(1S,5S)-4,7,7-trimethylbicyclo[3.2.0]hept-3-en-6-one

Details

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Internal ID 25d50bdd-3c31-4390-9aff-3751abb128c7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,5S)-4,7,7-trimethylbicyclo[3.2.0]hept-3-en-6-one
SMILES (Canonical) CC1=CCC2C1C(=O)C2(C)C
SMILES (Isomeric) CC1=CC[C@H]2[C@@H]1C(=O)C2(C)C
InChI InChI=1S/C10H14O/c1-6-4-5-7-8(6)9(11)10(7,2)3/h4,7-8H,5H2,1-3H3/t7-,8+/m0/s1
InChI Key JVEJBTZZORGEKF-JGVFFNPUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.70

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,5S)-4,7,7-trimethylbicyclo[3.2.0]hept-3-en-6-one

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.88% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.80% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.63% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.61% 91.11%
CHEMBL1871 P10275 Androgen Receptor 81.82% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.72% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.33% 100.00%
CHEMBL2581 P07339 Cathepsin D 80.15% 98.95%

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.
Laggera tomentosa

Cross-Links

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PubChem 131121698
LOTUS LTS0115578
wikiData Q105135632