(4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-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 8dd1401a-37b6-45ce-8825-dc337db1e99a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-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/C36H56O9/c1-31(2)13-15-36(30(42)43)16-14-34(5)20(21(36)17-31)7-8-24-32(3)11-10-25(33(4,19-38)23(32)9-12-35(24,34)6)45-29-28(41)27(40)26(39)22(18-37)44-29/h7,19,21-29,37,39-41H,8-18H2,1-6H3,(H,42,43)/t21-,22+,23+,24+,25-,26+,27-,28+,29-,32-,33-,34+,35+,36-/m0/s1
InChI Key CJJIRCAOHRWQEM-DLQTVUGOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H56O9
Molecular Weight 632.80 g/mol
Exact Mass 632.39243336 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.24
H-Bond Acceptor 8
H-Bond Donor 5
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,9S,10S,12aR,14bS)-9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-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 + 0.8287 82.87%
Caco-2 - 0.8422 84.22%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8922 89.22%
OATP2B1 inhibitior - 0.5765 57.65%
OATP1B1 inhibitior + 0.7299 72.99%
OATP1B3 inhibitior - 0.4453 44.53%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6224 62.24%
BSEP inhibitior + 0.6601 66.01%
P-glycoprotein inhibitior + 0.7090 70.90%
P-glycoprotein substrate - 0.8614 86.14%
CYP3A4 substrate + 0.6885 68.85%
CYP2C9 substrate - 0.8127 81.27%
CYP2D6 substrate - 0.8768 87.68%
CYP3A4 inhibition - 0.7980 79.80%
CYP2C9 inhibition - 0.8004 80.04%
CYP2C19 inhibition - 0.8872 88.72%
CYP2D6 inhibition - 0.9436 94.36%
CYP1A2 inhibition - 0.7486 74.86%
CYP2C8 inhibition + 0.5804 58.04%
CYP inhibitory promiscuity - 0.9181 91.81%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7059 70.59%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9278 92.78%
Skin irritation - 0.5845 58.45%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.7870 78.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7071 70.71%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.8875 88.75%
skin sensitisation - 0.9026 90.26%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6814 68.14%
Acute Oral Toxicity (c) III 0.7818 78.18%
Estrogen receptor binding + 0.6681 66.81%
Androgen receptor binding + 0.7239 72.39%
Thyroid receptor binding - 0.5546 55.46%
Glucocorticoid receptor binding + 0.6638 66.38%
Aromatase binding + 0.6478 64.78%
PPAR gamma + 0.6452 64.52%
Honey bee toxicity - 0.7843 78.43%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7155 71.55%
Fish aquatic toxicity + 0.9814 98.14%

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 96.08% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.71% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.31% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.27% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.10% 95.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.78% 95.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.78% 93.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.71% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.33% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.60% 96.21%
CHEMBL2581 P07339 Cathepsin D 82.46% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.46% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.96% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.86% 89.00%
CHEMBL5255 O00206 Toll-like receptor 4 81.41% 92.50%
CHEMBL5028 O14672 ADAM10 81.08% 97.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.10% 95.50%

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.
Luffa aegyptiaca

Cross-Links

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PubChem 21609769
LOTUS LTS0250174
wikiData Q104961225