(1R,2S,5R)-2-Isopropyl-5-methy
lcyclohexyl 3-((((S)-1-amino-1-oxobutan-2-yl)amino)methyl)hexanoate- 询价
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- 2025年07月11日
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- 英文名：
(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 3-((((S)-1-amino-1-oxobutan-2-yl)amino)methyl)hexanoate
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
2650518-20-8
(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 3-((((S)-1-amino-1-oxobutan-2-yl)amino)methyl)hexanoate
2650518-20-8
C21H40N2O3
368.55
No Data Available
No Data Available
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文献和实验(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 3-((((S)-1-amino-1-oxobutan-2-yl)amino)methyl)hexanoate
2650518-20-8
C21H40N2O3
368.55
No Data Available
No Data Available
Enzymatic Synthesis of (S)-Phenylalanine and Related (S)-Amino Acids by Phenylalanine Dehydrogenase
substituents in the reductive amination reaction. Optically pure (S)-phe and other (S)-amino acids are quantitatively synthesized from their oxo-analogs using PheDH, with a regeneration of NADH by formate dehydrogenase from Candida boidinii No. 2201. Acetone
In an effort to produce renm mhibttory peptides, the preparation of (2 S ,4 S ,5 S )-5-( t -Butoxycarbonylamino)-4-( t -butyldimethylsilyloxy)-2-isopropyl-7-methyl octanotc acid, 15 , was carried out ( 1 ). This pseudo-dipeptide was used
Chiral Benzofurazan-Derived Derivatization Reagents for Indirect Enantioseparations by HPLC
The separation of enantiomers of biologically important molecules, such as chiral pharmaceuticals and amino acids, is an important issue because a significant difference in the activity of the enantiomers is usually observed in biological
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