(4,6,8,16-Tetramethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-18-yl) acetate

Details

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Internal ID 70af1dd7-fa63-4d32-95fb-24bf5aeccd6e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Aconitane-type diterpenoid alkaloids
IUPAC Name (4,6,8,16-tetramethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-18-yl) acetate
SMILES (Canonical) CC(=O)OC1C2C3C4(C1C(CCC4OC)(CN3)C)C5CC6C(CC2(C5C6OC)OC)OC
SMILES (Isomeric) CC(=O)OC1C2C3C4(C1C(CCC4OC)(CN3)C)C5CC6C(CC2(C5C6OC)OC)OC
InChI InChI=1S/C25H39NO6/c1-12(27)32-20-18-22-25(16(29-4)7-8-23(2,11-26-22)21(20)25)14-9-13-15(28-3)10-24(18,31-6)17(14)19(13)30-5/h13-22,26H,7-11H2,1-6H3
InChI Key HOBLCKNCLIEATR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H39NO6
Molecular Weight 449.60 g/mol
Exact Mass 449.27773796 g/mol
Topological Polar Surface Area (TPSA) 75.20 Ų
XlogP 1.40

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4,6,8,16-Tetramethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-18-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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 98.18% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.35% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.27% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 94.49% 94.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.70% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 92.02% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.30% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.48% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.88% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.03% 97.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.95% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 87.86% 92.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.25% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.18% 96.77%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 87.09% 92.88%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.36% 82.69%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 86.33% 98.99%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.09% 91.03%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.71% 97.28%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.76% 93.04%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.99% 100.00%
CHEMBL204 P00734 Thrombin 80.05% 96.01%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.02% 95.89%

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.
Delphinium gueneri

Cross-Links

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PubChem 162844294
LOTUS LTS0180448
wikiData Q105031162