Arginine derivatives Asparagine derivatives Aspartic acid derivatives Cysteine derivatives Glutamine derivatives Glutamic acid derivatives Glycine derivative Histidine derivatives Isoleucine derivatives Leucine derivatives Lysine derivatives Methionine derivatives Phenylalanine derivatives Proline derivatives Serine derivatives Threonine derivatives Tryptophan derivatives Tyrosine derivatives Valine derivatives Alanine derivatives Methionine derivatives BOC-amino acid Cbz-amino acid FMOC-amino acid α-Amino acid Other Amino Acid Protection Amino alcohol derivative Amino acid salts Amino acid esters Other amino acid derivatives Natural amino acids and derivatives
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Amino Acids and Derivatives

Arginine derivatives Asparagine derivatives Aspartic acid derivatives Cysteine derivatives Glutamine derivatives Glutamic acid derivatives Glycine derivative Histidine derivatives Isoleucine derivatives Leucine derivatives Lysine derivatives Methionine derivatives Phenylalanine derivatives Proline derivatives Serine derivatives Threonine derivatives Tryptophan derivatives Tyrosine derivatives Valine derivatives Alanine derivatives Methionine derivatives BOC-amino acid Cbz-amino acid FMOC-amino acid α-Amino acid Other Amino Acid Protection Amino alcohol derivative Amino acid salts Amino acid esters Other amino acid derivatives Natural amino acids and derivatives
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Amino acids and their derivatives belong to a compound containing both amino group and carboxyl group. They are presented in both the form of free-state and bound-state in vivo. Free amino acids are distributed in all kinds of animal cells and body fluids with the bound amino acids being the mainly basic components of proteins and peptides.

Natural amino acids act as colorless crystalline materials with relatively high melting points being mostly above 200 ℃. They are usually soluble in water but insoluble in non-polar organic solvents. However, tyrosine and cystine are insoluble in water; proline and hydroxyl proline are soluble in ethanol and ether. All amino acids are soluble in strong acid and alkali solution.

According to the polar characterization of the R group of the side chain of the α-amino acid; those 20 common amino acids that constitute protein can be divided into four groups:
① Amino acids with R group being non-polar; There are 8 kinds in total, wherein five kinds have aliphatic side chains, namely alanine, leucine, isoleucine, valine and proline; two kinds are aromatic amino acids, phenylalanine and tryptophan; one kind belongs to sulfur-containing amino acid, namely methionine; amino acids belonging to this group have lower water solubility than polar R-group amino acid; proline is generally different with α-amino acid, it is formed through the substitution of one hydrogen atom of the amino acid with the side chains of the α- amino acid, belonging actually to imino acid.
② Amino acids with polar but non-charged R group; There are seven kinds in total, namely serine, threonine and tyrosine with R group having hydroxy group; cysteine with R group having a mercapto group of cysteine; glutamine and asparagine with R-group containing amide group, another amino acid is glycine ; glycine molecule has no R group, but having certain polarity, and thus being classified into this group; the side chains in this group of amino acid contain unassociated polar groups and can form hydrogen bonds with water, and is easily soluble in water.
③Amino acids with R group being positively charged amino acids. There are three kinds in total, namely, lysine, arginine, and histidine; they carry positive charge at pH7.0 and are also known as alkaline amino acids.
④Amino acids with R group being negatively charged. There are two kinds in total, namely glutamate and aspartate; at pH7.0, the molecules are negatively charged, also known as acidic amino acids. The formula, abbreviations symbols and related constants of 20 kinds of amino acid structures can be seen from the table. In addition to the 20 common amino acids mentioned above, there are also diiodotyrosine, thyroxine, hydroxyproline and hydroxylysine existing in certain proteins. In addition to amino acids involved in protein composition, it has been also found of more than 200 kinds of other kinds amino acids in a variety of tissues and cells; these amino acids are mostly derivatives of those α- amino acid composition of proteins.

However, there are some β-, γ- or δ- amino acids and some amino acids belong to D-type amino acids such as [beta]-alanine, [gamma]-aminobutyric acid and the phenylalanine contained in the antibiotics gramicidin-S, the D-alanine and D-glutamate contained in Gram-positive bacteria cell wall. Some non-protein amino acids can act as metabolically important precursors or intermediates, wherein β-alanine is the precursors of vitamin pantothenic acid; ornithine, and citrulline are the precursors in the synthesis of arginine; [gamma]-aminobutyric acid is the chemical neurotransmitter. Plants contain a large amount of non-protein amino acids, belonging to plant secondary substances, such as theanine, canavanine, djenkolic acid, β- Cyanoalanine and so on.

In addition to 20 kinds of amino acids found in the body and animal protein products, it has been found of nearly 200 kinds of other kinds of amino acids in nature. Most of them have been discovered in the plant kingdom and have complex molecular structures with no relation with the protein metabolism. There have been less that have been seen in the animal kingdom with some of them being originated from the chemical modification of certain incorporated amino acids in the specific proteins, for example, the proline and lysine contained in collagen protein are often partially subject to re-hydroxylation of hydroxyproline and hydroxylysine; Another example is that there are often a small amount of lysine and histidine contained in actin and myosin protein containing hypermethylated εN methyl-lysine and 3N-histidine; it has been also found in the histone protein that the ∈ amino group contained in lysine is acetylated and the OH group in the serine is phosphorylated; thyroglobulin contains iodinated tyrosine and thyronine iodide; The heavy chain of τ myosin and the N-terminal of certain proteins contain pyroglutamate formed by glutamine; there also exists the cystine constituting of two cysteine molecules in the general protein.

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Structure:
Chemical Name:
FMOC-SER(GALNAC(AC)3-ALPHA-D)-OH
CAS:
120173-57-1
MF:
C32H36N2O13
Structure:
Chemical Name:
H-GAMMA-GLU-GLU-OH
CAS:
1116-22-9
MF:
C10H16N2O7
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(2-METHYL-PHENYL)-PROPIONIC ACID
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507472-27-7
MF:
C25H23NO4
Structure:
Chemical Name:
H-DAP(BOC)-OME HCL
CAS:
114559-25-0
MF:
C9H19ClN2O4
Structure:
Chemical Name:
3-Aminopyrrolidine-3-carboxylic acid
CAS:
80546-88-9
MF:
C5H10N2O2
Structure:
Chemical Name:
DABSYL-L-TRYPTOPHAN
CAS:
97685-00-2
MF:
C25H25N5O4S
Structure:
Chemical Name:
FMOC-D-TYR-OH
CAS:
112883-29-1
MF:
C24H21NO5
Structure:
Chemical Name:
FMOC-DAP(FMOC)-OH
CAS:
201473-90-7
MF:
C33H28N2O6
Structure:
Chemical Name:
8-HYDROXY-DPAT HYDROBROMIDE
CAS:
87394-87-4
MF:
C16H26BrNO
Structure:
Chemical Name:
Z-D-HOMOPHE-OH
CAS:
138812-70-1
MF:
C18H19NO4
Structure:
Chemical Name:
FMOC-D-2-(5-BROMOTHIENYL)ALANINE
CAS:
220497-83-6
MF:
C22H18BrNO4S
Structure:
Chemical Name:
BOC-D-DAP(ALOC)-OH DCHA
CAS:
204197-26-2
MF:
C24H43N3O6
Structure:
Chemical Name:
BOC-D-ALLYLGLYCINE DCHA SALT
CAS:
221352-64-3
MF:
C22H40N2O4
Structure:
Chemical Name:
BOC-ALPHA-METHYL-D-PHE
CAS:
53940-88-8
MF:
C15H21NO4
Structure:
Chemical Name:
DNP-L-THREONINE
CAS:
1655-65-8
MF:
C10H11N3O7
Structure:
Chemical Name:
FAPGG
CAS:
64566-61-6
MF:
C20H21N3O6
Structure:
Chemical Name:
(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)-2-METHYLHEPT-6-ENOIC ACID
CAS:
288617-73-2
MF:
C23H25NO4
Structure:
Chemical Name:
L-TYROSINE DISODIUM SALT
CAS:
69847-45-6
MF:
C9H9NNa2O3
Structure:
Chemical Name:
H-D-TYR-OTBU
CAS:
87553-74-0
MF:
C13H19NO3
Structure:
Chemical Name:
DL-O-TYROSINE
CAS:
2370-61-8
MF:
C9H11NO3
Structure:
Chemical Name:
5-Methyl-L-norleucine
CAS:
31872-98-7
MF:
C7H15NO2
Structure:
Chemical Name:
3-Bromo-D-phenylalanine
CAS:
99295-78-0
MF:
C9H10BrNO2
Structure:
Chemical Name:
H-D-His-OMe 2HCl
CAS:
4467-54-3
MF:
C7H12ClN3O2
Structure:
Chemical Name:
S-ADENOSYL-L-METHIONINE IODIDE SALT
CAS:
3493-13-8
MF:
C15H23IN6O5S
Structure:
Chemical Name:
ENTEROSTATIN (PIG, RAT)
CAS:
117137-85-6
MF:
C25H42N8O8
Structure:
Chemical Name:
FMOC-CYS(2-HYDROXYETHYL)-OH
CAS:
200354-35-4
MF:
C20H21NO5S
Structure:
Chemical Name:
3,5-DIIODO-D-TYROSINE HYDROCHLORIDE
CAS:
16711-71-0
MF:
C9H9I2NO3
Structure:
Chemical Name:
2-AMINO-3-P-TOLYL-PROPIONIC ACID
CAS:
4599-47-7
MF:
C10H13NO2
Structure:
Chemical Name:
H-HYP-OBZL HCL
CAS:
62147-27-7
MF:
C12H16ClNO3
Structure:
Chemical Name:
BOC-(S)-3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID
CAS:
500770-71-8
MF:
C14H18FNO4
Structure:
Chemical Name:
(S)-3-AMINO-5-HEXYNOIC ACID HYDROCHLORIDE
CAS:
270596-46-8
MF:
C6H9NO2
Structure:
Chemical Name:
H-D-GLU(GLY-OH)-OH
CAS:
6729-55-1
MF:
C7H12N2O5
Structure:
Chemical Name:
L-BAME
CAS:
1784-04-9
MF:
C15H22N4O6
Structure:
Chemical Name:
N-Methacryloylglycine
CAS:
23578-45-2
MF:
C6H9NO3
Structure:
Chemical Name:
FMOC-HYP(BZL)-OH
CAS:
174800-02-3
MF:
C27H25NO5
Structure:
Chemical Name:
H-4-NITRO-PHE-OET HCL
CAS:
58816-66-3
MF:
C11H15ClN2O4
Structure:
Chemical Name:
FMOC-L-PIPECOLIC ACID
CAS:
86069-86-5
MF:
C21H21NO4
Structure:
Chemical Name:
(R)-2-Amino-3-methoxylpropanoic acid
CAS:
86118-11-8
MF:
C4H9NO3
Structure:
Chemical Name:
N-Cbz-L-glutamic acid 5-ethyl ester
CAS:
35726-62-6
MF:
C15H19NO6
Structure:
Chemical Name:
FMOC-CYS(ME)-OH
CAS:
138021-87-1
MF:
C19H19NO4S
Structure:
Chemical Name:
H-L-METHR-OH HCL
CAS:
2812-28-4
MF:
C5H11NO3
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID
CAS:
507472-13-1
MF:
C24H20FNO4
Structure:
Chemical Name:
DANSYL-L-LEUCINE
CAS:
1100-22-7
MF:
C18H24N2O4S
Structure:
Chemical Name:
BOC-CYS(FM)-OH
CAS:
84888-35-7
MF:
C22H25NO4S
Structure:
Chemical Name:
DL-ALPHA-METHYLTRYPTOPHAN METHYL ESTER HYDROCHLORIDE
CAS:
114524-80-0
MF:
C13H16N2O2
Structure:
Chemical Name:
(2RS,3RS)-2-AMINO-3-(3,4-DIHYDROXY-PHENYL)-3-HYDROXY-PROPIONIC ACID
CAS:
3916-18-5
MF:
C9H11NO5
Structure:
Chemical Name:
FMOC-L-TRYPTOPHANOL
CAS:
153815-60-2
MF:
C26H24N2O3
Structure:
Chemical Name:
FMOC-1,4-TRANS-ACHC-OH
CAS:
147900-46-7
MF:
C22H23NO4
Structure:
Chemical Name:
H-DL-TRP-NH2 HCL
CAS:
67607-61-8
MF:
C11H14ClN3O
Structure:
Chemical Name:
FMOC-LYS(ME)2-OH HCL
CAS:
252049-10-8
MF:
C23H29ClN2O4
Structure:
Chemical Name:
Z-ARG-AMC HCL
CAS:
70375-22-3
MF:
C24H28ClN5O5
Structure:
Chemical Name:
Poly-alpha,beta-(N-2-hydroxyethyl)-DL-aspartamide
CAS:
70679-99-1
MF:
C12H26N6O6
Structure:
Chemical Name:
BOC-L-2-AMINO-5-PHENYL-PENTANOIC ACID DCHA SALT
CAS:
113756-89-1
MF:
C28H46N2O4
Structure:
Chemical Name:
(R)-3-AMINO-4-(3-TRIFLUOROMETHYLPHENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
269726-73-0
MF:
C11H12F3NO2
Structure:
Chemical Name:
D-2-HYDROXYPENTANEDIOIC ACID DISODIUM SALT
CAS:
103404-90-6
MF:
C5H9NaO5
Structure:
Chemical Name:
N-2-NITROPHENYLSULFENYL-L-ISOLEUCINE DICYCLOHEXYLAMMONIUM SALT
CAS:
7675-49-2
MF:
C24H39N3O4S
Structure:
Chemical Name:
POLY-EPSILON-CBZ-L-LYSINE
CAS:
25931-47-9
MF:
C14H20N2O4
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(3-TRIFLUOROMETHYL-PHENYL)-PROPIONIC ACID
CAS:
517905-87-2
MF:
C25H20F3NO4
Structure:
Chemical Name:
4-CHLOROBENZOYL-L-TRYPTOPHAN CALCIUM SALT
CAS:
56116-62-2
MF:
C36H28CaCl2N4O6
Structure:
Chemical Name:
BOC-4,4-DIFLUORO-L-PROLINE METHYL ESTER
CAS:
203866-17-5
MF:
C11H17F2NO4
Structure:
Chemical Name:
H-LYS-LYS-OH 2HCL
CAS:
52123-30-5
MF:
C12H27ClN4O3
Structure:
Chemical Name:
FMOC-D-4-AMINOMETHYLPHENYLALANINE(BOC)
CAS:
268731-06-2
MF:
C30H32N2O6
Structure:
Chemical Name:
BOC-(R)-3-AMINO-4-(3-CHLORO-PHENYL)-BUTYRIC ACID
CAS:
331763-56-5
MF:
C15H20ClNO4
Structure:
Chemical Name:
TRANS-4-CYCLOHEXYL-L-PROLINE
CAS:
130092-20-5
MF:
C11H19NO2
Structure:
Chemical Name:
L-Phenylalaninamide hydrochloride
CAS:
65864-22-4
MF:
C9H13ClN2O
Structure:
Chemical Name:
N-BOC-N-[3-(BOC-AMINO)PROPYL]GLYCINE
CAS:
192124-66-6
MF:
C15H28N2O6
Structure:
Chemical Name:
(R)-3-AMINO-4-(2-BROMO-PHENYL)-BUTYRIC ACID HCL
CAS:
401915-60-4
MF:
C10H13BrClNO2
Structure:
Chemical Name:
DL-ALANYL-L-ALANINE
CAS:
59247-16-4
MF:
C6H12N2O3
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-3-(3-BROMO-PHENYL)-PROPIONIC ACID
CAS:
507472-18-6
MF:
C24H20BrNO4
Structure:
Chemical Name:
P-NITROBENZOYL-L-GLUTAMIC ACID
CAS:
6758-40-3
MF:
C12H12N2O7
Structure:
Chemical Name:
3-AMINOPENTANE-3-CARBOXYLIC ACID
CAS:
2566-29-2
MF:
C6H13NO2
Structure:
Chemical Name:
6-AMINO-PYRIMIDINE-4-CARBOXYLIC ACID
CAS:
38214-46-9
MF:
C5H5N3O2
Structure:
Chemical Name:
3-(1-NAPHTHYL)-D-ALANINE HYDROCHLORIDE
CAS:
122745-09-9
MF:
C13H14ClNO2
Structure:
Chemical Name:
BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE
CAS:
121505-93-9
MF:
C9H18N2O4
Structure:
Chemical Name:
S-Methyl-L-cysteine sulfoxide
CAS:
6853-87-8
MF:
C4H9NO3S
Structure:
Chemical Name:
DABSYL-GLYCINE
CAS:
89131-05-5
MF:
C16H18N4O4S
Structure:
Chemical Name:
4-Phosphonophenylglycine
CAS:
120667-15-4
MF:
C8H10NO5P
Structure:
Chemical Name:
N-(3-Indolylacetyl)-L-alanine
CAS:
57105-39-2
MF:
C13H14N2O3
Structure:
Chemical Name:
N,N-BIS(2-HYDROXYETHYL)GLYCINE SODIUM SALT
CAS:
139-41-3
MF:
C6H14NNaO4
Structure:
Chemical Name:
Z-HIS(BZL)-OH
CAS:
21929-66-8
MF:
C21H21N3O4
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(4-HYDROXY-PHENYL)-PROPIONIC ACID
CAS:
511272-36-9
MF:
C24H21NO5
Structure:
Chemical Name:
D-Glutamic acid 1-tert-butyl ester
CAS:
25456-76-2
MF:
C9H17NO4
Structure:
Chemical Name:
AMINO-(2-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID
CAS:
240490-00-0
MF:
C9H8F3NO2
Structure:
Chemical Name:
Nalpha-Acetyl-D-asparagine
CAS:
26117-27-1
MF:
C6H10N2O4
Structure:
Chemical Name:
Boc-L-2,4-diaminobutyric acid
CAS:
25691-37-6
MF:
C9H18N2O4
Structure:
Chemical Name:
Boc-2-Methyl-D-beta-phenylalanine
CAS:
499995-74-3
MF:
C15H21NO4
Structure:
Chemical Name:
Boc-3-Methyl-D-beta-phenylalanine
CAS:
499995-75-4
MF:
C15H21NO4
Structure:
Chemical Name:
Fmoc-D-beta-homophenylalanine
CAS:
209252-16-4
MF:
C25H23NO4
Structure:
Chemical Name:
BOC-D-PHE(3-I)-OH
CAS:
478183-66-3
MF:
C14H18INO4
Structure:
Chemical Name:
CHLOROACETYL-DL-ISOLEUCINE
CAS:
1115-24-8
MF:
C8H14ClNO3
Structure:
Chemical Name:
Boc-O-Benzyl-L-tyrosine hydroxysuccinimide ester
CAS:
34805-19-1
MF:
C25H28N2O7
Structure:
Chemical Name:
L-6-HYDROXYNORLEUCINE
CAS:
6033-32-5
MF:
C6H13NO3
Structure:
Chemical Name:
BOC-L-4-AMINOMETHYLPHENYLALANINE(FMOC)
CAS:
170157-61-6
MF:
C30H32N2O6
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-5-HEXYNOIC ACID
CAS:
270596-48-0
MF:
C21H19NO4
Structure:
Chemical Name:
BOC-(R)-3-AMINO-4-(PENTAFLUORO-PHENYL)-BUTYRIC ACID
CAS:
269398-93-8
MF:
C15H16F5NO4
Structure:
Chemical Name:
L-Glutamic acid alpha-amide
CAS:
636-65-7
MF:
C5H10N2O3
Structure:
Chemical Name:
D-Cyclobutylglycine
CAS:
49607-10-5
MF:
C6H11NO2
Structure:
Chemical Name:
DANSYL-L-SERINE PIPERIDINIUM SALT
CAS:
35021-12-6
MF:
C15H18N2O5S
Structure:
Chemical Name:
2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid
CAS:
67776-06-1
MF:
C7H12N2O4S
Structure:
Chemical Name:
4-Hydroxyisoleucine
CAS:
21704-86-9
MF:
C6H13NO3