[(3aR,4R,6R,7Z,10Z,11aS)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] (2R)-2-methylbutanoate

Details

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Internal ID d6ae751e-c714-4d47-a036-312b11a1e970
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Germacranolides and derivatives
IUPAC Name [(3aR,4R,6R,7Z,10Z,11aS)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] (2R)-2-methylbutanoate
SMILES (Canonical) CCC(C)C(=O)OC1CC(C=CC(=O)C(=CC2C1C(=C)C(=O)O2)C)(C)O
SMILES (Isomeric) CC[C@@H](C)C(=O)O[C@@H]1C[C@@](/C=C\C(=O)/C(=C\[C@H]2[C@@H]1C(=C)C(=O)O2)/C)(C)O
InChI InChI=1S/C20H26O6/c1-6-11(2)18(22)26-16-10-20(5,24)8-7-14(21)12(3)9-15-17(16)13(4)19(23)25-15/h7-9,11,15-17,24H,4,6,10H2,1-3,5H3/b8-7-,12-9-/t11-,15+,16-,17+,20+/m1/s1
InChI Key XUPGTXZVXSSFBQ-AUIFUDINSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O6
Molecular Weight 362.40 g/mol
Exact Mass 362.17293854 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(3aR,4R,6R,7Z,10Z,11aS)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] (2R)-2-methylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.7095 70.95%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4620 46.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8668 86.68%
OATP1B3 inhibitior + 0.9138 91.38%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5255 52.55%
P-glycoprotein inhibitior + 0.6212 62.12%
P-glycoprotein substrate - 0.6540 65.40%
CYP3A4 substrate + 0.6427 64.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9150 91.50%
CYP3A4 inhibition - 0.6245 62.45%
CYP2C9 inhibition - 0.8683 86.83%
CYP2C19 inhibition - 0.8476 84.76%
CYP2D6 inhibition - 0.9577 95.77%
CYP1A2 inhibition - 0.8405 84.05%
CYP2C8 inhibition - 0.6594 65.94%
CYP inhibitory promiscuity - 0.8876 88.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4666 46.66%
Eye corrosion - 0.9633 96.33%
Eye irritation - 0.8883 88.83%
Skin irritation - 0.5659 56.59%
Skin corrosion - 0.8932 89.32%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3779 37.79%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.6304 63.04%
skin sensitisation - 0.5727 57.27%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7020 70.20%
Acute Oral Toxicity (c) III 0.4880 48.80%
Estrogen receptor binding + 0.6646 66.46%
Androgen receptor binding + 0.5624 56.24%
Thyroid receptor binding + 0.5905 59.05%
Glucocorticoid receptor binding + 0.6638 66.38%
Aromatase binding - 0.5510 55.10%
PPAR gamma - 0.5576 55.76%
Honey bee toxicity - 0.8110 81.10%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9494 94.94%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.26% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.88% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.26% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.12% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 90.60% 90.17%
CHEMBL2581 P07339 Cathepsin D 89.47% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 87.43% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.07% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.44% 97.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.85% 96.47%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.74% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.02% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.56% 99.23%
CHEMBL4072 P07858 Cathepsin B 84.03% 93.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.50% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.73% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.88% 93.56%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 80.75% 96.37%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.24% 94.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.04% 97.33%

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.
Serratula coronata
Silene turkestanica
Tithonia diversifolia

Cross-Links

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PubChem 163035861
LOTUS LTS0209999
wikiData Q105138639