953-69-5

Usage

Uses

Used in Pharmaceutical and Medicinal Chemistry:
Bicyclo[2.2.2]octane-1-carboxylic acid, 4-phenylis used as a building block for the synthesis of various derivatives with potential therapeutic properties. Its unique bicyclic structure and functional groups may contribute to its biological activities, making it a promising candidate for the development of new drugs and pharmaceutical agents.

Upstream product

• 950-22-1 1-cyano-4-phenylbicyclo<2.2.2>octane 
• 714-68-1 1-bromo-4-phenylbicyclo<2.2.2>octane 
• 23062-51-3 methyl 4-bromo-bicyclo[2.2.2]octane-1-carboxylate 
• 18720-35-9 bicyclo[2.2.2]octane-1,4-dicarboxylic acid monomethyl ester 
• 23062-52-4 methyl 4-phenylbicyclo<2.2.2>octane-1-carboxylate 

Downstream Products

• 23760-80-7 4-phenylbicyclo<2.2.2>octane-1-methanol 
• 942999-69-1 2-diazo-1-(4-phenylbicyclo[2.2.2]oct-1-yl)ethanone 
• 70631-58-2 methyl 2-(4-phenylbicyclo[2.2.2]octan-1-yl)acetate 
• 1620074-83-0 C₁₇H₂₁BrO₂ 
• 1055926-26-5 N'-[4-(benzyloxy)-2-(trifluoromethyl)benzoyl]-4-phenylbicyclo[2.2.2]octane-1-carbohydrazide 
• 719274-60-9 2-[4-(benzyloxy)-2-(trifluoromethyl)phenyl]-5-(4-phenylbicyclo[2.2.2]oct-1-yl)-1,3,4-oxadiazole 
• 719272-76-1 4-[4-Methyl-5-(4-phenylbicyclo[2.2.2]oct-1-yl)-4H-1,2,4-triazol-3-yl]-3-(trifluoromethyl)phenol 
• 909912-83-0 4-phenylbicyclo[2.2.2]octane-1-carboxylic acid chloride 
• 94993-94-9 1-(2,2-Difluoro-vinyl)-4-phenyl-bicyclo[2.2.2]octane 
• 94994-29-3 4-phenylbicyclo<2.2.2>octane-1-carboxaldehyde 
• 94994-25-9 4-carbomethoxybicyclo<2.2.2>octane-1-carboxaldehyde 
• 94994-15-7 4-hydroxymethyl-bicyclo[2.2.2]octane-1-carboxylic acid methyl ester 
• 18720-35-9 bicyclo[2.2.2]octane-1,4-dicarboxylic acid monomethyl ester 

Relevant academic research and scientific papers

LYSOPHOSPHATIDIC ACID RECEPTOR ANTAGONISTS

Compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases, disorders, or conditions associated with one or more of the lysophosphatidic acid receptors are provided.

Discovery of a potent, selective, and orally efficacious pyrimidinooxazinyl bicyclooctaneacetic acid diacylglycerol acyltransferase-1 inhibitor

Inhibition of DGAT-1 is increasingly seen as an attractive mechanism with the potential for treatment of obesity and other elements of the metabolic syndrome. We report here a bicyclooctaneacetic acid derivative in the pyrimidinooxazine structural class o

PYRIMIDO- [4, 5-B] -OXAZINES FOR USE AS DGAT INHIBITORS

Formula (I). Compounds of formula (I) or salts thereof, wherein A1, and R1 to R5 are as defined in the specification, are DGAT-1 inhibitors and are thereby useful in the treatment of, for example, obesity. Processes to make compounds of formula (I) are also described.

Triazole derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1

Triazole derivatives of structural formula I are selective inhibitors of the 11β-hydroxysteroid dehydrogenase-1. The compounds are useful for the treatment of diabetes, such as noninsulin-dependent diabetes (NIDDM), hyperglycemia, obesity, insulin resista