5-[6-Carboxy-4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-22-oxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-yl]oxy]oxane-2-carboxylic acid

Details

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Internal ID f0c6201b-f273-49ee-a4ee-852e9d09c684
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name 5-[6-carboxy-4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-22-oxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-yl]oxy]oxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C48H72O20/c1-19-26(50)27(51)32(56)39(62-19)67-36-31(55)29(53)34(38(59)60)66-41(36)68-35-30(54)28(52)33(37(57)58)65-40(35)63-24-11-12-45(4)22(46(24,5)18-49)10-13-48(7)23(45)9-8-20-21-16-43(2)17-25(64-42(43)61)44(21,3)14-15-47(20,48)6/h8,19,21-36,39-41,49-56H,9-18H2,1-7H3,(H,57,58)(H,59,60)
InChI Key ZUOJCKGXPVRRBE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C48H72O20
Molecular Weight 969.10 g/mol
Exact Mass 968.46169468 g/mol
Topological Polar Surface Area (TPSA) 318.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 0.34
H-Bond Acceptor 18
H-Bond Donor 10
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-[6-Carboxy-4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-22-oxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-yl]oxy]oxane-2-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 + 0.8075 80.75%
Caco-2 - 0.8932 89.32%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8366 83.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8395 83.95%
OATP1B3 inhibitior + 0.9301 93.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5271 52.71%
BSEP inhibitior + 0.7959 79.59%
P-glycoprotein inhibitior + 0.7507 75.07%
P-glycoprotein substrate - 0.5682 56.82%
CYP3A4 substrate + 0.7270 72.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8832 88.32%
CYP3A4 inhibition - 0.8745 87.45%
CYP2C9 inhibition - 0.8654 86.54%
CYP2C19 inhibition - 0.9163 91.63%
CYP2D6 inhibition - 0.9428 94.28%
CYP1A2 inhibition - 0.8020 80.20%
CYP2C8 inhibition + 0.7259 72.59%
CYP inhibitory promiscuity - 0.9026 90.26%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4706 47.06%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9037 90.37%
Skin irritation + 0.5707 57.07%
Skin corrosion - 0.9325 93.25%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7230 72.30%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.9163 91.63%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6340 63.40%
Acute Oral Toxicity (c) III 0.5907 59.07%
Estrogen receptor binding + 0.8047 80.47%
Androgen receptor binding + 0.7395 73.95%
Thyroid receptor binding - 0.5848 58.48%
Glucocorticoid receptor binding + 0.7319 73.19%
Aromatase binding + 0.6036 60.36%
PPAR gamma + 0.8096 80.96%
Honey bee toxicity - 0.7433 74.33%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9769 97.69%

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
CHEMBL3714130 P46095 G-protein coupled receptor 6 95.35% 97.36%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.28% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.26% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.73% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.40% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.94% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.44% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.80% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.61% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.39% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.15% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.75% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.08% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 80.35% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.03% 94.33%

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.
Albizia myriophylla

Cross-Links

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PubChem 73799329
LOTUS LTS0110627
wikiData Q105383911