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

Details

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Internal ID 4f26840c-8f3f-4ea5-8e04-9ed00c617688
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name [(2S,3S,4aR,5R,8aS)-3-[(2R,3S,4S,5R,6S)-5-acetyloxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,1,4a,6-tetramethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl] (Z)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H52O9/c1-10-19(3)30(38)42-29-24(41-31-27(37)26(36)28(21(5)39-31)40-22(6)35)17-33(9)23(13-11-18(2)15-16-34)20(4)12-14-25(33)32(29,7)8/h10,12,15,21,23-29,31,34,36-37H,11,13-14,16-17H2,1-9H3/b18-15+,19-10-/t21-,23+,24-,25+,26-,27-,28-,29+,31+,33+/m0/s1
InChI Key IUPUSRDATISFTN-XVCRJXONSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C33H52O9
Molecular Weight 592.80 g/mol
Exact Mass 592.36113323 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3S,4aR,5R,8aS)-3-[(2R,3S,4S,5R,6S)-5-acetyloxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,1,4a,6-tetramethyl-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 + 0.8464 84.64%
Caco-2 - 0.7901 79.01%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.8778 87.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8248 82.48%
OATP1B3 inhibitior + 0.8097 80.97%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.9151 91.51%
P-glycoprotein inhibitior + 0.7702 77.02%
P-glycoprotein substrate - 0.5360 53.60%
CYP3A4 substrate + 0.7062 70.62%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8973 89.73%
CYP3A4 inhibition - 0.7747 77.47%
CYP2C9 inhibition - 0.8484 84.84%
CYP2C19 inhibition - 0.8752 87.52%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition - 0.5964 59.64%
CYP2C8 inhibition + 0.5709 57.09%
CYP inhibitory promiscuity - 0.9153 91.53%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6756 67.56%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9302 93.02%
Skin irritation - 0.5459 54.59%
Skin corrosion - 0.9530 95.30%
Ames mutagenesis - 0.6970 69.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6774 67.74%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.6892 68.92%
skin sensitisation - 0.8770 87.70%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6387 63.87%
Acute Oral Toxicity (c) III 0.7317 73.17%
Estrogen receptor binding + 0.7419 74.19%
Androgen receptor binding + 0.5794 57.94%
Thyroid receptor binding - 0.5310 53.10%
Glucocorticoid receptor binding + 0.7241 72.41%
Aromatase binding + 0.6904 69.04%
PPAR gamma + 0.7124 71.24%
Honey bee toxicity - 0.6859 68.59%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9798 97.98%

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 98.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.36% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.58% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.01% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.20% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.16% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.53% 99.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.23% 100.00%
CHEMBL2581 P07339 Cathepsin D 88.22% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.12% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.92% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.72% 95.89%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.90% 91.24%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.59% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.92% 97.36%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.53% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.99% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.87% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.62% 99.23%

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 163023381
LOTUS LTS0090037
wikiData Q105120767