Propanoic acid, 2-methyl-, 3,6-bis(acetyloxy)-2,3,3a,4,5,6,6a,7,9a,9b-decahydro-3,6,9-trimethyl-2-oxoazuleno(4,5-b)furan-4-yl ester, (3S-(3alpha,3aalpha,4alpha,6beta,6abeta,9abeta,9balpha))-

Details

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Internal ID 2b6faede-3ff3-4b72-b9d0-31e14ca6d63d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Guaianolides and derivatives
IUPAC Name (3,6-diacetyloxy-3,6,9-trimethyl-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-methylpropanoate
SMILES (Canonical) CC1=CCC2C1C3C(C(CC2(C)OC(=O)C)OC(=O)C(C)C)C(C(=O)O3)(C)OC(=O)C
SMILES (Isomeric) CC1=CCC2C1C3C(C(CC2(C)OC(=O)C)OC(=O)C(C)C)C(C(=O)O3)(C)OC(=O)C
InChI InChI=1S/C23H32O8/c1-11(2)20(26)28-16-10-22(6,30-13(4)24)15-9-8-12(3)17(15)19-18(16)23(7,21(27)29-19)31-14(5)25/h8,11,15-19H,9-10H2,1-7H3
InChI Key YNZANXMCWKBMJS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H32O8
Molecular Weight 436.50 g/mol
Exact Mass 436.20971797 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Propanoic acid, 2-methyl-, 3,6-bis(acetyloxy)-2,3,3a,4,5,6,6a,7,9a,9b-decahydro-3,6,9-trimethyl-2-oxoazuleno(4,5-b)furan-4-yl ester, (3S-(3alpha,3aalpha,4alpha,6beta,6abeta,9abeta,9balpha))-

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 + 0.5297 52.97%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6068 60.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8987 89.87%
OATP1B3 inhibitior + 0.8664 86.64%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7365 73.65%
P-glycoprotein inhibitior + 0.8255 82.55%
P-glycoprotein substrate - 0.6244 62.44%
CYP3A4 substrate + 0.6510 65.10%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8650 86.50%
CYP3A4 inhibition - 0.6341 63.41%
CYP2C9 inhibition - 0.8188 81.88%
CYP2C19 inhibition - 0.7770 77.70%
CYP2D6 inhibition - 0.9565 95.65%
CYP1A2 inhibition - 0.6302 63.02%
CYP2C8 inhibition - 0.7037 70.37%
CYP inhibitory promiscuity - 0.8841 88.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5020 50.20%
Eye corrosion - 0.9708 97.08%
Eye irritation - 0.9067 90.67%
Skin irritation - 0.6232 62.32%
Skin corrosion - 0.9103 91.03%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4125 41.25%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.6995 69.95%
skin sensitisation - 0.6462 64.62%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.6944 69.44%
Acute Oral Toxicity (c) III 0.4382 43.82%
Estrogen receptor binding + 0.8713 87.13%
Androgen receptor binding + 0.7071 70.71%
Thyroid receptor binding + 0.5953 59.53%
Glucocorticoid receptor binding + 0.7993 79.93%
Aromatase binding + 0.5749 57.49%
PPAR gamma + 0.6898 68.98%
Honey bee toxicity - 0.6146 61.46%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9874 98.74%

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 96.34% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 94.43% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.36% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.07% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.16% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.15% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.53% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.87% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.73% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.57% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 85.52% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 84.59% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.50% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.15% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.82% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.31% 95.71%

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.
Echinacea angustifolia

Cross-Links

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PubChem 155119
LOTUS LTS0176643
wikiData Q105309274