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

Details

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Internal ID 50d85eba-aec8-4393-9655-81132254da1f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-2-hydroxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid
SMILES (Canonical) CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C
SMILES (Isomeric) C[C@@]12CC[C@@H]3[C@@]([C@H]1CC=C4[C@]2(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O)C)(C[C@@H]([C@@H](C3(C)C)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)C(=O)O)O)O)O)O)C
InChI InChI=1S/C36H56O10/c1-31(2)12-14-36(30(43)44)15-13-34(6)18(19(36)16-31)8-9-22-33(5)17-20(37)27(32(3,4)21(33)10-11-35(22,34)7)46-29-25(40)23(38)24(39)26(45-29)28(41)42/h8,19-27,29,37-40H,9-17H2,1-7H3,(H,41,42)(H,43,44)/t19-,20-,21-,22+,23-,24-,25+,26-,27-,29-,33-,34+,35+,36-/m0/s1
InChI Key NERHQGKEBFWBNZ-JFXLBYTDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H56O10
Molecular Weight 648.80 g/mol
Exact Mass 648.38734798 g/mol
Topological Polar Surface Area (TPSA) 174.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.12
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 4

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-[[(2S,3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-2-hydroxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,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 + 0.9091 90.91%
Caco-2 - 0.8539 85.39%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8089 80.89%
OATP2B1 inhibitior - 0.7248 72.48%
OATP1B1 inhibitior + 0.8001 80.01%
OATP1B3 inhibitior - 0.2300 23.00%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5071 50.71%
BSEP inhibitior - 0.6585 65.85%
P-glycoprotein inhibitior + 0.7158 71.58%
P-glycoprotein substrate - 0.7957 79.57%
CYP3A4 substrate + 0.6809 68.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8798 87.98%
CYP3A4 inhibition - 0.6587 65.87%
CYP2C9 inhibition - 0.8579 85.79%
CYP2C19 inhibition - 0.8754 87.54%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.8345 83.45%
CYP2C8 inhibition + 0.6548 65.48%
CYP inhibitory promiscuity - 0.9685 96.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6704 67.04%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9166 91.66%
Skin irritation + 0.5075 50.75%
Skin corrosion - 0.9255 92.55%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4394 43.94%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.8054 80.54%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.5526 55.26%
Acute Oral Toxicity (c) IV 0.4349 43.49%
Estrogen receptor binding + 0.6474 64.74%
Androgen receptor binding + 0.7218 72.18%
Thyroid receptor binding - 0.5723 57.23%
Glucocorticoid receptor binding + 0.6671 66.71%
Aromatase binding + 0.6929 69.29%
PPAR gamma + 0.6682 66.82%
Honey bee toxicity - 0.7878 78.78%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9859 98.59%

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 97.49% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.70% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.91% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.40% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.17% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.08% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.15% 93.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.79% 96.77%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.62% 91.07%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.59% 97.36%
CHEMBL221 P23219 Cyclooxygenase-1 83.51% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.78% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.96% 100.00%

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.
Caryocar glabrum
Medicago arabica

Cross-Links

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PubChem 11549167
LOTUS LTS0091473
wikiData Q105178132