28-Glucosyloleanolic acid 3-arabinoside

Details

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Internal ID 2f13ad2a-5366-40be-9475-9838ceb12bd9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name [3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H66O12/c1-36(2)14-16-41(35(49)53-34-32(48)30(46)29(45)24(19-42)51-34)17-15-39(6)21(22(41)18-36)8-9-26-38(5)12-11-27(37(3,4)25(38)10-13-40(26,39)7)52-33-31(47)28(44)23(43)20-50-33/h8,22-34,42-48H,9-20H2,1-7H3
InChI Key VXRNZMDDBZNPKJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C41H66O12
Molecular Weight 751.00 g/mol
Exact Mass 750.45542754 g/mol
Topological Polar Surface Area (TPSA) 196.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 2.96
H-Bond Acceptor 12
H-Bond Donor 7
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 28-Glucosyloleanolic acid 3-arabinoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7891 78.91%
Caco-2 - 0.8702 87.02%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8567 85.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.6952 69.52%
OATP1B3 inhibitior - 0.5700 57.00%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6276 62.76%
BSEP inhibitior - 0.5383 53.83%
P-glycoprotein inhibitior + 0.7492 74.92%
P-glycoprotein substrate - 0.8428 84.28%
CYP3A4 substrate + 0.7178 71.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition - 0.9300 93.00%
CYP2C9 inhibition - 0.8838 88.38%
CYP2C19 inhibition - 0.9101 91.01%
CYP2D6 inhibition - 0.9422 94.22%
CYP1A2 inhibition - 0.8933 89.33%
CYP2C8 inhibition + 0.6068 60.68%
CYP inhibitory promiscuity - 0.9668 96.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6254 62.54%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9111 91.11%
Skin irritation - 0.6103 61.03%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6518 65.18%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.9875 98.75%
skin sensitisation - 0.8917 89.17%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.9005 90.05%
Acute Oral Toxicity (c) III 0.7945 79.45%
Estrogen receptor binding + 0.6673 66.73%
Androgen receptor binding + 0.7194 71.94%
Thyroid receptor binding - 0.5830 58.30%
Glucocorticoid receptor binding + 0.6447 64.47%
Aromatase binding + 0.6356 63.56%
PPAR gamma + 0.6959 69.59%
Honey bee toxicity - 0.7168 71.68%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6305 63.05%
Fish aquatic toxicity + 0.9411 94.11%

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 98.24% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.64% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.53% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.23% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.36% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.94% 95.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.35% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.93% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.53% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 84.54% 92.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.46% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.68% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.65% 96.21%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.59% 97.36%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.31% 86.92%

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.
Lafoensia glyptocarpa

Cross-Links

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PubChem 74951269
LOTUS LTS0057503
wikiData Q105298718