(2S,4aS,6aS,6aS,6bR,8aR,10R,12aR,14bR)-10-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-methoxycarbonyl-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

Details

• Internal ID: 04bd3158-016b-4f56-b9a7-5be898c149a9
• Taxonomy: Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
• IUPAC Name: (2S,4aS,6aS,6aS,6bR,8aR,10R,12aR,14bR)-10-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-methoxycarbonyl-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
• SMILES (Canonical): CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)C)CC=C6C3(CCC7(C6CC(CC7)(C)C(=O)OC)C(=O)O)C)C)C
• SMILES (Isomeric): C[C@@]1(CC[C@]2(CC[C@@]3(C(=CC[C@@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@H](C5(C)C)O[C@H]6[C@@H]([C@@H]([C@H]([C@H](O6)CO)O)O)O[C@H]7[C@@H]([C@@H]([C@@H]([C@H](O7)CO)O)O)O)C)C)[C@H]2C1)C)C(=O)O)C(=O)OC
• InChI: InChI=1S/C43H68O15/c1-38(2)25-10-13-42(6)26(9-8-21-22-18-39(3,37(53)54-7)14-16-43(22,36(51)52)17-15-41(21,42)5)40(25,4)12-11-27(38)57-35-33(31(49)29(47)24(20-45)56-35)58-34-32(50)30(48)28(46)23(19-44)55-34/h8,22-35,44-50H,9-20H2,1-7H3,(H,51,52)/t22-,23-,24-,25+,26+,27-,28-,29+,30-,31-,32-,33-,34+,35+,39+,40+,41-,42-,43-/m1/s1
• InChI Key: RGDJCYRXKJVXKD-ZPAQCIBDSA-N
• Popularity: 0 references in papers

Physical and Chemical Properties

• Molecular Formula: C₄₃H₆₈O₁₅
• Molecular Weight: 825.00 g/mol
• Exact Mass: 824.45582146 g/mol
• Topological Polar Surface Area (TPSA): 242.00 Ų
• XlogP: 3.00
• Atomic LogP (AlogP): 2.04
• H-Bond Acceptor: 14
• H-Bond Donor: 8
• Rotatable Bonds: 8

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.7095	70.95%
Caco-2	-	0.8831	88.31%
Blood Brain Barrier	-	0.6250	62.50%
Human oral bioavailability	-	0.7429	74.29%
Subcellular localzation	Mitochondria	0.8703	87.03%
OATP2B1 inhibitior	-	0.8806	88.06%
OATP1B1 inhibitior	-	0.3428	34.28%
OATP1B3 inhibitior	-	0.3603	36.03%
MATE1 inhibitior	-	1.0000	100.00%
OCT2 inhibitior	+	0.5250	52.50%
BSEP inhibitior	-	0.5131	51.31%
P-glycoprotein inhibitior	+	0.7620	76.20%
P-glycoprotein substrate	-	0.8344	83.44%
CYP3A4 substrate	+	0.7190	71.90%
CYP2C9 substrate	-	1.0000	100.00%
CYP2D6 substrate	-	0.8825	88.25%
CYP3A4 inhibition	-	0.9142	91.42%
CYP2C9 inhibition	-	0.8703	87.03%
CYP2C19 inhibition	-	0.8926	89.26%
CYP2D6 inhibition	-	0.9480	94.80%
CYP1A2 inhibition	-	0.8810	88.10%
CYP2C8 inhibition	+	0.6865	68.65%
CYP inhibitory promiscuity	-	0.9614	96.14%
UGT catelyzed	-	0.6000	60.00%
Carcinogenicity (binary)	-	0.9700	97.00%
Carcinogenicity (trinary)	Non-required	0.6024	60.24%
Eye corrosion	-	0.9884	98.84%
Eye irritation	-	0.9118	91.18%
Skin irritation	-	0.6660	66.60%
Skin corrosion	-	0.9449	94.49%
Ames mutagenesis	-	0.8470	84.70%
Human Ether-a-go-go-Related Gene inhibition	-	0.4167	41.67%
Micronuclear	-	0.7800	78.00%
Hepatotoxicity	-	0.9256	92.56%
skin sensitisation	-	0.8977	89.77%
Respiratory toxicity	+	0.5222	52.22%
Reproductive toxicity	+	0.8889	88.89%
Mitochondrial toxicity	-	0.6125	61.25%
Nephrotoxicity	+	0.4497	44.97%
Acute Oral Toxicity (c)	III	0.7305	73.05%
Estrogen receptor binding	+	0.7483	74.83%
Androgen receptor binding	+	0.7326	73.26%
Thyroid receptor binding	-	0.6372	63.72%
Glucocorticoid receptor binding	+	0.6597	65.97%
Aromatase binding	+	0.6306	63.06%
PPAR gamma	+	0.7364	73.64%
Honey bee toxicity	-	0.7085	70.85%
Biodegradation	-	0.6750	67.50%
Crustacea aquatic toxicity	-	0.6300	63.00%
Fish aquatic toxicity	+	0.9479	94.79%

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	98.65%	91.11%
CHEMBL3251	P19838	Nuclear factor NF-kappa-B p105 subunit	96.24%	96.09%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	91.49%	94.45%
CHEMBL3880	P07900	Heat shock protein HSP 90-alpha	90.63%	96.21%
CHEMBL3137262	O60341	LSD1/CoREST complex	90.59%	97.09%
CHEMBL3714130	P46095	G-protein coupled receptor 6	90.35%	97.36%
CHEMBL5255	O00206	Toll-like receptor 4	87.73%	92.50%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	87.22%	95.56%
CHEMBL2111367	P27986	PI3-kinase p110-alpha/p85-alpha	86.37%	94.33%
CHEMBL3060	Q9Y345	Glycine transporter 2	86.08%	99.17%
CHEMBL5608	Q16288	NT-3 growth factor receptor	84.92%	95.89%
CHEMBL2581	P07339	Cathepsin D	83.83%	98.95%
CHEMBL4187	Q99250	Sodium channel protein type II alpha subunit	82.66%	95.50%
CHEMBL5028	O14672	ADAM10	82.15%	97.50%
CHEMBL340	P08684	Cytochrome P450 3A4	81.05%	91.19%

Plants that contains it

• Phytolacca icosandra

Cross-Links

• PubChem: 162954956
• LOTUS: LTS0024984
• wikiData: Q105235779