[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,17R,18R)-18-acetyloxy-6,8,9-trimethoxy-13-methyl-16-oxo-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate

Details

Top
Internal ID a89dbf67-8b3d-4e08-b84c-c9963d569310
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Aconitane-type diterpenoid alkaloids
IUPAC Name [(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,17R,18R)-18-acetyloxy-6,8,9-trimethoxy-13-methyl-16-oxo-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H37NO8/c1-12(28)34-19-14-9-15-18(19)24(32-5,10-16(14)31-4)26(33-6)21(35-13(2)29)20-23(3)8-7-17(30)25(15,20)22(26)27-11-23/h14-16,18-22,27H,7-11H2,1-6H3/t14-,15-,16+,18-,19+,20-,21-,22+,23+,24-,25+,26-/m1/s1
InChI Key KHLANGIAWTYCRD-ASDYVBNUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H37NO8
Molecular Weight 491.60 g/mol
Exact Mass 491.25191714 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 0.10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,17R,18R)-18-acetyloxy-6,8,9-trimethoxy-13-methyl-16-oxo-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

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

Targets

Top

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 97.63% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.48% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.27% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.97% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.66% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.71% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.04% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 89.88% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.91% 96.77%
CHEMBL340 P08684 Cytochrome P450 3A4 88.81% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.55% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.26% 92.94%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.11% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.77% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 87.40% 97.79%
CHEMBL299 P17252 Protein kinase C alpha 86.93% 98.03%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.87% 96.95%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 86.74% 90.48%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.22% 92.29%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.45% 82.69%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.20% 92.62%
CHEMBL2581 P07339 Cathepsin D 82.57% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.15% 86.33%
CHEMBL204 P00734 Thrombin 81.02% 96.01%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.90% 94.78%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.77% 100.00%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 80.32% 95.71%

Plants that contains it

Top
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 peregrinum

Cross-Links

Top
PubChem 162960359
LOTUS LTS0083613
wikiData Q105141193