2-[2-[3,5-Dihydroxy-2-(hydroxymethyl)-6-[[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]oxan-4-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol

Details

• Internal ID: c37f5442-833e-477b-a871-287f64ce4399
• Taxonomy: Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
• IUPAC Name: 2-[2-[3,5-dihydroxy-2-(hydroxymethyl)-6-[[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]oxan-4-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol
• SMILES (Canonical): CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O
• SMILES (Isomeric): CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O
• InChI: InChI=1S/C51H84O23/c1-20(19-66-45-40(62)38(60)34(56)29(16-52)69-45)8-13-51(65)21(2)32-28(74-51)15-27-25-7-6-23-14-24(9-11-49(23,4)26(25)10-12-50(27,32)5)68-47-42(64)43(36(58)31(18-54)70-47)72-48-44(39(61)35(57)30(17-53)71-48)73-46-41(63)37(59)33(55)22(3)67-46/h6,20-22,24-48,52-65H,7-19H2,1-5H3
• InChI Key: QUMAKTXJGFOROP-UHFFFAOYSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₅₁H₈₄O₂₃
• Molecular Weight: 1065.20 g/mol
• Exact Mass: 1064.54033892 g/mol
• Topological Polar Surface Area (TPSA): 366.00 Ų
• XlogP: -1.20
• Atomic LogP (AlogP): -3.01
• H-Bond Acceptor: 23
• H-Bond Donor: 14
• Rotatable Bonds: 15

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.7571	75.71%
Caco-2	-	0.8835	88.35%
Blood Brain Barrier	-	0.6750	67.50%
Human oral bioavailability	-	0.8429	84.29%
Subcellular localzation	Mitochondria	0.7376	73.76%
OATP2B1 inhibitior	-	1.0000	100.00%
OATP1B1 inhibitior	+	0.8789	87.89%
OATP1B3 inhibitior	+	0.8994	89.94%
MATE1 inhibitior	-	0.9612	96.12%
OCT2 inhibitior	-	0.5500	55.00%
BSEP inhibitior	+	0.7398	73.98%
P-glycoprotein inhibitior	+	0.7406	74.06%
P-glycoprotein substrate	+	0.6786	67.86%
CYP3A4 substrate	+	0.7494	74.94%
CYP2C9 substrate	-	0.8020	80.20%
CYP2D6 substrate	-	0.8336	83.36%
CYP3A4 inhibition	-	0.9268	92.68%
CYP2C9 inhibition	-	0.9182	91.82%
CYP2C19 inhibition	-	0.9234	92.34%
CYP2D6 inhibition	-	0.9343	93.43%
CYP1A2 inhibition	-	0.9102	91.02%
CYP2C8 inhibition	+	0.7324	73.24%
CYP inhibitory promiscuity	-	0.9302	93.02%
UGT catelyzed	-	0.6000	60.00%
Carcinogenicity (binary)	-	0.9900	99.00%
Carcinogenicity (trinary)	Non-required	0.5116	51.16%
Eye corrosion	-	0.9898	98.98%
Eye irritation	-	0.9049	90.49%
Skin irritation	+	0.4929	49.29%
Skin corrosion	-	0.9426	94.26%
Ames mutagenesis	-	0.9300	93.00%
Human Ether-a-go-go-Related Gene inhibition	+	0.8123	81.23%
Micronuclear	-	0.8700	87.00%
Hepatotoxicity	-	0.8625	86.25%
skin sensitisation	-	0.9214	92.14%
Respiratory toxicity	+	0.7333	73.33%
Reproductive toxicity	+	0.9222	92.22%
Mitochondrial toxicity	+	0.5375	53.75%
Nephrotoxicity	-	0.9020	90.20%
Acute Oral Toxicity (c)	I	0.5904	59.04%
Estrogen receptor binding	+	0.8588	85.88%
Androgen receptor binding	+	0.6978	69.78%
Thyroid receptor binding	+	0.5496	54.96%
Glucocorticoid receptor binding	+	0.6792	67.92%
Aromatase binding	+	0.6795	67.95%
PPAR gamma	+	0.7982	79.82%
Honey bee toxicity	-	0.6115	61.15%
Biodegradation	-	0.6500	65.00%
Crustacea aquatic toxicity	-	0.5900	59.00%
Fish aquatic toxicity	+	0.9176	91.76%

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	98.75%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	98.74%	96.09%
CHEMBL226	P30542	Adenosine A1 receptor	98.02%	95.93%
CHEMBL3137262	O60341	LSD1/CoREST complex	93.46%	97.09%
CHEMBL1994	P08235	Mineralocorticoid receptor	92.63%	100.00%
CHEMBL3359	P21462	Formyl peptide receptor 1	92.57%	93.56%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	92.30%	94.45%
CHEMBL1907603	Q05586	Glutamate NMDA receptor; GRIN1/GRIN2B	91.67%	95.89%
CHEMBL1806	P11388	DNA topoisomerase II alpha	91.02%	89.00%
CHEMBL1293249	Q13887	Kruppel-like factor 5	90.03%	86.33%
CHEMBL253	P34972	Cannabinoid CB2 receptor	89.78%	97.25%
CHEMBL5608	Q16288	NT-3 growth factor receptor	88.78%	95.89%
CHEMBL2581	P07339	Cathepsin D	88.60%	98.95%
CHEMBL2955	O95136	Sphingosine 1-phosphate receptor Edg-5	88.51%	92.86%
CHEMBL4681	P42330	Aldo-keto-reductase family 1 member C3	87.49%	89.05%
CHEMBL218	P21554	Cannabinoid CB1 receptor	85.75%	96.61%
CHEMBL2094135	Q96BI3	Gamma-secretase	85.60%	98.05%
CHEMBL2140	P48775	Tryptophan 2,3-dioxygenase	85.49%	98.46%
CHEMBL1937	Q92769	Histone deacetylase 2	84.86%	94.75%
CHEMBL4227	P25090	Lipoxin A4 receptor	84.42%	100.00%
CHEMBL1821	P08173	Muscarinic acetylcholine receptor M4	82.84%	94.08%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	82.69%	94.00%
CHEMBL2335	P42785	Lysosomal Pro-X carboxypeptidase	82.33%	100.00%
CHEMBL2360	P00492	Hypoxanthine-guanine phosphoribosyltransferase	82.27%	87.38%
CHEMBL242	Q92731	Estrogen receptor beta	81.45%	98.35%
CHEMBL1914	P06276	Butyrylcholinesterase	81.36%	95.00%
CHEMBL216	P11229	Muscarinic acetylcholine receptor M1	81.06%	94.23%
CHEMBL4581	P52732	Kinesin-like protein 1	80.56%	93.18%
CHEMBL5255	O00206	Toll-like receptor 4	80.54%	92.50%
CHEMBL2996	Q05655	Protein kinase C delta	80.35%	97.79%

Plants that contains it

• Lilium regale

Cross-Links

• PubChem: 162883196
• LOTUS: LTS0189723
• wikiData: Q105228266