30715-50-5

Upstream product

• 591-20-8 3-Bromophenol 
• 75-65-0 tert-butyl alcohol 
• 106-41-2 4-bromo-phenol 
• 31951-06-1 4-bromo-1-tert-butyl-2-nitro-benzene 
• 30788-02-4 5-Bromo-2-(1,1-dimethylethyl)-1-methoxybenzene 
• 857595-32-5 5-bromo-2-tert-butyl-aniline 

Downstream Products

• 159390-39-3 2,2'-Methylenebis<3-bromo-6-(1,1-dimethylethyl)phenol> 
• 173336-28-2 4-tert-butyl-3-(3-methoxypropyloxy)-bromobenzene 

Relevant academic research and scientific papers

Method for inhibiting gene expression promoted by AP1 protein with RAR beta selective retinoids and method for treatment of diseases and conditions with such retinoids

Retinoid compounds which repress expression of the gene promoted by AP1 protein but which do not significantly activate expression of the genes having RA-responsive elements in their promoter region through RAR alpha and RAR GAMMA receptor subtypes, are u

Substituted diaryl or diheteroaryl methanes, ethers and amines having retinoid agonist, antagonist or inverse agonist type biological activity

Compounds of the formula where the symbols have the meaning defined in the specification, have retinoid, retinoid antagonist or retinoid inverse agonist type biological activity.

Acetylenes disubstituted with 2-tetrahydropyranoxyaryl and aryl or heteroaryl groups having retinoid-like biological activity

Compounds of the formula STR1 wherein R1 -R5, X, Y, A, B are as defined in the specification have retinoid-like biological activity.

Synthesis and Structure of 2,2'-Dihydroxybenzophenones and 1,8-Dihydroxyfluorenones

Derivatives of 2,2'-dihydroxybenzophenone and 1,8-dihydroxyfluorenone are interesting because their structures juxtapose a carbonyl group and two hydroxyl groups, thereby permitting them to be used to study the double electrophilic activation of carbonyl