3-amino-2-hydroxy-4-phenylbutanoic acid and 5,5-dimethylthiazolidine-4-carboxylic acid

3-amino-2-hydroxy-4-phenylbutanoic acid has been researched along with 5,5-dimethylthiazolidine-4-carboxylic acid in 1 studies

Compound Research Comparison

Studies (3-amino-2-hydroxy-4-phenylbutanoic acid)	Trials (3-amino-2-hydroxy-4-phenylbutanoic acid)	Recent Studies (post-2010) (3-amino-2-hydroxy-4-phenylbutanoic acid)	Studies (5,5-dimethylthiazolidine-4-carboxylic acid)	Trials (5,5-dimethylthiazolidine-4-carboxylic acid)	Recent Studies (post-2010) (5,5-dimethylthiazolidine-4-carboxylic acid)
42	0	3	5	0	0

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ami, E; Hamada, Y; Hayashi, Y; Hidaka, K; Hori, Y; Kimura, T; Kiso, Y; Nagai, A; Nakahara, K; Nakatani, S; Nguyen, JT; Ohnishi, N; Sato, A	1

Other Studies

1 other study(ies) available for 3-amino-2-hydroxy-4-phenylbutanoic acid and 5,5-dimethylthiazolidine-4-carboxylic acid

Article	Year
Combination of non-natural D-amino acid derivatives and allophenylnorstatine-dimethylthioproline scaffold in HIV protease inhibitors have high efficacy in mutant HIV. Journal of medicinal chemistry, 2008, May-22, Volume: 51, Issue:10 Topics: Amino Acids; Drug Resistance, Viral; HIV Protease; HIV Protease Inhibitors; HIV-1; Models, Molecular; Mutation; Phenylbutyrates; Stereoisomerism; Structure-Activity Relationship; Thiazoles	2008

Article

Year

Combination of non-natural D-amino acid derivatives and allophenylnorstatine-dimethylthioproline scaffold in HIV protease inhibitors have high efficacy in mutant HIV.

Journal of medicinal chemistry, 2008, May-22, Volume: 51, Issue:10

Topics: Amino Acids; Drug Resistance, Viral; HIV Protease; HIV Protease Inhibitors; HIV-1; Models, Molecular; Mutation; Phenylbutyrates; Stereoisomerism; Structure-Activity Relationship; Thiazoles

2008