[(2S,3S,4aS,5R,8aS)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,1,4a,6-tetramethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,8,8a-hexahydronaphthalen-2-yl] (Z)-2-methylbut-2-enoate

Details

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Internal ID 73e3640a-61e0-4879-9037-7dcbadb2af4d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name [(2S,3S,4aS,5R,8aS)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,1,4a,6-tetramethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,8,8a-hexahydronaphthalen-2-yl] (Z)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H50O8/c1-9-18(3)28(36)39-27-22(38-29-26(35)25(34)24(33)20(5)37-29)16-31(8)21(12-10-17(2)14-15-32)19(4)11-13-23(31)30(27,6)7/h9,11,14,20-27,29,32-35H,10,12-13,15-16H2,1-8H3/b17-14+,18-9-/t20-,21+,22-,23+,24+,25+,26-,27+,29+,31-/m0/s1
InChI Key ABAMJPLUWDIGKU-QWUHJACOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H50O8
Molecular Weight 550.70 g/mol
Exact Mass 550.35056855 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.81
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3S,4aS,5R,8aS)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,1,4a,6-tetramethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,8,8a-hexahydronaphthalen-2-yl] (Z)-2-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7645 76.45%
Caco-2 - 0.7597 75.97%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.8280 82.80%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.8440 84.40%
OATP1B3 inhibitior - 0.2551 25.51%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8794 87.94%
P-glycoprotein inhibitior + 0.7097 70.97%
P-glycoprotein substrate - 0.5778 57.78%
CYP3A4 substrate + 0.6939 69.39%
CYP2C9 substrate - 0.8033 80.33%
CYP2D6 substrate - 0.8830 88.30%
CYP3A4 inhibition - 0.8996 89.96%
CYP2C9 inhibition - 0.8458 84.58%
CYP2C19 inhibition - 0.8568 85.68%
CYP2D6 inhibition - 0.9293 92.93%
CYP1A2 inhibition - 0.6714 67.14%
CYP2C8 inhibition + 0.5724 57.24%
CYP inhibitory promiscuity - 0.8762 87.62%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7099 70.99%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9404 94.04%
Skin irritation - 0.5875 58.75%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.6870 68.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7346 73.46%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7642 76.42%
skin sensitisation - 0.8647 86.47%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6973 69.73%
Acute Oral Toxicity (c) III 0.7715 77.15%
Estrogen receptor binding + 0.7144 71.44%
Androgen receptor binding + 0.5607 56.07%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6850 68.50%
Aromatase binding + 0.6818 68.18%
PPAR gamma + 0.6525 65.25%
Honey bee toxicity - 0.6930 69.30%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9646 96.46%

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 98.60% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.34% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 93.55% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.18% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.32% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.67% 99.17%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.43% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.86% 95.56%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 87.77% 91.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.16% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.89% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.49% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.28% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.97% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.41% 97.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.32% 91.07%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.05% 93.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.49% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163017711
LOTUS LTS0152071
wikiData Q104908495