[3,4-Diacetyloxy-5-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[16-hydroxy-5',7,9,13-tetramethyl-3'-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-2-yl]methyl acetate

Details

• Internal ID: e1cf2895-d8bb-45ca-bae2-8fa3ba5b5eca
• Taxonomy: Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
• IUPAC Name: [3,4-diacetyloxy-5-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[16-hydroxy-5',7,9,13-tetramethyl-3'-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-2-yl]methyl acetate
• SMILES (Canonical): CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O
• SMILES (Isomeric): CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O
• InChI: InChI=1S/C57H88O27/c1-21-13-37(81-51-44(69)42(67)40(65)33(17-58)77-51)57(73-19-21)22(2)38-32(84-57)16-31-29-10-9-27-14-28(63)15-36(56(27,8)30(29)11-12-55(31,38)7)80-54-50(49(76-26(6)62)47(75-25(5)61)35(79-54)20-72-24(4)60)83-53-46(71)48(39(64)23(3)74-53)82-52-45(70)43(68)41(66)34(18-59)78-52/h9,21-23,28-54,58-59,63-71H,10-20H2,1-8H3
• InChI Key: YWDANXPOTPLHIH-UHFFFAOYSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₅₇H₈₈O₂₇
• Molecular Weight: 1205.30 g/mol
• Exact Mass: 1204.55129753 g/mol
• Topological Polar Surface Area (TPSA): 394.00 Ų
• XlogP: -1.00
• Atomic LogP (AlogP): -2.31
• H-Bond Acceptor: 27
• H-Bond Donor: 11
• Rotatable Bonds: 14

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.8056	80.56%
Caco-2	-	0.8723	87.23%
Blood Brain Barrier	-	0.5250	52.50%
Human oral bioavailability	-	0.7429	74.29%
Subcellular localzation	Mitochondria	0.8501	85.01%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8385	83.85%
OATP1B3 inhibitior	+	0.9025	90.25%
MATE1 inhibitior	-	1.0000	100.00%
OCT2 inhibitior	-	0.5521	55.21%
BSEP inhibitior	+	0.9696	96.96%
P-glycoprotein inhibitior	+	0.7486	74.86%
P-glycoprotein substrate	+	0.6400	64.00%
CYP3A4 substrate	+	0.7607	76.07%
CYP2C9 substrate	-	1.0000	100.00%
CYP2D6 substrate	-	0.8766	87.66%
CYP3A4 inhibition	-	0.8389	83.89%
CYP2C9 inhibition	-	0.9095	90.95%
CYP2C19 inhibition	-	0.9382	93.82%
CYP2D6 inhibition	-	0.9468	94.68%
CYP1A2 inhibition	-	0.9168	91.68%
CYP2C8 inhibition	+	0.7946	79.46%
CYP inhibitory promiscuity	-	0.9561	95.61%
UGT catelyzed	+	0.9000	90.00%
Carcinogenicity (binary)	-	0.9900	99.00%
Carcinogenicity (trinary)	Non-required	0.4754	47.54%
Eye corrosion	-	0.9897	98.97%
Eye irritation	-	0.8998	89.98%
Skin irritation	+	0.5722	57.22%
Skin corrosion	-	0.9383	93.83%
Ames mutagenesis	-	0.7800	78.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.7878	78.78%
Micronuclear	-	0.7900	79.00%
Hepatotoxicity	-	0.8195	81.95%
skin sensitisation	-	0.9306	93.06%
Respiratory toxicity	+	0.7556	75.56%
Reproductive toxicity	+	0.9556	95.56%
Mitochondrial toxicity	+	0.6500	65.00%
Nephrotoxicity	-	0.6429	64.29%
Acute Oral Toxicity (c)	III	0.4809	48.09%
Estrogen receptor binding	+	0.8100	81.00%
Androgen receptor binding	+	0.7513	75.13%
Thyroid receptor binding	+	0.6050	60.50%
Glucocorticoid receptor binding	+	0.7875	78.75%
Aromatase binding	+	0.6318	63.18%
PPAR gamma	+	0.8309	83.09%
Honey bee toxicity	-	0.5751	57.51%
Biodegradation	-	0.7500	75.00%
Crustacea aquatic toxicity	+	0.5945	59.45%
Fish aquatic toxicity	+	0.9587	95.87%

Targets

Proven Targets:

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	99.04%	96.09%
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	97.02%	91.11%
CHEMBL1293249	Q13887	Kruppel-like factor 5	96.44%	86.33%
CHEMBL5255	O00206	Toll-like receptor 4	95.61%	92.50%
CHEMBL226	P30542	Adenosine A1 receptor	95.15%	95.93%
CHEMBL1806	P11388	DNA topoisomerase II alpha	94.98%	89.00%
CHEMBL1994	P08235	Mineralocorticoid receptor	94.49%	100.00%
CHEMBL253	P34972	Cannabinoid CB2 receptor	94.35%	97.25%
CHEMBL218	P21554	Cannabinoid CB1 receptor	93.05%	96.61%
CHEMBL1907603	Q05586	Glutamate NMDA receptor; GRIN1/GRIN2B	92.10%	95.89%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	92.05%	94.45%
CHEMBL3137262	O60341	LSD1/CoREST complex	91.54%	97.09%
CHEMBL1914	P06276	Butyrylcholinesterase	90.21%	95.00%
CHEMBL3351	Q13085	Acetyl-CoA carboxylase 1	86.38%	93.04%
CHEMBL1871	P10275	Androgen Receptor	85.97%	96.43%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	85.79%	94.00%
CHEMBL3401	O75469	Pregnane X receptor	84.23%	94.73%
CHEMBL340	P08684	Cytochrome P450 3A4	83.61%	91.19%
CHEMBL4227	P25090	Lipoxin A4 receptor	83.44%	100.00%
CHEMBL1075094	Q16236	Nuclear factor erythroid 2-related factor 2	83.27%	96.00%
CHEMBL241	Q14432	Phosphodiesterase 3A	83.02%	92.94%
CHEMBL3359	P21462	Formyl peptide receptor 1	82.73%	93.56%
CHEMBL5608	Q16288	NT-3 growth factor receptor	82.28%	95.89%
CHEMBL3922	P50579	Methionine aminopeptidase 2	82.02%	97.28%
CHEMBL1907602	P06493	Cyclin-dependent kinase 1/cyclin B1	81.68%	91.24%
CHEMBL2581	P07339	Cathepsin D	81.51%	98.95%
CHEMBL4187	Q99250	Sodium channel protein type II alpha subunit	80.73%	95.50%
CHEMBL5028	O14672	ADAM10	80.28%	97.50%

Plants that contains it

• Ruscus aculeatus

Cross-Links

• PubChem: 78178018
• LOTUS: LTS0027467
• wikiData: Q105366453