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:
AC-LYS (BOC)-OH
CAS:
23500-04-1
MF:
C13H24N2O5
Structure:
Chemical Name:
L-2-AMINO-3-GUANIDINOPROPIONIC ACID HYDROCHLORIDE
CAS:
1482-99-1
MF:
C4H11ClN4O2
Structure:
Chemical Name:
(R)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID HYDROCHLORIDE
CAS:
270596-35-5
MF:
C12H15NO2
Structure:
Chemical Name:
L-2-AMINO-5-PHENYL-PENTANOIC ACID
CAS:
62777-25-7
MF:
C11H15NO2
Structure:
Chemical Name:
BOC-(R)-3-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID
CAS:
500788-85-2
MF:
C15H21NO5
Structure:
Chemical Name:
(H-CYS-BETANA)2
CAS:
1259-69-4
MF:
C26H26N4O2S2
Structure:
Chemical Name:
BOC-(R)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID
CAS:
500789-07-1
MF:
C14H18BrNO4
Structure:
Chemical Name:
N-(2-NITROPHENYLSULFENYL)-S-BENZYL-L-CYSTEINE DICYCLOHEXYLAMMONIUM SALT
CAS:
7675-65-2
MF:
C28H39N3O4S2
Structure:
Chemical Name:
METHYL 5-AMINO-2-FUROATE
CAS:
22600-30-2
MF:
C6H7NO3
Structure:
Chemical Name:
DABSYL-L-PROLINE
CAS:
89131-09-9
MF:
C19H22N4O4S
Structure:
Chemical Name:
LYS-ARG-PRO-PRO-GLY-PHE-SER-PRO-PHE
CAS:
71800-36-7
MF:
C50H73N13O11
Structure:
Chemical Name:
N-Boc-N'-xanthyl-L-asparagine
CAS:
65420-40-8
MF:
C22H24N2O6
Structure:
Chemical Name:
(1R,2S)-1-BOC-AMINO-2-VINYLCYCLOPROPANECARBOXYLIC ACID ETHYL ESTER
CAS:
213316-49-5
MF:
C13H21NO4
Structure:
Chemical Name:
MEOSUC-ALA-ALA-PRO-VAL-AMC
CAS:
72252-90-5
MF:
C31H41N5O9
Structure:
Chemical Name:
(S)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID HYDROCHLORIDE
CAS:
270263-08-6
MF:
C12H15NO2
Structure:
Chemical Name:
Boc-3-Methyl-L-beta-phenylalanine
CAS:
464930-76-5
MF:
C15H21NO4
Structure:
Chemical Name:
L-Arginine hydrochloride
CAS:
15595-35-4
MF:
C6H15ClN4O2
Structure:
Chemical Name:
Boc-beta-(R)-4-methoxyphenylalanine
CAS:
500788-87-4
MF:
C15H21NO5
Structure:
Chemical Name:
TYRPHOSTIN A51
CAS:
122520-90-5
MF:
C13H8N4O3
Structure:
Chemical Name:
TRANS-2-AMINO-1-CYCLOHEXANECARBOXYLIC ACID
CAS:
5691-19-0
MF:
C7H13NO2
Structure:
Chemical Name:
BOC-PHE-SER-ARG-AMC ACETATE SALT
CAS:
73554-90-2
MF:
C33H43N7O8
Structure:
Chemical Name:
BOC-TRANEXAMIC ACID
CAS:
27687-14-5
MF:
C13H23NO4
Structure:
Chemical Name:
H-D-THR(TBU)-OH
CAS:
201274-81-9
MF:
C8H17NO3
Structure:
Chemical Name:
FMOC-(S)-2-TETRAHYDROISOQUINOLINE ACETIC ACID
CAS:
270062-99-2
MF:
C26H23NO4
Structure:
Chemical Name:
DANSYL-L-PROLINE
CAS:
1239-94-7
MF:
C17H20N2O4S
Structure:
Chemical Name:
4-AMINO-2-BUTANOL
CAS:
39884-48-5
MF:
C4H11NO
Structure:
Chemical Name:
AC-NLE-OH
CAS:
15891-49-3
MF:
C8H15NO3
Structure:
Chemical Name:
AC-NVA-OH
CAS:
15891-50-6
MF:
C7H13NO3
Structure:
Chemical Name:
BOC-PHE(2-I)-OH
CAS:
273221-78-6
MF:
C14H18INO4
Structure:
Chemical Name:
(-)-(1S,4R)-N-FMOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID
CAS:
220497-65-4
MF:
C21H19NO4
Structure:
Chemical Name:
(S)-3-AMINO-4-(2-THIENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
270065-91-3
MF:
C8H11NO2S
Structure:
Chemical Name:
DL-ALANYL-L-LEUCINE
CAS:
1638-60-4
MF:
C9H18N2O3
Structure:
Chemical Name:
H-D-GLU(OME)-OH
CAS:
6461-04-7
MF:
C6H11NO4
Structure:
Chemical Name:
Boc-5-aminopentanoic acid
CAS:
27219-07-4
MF:
C10H19NO4
Structure:
Chemical Name:
H-D-SER-OET HCL
CAS:
104055-46-1
MF:
C5H12ClNO3
Structure:
Chemical Name:
MAGNESIUM L-GLUTAMATE TETRAHYDRATE
CAS:
18543-68-5
MF:
C10H13MgN2O8-
Structure:
Chemical Name:
BOC-ORN-OH
CAS:
21887-64-9
MF:
C10H20N2O4
Structure:
Chemical Name:
FMOC-D-ALANINOL
CAS:
202751-95-9
MF:
C18H19NO3
Structure:
Chemical Name:
Z-GLY-PHE-OH
CAS:
1170-76-9
MF:
C19H20N2O5
Structure:
Chemical Name:
Z-DAB(BOC)-OH
CAS:
3350-13-8
MF:
C17H24N2O6
Structure:
Chemical Name:
3-THIOPHENEPROPIONIC ACID
CAS:
3685-48-1
MF:
C7H9NO2S
Structure:
Chemical Name:
Z-ALA-OME
CAS:
28819-05-8
MF:
C12H15NO4
Structure:
Chemical Name:
7-BENZYLOXYGRAMINE
CAS:
94067-27-3
MF:
C18H20N2O
Structure:
Chemical Name:
BOC-D-MEVAL-OH
CAS:
89536-85-6
MF:
C11H21NO4
Structure:
Chemical Name:
PHENYLTHIOHYDANTOIN-DELTA-THREONINE
CAS:
5800-50-0
MF:
C11H10N2OS
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID
CAS:
331763-76-9
MF:
C25H22BrNO4
Structure:
Chemical Name:
AMINO-(2-METHOXY-PHENYL)-ACETIC ACID
CAS:
271583-17-6
MF:
C9H11NO3
Structure:
Chemical Name:
4-AMINO-2-METHYLTHIO-5-THIAZOLECARBOXYLIC ACID METHYL ESTER
CAS:
60093-05-2
MF:
C6H8N2O2S2
Structure:
Chemical Name:
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL
CAS:
51096-49-2
MF:
C15H17NO
Structure:
Chemical Name:
L-Alanyl-L-leucine
CAS:
3303-34-2
MF:
C9H18N2O3
Structure:
Chemical Name:
FMOC-HIS-OH
CAS:
116611-64-4
MF:
C21H19N3O4
Structure:
Chemical Name:
H-ALPHA-ME-D-VAL-OH
CAS:
53940-82-2
MF:
C6H13NO2
Structure:
Chemical Name:
L-Glutamic acid 1-tert-Butyl ester hydrochloride
CAS:
144313-55-3
MF:
C9H18ClNO4
Structure:
Chemical Name:
DL-CYSTEIC ACID
CAS:
3024-83-7
MF:
C3H7NO5S
Structure:
Chemical Name:
H-D-MET-OET HCL
CAS:
7512-43-8
MF:
C7H16ClNO2S
Structure:
Chemical Name:
D-TERT-LEUCINE HYDROCHLORIDE
CAS:
112720-39-5
MF:
C6H14ClNO2
Structure:
Chemical Name:
H-D-CHA-OH
CAS:
58717-02-5
MF:
C9H17NO2
Structure:
Chemical Name:
AC-ALA-GLN-OH
CAS:
121574-43-4
MF:
C10H17N3O5
Structure:
Chemical Name:
O-ACETYL-L-SERINE
CAS:
5147-00-2
MF:
C5H9NO4
Structure:
Chemical Name:
BOC-(R)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID
CAS:
332064-73-0
MF:
C17H23NO4
Structure:
Chemical Name:
DL-GLUTAMIC ACID HYDROCHLORIDE
CAS:
15767-75-6
MF:
C5H10ClNO4
Structure:
Chemical Name:
Z-D-PYR-OH
CAS:
78339-57-8
MF:
C13H13NO5
Structure:
Chemical Name:
H-GLY-MET-OH
CAS:
554-94-9
MF:
C7H14N2O3S
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-3-(2,4-DICHLORO-PHENYL)-PROPIONIC ACID
CAS:
501015-34-5
MF:
C24H19Cl2NO4
Structure:
Chemical Name:
CHLOROACETYL-DL-SERINE
CAS:
67206-28-4
MF:
C5H8ClNO4
Structure:
Chemical Name:
N-(3-Indolylacetyl)-L-isoleucine
CAS:
57105-45-0
MF:
C16H20N2O3
Structure:
Chemical Name:
3,5-Diiodo-DL-tyrosine
CAS:
66-02-4
MF:
C9H9I2NO3
Structure:
Chemical Name:
4-Amino-2-methylquinoline-6-carboxylic acid
CAS:
99984-73-3
MF:
C11H10N2O2
Structure:
Chemical Name:
BOC-SER-OH H2O
CAS:
204191-40-2
MF:
C8H17NO6
Structure:
Chemical Name:
H-D-TRP-OBZL HCL
CAS:
22839-16-3
MF:
C18H19ClN2O2
Structure:
Chemical Name:
NALPHA,NOMEGA-DICARBOBENZOXY-L-ARGININE
CAS:
53934-75-1
MF:
C22H26N4O6
Structure:
Chemical Name:
N,N-DIETHYLGLYCINE METHYL ESTER
CAS:
30280-35-4
MF:
C7H15NO2
Structure:
Chemical Name:
(R)-3-AMINO-4-(3,4-DIFLUOROPHENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
269396-58-9
MF:
C10H11F2NO2
Structure:
Chemical Name:
N,N′-Bis-tert-butoxycarbonylthiourea
CAS:
145013-05-4
MF:
C11H20N2O4S
Structure:
Chemical Name:
VINYL ACCA
CAS:
159622-10-3
MF:
C11H17NO4
Structure:
Chemical Name:
5-AMINO-2-METHOXYBENZOIC ACID
CAS:
3403-47-2
MF:
C8H9NO3
Structure:
Chemical Name:
DL-ALLO-ISOLEUCINE
CAS:
3107-04-8
MF:
C6H13NO2
Structure:
Chemical Name:
DL-CYCLOSERINE
CAS:
68-39-3
MF:
C3H6N2O2
Structure:
Chemical Name:
Boc-N-methyl-D-leucine
CAS:
89536-84-5
MF:
C12H23NO4
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID
CAS:
332064-75-2
MF:
C27H25NO4
Structure:
Chemical Name:
4-DIMETHYLAMINOBUTYRIC ACID HYDROCHLORIDE
CAS:
69954-66-1
MF:
C6H14ClNO2
Structure:
Chemical Name:
BZ-DL-ARG-BETANA HCL
CAS:
913-04-2
MF:
C23H26ClN5O2
Structure:
Chemical Name:
BOC-ALLO-ILE-OH
CAS:
35264-07-4
MF:
C11H21NO4
Structure:
Chemical Name:
N,N-BIS(CARBOXYLATOMETHYL)ALANINE TRISODIUM SALT
CAS:
164462-16-2
MF:
C7H12NNaO6
Structure:
Chemical Name:
NG-MONOMETHYL-D-ARGININE MONOACETATE
CAS:
137694-75-8
MF:
C9H20N4O4
Structure:
Chemical Name:
BOC-D-TIC-OH
CAS:
115962-35-1
MF:
C15H19NO4
Structure:
Chemical Name:
AC-DL-HIS-OH H2O
CAS:
213178-97-3
MF:
C8H13N3O4
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-5-HEXYNOIC ACID
CAS:
332064-94-5
MF:
C21H19NO4
Structure:
Chemical Name:
Fmoc-Gly-Gly-OH
CAS:
35665-38-4
MF:
C19H18N2O5
Structure:
Chemical Name:
3,4-DICHLORO-DL-PHENYLALANINE
CAS:
5472-67-3
MF:
C9H9Cl2NO2
Structure:
Chemical Name:
N-Acetyl-D-glutamic acid
CAS:
19146-55-5
MF:
C7H11NO5
Structure:
Chemical Name:
Z-GLY-GLY-LEU-OH
CAS:
13347-77-8
MF:
C18H25N3O6
Structure:
Chemical Name:
D-PROPARGYLGLYCINE
CAS:
23235-03-2
MF:
C5H7NO2
Structure:
Chemical Name:
N-(TERT-BUTOXYCARBONYL)-D-PROLINAL
CAS:
73365-02-3
MF:
C10H17NO3
Structure:
Chemical Name:
DMOG
CAS:
89464-63-1
MF:
C6H9NO5
Structure:
Chemical Name:
4-(Boc-amino)-1-(Fmoc-piperidinyl)-4-carboxylic Acid
CAS:
368866-07-3
MF:
C26H30N2O6
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID
CAS:
511272-53-0
MF:
C24H20ClNO4
Structure:
Chemical Name:
BOC-ARG(Z)-OH
CAS:
51219-18-2
MF:
C19H28N4O6
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID
CAS:
270596-45-7
MF:
C27H25NO4
Structure:
Chemical Name:
N-tert-Butoxycarbonyl-N'-benzyloxycarbonyl-L-ornithine
CAS:
2480-93-5
MF:
C18H26N2O6