[(1S,2S,4R,8S,9R,11R)-1-ethoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate

Details

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Internal ID ac782af4-e299-4ab8-9591-6ddacfeacd13
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Germacranolides and derivatives
IUPAC Name [(1S,2S,4R,8S,9R,11R)-1-ethoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate
SMILES (Canonical) CCOC12CCC(O1)(CC(C3C(CC2C)OC(=O)C3=C)OC(=O)C(C)C)C
SMILES (Isomeric) CCO[C@@]12CC[C@@](O1)(C[C@H]([C@@H]3[C@@H](C[C@@H]2C)OC(=O)C3=C)OC(=O)C(C)C)C
InChI InChI=1S/C21H32O6/c1-7-24-21-9-8-20(6,27-21)11-16(26-18(22)12(2)3)17-14(5)19(23)25-15(17)10-13(21)4/h12-13,15-17H,5,7-11H2,1-4,6H3/t13-,15+,16+,17-,20+,21-/m0/s1
InChI Key CASQLMHFEQKREM-KESHLRAWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O6
Molecular Weight 380.50 g/mol
Exact Mass 380.21988874 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 6
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 [(1S,2S,4R,8S,9R,11R)-1-ethoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.6874 68.74%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7208 72.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8618 86.18%
OATP1B3 inhibitior + 0.8470 84.70%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.7126 71.26%
P-glycoprotein inhibitior - 0.5501 55.01%
P-glycoprotein substrate - 0.5645 56.45%
CYP3A4 substrate + 0.6701 67.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8937 89.37%
CYP3A4 inhibition - 0.5842 58.42%
CYP2C9 inhibition - 0.6731 67.31%
CYP2C19 inhibition - 0.7227 72.27%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.6183 61.83%
CYP2C8 inhibition - 0.6802 68.02%
CYP inhibitory promiscuity - 0.8305 83.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5545 55.45%
Eye corrosion - 0.9775 97.75%
Eye irritation - 0.8369 83.69%
Skin irritation - 0.5573 55.73%
Skin corrosion - 0.9259 92.59%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3923 39.23%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5767 57.67%
skin sensitisation - 0.7924 79.24%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5563 55.63%
Acute Oral Toxicity (c) III 0.6541 65.41%
Estrogen receptor binding + 0.8986 89.86%
Androgen receptor binding + 0.6438 64.38%
Thyroid receptor binding + 0.7535 75.35%
Glucocorticoid receptor binding + 0.8207 82.07%
Aromatase binding + 0.7296 72.96%
PPAR gamma + 0.8129 81.29%
Honey bee toxicity - 0.6662 66.62%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9964 99.64%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.05% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.32% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.86% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.34% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.10% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 89.55% 97.79%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 89.51% 85.30%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.26% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.47% 99.23%
CHEMBL299 P17252 Protein kinase C alpha 87.37% 98.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.08% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.88% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.41% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.77% 95.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.68% 85.14%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.75% 95.71%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.39% 96.47%
CHEMBL340 P08684 Cytochrome P450 3A4 81.78% 91.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.66% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.83% 97.14%

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.
Blumea densiflora

Cross-Links

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PubChem 163011911
LOTUS LTS0040590
wikiData Q104951870