专利号:US-9499472-B2 优先权日:2012-03-05 标题:Aspartylamide inhibitors of excitatory amino acid transporters 发明人:GERDES JOHN M; BRIDGES RICHARD J; AHMED SYED K; PATEL SARJUBHAI 权利人:THE UNIV OF MONTANA 摘要:The compounds of the invention are inhibitors of excitatory amino acid transporters (EAAT) that penetrate the blood-brain barrier to access the central nervous system. The compounds of the invention follow the structural formula: n nor a salt, ester or prodrug thereof, wherein X is a halogen, such as fluorine, or a radionuclide, such as fluorine-18. The compounds and methods described herein can be used for the treatment of, e.g., neurodegenerative disorders (e.g., amyotrophic lateral sclerosis), ischemia, spinal cord injury, and traumatic brain injury in a patient (e.g., a human). The invention further provides compounds and methods for the synthesis and use of radiographic tracers to diagnose and follow the progression of such disorders.
专利号:WO-2024097744-A2 优先权日:2022-11-01 标题 :Dna-compatible wittig olefination of on-dna peptidyl-ylides for development of on-dna peptidomimetics through diversity-oriented synthesis (dos)
专利号:WO-9012883-A1 优先权日:1989-04-24 标题:Enzymatic membrane method for the synthesis and separation of peptides
参考标题:Traceless Staudinger Ligation Of Glycosyl Azides With Triaryl Phosphines: Stereoselective Synthesis Of Glycosyl Amides 作者:Aldo Bianchi,Anna Bernardi |发布日期:2006.6.1 摘要:α-Glycosyl Amides Can Be Synthesized From The Corresponding O-Benzyl-α-Glycosyl Azides Using A Traceless Staudinger Ligation With Diphenylphosphanyl-Phenyl Esters 4. All The Phosphines Employed And Their Phenol Precursors Are Stable To Air At 4 °C For Months. Fast Intramolecular Trapping Of The Reduction Intermediates Results In The Direct Formation Of The Amide Link, Which, In Turn, Prevents Epimerisation
合成参考文献
摘要:Lubell, W. D.; Blankenship, J. W.; Fridkin, G.; Kaul, R., Science of Synthesis, (2005) 21, 722.