16-[5-[3-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one

Details

• Internal ID: 5cd5e1bb-784f-44c1-9680-357cba43aa71
• Taxonomy: Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
• IUPAC Name: 16-[5-[3-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one
• SMILES (Canonical): CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C)C)C)OC1
• SMILES (Isomeric): CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C)C)C)OC1
• InChI: InChI=1S/C56H90O29/c1-19-7-8-56(75-17-19)20(2)34-28(85-56)10-24-22-6-5-21-9-27(25(61)12-54(21,3)23(22)11-33(63)55(24,34)4)76-50-43(72)40(69)45(32(16-60)80-50)81-53-48(47(38(67)31(15-59)79-53)83-49-41(70)35(64)26(62)18-74-49)84-52-44(73)46(37(66)30(14-58)78-52)82-51-42(71)39(68)36(65)29(13-57)77-51/h19-32,34-53,57-62,64-73H,5-18H2,1-4H3
• InChI Key: XBVUBGLKNSANLK-UHFFFAOYSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₅₆H₉₀O₂₉
• Molecular Weight: 1227.30 g/mol
• Exact Mass: 1226.55677683 g/mol
• Topological Polar Surface Area (TPSA): 452.00 Ų
• XlogP: -4.60
• Atomic LogP (AlogP): -6.30
• H-Bond Acceptor: 29
• H-Bond Donor: 16
• Rotatable Bonds: 14

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.5734	57.34%
Caco-2	-	0.8737	87.37%
Blood Brain Barrier	-	0.7000	70.00%
Human oral bioavailability	-	0.8000	80.00%
Subcellular localzation	Mitochondria	0.7299	72.99%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8354	83.54%
OATP1B3 inhibitior	+	0.9419	94.19%
MATE1 inhibitior	-	1.0000	100.00%
OCT2 inhibitior	-	0.5000	50.00%
BSEP inhibitior	+	0.8504	85.04%
P-glycoprotein inhibitior	+	0.7423	74.23%
P-glycoprotein substrate	+	0.5095	50.95%
CYP3A4 substrate	+	0.7461	74.61%
CYP2C9 substrate	-	1.0000	100.00%
CYP2D6 substrate	-	0.8483	84.83%
CYP3A4 inhibition	-	0.9265	92.65%
CYP2C9 inhibition	-	0.9261	92.61%
CYP2C19 inhibition	-	0.9124	91.24%
CYP2D6 inhibition	-	0.9583	95.83%
CYP1A2 inhibition	-	0.9264	92.64%
CYP2C8 inhibition	+	0.7082	70.82%
CYP inhibitory promiscuity	-	0.9693	96.93%
UGT catelyzed	-	0.6000	60.00%
Carcinogenicity (binary)	-	1.0000	100.00%
Carcinogenicity (trinary)	Non-required	0.6417	64.17%
Eye corrosion	-	0.9922	99.22%
Eye irritation	-	0.9018	90.18%
Skin irritation	-	0.6168	61.68%
Skin corrosion	-	0.9490	94.90%
Ames mutagenesis	-	0.8000	80.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.8188	81.88%
Micronuclear	-	0.9100	91.00%
Hepatotoxicity	-	0.8375	83.75%
skin sensitisation	-	0.9422	94.22%
Respiratory toxicity	+	0.8000	80.00%
Reproductive toxicity	+	0.7444	74.44%
Mitochondrial toxicity	-	0.5250	52.50%
Nephrotoxicity	-	0.7595	75.95%
Acute Oral Toxicity (c)	I	0.7641	76.41%
Estrogen receptor binding	+	0.8718	87.18%
Androgen receptor binding	+	0.7445	74.45%
Thyroid receptor binding	+	0.5515	55.15%
Glucocorticoid receptor binding	+	0.6893	68.93%
Aromatase binding	+	0.6329	63.29%
PPAR gamma	+	0.7968	79.68%
Honey bee toxicity	-	0.5537	55.37%
Biodegradation	-	0.7500	75.00%
Crustacea aquatic toxicity	+	0.5100	51.00%
Fish aquatic toxicity	+	0.8173	81.73%

Targets

Proven Targets:

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	98.52%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	96.66%	96.09%
CHEMBL3137262	O60341	LSD1/CoREST complex	95.27%	97.09%
CHEMBL1293249	Q13887	Kruppel-like factor 5	91.98%	86.33%
CHEMBL1994	P08235	Mineralocorticoid receptor	91.49%	100.00%
CHEMBL218	P21554	Cannabinoid CB1 receptor	90.85%	96.61%
CHEMBL5255	O00206	Toll-like receptor 4	88.72%	92.50%
CHEMBL3351	Q13085	Acetyl-CoA carboxylase 1	88.07%	93.04%
CHEMBL4187	Q99250	Sodium channel protein type II alpha subunit	87.46%	95.50%
CHEMBL1907602	P06493	Cyclin-dependent kinase 1/cyclin B1	87.09%	91.24%
CHEMBL259	P32245	Melanocortin receptor 4	86.68%	95.38%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	85.58%	94.45%
CHEMBL241	Q14432	Phosphodiesterase 3A	84.81%	92.94%
CHEMBL1902	P62942	FK506-binding protein 1A	84.67%	97.05%
CHEMBL3476	O15111	Inhibitor of nuclear factor kappa B kinase alpha subunit	83.38%	95.83%
CHEMBL3880	P07900	Heat shock protein HSP 90-alpha	82.92%	96.21%
CHEMBL4016	P42262	Glutamate receptor ionotropic, AMPA 2	82.25%	86.92%
CHEMBL1937	Q92769	Histone deacetylase 2	82.11%	94.75%
CHEMBL226	P30542	Adenosine A1 receptor	82.03%	95.93%
CHEMBL2274	Q9H228	Sphingosine 1-phosphate receptor Edg-8	82.02%	100.00%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	80.86%	95.56%
CHEMBL253	P34972	Cannabinoid CB2 receptor	80.67%	97.25%
CHEMBL233	P35372	Mu opioid receptor	80.13%	97.93%
CHEMBL4618	P09960	Leukotriene A4 hydrolase	80.02%	97.86%

Plants that contains it

• Allium obliquum

Cross-Links

• PubChem: 163003011
• LOTUS: LTS0118529
• wikiData: Q105324749