Soyasaponin I

Details

• Internal ID: 16b1f255-a484-4036-87ee-81ea6b0a597e
• 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-carboxylic acid
• 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)/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-N
• Popularity: 64 references in papers

Physical and Chemical Properties

• Molecular Formula: C₄₈H₇₈O₁₈
• Molecular Weight: 943.10 g/mol
• Exact Mass: 942.51881563 g/mol
• Topological Polar Surface Area (TPSA): 295.00 Ų
• XlogP: 2.40
• Atomic LogP (AlogP): 0.70
• H-Bond Acceptor: 17
• H-Bond Donor: 11
• Rotatable Bonds: 9

Synonyms

• Soyasaponin Bb
• 51330-27-9
• SoyasaponinBb
• soyasaponin 1
• CCRIS 6617
• SCM 3B
• Soybean saponin fraction B1
• CHEBI:9211
• (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-carboxylic acid
• Oleanane, b-D-glucopyranosiduronic acid deriv.
• (3beta,22beta)-22,24-dihydroxyolean-12-en-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucopyranosiduronic acid
• (3beta,22beta)-22,24-dihydroxyolean-12-en-3-yl alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucopyranosiduronic acid
• beta-D-Glucopyranosiduronic acid, (3beta,4beta,22beta)-22,23-dihydroxyolean-12-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-2)-O-beta-D-galactopyranosyl-(1-2)-
• Soyasaponin-Bb
• C48H78O18
• SCHEMBL397064
• Soyasaponin Bb(Soyasaponin I)
• CHEMBL511016
• PTDAHAWQAGSZDD-IOVCITQVSA-N
• DTXSID901031429
• HY-N0310
• MFCD02752366
• AKOS030530134
• AC-34174
• MS-31761
• LS-175250
• CS-0008808
• O0587
• C08983
• Q-100575
• Q27108314
• 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[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]oxane-2-carboxylic acid
• b-D-Glucopyranosiduronic acid, (3b,4b,22b)-22,23-dihydroxyolean-12-en-3-yl O-6-deoxy-.alpha.-L-mannopyranosyl-(1.2)-O-.beta.-D-galactopyranosyl-(1.2)-

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.7891	78.91%
Caco-2	-	0.9373	93.73%
Blood Brain Barrier	-	0.6250	62.50%
Human oral bioavailability	-	0.8429	84.29%
Subcellular localzation	Mitochondria	0.8567	85.67%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8400	84.00%
OATP1B3 inhibitior	-	0.5700	57.00%
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	-	0.6924	69.24%
CYP3A4 substrate	+	0.7177	71.77%
CYP2C9 substrate	-	1.0000	100.00%
CYP2D6 substrate	-	0.8798	87.98%
CYP3A4 inhibition	-	0.9300	93.00%
CYP2C9 inhibition	-	0.8838	88.38%
CYP2C19 inhibition	-	0.9101	91.01%
CYP2D6 inhibition	-	0.9422	94.22%
CYP1A2 inhibition	-	0.8933	89.33%
CYP2C8 inhibition	+	0.7398	73.98%
CYP inhibitory promiscuity	-	0.9668	96.68%
UGT catelyzed	-	0.5000	50.00%
Carcinogenicity (binary)	-	0.9700	97.00%
Carcinogenicity (trinary)	Non-required	0.6254	62.54%
Eye corrosion	-	0.9900	99.00%
Eye irritation	-	0.9081	90.81%
Skin irritation	-	0.6103	61.03%
Skin corrosion	-	0.9480	94.80%
Ames mutagenesis	-	0.9400	94.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.7702	77.02%
Micronuclear	-	0.8600	86.00%
Hepatotoxicity	-	0.8500	85.00%
skin sensitisation	-	0.8917	89.17%
Respiratory toxicity	-	0.7778	77.78%
Reproductive toxicity	+	0.9000	90.00%
Mitochondrial toxicity	-	0.7625	76.25%
Nephrotoxicity	-	0.8449	84.49%
Acute Oral Toxicity (c)	III	0.7945	79.45%
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	-	0.7276	72.76%
Biodegradation	-	0.7750	77.50%
Crustacea aquatic toxicity	-	0.5800	58.00%
Fish aquatic toxicity	+	0.9411	94.11%

Targets

Proven Targets:

No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID	UniProt ID	Name	Probability	Model accuracy
CHEMBL3714130	P46095	G-protein coupled receptor 6	97.60%	97.36%
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	95.85%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	91.89%	96.09%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	91.38%	95.56%
CHEMBL3807	P17706	T-cell protein-tyrosine phosphatase	90.28%	93.00%
CHEMBL1293249	Q13887	Kruppel-like factor 5	89.20%	86.33%
CHEMBL1806	P11388	DNA topoisomerase II alpha	85.71%	89.00%
CHEMBL3137262	O60341	LSD1/CoREST complex	85.33%	97.09%
CHEMBL1994	P08235	Mineralocorticoid receptor	84.17%	100.00%
CHEMBL5608	Q16288	NT-3 growth factor receptor	84.03%	95.89%
CHEMBL3060	Q9Y345	Glycine transporter 2	83.38%	99.17%
CHEMBL2581	P07339	Cathepsin D	82.74%	98.95%
CHEMBL5028	O14672	ADAM10	81.99%	97.50%
CHEMBL221	P23219	Cyclooxygenase-1	81.73%	90.17%
CHEMBL253	P34972	Cannabinoid CB2 receptor	80.54%	97.25%
CHEMBL2007	P16234	Platelet-derived growth factor receptor alpha	80.25%	91.07%
CHEMBL4187	Q99250	Sodium channel protein type II alpha subunit	80.11%	95.50%
CHEMBL5255	O00206	Toll-like receptor 4	80.04%	92.50%

Plants that contains it

• Achillea pseudopectinata
• Aglaia australiensis
• Allagopappus viscosissimus
• Arachis hypogaea
• Asimina parviflora
• Astragalus condensatus
• Astragalus mongholicus
• Astragalus pterocephalus
• Astragalus sikokianus
• Astragalus spinosus
• Astragalus trimestris
• Atraphaxis spinosa
• Atuna excelsa subsp. racemosa
• Baccharis neglecta
• Berberis floribunda
• Bertya dimerostigma
• Bonamia spectabilis
• Centaurea cuneifolia subsp. cuneifolia
• Chondrodendron tomentosum
• Clerodendrum bungei
• Crotalaria albida
• Cymodocea nodosa
• Delphinium barbeyi
• Diospyros ebenum
• Diplacus longiflorus
• Embelia parviflora
• Embelia schimperi
• Ephedra sinica
• Epilobium hirsutum
• Erysimum leptophyllum
• Erythrina melanacantha
• Esenbeckia leiocarpa
• Euphorbia jolkinii
• Faramea multiflora
• Fumaria densiflora
• Glycine max
• Glycyrrhiza glabra
• Grona styracifolia
• Gymnocalycium schickendantzii
• Haplophyllum obtusifolium
• Hedysarum polybotrys
• Helichrysum tenuifolium
• Hydrangea serrata
• Hypericum styphelioides
• Impatiens siculifera
• Isoberlinia tomentosa
• Jamesoniella colorata
• Lepidosperma ustulatum
• Linnaea chinensis
• Lunularia cruciata
• Lupinus angustifolius
• Lupinus oreophilus
• Lupinus polyphyllus
• Lythrum salicaria
• Macadamia ternifolia
• Medicago arabica
• Medicago arborea
• Medicago polymorpha
• Medicago sativa
• Medicago truncatula
• Melilotus officinalis
• Melilotus officinalis
• Monsonia senegalensis
• Myrica rubra
• Onopordum acanthium
• Oreomecon alpina
• Pancratium sickenbergeri
• Peltogyne paniculata subsp. pubescens
• Phaseolus vulgaris
• Pinalia anomala
• Piper regnellii
• Plathymenia reticulata
• Pogostemon cablin
• Pteridium esculentum
• Pterodon emarginatus
• Pueraria montana var. lobata
• Pueraria montana var. thomsonii
• Pulsatilla campanella
• Pyrola japonica
• Ranunculus peltatus
• Rosulabryum capillare
• Rothia indica
• Salvia miltiorrhiza
• Saracha nigribaccata
• Simarouba glauca
• Sophora flavescens
• Sophora tonkinensis
• Stenocereus laevigatus
• Styphnolobium japonicum
• Syzygium nervosum
• Syzygium polycephaloides
• Trifolium alexandrinum
• Trifolium incarnatum
• Trifolium repens
• Trifolium resupinatum
• Varronia leucocephala
• Vellozia nanuzae
• Vernonanthura fagifolia
• Vigna mungo
• Wisteria brachybotrys

Cross-Links

• PubChem: 122097
• NPASS: NPC236657
• LOTUS: LTS0182499
• wikiData: Q27108314