(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one

Details

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Internal ID 62bf6b28-b8da-4103-8f90-9f08b698b4d4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one
SMILES (Canonical) CC1=CC(=O)C2CC1C2(C)C
SMILES (Isomeric) CC1=CC(=O)[C@@H]2C[C@@H]1C2(C)C
InChI InChI=1S/C10H14O/c1-6-4-9(11)8-5-7(6)10(8,2)3/h4,7-8H,5H2,1-3H3/t7-,8-/m0/s1
InChI Key DCSCXTJOXBUFGB-YUMQZZPRSA-N
Popularity 72 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 1.60

Synonyms

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(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one

2D Structure

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2D Structure of (1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-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 90.23% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.26% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.03% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.61% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.58% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.91% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.87% 97.09%
CHEMBL2581 P07339 Cathepsin D 81.45% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.07% 99.23%

Cross-Links

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PubChem 6973628
LOTUS LTS0177954
wikiData Q104253227