[(3aS,4S,6S,9S,10R,11aR)-6-acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,8,9,10,11,11a-octahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate

Details

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Internal ID cd6247c9-1c48-41f6-a622-f06a5e97bc53
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Germacranolides and derivatives
IUPAC Name [(3aS,4S,6S,9S,10R,11aR)-6-acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,8,9,10,11,11a-octahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1CC(C(=O)CC(C(CC2C1C(=C)C(=O)O2)C)O)(C)OC(=O)C
SMILES (Isomeric) C/C=C(/C)\C(=O)O[C@H]1C[C@](C(=O)C[C@@H]([C@@H](C[C@@H]2[C@@H]1C(=C)C(=O)O2)C)O)(C)OC(=O)C
InChI InChI=1S/C22H30O8/c1-7-11(2)20(26)29-17-10-22(6,30-14(5)23)18(25)9-15(24)12(3)8-16-19(17)13(4)21(27)28-16/h7,12,15-17,19,24H,4,8-10H2,1-3,5-6H3/b11-7-/t12-,15+,16-,17+,19+,22+/m1/s1
InChI Key QHGWZSLYSOBOIR-HIIGEEJOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O8
Molecular Weight 422.50 g/mol
Exact Mass 422.19406791 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.03
H-Bond Acceptor 8
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 [(3aS,4S,6S,9S,10R,11aR)-6-acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,8,9,10,11,11a-octahydrocyclodeca[b]furan-4-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 + 0.9897 98.97%
Caco-2 + 0.5832 58.32%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6172 61.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8574 85.74%
OATP1B3 inhibitior + 0.8734 87.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6485 64.85%
P-glycoprotein inhibitior + 0.6933 69.33%
P-glycoprotein substrate - 0.6052 60.52%
CYP3A4 substrate + 0.6631 66.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9008 90.08%
CYP3A4 inhibition - 0.6069 60.69%
CYP2C9 inhibition - 0.8535 85.35%
CYP2C19 inhibition - 0.8289 82.89%
CYP2D6 inhibition - 0.9661 96.61%
CYP1A2 inhibition - 0.6470 64.70%
CYP2C8 inhibition - 0.5652 56.52%
CYP inhibitory promiscuity - 0.9743 97.43%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5610 56.10%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.9231 92.31%
Skin irritation + 0.5085 50.85%
Skin corrosion - 0.9221 92.21%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6713 67.13%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7536 75.36%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.8680 86.80%
Acute Oral Toxicity (c) III 0.3059 30.59%
Estrogen receptor binding + 0.7171 71.71%
Androgen receptor binding + 0.6179 61.79%
Thyroid receptor binding + 0.5568 55.68%
Glucocorticoid receptor binding + 0.7171 71.71%
Aromatase binding + 0.5955 59.55%
PPAR gamma + 0.5846 58.46%
Honey bee toxicity - 0.6272 62.72%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9901 99.01%

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 98.22% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.87% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 92.37% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.11% 99.23%
CHEMBL221 P23219 Cyclooxygenase-1 91.57% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.60% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.59% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.01% 95.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.87% 85.14%
CHEMBL299 P17252 Protein kinase C alpha 85.45% 98.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.97% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.16% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.59% 97.09%
CHEMBL1902 P62942 FK506-binding protein 1A 81.69% 97.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.11% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.90% 92.94%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.42% 91.24%
CHEMBL340 P08684 Cytochrome P450 3A4 80.40% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.23% 93.56%

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.
Eremanthus glomerulatus

Cross-Links

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PubChem 162876031
LOTUS LTS0031691
wikiData Q105220916