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:
D-Tyr-Ome
CAS:
3410-66-0
MF:
C10H13NO3
Structure:
Chemical Name:
1-Methyl-5-oxoproline methyl ester
CAS:
190783-99-4
MF:
C7H11NO3
Structure:
Chemical Name:
(4-FLUORO-PHENYLAMINO)-ACETIC ACID
CAS:
351-95-1
MF:
C8H8FNO2
Structure:
Chemical Name:
2-AMINO-3-METHOXYCARBONYL-5-NITROTHIOPHENE
CAS:
43028-48-4
MF:
C6H6N2O4S
Structure:
Chemical Name:
Diethyl N-[5-[N-[(3,4-dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl]-N-methylamino]-2-thenoyl]-L-glutamate
CAS:
132463-02-6
MF:
C25H30N4O6S
Structure:
Chemical Name:
Acetic acid, (1-methylhydrazino)-, 1,1-dimethylethyl ester (9CI)
CAS:
144036-71-5
MF:
C7H16N2O2
Structure:
Chemical Name:
DL-ALANYL-DL-ISOLEUCINE
CAS:
935399-25-0
MF:
C9H18N2O3
Structure:
Chemical Name:
DL-Cyclobutylalanine
CAS:
4426-06-6
MF:
C7H13NO2
Structure:
Chemical Name:
DL-Cyclopropylglycine
CAS:
10294-18-5
MF:
C5H9NO2
Structure:
Chemical Name:
Fmoc-2,4-Difluoro-L-Phenylalanine
MF:
C24H19F2NO4
Chemical Name:
L-ArginineMalate(1:1)
Structure:
Chemical Name:
N-BOC-1-AMINO-1-CYCLOPENTANEMETHANOL
CAS:
174889-22-6
MF:
C11H21NO2
Structure:
Chemical Name:
Benzeneacetic acid, alpha,4-diamino- (9CI)
CAS:
75176-85-1
MF:
C8H10N2O2
Structure:
Chemical Name:
ethyl DL-methionate hydrochloride
CAS:
6297-53-6
MF:
C7H16ClNO2S
Chemical Name:
ACETYL HEXAPEPTIDE-3
Structure:
Chemical Name:
4-AMINOQUINOLINE-3-CARBOXYLIC ACID
CAS:
68313-46-2
MF:
C10H8N2O2
Chemical Name:
L-2,6-diaminohexanoic acid monoactate
MF:
C8H18N2O4
Structure:
Chemical Name:
2-Ethoxy-5-Nitro-Phenylalanine
MF:
C11H14N2O5
Structure:
Chemical Name:
DL-N-BENZOYL-2-BENZYLSERINE
CAS:
52421-48-4
MF:
C17H17NO4
Structure:
Chemical Name:
FMOC-CYS(SO3H)-OH DISODIUM SALT
CAS:
163558-30-3
MF:
C18H18NNaO7S2
Structure:
Chemical Name:
(R)-2-AMINO-N-METHYL-SUCCINAMIC ACID
CAS:
7175-34-0
MF:
C5H10N2O3
Structure:
Chemical Name:
L-ALANINE (D7)
CAS:
74280-71-0
MF:
C3D7NO2
Structure:
Chemical Name:
BARIUM CIS-EPOXY-SUCCINATE
CAS:
36170-34-0
MF:
C4H6BaO5
Structure:
Chemical Name:
(S)-(-)-1-(N-(1-ETHOXYCARBONYL-3-PHEN&
CAS:
130414-30-1
MF:
C20H27F3N2O5
Structure:
Chemical Name:
L-LEUCINE ETHYL ESTER HYDROCHLORIDE
CAS:
2143-40-0
MF:
C8H18ClNO2
Structure:
Chemical Name:
D-TRYPTOPHAN BENZYL ESTER 98
CAS:
141595-98-4
MF:
C18H18N2O2
Structure:
Chemical Name:
ZPCK
CAS:
26049-94-5
MF:
C18H18ClNO3
Structure:
Chemical Name:
H-TYR-OBZL
CAS:
42406-77-9
MF:
C16H17NO3
Structure:
Chemical Name:
Z-DEVD-CMK
CAS:
250584-13-5
MF:
C27H35ClN4O12
Structure:
Chemical Name:
BOC-3-IODO-D-TYR-OH
CAS:
478183-68-5
MF:
C14H18INO5
Structure:
Chemical Name:
BOC-4-HYDROXY-D-PHENYLGLYCINE
CAS:
1217464-82-8
MF:
C11H17NO4
Structure:
Chemical Name:
(R)-3-(Boc-amino)-4-(3,4-dichlorophenyl)butyric acid
MF:
C15H19Cl2NO4
Structure:
Chemical Name:
Trans-L-3-Hydroxy-Proline
MF:
C5H9NO3
Structure:
Chemical Name:
DL-Cis-Hydroxyproline
MF:
C5H9NO3
Chemical Name:
DL-Glu(OBzl)-OBzl Tosoh
MF:
C19H21NO4·C7H8O3S
Structure:
Chemical Name:
L-Histidine ethyl ester hydrochloride
MF:
C8H14ClN3O2
Structure:
Chemical Name:
L-2-(5-Bromothienyl)alanine
CAS:
154593-58-5
MF:
C7H8BrNO2S
Structure:
Chemical Name:
FMOC-SER(BZL)-OH
CAS:
73724-46-6
MF:
C25H23NO5
Structure:
Chemical Name:
3-Thietanecarboxylicacid,3-amino-(9CI)
CAS:
138650-26-7
MF:
C4H7NO2S
Structure:
Chemical Name:
Z-ORN(BOC)-OH
CAS:
7733-29-1
MF:
C18H26N2O6
Structure:
Chemical Name:
GLY-PRO-7-AMINO-4-METHYLCOUMARIN
MF:
C17H19N3O4
Structure:
Chemical Name:
Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester
CAS:
787548-29-2
MF:
C8H13NO2
Structure:
Chemical Name:
methyl 2-{[(benzyloxy)carbonyl]amino}-3-hydroxypropanoate
CAS:
14464-15-4
MF:
C12H15NO5
Structure:
Chemical Name:
TOS-GLU-OH
CAS:
4216-80-2
MF:
C19H14O3
Structure:
Chemical Name:
N-(Phosphonomethyl)glycine monoammonium salt
CAS:
40465-66-5
MF:
C3H7NO5P.NH4
Structure:
Chemical Name:
2-[METHYL(PHENYL)AMINO]ACETIC ACID
CAS:
40643-55-8
MF:
C9H11NO2
Structure:
Chemical Name:
N-([3-(TRIFLUOROMETHYL)PHENYL]SULFONYL)PHENYLALANINE
CAS:
250714-63-7
MF:
C16H14F3NO4S
Structure:
Chemical Name:
N-2-Aminobenzoyl glycine benzyl ester
CAS:
150374-97-3
MF:
C16H16N2O3
Structure:
Chemical Name:
Dibenzyl L-aspartate
CAS:
2791-79-9
MF:
C18H19NO4
Structure:
Chemical Name:
Z-ASN-ONP
CAS:
3256-57-3
MF:
C18H17N3O7
Structure:
Chemical Name:
H-GLN-ONB HBR
CAS:
14349-18-9
MF:
C12H16BrN3O5
Structure:
Chemical Name:
H-DL-TIC-OH
CAS:
67123-97-1
MF:
C10H11NO2
Structure:
Chemical Name:
N-(TERT-BUTOXYCARBONYL)-L-CYSTEINE METHYL ESTER
CAS:
55757-46-5
MF:
C9H17NO4S
Structure:
Chemical Name:
HIPPURYL-HIS-LEU FREE BASE
CAS:
207386-83-2
MF:
C21H31N5O5
Structure:
Chemical Name:
H-D-PHE-PRO-ARG-CHLOROMETHYLKETONE TRIFLUOROACETATE SALT
CAS:
71142-71-7
MF:
C21H31ClN6O3
Structure:
Chemical Name:
(R)-(+)-2-AMINO-4-METHYL-1,1-DIPHENYL-1-PENTANOL
CAS:
161832-74-2
MF:
C18H23NO
Structure:
Chemical Name:
L-GLUTAMIC ACID GAMMA-(2,2,2-TRICHLOROETHYL) ESTER
CAS:
92739-23-6
MF:
C7H10Cl3NO4
Structure:
Chemical Name:
DL-N-FMOC-2'-METHYLPHENYLALANINE
CAS:
135944-06-8
MF:
C25H23NO4
Structure:
Chemical Name:
(S)-ALPHA-BENZYL-PROLINE-HCL
CAS:
637020-57-6
MF:
C12H15NO2
Structure:
Chemical Name:
L-Alanine hydrochloride
CAS:
6003-05-0
MF:
C3H8ClNO2
Structure:
Chemical Name:
S-(2-THIAZOLYL)-L-CYSTEINE
CAS:
405150-20-1
MF:
C6H8N2O2S2
Structure:
Chemical Name:
(2S,4S)-4-METHYLGLUTAMIC ACID HYDROCHLORIDE
CAS:
160806-12-2
MF:
C6H11NO4.HCl
Structure:
Chemical Name:
L-LEUCINE TERT-BUTYL ESTER HYDROCHLORIDE
CAS:
21691-53-2
MF:
C10H21NO2
Chemical Name:
PROLINE, L-(RG)
Structure:
Chemical Name:
BOC-D-CYS(NPYS)-OH
CAS:
200350-73-8
MF:
C13H17N3O6S2
Structure:
Chemical Name:
D-ASPARTIC ACID ALPHA-T-BUTYL ESTER HYDROCHLORIDE
MF:
C8H16ClNO4
Structure:
Chemical Name:
N-TRIFLUOROACETYL-L-GLUTAMINE
CAS:
2419-34-3
MF:
C7H9F3N2O4
Chemical Name:
L-ALPHA-PHOSPHATIDYLSERINES, BRAIN, BOVINE
Structure:
Chemical Name:
3-CYCLOHEXYL-L-ALANINE HYDRATE
CAS:
307310-72-1
MF:
C9H19NO3
Structure:
Chemical Name:
L-arginine L-malate
CAS:
93964-77-3
MF:
C10H20N4O7
Structure:
Chemical Name:
sodium hydrogen N-(1-oxotetradecyl)-L-glutamate
CAS:
38517-37-2
MF:
C19H34NNaO5
Structure:
Chemical Name:
N-Methyl-L-Methionine
CAS:
42537-72-4
MF:
C6H13NO2S
Structure:
Chemical Name:
S-Adenosyl-methionine Chloride
MF:
C15H23ClN6O4S
Chemical Name:
α-amino-1- cyclohexenylpropionic acid
MF:
C9H15NO2
Structure:
Chemical Name:
Undecylenoyl phenylalanine
CAS:
175357-18-3
MF:
C20H29NO3
Structure:
Chemical Name:
Boc-Diethylglycine
CAS:
35264-04-1
MF:
C12H23NO4
Structure:
Chemical Name:
DL-Propargyl-cysteine
MF:
C6H9NO2S
Structure:
Chemical Name:
Glycine, alanyl-, methyl ester (9CI)
CAS:
438002-26-7
MF:
C6H12N2O3
Structure:
Chemical Name:
Cyclopropanecarboxylic acid, 1-amino-, ethyl ester (9CI)
CAS:
72784-47-5
MF:
C6H11NO2
Structure:
Chemical Name:
1-{[(benzyloxy)carbonyl]amino}cyclohexanecarboxylic acid
CAS:
17191-43-4
MF:
C15H19NO4
Structure:
Chemical Name:
2-[(tert-butoxycarbonyl)amino]-3-(5-bromo-1H-indol-3-yl)propanoic acid
CAS:
67308-26-3
MF:
C16H19BrN2O4
Structure:
Chemical Name:
L(+)-FMOC-ORNITHINE HCL
CAS:
201046-57-3
MF:
C20H23ClN2O4
Structure:
Chemical Name:
ETHYL 6-N-BOC-D-LYSINATE HCL
CAS:
122456-82-0
MF:
C13H27ClN2O4
Structure:
Chemical Name:
5-Aminolevulinic Acid, Hydrochloride Salt
CAS:
925-45-1
MF:
C11H20O2
Structure:
Chemical Name:
3-(4-(METHYLSULFONYL)PHENYL)SERINE ETHYL ESTER
CAS:
31925-27-6
MF:
C12H17NO5S
Structure:
Chemical Name:
2,3,5-Trifluoro-L-phenylalanine
CAS:
873429-59-5
MF:
C9H8F3NO2
Chemical Name:
L-Arginine DL-Malate(1:1)
Structure:
Chemical Name:
L-Lysine Diisocyanate
CAS:
45172-15-4
MF:
C10H14N2O4
Structure:
Chemical Name:
N-BOC-3-CHLORO-D-TYROSINE
CAS:
478183-57-2
MF:
C14H18ClNO5
Structure:
Chemical Name:
(s)-2-amino-1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid
CAS:
104974-45-0
MF:
C11H13NO2
Structure:
Chemical Name:
N-(1-oxopropyl)-Glycine
CAS:
21709-90-0
MF:
C5H9NO3
Structure:
Chemical Name:
Ibuprofen lysinate
CAS:
57469-76-8
MF:
C19H32N2O4
Structure:
Chemical Name:
FMOC-DL-7-AZATRYPTOPHAN
MF:
C25H21N3O4
Structure:
Chemical Name:
(R)-N-BOC-2-CHLORO-BETA-PHENYLALANINE
CAS:
500789-05-9
MF:
C14H18ClNO4
Structure:
Chemical Name:
FMOC-2-(2-AMINOETHOXY)ETHANOL
CAS:
299430-87-8
MF:
C19H21NO4
Structure:
Chemical Name:
(R)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-2-METHYL-HEPT-6-ENOIC ACID
CAS:
288617-77-6
MF:
C23H25NO4
Structure:
Chemical Name:
(R)-METHYL 2-(TERT-BUTOXYCARBONYLAMINO)-3-IODOPROPANOATE
CAS:
889670-02-4
MF:
C9H16INO4
Structure:
Chemical Name:
4-Nitro-D-phenylalanine hydrochloride
CAS:
147065-06-3
MF:
C9H11ClN2O4
Structure:
Chemical Name:
O-(2-Nitrobenzyl)-L-tyrosine Hydrochloride
CAS:
207727-86-4
MF:
C16H17ClN2O5
Structure:
Chemical Name:
L-Norvaline, 5-hydroxy-N- [(phenylmethoxy)carbonyl]-, 1,1-dimethylethylester
CAS:
124620-51-5
MF:
C17H25NO5