42288-24-4

Upstream product

• 99-92-3 p-aminobenzophenone 
• 79-08-3 bromoacetic acid 
• 127-09-3 sodium acetate 
• 79-11-8 chloroacetic acid 
• 100-19-6 (4-nitrophenyl)ethanone 

Downstream Products

• 99972-78-8 3-(4-acetyl-phenyl)-oxazolidine-2,5-dione 
• 154136-93-3 [4-((E)-3-Pyridin-2-yl-acryloyl)-phenylamino]-acetic acid 
• 154136-95-5 N-<4-<3-(4-pyridyl)-2-propenoyl>phenyl>glycine 
• 154136-94-4 [4-((E)-3-Pyridin-3-yl-acryloyl)-phenylamino]-acetic acid 
• 154136-92-2 [4-((E)-3-Thiophen-2-yl-acryloyl)-phenylamino]-acetic acid 
• 139515-42-7 (4-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylamino)-acetic acid 
• 84968-84-3 N-nitroso-N-(4-acetylphenyl)glycine 
• 143391-20-2 {4-[(E)-3-(4-Chloro-phenyl)-acryloyl]-phenylamino}-acetic acid 
• 143391-22-4 {4-[(E)-3-(3-Nitro-phenyl)-acryloyl]-phenylamino}-acetic acid 
• 143391-21-3 {4-[(E)-3-(2-Bromo-phenyl)-acryloyl]-phenylamino}-acetic acid 
• 1062017-99-5 2-((4-acetylphenyl)amino)-1-(4-(4-methoxyphenyl)piperazin-1-yl)ethanone 
• 84968-94-5 3-<4-<3-(4-nitrophenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84969-02-8 C₁₉H₁₆N₂O₅ 
• 84968-92-3 3-<4-<3-(4-methoxyphenyl)-1-oxo-2-propenyl>-phenyl>sydnone 

Relevant academic research and scientific papers

Non-natural amino acid and application thereof Recombinant protein and recombinant protein conjugate comprising same

The invention provides a non-natural amino acid. A compound represented by formula (I) or an enantiomer thereof. The invention also provides application of the non-natural amino acid. Further, the present invention also provides a protein conjugate comprising the recombinant protein and of the non-natural amino acid prepared from the recombinant protein. The non-natural amino acid provided by the invention is simple and convenient to prepare, good in safety, not prone to inactivation during protein insertion, high in conjugate rate with a coupling part, and higher in stability of the obtained conjugate.

PIPERAZINE DERIVATIVES, COMPOSITIONS, AND USES RELATED THERETO

The disclosure relates to piperazine derivatives, compositions, and methods related thereto. In certain embodiments, the disclosure relates to inhibitors of NADPH-oxidase.

Synthesis and antimicrobial activity of 3-(substituted-phenyl)-sydnones

3-(3 or 4-Acetylphenyl)-sydnones 7, 8 have been synthesized by formation of the glycines 3, 4, followed by nitrosation to 5, 6 and cyclization with acetic anhydride to sydnones. Sydnone derivatives carrying chalcone moieties 15, 16 were prepared by format

Reactions of 3-(p-Acetylphenyl)sydnones: Part 1-Synthesis and Biological Evaluation of 3-(p-Acetylphenl)sydnone and Its Derivatives

3-(p-Acetylphenyl)sydnone (7) undergoes condensation with aryl aldehydes to give the corresponding cinnamoyl derivatives (11-25).The reaction of sydnones (7-9) with hydroxylamine, phenylhydrazine, dimethyl acetylene-dicarboxylate and bromine gives the ket