(4-Ethylidene-12-hydroxy-6,7-dimethyl-3-oxo-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecan-7-yl) acetate

Details

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Internal ID 704f43bb-ea52-4329-a7da-eaa60f24beed
Taxonomy Organoheterocyclic compounds > Pyrrolizidines
IUPAC Name (4-ethylidene-12-hydroxy-6,7-dimethyl-3-oxo-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecan-7-yl) acetate
SMILES (Canonical) CC=C1CC(C(COCC2C(CN3C2C(CC3)OC1=O)O)(C)OC(=O)C)C
SMILES (Isomeric) CC=C1CC(C(COCC2C(CN3C2C(CC3)OC1=O)O)(C)OC(=O)C)C
InChI InChI=1S/C20H31NO6/c1-5-14-8-12(2)20(4,27-13(3)22)11-25-10-15-16(23)9-21-7-6-17(18(15)21)26-19(14)24/h5,12,15-18,23H,6-11H2,1-4H3
InChI Key UIQMGOZIBSCNPE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H31NO6
Molecular Weight 381.50 g/mol
Exact Mass 381.21513771 g/mol
Topological Polar Surface Area (TPSA) 85.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4-Ethylidene-12-hydroxy-6,7-dimethyl-3-oxo-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecan-7-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9195 91.95%
Caco-2 + 0.5812 58.12%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4629 46.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8824 88.24%
OATP1B3 inhibitior + 0.9333 93.33%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8778 87.78%
P-glycoprotein inhibitior - 0.6825 68.25%
P-glycoprotein substrate + 0.6423 64.23%
CYP3A4 substrate + 0.6640 66.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8168 81.68%
CYP3A4 inhibition - 0.8848 88.48%
CYP2C9 inhibition - 0.9320 93.20%
CYP2C19 inhibition - 0.9251 92.51%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition - 0.9016 90.16%
CYP2C8 inhibition - 0.7539 75.39%
CYP inhibitory promiscuity - 0.9846 98.46%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.7168 71.68%
Eye corrosion - 0.9835 98.35%
Eye irritation - 0.9908 99.08%
Skin irritation - 0.7243 72.43%
Skin corrosion - 0.9210 92.10%
Ames mutagenesis - 0.5378 53.78%
Human Ether-a-go-go-Related Gene inhibition - 0.3919 39.19%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.8479 84.79%
skin sensitisation - 0.8394 83.94%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.7596 75.96%
Acute Oral Toxicity (c) III 0.6586 65.86%
Estrogen receptor binding + 0.6421 64.21%
Androgen receptor binding - 0.5662 56.62%
Thyroid receptor binding - 0.6288 62.88%
Glucocorticoid receptor binding + 0.5435 54.35%
Aromatase binding - 0.5800 58.00%
PPAR gamma - 0.6212 62.12%
Honey bee toxicity - 0.6358 63.58%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.7409 74.09%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.63% 96.09%
CHEMBL325 Q13547 Histone deacetylase 1 96.29% 95.92%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.55% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.26% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.39% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.15% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.91% 99.23%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 89.80% 94.78%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.86% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.39% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.24% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.67% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.55% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.02% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.96% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.45% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.96% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.64% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 83.47% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 82.92% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.79% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.38% 97.14%
CHEMBL5028 O14672 ADAM10 81.20% 97.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.23% 93.04%

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.
Senecio syringifolius

Cross-Links

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PubChem 163060817
LOTUS LTS0163446
wikiData Q105273536