(1R,3R,4R,5R,8R,9S,11S,13R,14S,16S,17R,18R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,4,13,18-tetrol

Details

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Internal ID 1a677aaf-2615-4fc7-8326-dd6696dbdea4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Villanovane, atisane, trachylobane or helvifulvane diterpenoids > Atisane diterpenoids > Hetisine-type diterpenoid alkaloids
IUPAC Name (1R,3R,4R,5R,8R,9S,11S,13R,14S,16S,17R,18R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,4,13,18-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H27NO4/c1-8-9-3-10-14-19-6-12(22)16(24)17(2)7-21(14)11(13(17)19)5-18(10,15(8)23)20(19,25)4-9/h9-16,22-25H,1,3-7H2,2H3/t9-,10+,11-,12+,13+,14+,15+,16-,17-,18-,19+,20-/m0/s1
InChI Key IZAMPMCOQUBWAE-RUHQHNFMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H27NO4
Molecular Weight 345.40 g/mol
Exact Mass 345.19400834 g/mol
Topological Polar Surface Area (TPSA) 84.20 Ų
XlogP -0.70

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,3R,4R,5R,8R,9S,11S,13R,14S,16S,17R,18R)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,4,13,18-tetrol

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 97.18% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.42% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.53% 85.14%
CHEMBL1871 P10275 Androgen Receptor 84.72% 96.43%
CHEMBL259 P32245 Melanocortin receptor 4 84.56% 95.38%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.28% 92.86%
CHEMBL226 P30542 Adenosine A1 receptor 82.59% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.38% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.22% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.16% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.93% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.81% 82.69%

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.
Aconitum japonicum

Cross-Links

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PubChem 162931579
LOTUS LTS0133771
wikiData Q105123093