Ramarin B

Details

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Internal ID 3202aaa5-559d-4627-8749-10ec3d6d5adb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Aristolane sesquiterpenoids
IUPAC Name (1S,1aS,7S,7aS,7bS)-1-(hydroxymethyl)-1,7,7a-trimethyl-1a,4,5,6,7,7b-hexahydrocyclopropa[a]naphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-9-5-4-6-10-7-11(17)12-13(15(9,10)3)14(12,2)8-16/h7,9,12-13,16H,4-6,8H2,1-3H3/t9-,12-,13+,14+,15+/m0/s1
InChI Key LIVASJQCBXDCNE-NJEAUENSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.40

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ramarin B

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
CHEMBL2581 P07339 Cathepsin D 94.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.70% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.14% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.82% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.18% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.92% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.31% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 87.44% 95.93%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.91% 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.
There are no matching plants.

Cross-Links

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PubChem 122384787
LOTUS LTS0124707
wikiData Q77419828