78461-92-4

Upstream product

• 22809-37-6 6-bromohexanoyl chloride 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 4224-70-8 6-bromohexanoic acid 
• 151823-76-6 C₉H₁₅BrO₄ 

Downstream Products

• 78461-94-6 R-6-(3-thiazolidinyl)hexanoic acid N-α-methylbenzylamide 
• 146919-28-0 1-[5-((R)-1-Phenyl-ethylcarbamoyl)-pentyl]-pyridinium; bromide 
• 1226496-91-8 C₃₁H₄₀N₂O₂S₅ 
• 78461-96-8 6-(2-{2-[5-((R)-1-Phenyl-ethylcarbamoyl)-pentylamino]-ethyldisulfanyl}-ethylamino)-hexanoic acid ((R)-1-phenyl-ethyl)-amide 
• 78461-98-0 R,R-N,N'-bis<6-(α-methylbenzyl)aminohexyl>cystamine 
• 146919-26-8 Trimethyl-[5-((R)-1-phenyl-ethylcarbamoyl)-pentyl]-ammonium; bromide 

Relevant academic research and scientific papers

An enantiomeric discrimination in aqueous mixed chiral micelles through hydrogen bonding

Self-assembling molecular receptor comprising a chiral surfactant amide placed in a rigid micellar environment recognizes the different amide enantiomeric forms in water solutions by means of hydrogen bonding.

Structural modifications of the serotonin 5-HT7 receptor agonist N -(4-cyanophenylmethyl)-4-(2-biphenyl)-1-piperazinehexanamide (LP-211) to improve in vitro microsomal stability: A case study

The 5-HT7 serotonin receptor is revealing a promising target for innovative therapeutic strategies of neurodevelopmental and neuropsychiatric disorders. Here, we report the synthesis of thirty long-chain arylpiperazine analogs of the selective

Structural requirements for adrenergic α-receptor covalent occupancy by chiral tetramine disulfides

Chiral tetramine disulfides, designed to study the molecular properties of the active site of the adrenergic α-receptor, were synthesized and tested on rat vas deferens preparation. The activity of the three optical isomers showed that the receptor displa