(4aR,5R,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxycarbonyloxan-2-yl]oxy-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 2acebbcd-2d2e-4ae5-bd3a-c08a25263efb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (4aR,5R,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxycarbonyloxan-2-yl]oxy-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/C37H58O11/c1-32(2)14-15-37(31(44)45)20(16-32)19-8-9-22-33(3)12-11-24(47-30-27(42)25(40)26(41)28(48-30)29(43)46-7)34(4,18-38)21(33)10-13-35(22,5)36(19,6)17-23(37)39/h8,20-28,30,38-42H,9-18H2,1-7H3,(H,44,45)/t20-,21+,22+,23+,24-,25-,26-,27+,28-,30+,33-,34+,35+,36+,37+/m0/s1
InChI Key WHNZFHPZVSSPNC-PXNIFYFQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H58O11
Molecular Weight 678.80 g/mol
Exact Mass 678.39791266 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aR,5R,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxycarbonyloxan-2-yl]oxy-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 + 0.8518 85.18%
Caco-2 - 0.8568 85.68%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8570 85.70%
OATP2B1 inhibitior - 0.7277 72.77%
OATP1B1 inhibitior + 0.8530 85.30%
OATP1B3 inhibitior - 0.2561 25.61%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5542 55.42%
BSEP inhibitior - 0.4632 46.32%
P-glycoprotein inhibitior + 0.7584 75.84%
P-glycoprotein substrate - 0.6266 62.66%
CYP3A4 substrate + 0.7184 71.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8825 88.25%
CYP3A4 inhibition - 0.6909 69.09%
CYP2C9 inhibition - 0.8107 81.07%
CYP2C19 inhibition - 0.8685 86.85%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.8058 80.58%
CYP2C8 inhibition + 0.6761 67.61%
CYP inhibitory promiscuity - 0.9563 95.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6994 69.94%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9187 91.87%
Skin irritation - 0.5927 59.27%
Skin corrosion - 0.9460 94.60%
Ames mutagenesis - 0.7524 75.24%
Human Ether-a-go-go-Related Gene inhibition + 0.7123 71.23%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.8642 86.42%
skin sensitisation - 0.8980 89.80%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5812 58.12%
Acute Oral Toxicity (c) III 0.7290 72.90%
Estrogen receptor binding + 0.6466 64.66%
Androgen receptor binding + 0.7277 72.77%
Thyroid receptor binding - 0.5838 58.38%
Glucocorticoid receptor binding + 0.7004 70.04%
Aromatase binding + 0.6752 67.52%
PPAR gamma + 0.6948 69.48%
Honey bee toxicity - 0.7875 78.75%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9479 94.79%

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 93.72% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.97% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.50% 96.09%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 88.55% 91.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.80% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.00% 97.09%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.57% 94.33%
CHEMBL221 P23219 Cyclooxygenase-1 85.95% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.86% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.24% 92.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.12% 91.07%
CHEMBL5028 O14672 ADAM10 84.54% 97.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.75% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.24% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.12% 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.
Prunella vulgaris

Cross-Links

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PubChem 16105450
LOTUS LTS0223189
wikiData Q105305473