[(3S,8R,9S,10R,12R,13S,14S,17S)-17-acetyl-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-12-yl] (E)-2-methylbut-2-enoate

Details

• Internal ID: 7abd313d-87f4-4021-b3b4-21009ee48321
• Taxonomy: Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
• IUPAC Name: [(3S,8R,9S,10R,12R,13S,14S,17S)-17-acetyl-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-12-yl] (E)-2-methylbut-2-enoate
• SMILES (Canonical): CC=C(C)C(=O)OC1CC2C(CC=C3C2(CCC(C3)OC4CC(C(C(O4)C)OC5CC(C(C(O5)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)C)O)OC)O)OC)O)OC)OC)C)C8(C1(C(CC8)C(=O)C)C)O
• SMILES (Isomeric): C/C=C(\C)/C(=O)O[C@@H]1C[C@H]2[C@@H](CC=C3[C@@]2(CC[C@@H](C3)O[C@H]4C[C@@H]([C@@H]([C@H](O4)C)O[C@H]5C[C@@H]([C@@H]([C@H](O5)C)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)C)O)OC)O)OC)O)OC)OC)C)[C@@]8([C@]1([C@H](CC8)C(=O)C)C)O
• InChI: InChI=1S/C54H86O19/c1-14-25(2)49(59)70-38-22-35-34(54(60)20-18-33(26(3)55)53(38,54)9)16-15-31-21-32(17-19-52(31,35)8)69-39-23-36(61-10)44(28(5)65-39)71-40-24-37(62-11)45(29(6)66-40)72-51-43(58)48(64-13)46(30(7)68-51)73-50-42(57)47(63-12)41(56)27(4)67-50/h14-15,27-30,32-48,50-51,56-58,60H,16-24H2,1-13H3/b25-14+/t27-,28-,29-,30-,32+,33-,34-,35+,36+,37+,38-,39+,40+,41-,42-,43-,44-,45-,46-,47+,48-,50+,51+,52+,53+,54+/m1/s1
• InChI Key: NGOPWLMMSZURID-YHDNGIKKSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₅₄H₈₆O₁₉
• Molecular Weight: 1039.20 g/mol
• Exact Mass: 1038.57633051 g/mol
• Topological Polar Surface Area (TPSA): 235.00 Ų
• XlogP: 2.90
• Atomic LogP (AlogP): 4.20
• H-Bond Acceptor: 19
• H-Bond Donor: 4
• Rotatable Bonds: 15

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9426	94.26%
Caco-2	-	0.8659	86.59%
Blood Brain Barrier	-	0.5250	52.50%
Human oral bioavailability	-	0.7286	72.86%
Subcellular localzation	Mitochondria	0.7305	73.05%
OATP2B1 inhibitior	-	0.8738	87.38%
OATP1B1 inhibitior	+	0.8613	86.13%
OATP1B3 inhibitior	+	0.9218	92.18%
MATE1 inhibitior	-	0.9600	96.00%
OCT2 inhibitior	-	0.6374	63.74%
BSEP inhibitior	+	0.9854	98.54%
P-glycoprotein inhibitior	+	0.7525	75.25%
P-glycoprotein substrate	+	0.7479	74.79%
CYP3A4 substrate	+	0.7382	73.82%
CYP2C9 substrate	-	0.8019	80.19%
CYP2D6 substrate	-	0.9048	90.48%
CYP3A4 inhibition	-	0.8515	85.15%
CYP2C9 inhibition	-	0.9153	91.53%
CYP2C19 inhibition	-	0.9382	93.82%
CYP2D6 inhibition	-	0.9466	94.66%
CYP1A2 inhibition	-	0.8666	86.66%
CYP2C8 inhibition	+	0.6792	67.92%
CYP inhibitory promiscuity	-	0.9532	95.32%
UGT catelyzed	+	0.6000	60.00%
Carcinogenicity (binary)	-	0.9800	98.00%
Carcinogenicity (trinary)	Non-required	0.5261	52.61%
Eye corrosion	-	0.9910	99.10%
Eye irritation	-	0.9026	90.26%
Skin irritation	+	0.5649	56.49%
Skin corrosion	-	0.9199	91.99%
Ames mutagenesis	-	0.6954	69.54%
Human Ether-a-go-go-Related Gene inhibition	+	0.7754	77.54%
Micronuclear	-	0.6900	69.00%
Hepatotoxicity	-	0.6676	66.76%
skin sensitisation	-	0.8778	87.78%
Respiratory toxicity	+	0.6889	68.89%
Reproductive toxicity	+	0.9889	98.89%
Mitochondrial toxicity	+	0.8875	88.75%
Nephrotoxicity	-	0.6664	66.64%
Acute Oral Toxicity (c)	I	0.3844	38.44%
Estrogen receptor binding	+	0.8394	83.94%
Androgen receptor binding	+	0.7433	74.33%
Thyroid receptor binding	+	0.6140	61.40%
Glucocorticoid receptor binding	+	0.8191	81.91%
Aromatase binding	+	0.7223	72.23%
PPAR gamma	+	0.8490	84.90%
Honey bee toxicity	-	0.6236	62.36%
Biodegradation	-	0.8500	85.00%
Crustacea aquatic toxicity	+	0.5845	58.45%
Fish aquatic toxicity	+	0.9550	95.50%

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	98.57%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	98.11%	96.09%
CHEMBL1806	P11388	DNA topoisomerase II alpha	95.42%	89.00%
CHEMBL1994	P08235	Mineralocorticoid receptor	93.46%	100.00%
CHEMBL5608	Q16288	NT-3 growth factor receptor	89.41%	95.89%
CHEMBL241	Q14432	Phosphodiesterase 3A	89.34%	92.94%
CHEMBL1293249	Q13887	Kruppel-like factor 5	89.14%	86.33%
CHEMBL340	P08684	Cytochrome P450 3A4	88.32%	91.19%
CHEMBL1907603	Q05586	Glutamate NMDA receptor; GRIN1/GRIN2B	87.46%	95.89%
CHEMBL1937	Q92769	Histone deacetylase 2	86.10%	94.75%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	85.76%	95.56%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	84.83%	94.45%
CHEMBL3137262	O60341	LSD1/CoREST complex	84.43%	97.09%
CHEMBL2581	P07339	Cathepsin D	83.81%	98.95%
CHEMBL2007	P16234	Platelet-derived growth factor receptor alpha	83.17%	91.07%
CHEMBL226	P30542	Adenosine A1 receptor	82.91%	95.93%
CHEMBL5028	O14672	ADAM10	82.33%	97.50%
CHEMBL3038477	P67870	Casein kinase II alpha/beta	82.15%	99.23%
CHEMBL2035	P08912	Muscarinic acetylcholine receptor M5	81.10%	94.62%
CHEMBL1907601	P11802	Cyclin-dependent kinase 4/cyclin D1	80.20%	98.99%
CHEMBL4478	Q00975	Voltage-gated N-type calcium channel alpha-1B subunit	80.13%	97.14%

Plants that contains it

• Hoodia gordonii

Cross-Links

• PubChem: 16733113
• LOTUS: LTS0127041
• wikiData: Q105179050