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

Details

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Internal ID ee2763cc-12b4-4165-a284-da6d011771ba
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4-acetyloxy-3,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H58O9/c1-21(39)45-29-24(40)19-44-30(28(29)41)46-27-11-12-33(4)25(34(27,5)20-38)10-13-36(7)26(33)9-8-22-23-18-32(2,3)14-16-37(23,31(42)43)17-15-35(22,36)6/h8,23-30,38,40-41H,9-20H2,1-7H3,(H,42,43)/t23-,24-,25+,26+,27-,28+,29-,30-,33-,34-,35+,36+,37-/m0/s1
InChI Key GZHUOZHHOSNNHO-JBCPEALYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H58O9
Molecular Weight 646.80 g/mol
Exact Mass 646.40808342 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.24
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4-acetyloxy-3,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-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 + 0.8845 88.45%
Caco-2 - 0.8374 83.74%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8576 85.76%
OATP2B1 inhibitior - 0.5748 57.48%
OATP1B1 inhibitior + 0.6946 69.46%
OATP1B3 inhibitior - 0.2968 29.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5224 52.24%
BSEP inhibitior + 0.7556 75.56%
P-glycoprotein inhibitior + 0.7584 75.84%
P-glycoprotein substrate - 0.6184 61.84%
CYP3A4 substrate + 0.7194 71.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8855 88.55%
CYP3A4 inhibition - 0.7485 74.85%
CYP2C9 inhibition - 0.8418 84.18%
CYP2C19 inhibition - 0.8896 88.96%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition - 0.8451 84.51%
CYP2C8 inhibition + 0.6342 63.42%
CYP inhibitory promiscuity - 0.9366 93.66%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6779 67.79%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9209 92.09%
Skin irritation - 0.5771 57.71%
Skin corrosion - 0.9484 94.84%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6556 65.56%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.9009 90.09%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5332 53.32%
Acute Oral Toxicity (c) III 0.8052 80.52%
Estrogen receptor binding + 0.6563 65.63%
Androgen receptor binding + 0.7157 71.57%
Thyroid receptor binding - 0.5857 58.57%
Glucocorticoid receptor binding + 0.6723 67.23%
Aromatase binding + 0.6746 67.46%
PPAR gamma + 0.6402 64.02%
Honey bee toxicity - 0.7737 77.37%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6150 61.50%
Fish aquatic toxicity + 0.9607 96.07%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 98.90% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.56% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.54% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.77% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.54% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.77% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.80% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.13% 91.07%
CHEMBL2581 P07339 Cathepsin D 84.12% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.72% 95.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.63% 96.77%
CHEMBL5028 O14672 ADAM10 83.19% 97.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.01% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.69% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.12% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.26% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.17% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11285192
LOTUS LTS0089229
wikiData Q105024387