(1S,4aS,6R,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-5,5,8a-trimethyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4,4a,6,7,8-hexahydronaphthalene-2-carboxylic acid

Details

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Internal ID cd152c54-d7aa-4e73-8781-24c7dea39cf4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name (1S,4aS,6R,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-5,5,8a-trimethyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4,4a,6,7,8-hexahydronaphthalene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H44O9/c1-14(10-12-27)5-7-16-15(23(32)33)6-8-18-25(2,3)19(9-11-26(16,18)4)35-24-22(31)21(30)20(29)17(13-28)34-24/h6,14,16-22,24,27-31H,5,7-13H2,1-4H3,(H,32,33)/t14-,16+,17+,18+,19+,20+,21-,22+,24-,26+/m0/s1
InChI Key LTEZVUVZFATCKC-NTFYDHSXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H44O9
Molecular Weight 500.60 g/mol
Exact Mass 500.29853298 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.44
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4aS,6R,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-5,5,8a-trimethyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4,4a,6,7,8-hexahydronaphthalene-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 + 0.7768 77.68%
Caco-2 - 0.7642 76.42%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8337 83.37%
OATP2B1 inhibitior - 0.7157 71.57%
OATP1B1 inhibitior + 0.8229 82.29%
OATP1B3 inhibitior - 0.3365 33.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6776 67.76%
BSEP inhibitior - 0.6124 61.24%
P-glycoprotein inhibitior - 0.5549 55.49%
P-glycoprotein substrate - 0.7607 76.07%
CYP3A4 substrate + 0.6663 66.63%
CYP2C9 substrate - 0.8020 80.20%
CYP2D6 substrate - 0.8963 89.63%
CYP3A4 inhibition - 0.9021 90.21%
CYP2C9 inhibition - 0.8375 83.75%
CYP2C19 inhibition - 0.8403 84.03%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.8126 81.26%
CYP2C8 inhibition - 0.6701 67.01%
CYP inhibitory promiscuity - 0.9527 95.27%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7155 71.55%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9581 95.81%
Skin irritation - 0.6357 63.57%
Skin corrosion - 0.9537 95.37%
Ames mutagenesis - 0.7670 76.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3764 37.64%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.7948 79.48%
skin sensitisation - 0.8817 88.17%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6858 68.58%
Acute Oral Toxicity (c) III 0.7381 73.81%
Estrogen receptor binding + 0.6537 65.37%
Androgen receptor binding + 0.5924 59.24%
Thyroid receptor binding - 0.4905 49.05%
Glucocorticoid receptor binding + 0.6034 60.34%
Aromatase binding + 0.5806 58.06%
PPAR gamma + 0.6223 62.23%
Honey bee toxicity - 0.7354 73.54%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6850 68.50%
Fish aquatic toxicity + 0.9438 94.38%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.06% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.33% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 92.64% 90.17%
CHEMBL2581 P07339 Cathepsin D 91.59% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.72% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.01% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.35% 97.25%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.15% 94.08%
CHEMBL5255 O00206 Toll-like receptor 4 86.08% 92.50%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 85.82% 94.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.44% 95.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.03% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.03% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.70% 99.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.93% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.91% 95.89%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.60% 94.62%
CHEMBL5028 O14672 ADAM10 81.25% 97.50%
CHEMBL237 P41145 Kappa opioid receptor 81.23% 98.10%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.39% 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.
Aristeguietia glutinosa

Cross-Links

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PubChem 163041562
LOTUS LTS0090608
wikiData Q105156916