(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8-oxo-1,2,3,4a,5,6,7,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Details

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Internal ID 439ef797-d97c-43f4-a55c-72487e802328
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8-oxo-1,2,3,4a,5,6,7,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid
SMILES (Canonical) CC1(CCC2C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C
SMILES (Isomeric) C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC(=O)[C@@H]5[C@H]4CC(CC5)(C)C)C)C)(C)C)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)C(=O)O)O)O)O
InChI InChI=1S/C35H54O8/c1-31(2)13-10-18-19(16-31)20-8-9-23-33(5)14-12-24(42-30-27(39)25(37)26(38)28(43-30)29(40)41)32(3,4)22(33)11-15-34(23,6)35(20,7)17-21(18)36/h8,18-19,22-28,30,37-39H,9-17H2,1-7H3,(H,40,41)/t18-,19+,22-,23+,24-,25-,26-,27+,28-,30+,33-,34+,35+/m0/s1
InChI Key VOPSFXLIPFJEHR-HFZRVDPXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C35H54O8
Molecular Weight 602.80 g/mol
Exact Mass 602.38186868 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8-oxo-1,2,3,4a,5,6,7,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-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 + 0.9119 91.19%
Caco-2 - 0.8188 81.88%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7888 78.88%
OATP2B1 inhibitior - 0.5802 58.02%
OATP1B1 inhibitior + 0.7589 75.89%
OATP1B3 inhibitior + 0.8541 85.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.5767 57.67%
P-glycoprotein inhibitior + 0.7215 72.15%
P-glycoprotein substrate - 0.8192 81.92%
CYP3A4 substrate + 0.7080 70.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8839 88.39%
CYP3A4 inhibition - 0.7510 75.10%
CYP2C9 inhibition - 0.8779 87.79%
CYP2C19 inhibition - 0.9169 91.69%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.7652 76.52%
CYP2C8 inhibition + 0.6645 66.45%
CYP inhibitory promiscuity - 0.9557 95.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6429 64.29%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9297 92.97%
Skin irritation - 0.5247 52.47%
Skin corrosion - 0.9256 92.56%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6754 67.54%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.7663 76.63%
skin sensitisation - 0.7682 76.82%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6595 65.95%
Acute Oral Toxicity (c) IV 0.4895 48.95%
Estrogen receptor binding + 0.6139 61.39%
Androgen receptor binding + 0.7348 73.48%
Thyroid receptor binding - 0.5691 56.91%
Glucocorticoid receptor binding + 0.6717 67.17%
Aromatase binding + 0.6905 69.05%
PPAR gamma + 0.6290 62.90%
Honey bee toxicity - 0.7778 77.78%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9878 98.78%

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 96.51% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.49% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.95% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.56% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.49% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.00% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.21% 95.89%
CHEMBL2581 P07339 Cathepsin D 85.02% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.09% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.73% 94.45%
CHEMBL5255 O00206 Toll-like receptor 4 82.65% 92.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.52% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.55% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.27% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.65% 86.33%

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.
Aster auriculatus

Cross-Links

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PubChem 101935943
LOTUS LTS0041528
wikiData Q105290336