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:
Boc-3,3-Diphenyl-L-alanine
CAS:
138662-63-2
MF:
C20H23NO4
Structure:
Chemical Name:
D-2-Aminobutyric acid
CAS:
2623-91-8
MF:
C4H9NO2
Structure:
Chemical Name:
L-Cysteine methyl ester hydrochloride
CAS:
18598-63-5
MF:
C4H10ClNO2S
Structure:
Chemical Name:
BOC-D-3-Trifluoromethylphe
CAS:
82317-82-6
MF:
C15H18F3NO4
Structure:
Chemical Name:
Z-ARG(Z)2-OH
CAS:
14611-34-8
MF:
C30H32N4O8
Structure:
Chemical Name:
BOC-HIS(Z)-OH
CAS:
50305-43-6
MF:
C19H23N3O6
Structure:
Chemical Name:
3,3-Diphenyl-L-alanine
CAS:
149597-92-2
MF:
C15H15NO2
Structure:
Chemical Name:
D-LEUCYL-GLYCYL-GLYCINE
CAS:
18625-22-4
MF:
C10H19N3O4
Structure:
Chemical Name:
Boc-3-(2-thienyl)-L-alanine
CAS:
56675-37-7
MF:
C12H17NO4S
Structure:
Chemical Name:
3-AMINO-2,5,6-TRIFLUOROBENZOIC ACID
CAS:
133622-65-8
MF:
C7H4F3NO2
Structure:
Chemical Name:
FMOC-L-Valine
CAS:
68858-20-8
MF:
C20H21NO4
Structure:
Chemical Name:
1-Amino-1-cyclohexanecarboxylic acid
CAS:
2756-85-6
MF:
C7H13NO2
Structure:
Chemical Name:
4-Methylphenyl-L-alanine
CAS:
1991-87-3
MF:
C10H13NO2
Structure:
Chemical Name:
BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID
CAS:
270065-80-0
MF:
C16H20F3NO4
Structure:
Chemical Name:
L-Glutamic acid 5-methyl ester
CAS:
1499-55-4
MF:
C6H11NO4
Structure:
Chemical Name:
tert-Butyl 3-phenyl-L-alaninate hydrochloride
CAS:
15100-75-1
MF:
C13H20ClNO2
Structure:
Chemical Name:
Boc-beta-alanine
CAS:
3303-84-2
MF:
C8H15NO4
Structure:
Chemical Name:
BOC-D-4-Fluorophe
CAS:
57292-45-2
MF:
C14H18FNO4
Structure:
Chemical Name:
D-ASPARTIC ACID DIMETHYL ESTER HYDROCHLORIDE
CAS:
69630-50-8
MF:
C6H12ClNO4
Structure:
Chemical Name:
Methyl L-argininate dihydrochloride
CAS:
26340-89-6
MF:
C7H18Cl2N4O2
Structure:
Chemical Name:
2-Hydroxy-4-amino butanoic acid
CAS:
13477-53-7
MF:
C4H9NO3
Structure:
Chemical Name:
DL-4-HYDROXYPHENYLGLYCINE
CAS:
938-97-6
MF:
C8H9NO3
Structure:
Chemical Name:
DL-Lysine monohydrochloride
CAS:
70-53-1
MF:
C6H15ClN2O2
Structure:
Chemical Name:
L-Tyrosine benzyl ester p-toluenesulfonate
CAS:
53587-11-4
MF:
C23H25NO6S
Structure:
Chemical Name:
1-Hydroxybenzotriazole
CAS:
2592-95-2
MF:
C6H5N3O
Structure:
Chemical Name:
Boc-L-Histidine(Tosyl)
CAS:
35899-43-5
MF:
C18H23N3O6S
Structure:
Chemical Name:
N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine
CAS:
54613-99-9
MF:
C19H27ClN2O6
Structure:
Chemical Name:
tert-Butyl L-prolinate hydrochloride
CAS:
5497-76-7
MF:
C9H18ClNO2
Structure:
Chemical Name:
3-FLUORO-L-TYROSINE
CAS:
7423-96-3
MF:
C9H10FNO3
Structure:
Chemical Name:
BOC-D-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID
CAS:
123910-26-9
MF:
C17H20N2O4
Structure:
Chemical Name:
N-alpha-Cbz-L-lysine
CAS:
2212-75-1
MF:
C14H20N2O4
Structure:
Chemical Name:
BOC-L-4-Methylphe
CAS:
80102-26-7
MF:
C15H21NO4
Structure:
Chemical Name:
DL-4-Chlorophenylalanine methyl ester hydrochloride
CAS:
14173-40-1
MF:
C10H13Cl2NO2
Structure:
Chemical Name:
(-)-(1S,4R)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID
CAS:
151907-79-8
MF:
C11H17NO4
Structure:
Chemical Name:
L-2,4-DICHLOROPHENYLALANINE
CAS:
111119-36-9
MF:
C9H9Cl2NO2
Structure:
Chemical Name:
L-2-FURYLALANINE
CAS:
127682-08-0
MF:
C7H9NO3
Structure:
Chemical Name:
Oxaceprol
CAS:
33996-33-7
MF:
C7H11NO4
Structure:
Chemical Name:
4-(Methylamino)benzoic acid
CAS:
10541-83-0
MF:
C8H9NO2
Structure:
Chemical Name:
D-4,4'-BIPHENYLALANINE
CAS:
170080-13-4
MF:
C15H15NO2
Structure:
Chemical Name:
N-Acetylglycine
CAS:
543-24-8
MF:
C4H7NO3
Structure:
Chemical Name:
H-D-PHG-OME HCL
CAS:
19883-41-1
MF:
C9H12ClNO2
Structure:
Chemical Name:
(R)-N-BOC-2-Bromophenylalanine
CAS:
261360-76-3
MF:
C14H18BrNO4
Structure:
Chemical Name:
BOC-D-DAB(FMOC)-OH
CAS:
131570-57-5
MF:
C24H28N2O6
Structure:
Chemical Name:
TOS-ARG-OME HCL
CAS:
1784-03-8
MF:
C14H23ClN4O4S
Structure:
Chemical Name:
(S)-N-BOC-2-Bromophenylalanine
CAS:
261165-02-0
MF:
C14H18BrNO4
Structure:
Chemical Name:
4-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER
CAS:
183673-66-7
MF:
C26H30N2O6
Structure:
Chemical Name:
3-AMINOPHTHALIC ACID
CAS:
5434-20-8
MF:
C8H7NO4
Structure:
Chemical Name:
(S)-N-Boc-allylglycine
CAS:
90600-20-7
MF:
C10H17NO4
Structure:
Chemical Name:
(R)-3-Amino-1,2-propanediol
CAS:
66211-46-9
MF:
C3H9NO2
Structure:
Chemical Name:
Fmoc-O-trityl-L-threonine
CAS:
133180-01-5
MF:
C38H33NO5
Structure:
Chemical Name:
Boc-D-Allylglycine
CAS:
170899-08-8
MF:
C10H17NO4
Structure:
Chemical Name:
DL-Pyroglutamic acid
CAS:
149-87-1
MF:
C5H7NO3
Structure:
Chemical Name:
BENZOYL-DL-LEUCINE
CAS:
17966-67-5
MF:
C13H17NO3
Structure:
Chemical Name:
BOC-L-4,4'-BIPHENYLALANINE
CAS:
147923-08-8
MF:
C20H23NO4
Structure:
Chemical Name:
N-Cbz-L-Aspartic acid 4-benzyl ester
CAS:
3479-47-8
MF:
C19H19NO6
Structure:
Chemical Name:
AC-D-PRO-OH
CAS:
59785-68-1
MF:
C7H11NO3
Structure:
Chemical Name:
Boc-D-Valine
CAS:
22838-58-0
MF:
C10H19NO4
Structure:
Chemical Name:
Fmoc-D-Asn(Trt)-OH
CAS:
180570-71-2
MF:
C38H32N2O5
Structure:
Chemical Name:
H-TYR(BZL)-OH
CAS:
16652-64-5
MF:
C16H17NO3
Structure:
Chemical Name:
BOC-L-3-CYANOPHENYLALANINE
CAS:
131980-30-8
MF:
C15H18N2O4
Structure:
Chemical Name:
BOC-PHE(4-NHFMOC)-OH
CAS:
114346-31-5
MF:
C29H30N2O6
Structure:
Chemical Name:
FMOC-L-Arginine
CAS:
91000-69-0
MF:
C21H24N4O4
Structure:
Chemical Name:
D-(-)-A-4-HYDROXYPHENYLGLYCINE DANE SALT METHYL POTASSIUM
CAS:
69416-61-1
MF:
C13H16KNO5
Structure:
Chemical Name:
Nalpha-Cbz-L-Arginine
CAS:
1234-35-1
MF:
C14H20N4O4
Structure:
Chemical Name:
Methyl L-pyroglutamate
CAS:
4931-66-2
MF:
C6H9NO3
Structure:
Chemical Name:
H-D-MET-OME HCL
CAS:
69630-60-0
MF:
C6H14ClNO2S
Structure:
Chemical Name:
L(+)-Leucinol
CAS:
7533-40-6
MF:
C6H15NO
Structure:
Chemical Name:
L-Cyclopropylglycine
CAS:
49606-99-7
MF:
C5H9NO2
Structure:
Chemical Name:
Fmoc-D-glutamic acid gamma-tert-butyl ester
CAS:
104091-08-9
MF:
C24H27NO6
Structure:
Chemical Name:
D-Tyrosinol hydrochloride
CAS:
40829-04-7
MF:
C9H14ClNO2
Structure:
Chemical Name:
L-Homoserine
CAS:
672-15-1
MF:
C4H9NO3
Structure:
Chemical Name:
Ornipressin
CAS:
3397-23-7
MF:
C45H63N13O12S2
Structure:
Chemical Name:
BOC-D-PRO-OSU
CAS:
102185-34-2
MF:
C14H20N2O6
Structure:
Chemical Name:
Rink Amide Linker
CAS:
145069-56-3
MF:
C32H29NO7
Structure:
Chemical Name:
N-Acetyl-L-isoleucine
CAS:
3077-46-1
MF:
C8H15NO3
Structure:
Chemical Name:
Z-D-ASP(OTBU)-OH H2O
CAS:
71449-08-6
MF:
C16H21NO6
Structure:
Chemical Name:
BOC-(S)-3-AMINO-4-(4-FLUORO-PHENYL)-BUTYRIC ACID
CAS:
218608-97-0
MF:
C15H20FNO4
Structure:
Chemical Name:
Methyl L-prolinate hydrochloride
CAS:
2133-40-6
MF:
C6H12ClNO2
Structure:
Chemical Name:
L-Pyroglutaminol
CAS:
17342-08-4
MF:
C5H9NO2
Structure:
Chemical Name:
BOC-MET(O)-OH
CAS:
34805-21-5
MF:
C10H19NO5S
Structure:
Chemical Name:
Fmoc-D-tryptophan
CAS:
86123-11-7
MF:
C26H22N2O4
Structure:
Chemical Name:
N2-1[(1S)-Ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysyl-L-proline
CAS:
103300-91-0
MF:
C25H34F3N3O6
Structure:
Chemical Name:
BOC-D-2-PYRIDYLALANINE
CAS:
98266-32-1
MF:
C13H18N2O4
Structure:
Chemical Name:
Benzyl L-tryptophanate hydrochloride
CAS:
35858-81-2
MF:
C18H19ClN2O2
Structure:
Chemical Name:
Boc-D-Glu-OBzl
CAS:
34404-30-3
MF:
C17H23NO6
Structure:
Chemical Name:
4-Iodo-DL-phenylalanine
CAS:
14173-41-2
MF:
C9H10INO2
Structure:
Chemical Name:
BOC-D-BETA-HOMOPHENYLALANINE
CAS:
101555-61-7
MF:
C15H21NO4
Structure:
Chemical Name:
NG-MONOMETHYL-L-ARGININE ACETATE
CAS:
53308-83-1
MF:
C9H20N4O4
Structure:
Chemical Name:
FMOC-L-2-Methylphe
CAS:
211637-75-1
MF:
C25H23NO4
Structure:
Chemical Name:
L-Aspartic acid
CAS:
56-84-8
MF:
C4H7NO4
Structure:
Chemical Name:
BOC-D-3-Fluorophe
CAS:
114873-11-9
MF:
C14H18FNO4
Structure:
Chemical Name:
Boc-L-beta-glutamic acid 5-benzyl ester
CAS:
254101-10-5
MF:
C17H23NO6
Structure:
Chemical Name:
N-CARBOBENZOXY-DL-SERINE
CAS:
2768-56-1
MF:
C11H13NO5
Structure:
Chemical Name:
Benzylaminoacetic acid hydrochloride
CAS:
7689-50-1
MF:
C9H12ClNO2
Structure:
Chemical Name:
(S)-N-Boc-3-aminobutyric acid
CAS:
158851-30-0
MF:
C9H17NO4
Structure:
Chemical Name:
FMOC-L-2-Chlorophe
CAS:
198560-41-7
MF:
C24H20ClNO4
Structure:
Chemical Name:
Ethyl L-alaninate hydrochloride
CAS:
1115-59-9
MF:
C5H12ClNO2
Structure:
Chemical Name:
FMOC-L-4,4'-BIPHENYLALANINE
CAS:
205526-38-1
MF:
C30H25NO4
Structure:
Chemical Name:
N-(4-Nitrobenzoyl)-beta-alanine
CAS:
59642-21-6
MF:
C10H10N2O5
Structure:
Chemical Name:
2,4-DIFLUORO-DL-PHENYLALANINE
CAS:
32133-35-0
MF:
C9H9F2NO2