[4,5-Dihydroxy-6-[4-hydroxy-6-(hydroxymethyl)-2-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate

Details

• Internal ID: 6189df0c-d304-4a97-a65c-de6df04e1639
• Taxonomy: Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
• IUPAC Name: [4,5-dihydroxy-6-[4-hydroxy-6-(hydroxymethyl)-2-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate
• InChI: InChI=1S/C53H86O23/c1-21(20-67-47-40(62)38(60)36(58)32(18-54)72-47)10-15-53(66)22(2)34-31(76-53)17-30-28-9-8-26-16-27(11-13-51(26,6)29(28)12-14-52(30,34)7)71-50-46(75-49-42(64)39(61)44(24(4)69-49)70-25(5)56)43(65)45(33(19-55)73-50)74-48-41(63)37(59)35(57)23(3)68-48/h8,21-24,27-50,54-55,57-66H,9-20H2,1-7H3
• InChI Key: ODCDMFLMGYBFKH-UHFFFAOYSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₅₃H₈₆O₂₃
• Molecular Weight: 1091.20 g/mol
• Exact Mass: 1090.55598899 g/mol
• Topological Polar Surface Area (TPSA): 352.00 Ų
• XlogP: -0.70
• Atomic LogP (AlogP): -1.41
• H-Bond Acceptor: 23
• H-Bond Donor: 12
• Rotatable Bonds: 15

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.8294	82.94%
Caco-2	-	0.8827	88.27%
Blood Brain Barrier	-	0.6750	67.50%
Human oral bioavailability	-	0.8429	84.29%
Subcellular localzation	Mitochondria	0.8220	82.20%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8626	86.26%
OATP1B3 inhibitior	+	0.8670	86.70%
MATE1 inhibitior	-	0.9812	98.12%
OCT2 inhibitior	-	0.6500	65.00%
BSEP inhibitior	+	0.9247	92.47%
P-glycoprotein inhibitior	+	0.7443	74.43%
P-glycoprotein substrate	+	0.7037	70.37%
CYP3A4 substrate	+	0.7605	76.05%
CYP2C9 substrate	-	1.0000	100.00%
CYP2D6 substrate	-	0.8779	87.79%
CYP3A4 inhibition	-	0.9196	91.96%
CYP2C9 inhibition	-	0.9244	92.44%
CYP2C19 inhibition	-	0.9343	93.43%
CYP2D6 inhibition	-	0.9378	93.78%
CYP1A2 inhibition	-	0.9172	91.72%
CYP2C8 inhibition	+	0.7436	74.36%
CYP inhibitory promiscuity	-	0.9444	94.44%
UGT catelyzed	-	0.7000	70.00%
Carcinogenicity (binary)	-	0.9900	99.00%
Carcinogenicity (trinary)	Non-required	0.5179	51.79%
Eye corrosion	-	0.9902	99.02%
Eye irritation	-	0.9029	90.29%
Skin irritation	+	0.5497	54.97%
Skin corrosion	-	0.9408	94.08%
Ames mutagenesis	-	0.8500	85.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.7982	79.82%
Micronuclear	-	0.8700	87.00%
Hepatotoxicity	-	0.8375	83.75%
skin sensitisation	-	0.9231	92.31%
Respiratory toxicity	+	0.7444	74.44%
Reproductive toxicity	+	0.9556	95.56%
Mitochondrial toxicity	+	0.5250	52.50%
Nephrotoxicity	-	0.8752	87.52%
Acute Oral Toxicity (c)	I	0.4770	47.70%
Estrogen receptor binding	+	0.8583	85.83%
Androgen receptor binding	+	0.6996	69.96%
Thyroid receptor binding	+	0.6045	60.45%
Glucocorticoid receptor binding	+	0.7692	76.92%
Aromatase binding	+	0.7076	70.76%
PPAR gamma	+	0.8313	83.13%
Honey bee toxicity	-	0.5887	58.87%
Biodegradation	-	0.7750	77.50%
Crustacea aquatic toxicity	-	0.5855	58.55%
Fish aquatic toxicity	+	0.9416	94.16%

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	99.25%	96.09%
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	98.55%	91.11%
CHEMBL226	P30542	Adenosine A1 receptor	95.47%	95.93%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	94.85%	94.45%
CHEMBL1806	P11388	DNA topoisomerase II alpha	94.29%	89.00%
CHEMBL1907603	Q05586	Glutamate NMDA receptor; GRIN1/GRIN2B	94.27%	95.89%
CHEMBL2581	P07339	Cathepsin D	93.51%	98.95%
CHEMBL1994	P08235	Mineralocorticoid receptor	93.36%	100.00%
CHEMBL3359	P21462	Formyl peptide receptor 1	92.04%	93.56%
CHEMBL4681	P42330	Aldo-keto-reductase family 1 member C3	88.60%	89.05%
CHEMBL1293249	Q13887	Kruppel-like factor 5	88.22%	86.33%
CHEMBL5255	O00206	Toll-like receptor 4	88.06%	92.50%
CHEMBL1821	P08173	Muscarinic acetylcholine receptor M4	87.61%	94.08%
CHEMBL3137262	O60341	LSD1/CoREST complex	87.60%	97.09%
CHEMBL2955	O95136	Sphingosine 1-phosphate receptor Edg-5	87.13%	92.86%
CHEMBL253	P34972	Cannabinoid CB2 receptor	86.94%	97.25%
CHEMBL3892	Q99500	Sphingosine 1-phosphate receptor Edg-3	86.93%	97.29%
CHEMBL5608	Q16288	NT-3 growth factor receptor	86.16%	95.89%
CHEMBL4227	P25090	Lipoxin A4 receptor	85.48%	100.00%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	85.04%	94.00%
CHEMBL218	P21554	Cannabinoid CB1 receptor	84.46%	96.61%
CHEMBL2274	Q9H228	Sphingosine 1-phosphate receptor Edg-8	83.43%	100.00%
CHEMBL3401	O75469	Pregnane X receptor	83.24%	94.73%
CHEMBL5028	O14672	ADAM10	82.88%	97.50%
CHEMBL340	P08684	Cytochrome P450 3A4	82.75%	91.19%
CHEMBL1907602	P06493	Cyclin-dependent kinase 1/cyclin B1	82.47%	91.24%
CHEMBL2094135	Q96BI3	Gamma-secretase	81.54%	98.05%
CHEMBL237	P41145	Kappa opioid receptor	80.65%	98.10%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	80.18%	95.56%
CHEMBL5163	Q9NY46	Sodium channel protein type III alpha subunit	80.16%	96.90%
CHEMBL2140	P48775	Tryptophan 2,3-dioxygenase	80.16%	98.46%

Plants that contains it

• Smilax excelsa

Cross-Links

• PubChem: 163000454
• LOTUS: LTS0235570
• wikiData: Q105189743