[(1S,2R,6S,7S,8R,10R,12R,14S)-8-hydroxy-14-methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (E)-2-(acetyloxymethyl)but-2-enoate

Details

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Internal ID e754fc9b-8c8a-46c3-a968-7ed35dbb262d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Guaianolides and derivatives
IUPAC Name [(1S,2R,6S,7S,8R,10R,12R,14S)-8-hydroxy-14-methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (E)-2-(acetyloxymethyl)but-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O8/c1-6-12(8-27-11(4)23)21(26)29-19-15-10(3)20(25)28-18(15)16-13(9(2)17(19)24)7-14-22(16,5)30-14/h6,13-19,24H,2-3,7-8H2,1,4-5H3/b12-6+/t13-,14+,15-,16-,17+,18+,19-,22+/m0/s1
InChI Key JGHRVXZPUCLANB-PHZAAGGESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O8
Molecular Weight 418.40 g/mol
Exact Mass 418.16276778 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.23
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,6S,7S,8R,10R,12R,14S)-8-hydroxy-14-methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (E)-2-(acetyloxymethyl)but-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 + 0.9350 93.50%
Caco-2 - 0.7574 75.74%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6933 69.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8272 82.72%
OATP1B3 inhibitior + 0.8996 89.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4631 46.31%
P-glycoprotein inhibitior - 0.5109 51.09%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6743 67.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8960 89.60%
CYP3A4 inhibition - 0.6410 64.10%
CYP2C9 inhibition - 0.8656 86.56%
CYP2C19 inhibition - 0.8356 83.56%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.8204 82.04%
CYP2C8 inhibition - 0.6449 64.49%
CYP inhibitory promiscuity - 0.8563 85.63%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6314 63.14%
Eye corrosion - 0.9810 98.10%
Eye irritation - 0.8942 89.42%
Skin irritation - 0.6175 61.75%
Skin corrosion - 0.8998 89.98%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7292 72.92%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation - 0.7326 73.26%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.7232 72.32%
Acute Oral Toxicity (c) I 0.3535 35.35%
Estrogen receptor binding + 0.6843 68.43%
Androgen receptor binding + 0.6366 63.66%
Thyroid receptor binding + 0.5712 57.12%
Glucocorticoid receptor binding + 0.7979 79.79%
Aromatase binding + 0.5220 52.20%
PPAR gamma - 0.5336 53.36%
Honey bee toxicity - 0.6240 62.40%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9276 92.76%

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%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.96% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.47% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.09% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.93% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.30% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.79% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.65% 89.00%
CHEMBL2581 P07339 Cathepsin D 88.47% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 86.70% 97.79%
CHEMBL340 P08684 Cytochrome P450 3A4 85.20% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 84.77% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.64% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 83.86% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.55% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.87% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.64% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.90% 95.50%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.61% 89.34%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.31% 100.00%
CHEMBL5028 O14672 ADAM10 80.06% 97.50%

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.
Lasiolaena santosii

Cross-Links

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PubChem 163056061
LOTUS LTS0206425
wikiData Q105127364