非天然氨基酸是指那些在自然界中未发现或极少出现的氨基酸,通常通过化学合成或生物工程手段获得。这些氨基酸和其衍生物在生物化学、医药和材料科学等领域具有重要应用。它们可以用于设计和合成新型药物、开发抗体、制作生物材料,以及在蛋白质工程中引入特定功能,增加蛋白质的稳定性或活性。
常见的非天然氨基酸及其衍生物包括:
产品编号 | 结构式 | 项目名称规格 | 分子式 | 加入购物车 |
---|---|---|---|---|
D816068 |
![]() | 左旋苯甘氨酸, 95% D-2-Phenylglycine, 95% |
C8H9NO2 | |
A856518 |
![]() | 对羟基苯甘氨酸, 97% 2-Amino-2-(4-hydroxyphenyl)acetic acid, 97% |
C8H9NO3 | |
S869843 |
![]() | S-(2-羧乙基)-L-半胱氨酸, 98% S-(2-Carboxyethyl)-L-cysteine, 98% |
C6H11NO4S | |
N800425 |
![]() | N-乙酰-L-半胱氨酸, 99% N-Acetyl-L-Cysteine, 99% |
C5H9NO3S | |
M815979 |
![]() | α-甲基-D-苯丙氨酸, 98% α-Methyl-D-phenylalanine, 98% |
C10H13NO2 | |
C804188 |
![]() | L-4-氯苯丙氨酸, 98% 4-Chloro-Phe-OH, 98% |
C9H10ClNO2 | |
A800439 |
![]() | β-丙氨酸, 99% β-Alanine, 99% |
C3H7NO2 | |
S891635 |
![]() | H-β-(3-苯并噻蒽基)-丙氨酸-oH, 97% (S)-2-Amino-3-(benzo[b]thiophen-3-yl)propanoic acid, 97% |
C11H11NO2S | |
L805659 |
![]() | L-环丙基丙氨酸, 98% L-Cyclopropylalanine, 98% |
C6H11NO2 | |
D815816 |
![]() | D-焦谷氨酸, 98% D-Pyroglutamic acid, 98% |
C5H7NO3 | |
N814750 |
![]() | Nω-硝基-L-精氨酸, 98% Nω-Nitro-L-arginine, 98% |
C6H13N5O4 | |
N864275 |
![]() | Nω-单甲基-L-精氨酸乙酸盐, 98% Nω-Methyl-L-arginine Acetate, 98% |
C7H16N4O2·C2H4O2 | |
D868287 |
![]() | DL-邻酪氨酸, ≥98% DL-o-Tyrosine, ≥98% |
C9H11NO3 | |
L863998 |
![]() | L-间酪氨酸, 97% L-m-Tyrosine, 97% |
C9H11NO3 | |
O867607 |
![]() | O-磷酸基-L-酪氨酸, ≥97% O-Phospho-L-tyrosine, ≥97% |
C9H12NO6P | |
O835028 |
![]() | O-甲基-D-酪氨酸, >97% O-Methyl-D-tyrosine, >97% |
C10H13NO3 | |
D807812 |
![]() | D-叔亮氨酸, 98% D-tert-Leucine, 98% |
C6H13NO2 | |
D812309 |
![]() | DL-叔亮氨酸, 98% DL-tert-Leucine, 98% |
C6H13NO2 | |
D811960 |
![]() | D-别异亮氨酸, 98% D-allo-Isoleucine, 98% |
C6H13NO2 | |
C830431 |
![]() | 环亮氨酸, 98% Cycloleucine, 98% |
C6H11NO2 |