Estrogen receptor binding + 0.8044 80.44%
Androgen receptor binding + 0.7336 73.36%
Thyroid receptor binding - 0.6039 60.39%
Glucocorticoid receptor binding + 0.6854 68.54%
Aromatase binding + 0.6503 65.03%
PPAR gamma + 0.7934 79.34%
Honey bee toxicity - 0.7144 71.44%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5750 57.50%
Fish aquatic toxicity + 0.9411 94.11%

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
CHEMBL3714130 P46095 G-protein coupled receptor 6 97.82% 97.36%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.01% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.05% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.54% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.17% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.31% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.29% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.15% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.85% 89.00%
CHEMBL2581 P07339 Cathepsin D 84.10% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.73% 96.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.05% 94.45%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.58% 94.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.21% 99.17%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.39% 95.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.32% 91.07%
CHEMBL5255 O00206 Toll-like receptor 4 80.72% 92.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.43% 93.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.35% 91.24%
CHEMBL3401 O75469 Pregnane X receptor 80.04% 94.73%

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.
Abrus melanospermus subsp. melanospermus
Cicer arietinum
Glycine max
Sophora flavescens
Vicia lens

Cross-Links

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PubChem 53477584
NPASS NPC236658