8a-[3-[4-Acetyloxy-5-[4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3-hydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,8-dihydroxy-4-(hydroxymethyl)-6a,6b,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid

Details

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Internal ID 640bf0bb-69a7-4705-b1e2-c3ae31377dfc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name 8a-[3-[4-acetyloxy-5-[4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3-hydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,8-dihydroxy-4-(hydroxymethyl)-6a,6b,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4O)C)(CCC7C6(CC(C(C7(CO)C(=O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)O)O)O)OC(=O)C)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4O)C)(CCC7C6(CC(C(C7(CO)C(=O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)O)O)O)OC(=O)C)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O
InChI InChI=1S/C59H92O30/c1-23-40(85-46-38(72)41(29(66)19-79-46)86-50-44(74)57(78,20-61)22-81-50)42(83-24(2)63)39(73)48(82-23)87-43-34(68)28(65)18-80-49(43)89-52(77)58-13-12-53(3,4)14-26(58)25-8-9-31-54(5)15-27(64)45(88-47-37(71)36(70)35(69)30(17-60)84-47)59(21-62,51(75)76)32(54)10-11-55(31,6)56(25,7)16-33(58)67/h8,23,26-50,60-62,64-74,78H,9-22H2,1-7H3,(H,75,76)
InChI Key PLRQGYABNOAMAF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C59H92O30
Molecular Weight 1281.30 g/mol
Exact Mass 1280.56734151 g/mol
Topological Polar Surface Area (TPSA) 476.00 Ų
XlogP -3.20
Atomic LogP (AlogP) -4.72
H-Bond Acceptor 29
H-Bond Donor 16
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8a-[3-[4-Acetyloxy-5-[4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3-hydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,8-dihydroxy-4-(hydroxymethyl)-6a,6b,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8427 84.27%
Caco-2 - 0.8646 86.46%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.8733 87.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.6999 69.99%
OATP1B3 inhibitior + 0.8381 83.81%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9721 97.21%
P-glycoprotein inhibitior + 0.7435 74.35%
P-glycoprotein substrate + 0.7053 70.53%
CYP3A4 substrate + 0.7448 74.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8839 88.39%
CYP3A4 inhibition - 0.8187 81.87%
CYP2C9 inhibition - 0.8372 83.72%
CYP2C19 inhibition - 0.9259 92.59%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.9133 91.33%
CYP2C8 inhibition + 0.7928 79.28%
CYP inhibitory promiscuity - 0.9476 94.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4689 46.89%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8974 89.74%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9368 93.68%
Ames mutagenesis - 0.6370 63.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7703 77.03%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.9098 90.98%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6472 64.72%
Acute Oral Toxicity (c) III 0.6742 67.42%
Estrogen receptor binding + 0.7100 71.00%
Androgen receptor binding + 0.7574 75.74%
Thyroid receptor binding + 0.6889 68.89%
Glucocorticoid receptor binding + 0.7922 79.22%
Aromatase binding + 0.6451 64.51%
PPAR gamma + 0.8150 81.50%
Honey bee toxicity - 0.6583 65.83%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5550 55.50%
Fish aquatic toxicity + 0.9692 96.92%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
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 98.71% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.63% 95.17%
CHEMBL3714130 P46095 G-protein coupled receptor 6 95.26% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.60% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.86% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.20% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.10% 96.77%
CHEMBL1937 Q92769 Histone deacetylase 2 90.24% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.38% 94.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 88.48% 89.44%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.37% 99.23%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.98% 86.92%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.54% 100.00%
CHEMBL2581 P07339 Cathepsin D 86.68% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.58% 97.09%
CHEMBL5028 O14672 ADAM10 86.30% 97.50%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.18% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 85.72% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.68% 89.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.52% 94.33%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 85.52% 95.52%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.41% 93.00%
CHEMBL226 P30542 Adenosine A1 receptor 85.00% 95.93%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.80% 91.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.70% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.07% 91.07%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.27% 87.67%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.98% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.94% 95.89%
CHEMBL4618 P09960 Leukotriene A4 hydrolase 81.69% 97.86%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.12% 92.94%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.25% 81.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Platycodon grandiflorus

Cross-Links

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PubChem 137796334
LOTUS LTS0210109
wikiData Q105211168