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:
(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:
3-AMINOPENTANE-3-CARBOXYLIC ACID
CAS:
2566-29-2
MF:
C6H13NO2
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:
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:
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:
BOC-SAR-OH
CAS:
13734-36-6
MF:
C8H15NO4
Structure:
Chemical Name:
NEPSILON-CARBOBENZOXY-NALPHA-TOSYL-L-LYSINE
CAS:
34235-82-0
MF:
C21H26N2O6S
Structure:
Chemical Name:
N,N-DIMETHYLGLYCINE METHYL ESTER
CAS:
7148-06-3
MF:
C5H11NO2
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:
(S)-3-AMINO-4-(2-FURYL)-BUTYRIC ACID
CAS:
270263-05-3
MF:
C8H11NO3
Structure:
Chemical Name:
TYRPHOSTIN A9
CAS:
10537-47-0
MF:
C18H22N2O
Structure:
Chemical Name:
BOC-D-CHA-OH DCHA
CAS:
198470-07-4
MF:
C26H48N2O4
Structure:
Chemical Name:
POLY-L-GLUTAMIC ACID SODIUM SALT
CAS:
26247-79-0
MF:
C15H23N3O10
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID
CAS:
479064-99-8
MF:
C25H23NO4
Structure:
Chemical Name:
N-[3-(2-Furyl)acryloyl]-L-phenylalanyl-glycyl-glycine
CAS:
64967-39-1
MF:
C20H21N3O6
Structure:
Chemical Name:
Z-DEHYDRO-ALA-OME
CAS:
21149-17-7
MF:
C12H13NO4
Structure:
Chemical Name:
BOC-D-DAP(Z)-OH DCHA
CAS:
81306-94-7
MF:
C28H45N3O6
Structure:
Chemical Name:
3-(N-ACETYL-L-CYSTEIN-S-YL) ACETAMINOPHEN, SODIUM SALT
CAS:
52372-86-8
MF:
C13H16N2O5S
Structure:
Chemical Name:
BOC-(S)-3-AMINO-3-(2,4-DICHLORO-PHENYL)-PROPIONIC ACID
CAS:
499995-81-2
MF:
C14H17Cl2NO4
Structure:
Chemical Name:
FMOC-THR(GALNAC(AC)3-ALPHA-D)-OH
CAS:
116783-35-8
MF:
C33H38N2O13
Structure:
Chemical Name:
DL-2-AMINO-3-METHYL-1-BUTANOL
CAS:
16369-05-4
MF:
C5H13NO
Structure:
Chemical Name:
Fmoc-Pro-Pro-OH
CAS:
129223-22-9
MF:
C25H26N2O5
Structure:
Chemical Name:
N-L-gamma-Glutamyl-L-leucine
CAS:
2566-39-4
MF:
C11H20N2O5
Structure:
Chemical Name:
FMOC-L-STYRYLALANINE
CAS:
159610-82-9
MF:
C26H23NO4
Structure:
Chemical Name:
N-(TERT-BUTOXYCARBONYL)-3-(4-(1-PYRROLYL)PHENYL)-L-ALANINE
CAS:
312619-46-8
MF:
C18H22N2O4
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-4-(3-FLUORO-PHENYL)-BUTYRIC ACID
CAS:
331763-67-8
MF:
C25H22FNO4
Structure:
Chemical Name:
N-Boc-Trans-4-Hydroxy-D-proline methyl ester
CAS:
135042-17-0
MF:
C11H19NO5
Structure:
Chemical Name:
N-Carbobenzoxy-L-homoserine
CAS:
35677-88-4
MF:
C12H15NO5
Structure:
Chemical Name:
(2S,4S)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID
MF:
C25H28N2O6
Structure:
Chemical Name:
BOC-(S)-3-AMINO-3-(4-NITRO-PHENYL)-PROPIONIC ACID
CAS:
499995-73-2
MF:
C14H18N2O6
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID
CAS:
511272-35-8
MF:
C24H21NO5
Structure:
Chemical Name:
DL-ALPHA-METHYLLEUCINE
CAS:
144-24-1
MF:
C7H15NO2
Structure:
Chemical Name:
Z-GAMMA-ABU-OH
CAS:
5105-78-2
MF:
C12H15NO4
Structure:
Chemical Name:
PHT-GLY-OSU
CAS:
3397-29-3
MF:
C14H10N2O6
Structure:
Chemical Name:
3-TRIFLUOROMETHYL-L-PHENYLALANINE
CAS:
122839-48-9
MF:
C10H10F3NO2
Structure:
Chemical Name:
(S)-4-METHYLENE-PYRROLIDINE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER
CAS:
84348-38-9
MF:
C11H17NO4
Structure:
Chemical Name:
BOC-(R)-3-AMINO-5-HEXYNOIC ACID
CAS:
332064-91-2
MF:
C11H17NO4
Structure:
Chemical Name:
7-METHYL-DL-TRYPTOPHAN
CAS:
17332-70-6
MF:
C12H14N2O2
Structure:
Chemical Name:
Z-D-DAB(BOC)-OH DCHA
CAS:
214852-61-6
MF:
C29H47N3O6
Structure:
Chemical Name:
BOC-GLN-ONP
CAS:
15387-45-8
MF:
C16H21N3O7
Structure:
Chemical Name:
N-ME-TYR-OH
CAS:
537-49-5
MF:
C10H13NO3
Structure:
Chemical Name:
4-Hydroxy-L-isoleucine
CAS:
781658-23-9
MF:
C6H13NO3
Structure:
Chemical Name:
2-AMINO-3-PHENYLBUTANOIC ACID HYDROCHLORIDE
CAS:
80997-87-1
MF:
C10H14ClNO2
Structure:
Chemical Name:
FMOC-D-DAB(ALOC)-OH
CAS:
387824-78-4
MF:
C23H24N2O6
Structure:
Chemical Name:
BZ-PHE-OH
CAS:
2566-22-5
MF:
C16H15NO3
Structure:
Chemical Name:
Pemetrexed disodium hemipentahydrate
CAS:
357166-30-4
MF:
C20H24N5NaO7
Structure:
Chemical Name:
FMOC-PRO-ONP
CAS:
71989-32-7
MF:
C26H22N2O6
Structure:
Chemical Name:
PTH-ARGININE HYDROCHLORIDE
CAS:
117756-28-2
MF:
C13H18ClN5OS
Structure:
Chemical Name:
FMOC-D-LYS(Z)-OH
CAS:
110990-07-3
MF:
C29H30N2O6
Structure:
Chemical Name:
Z-D-ASP(OBZL)-OH
CAS:
5241-62-3
MF:
C19H19NO6
Structure:
Chemical Name:
H-ALA-SER-ALA-SER-SER-LEU-MET-ASP-LYS-GLU-ALA-VAL-TYR-PHE-ALA-HIS-LEU-ASP-ILE-ILE-TRP-OH
CAS:
121204-87-3
MF:
C109H163N25O32S
Structure:
Chemical Name:
Z-D-GLU(OME)-OH
CAS:
27025-24-7
MF:
C14H17NO6
Structure:
Chemical Name:
Fmoc-N-methyl-O-benzyl-L-threonine
CAS:
198561-81-8
MF:
C27H27NO5
Structure:
Chemical Name:
H-ALA-BETA-ALA-OH
CAS:
52788-02-0
MF:
C6H12N2O3
Structure:
Chemical Name:
Prostratin, PKC activator
CAS:
60857-08-1
MF:
C22H30O6
Structure:
Chemical Name:
N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE
CAS:
115186-37-3
MF:
C12H22N2O4
Structure:
Chemical Name:
L-ALPHA-(3-THIENYL)GLYCINE
CAS:
1194-87-2
MF:
C6H7NO2S
Structure:
Chemical Name:
BOC-O-DIBENZYLPHOSPHO-L-SERINE
CAS:
90013-45-9
MF:
C22H28NO8P
Structure:
Chemical Name:
N-BOC-ALPHA-METHYL-D-SERINE
CAS:
84311-18-2
MF:
C9H17NO5
Structure:
Chemical Name:
DL-Aspartic acid potassium salt
CAS:
14434-35-6
MF:
C4H6KNO4
Structure:
Chemical Name:
GLYCINE N-PROPYL ESTER HYDROCHLORIDE
CAS:
13049-01-9
MF:
C5H12ClNO2
Structure:
Chemical Name:
H-ALPHA-ME-D-PRO-OH
CAS:
63399-77-9
MF:
C6H11NO2
Structure:
Chemical Name:
O-BENZYL-L-SERINE METHYL ESTER HYDROCHLORIDE
CAS:
19525-87-2
MF:
C11H16ClNO3
Structure:
Chemical Name:
BOC-(S)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID
CAS:
270596-44-6
MF:
C17H23NO4
Structure:
Chemical Name:
NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER
CAS:
219968-28-2
MF:
C45H53N3O10
Structure:
Chemical Name:
L-PROLINE BETA-NAPHTHYLAMIDE HYDROCHLORIDE
CAS:
97216-16-5
MF:
C15H17ClN2O
Structure:
Chemical Name:
DI-DNP-L-LYSINE
CAS:
1655-49-8
MF:
C18H18N6O10
Structure:
Chemical Name:
FMOC-D-ARG-OH
CAS:
130752-32-8
MF:
C21H24N4O4
Structure:
Chemical Name:
H-MET-OIPR HCL
CAS:
85391-05-5
MF:
C8H18ClNO2S
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-4-(4-FLUORO-PHENYL)-BUTYRIC ACID
MF:
C25H22FNO4
Structure:
Chemical Name:
(S)-3-AMINO-4-(4-IODOPHENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
270065-70-8
MF:
C10H12INO2
Structure:
Chemical Name:
L-LEUCINE ALLYL ESTER P-TOLUENESULFONATE SALT
CAS:
88224-03-7
MF:
C16H25NO5S
Structure:
Chemical Name:
(R)-3-AMINO-4-(3-THIENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
269726-91-2
MF:
C8H11NO2S
Structure:
Chemical Name:
BOC-DAB(ALOC)-OH DCHA
CAS:
327156-92-3
MF:
C25H45N3O6
Structure:
Chemical Name:
PHENYLTHIOHYDANTOIN-GLUTAMINE
CAS:
10567-86-9
MF:
C12H13N3O2S
Structure:
Chemical Name:
H-PHE-LEU-OH
CAS:
3303-55-7
MF:
C15H22N2O3
Structure:
Chemical Name:
AC-WEHD-AMC
CAS:
189275-74-9
MF:
C38H40N8O11
Structure:
Chemical Name:
AC-D-NVA-OH
CAS:
57357-56-9
MF:
C7H13NO3
Structure:
Chemical Name:
FMOC-ARG(BOC)2-OH
CAS:
143824-77-5
MF:
C31H40N4O8
Chemical Name:
EC 1.4.1.3
CAS:
9029-11-2
MF:
NULL
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID
CAS:
511272-50-7
MF:
C24H20FNO4
Structure:
Chemical Name:
BOC-CYS(TBU)-OH
CAS:
56976-06-8
MF:
C12H23NO4S
Structure:
Chemical Name:
BOC-D-MEPHE-OH
CAS:
85466-66-6
MF:
C15H21NO4
Structure:
Chemical Name:
FMOC-TYR(2-BR-Z)-OH
CAS:
147688-40-2
MF:
C32H26BrNO7
Structure:
Chemical Name:
Potassium (R)-((3-ethoxy-1-methyl-3-oxoprop-1-enyl)amino)(4-hydroxyphenyl)acetate
CAS:
57938-86-0
MF:
C14H16KNO5
Structure:
Chemical Name:
2,4-Difluoro-D-phenylalanine
CAS:
266360-60-5
MF:
C9H9F2NO2
Structure:
Chemical Name:
N-α-Z-N-β-Boc-D-2,3-diaminopropionic acid
CAS:
62234-36-0
MF:
C16H22N2O6
Structure:
Chemical Name:
BOC-L-BETA-HOMOVALINE
CAS:
183990-64-9
MF:
C11H21NO4
Structure:
Chemical Name:
5-Benzothiazolecarboxylicacid,2-amino-
CAS:
101084-95-1
MF:
C8H6N2O2S
Structure:
Chemical Name:
N-ACETYL-S-GERANYLGERANYL-L-CYSTEINE
CAS:
139332-94-8
MF:
C25H41NO3S
Structure:
Chemical Name:
(S)-(+)-N-(3,5-DINITROBENZOYL)-ALPHA-PHENYLGLYCINE
CAS:
90761-62-9
MF:
C15H11N3O7
Structure:
Chemical Name:
AC-DMQD-CHO
CAS:
259199-63-8
MF:
C20H31N5O10S
Structure:
Chemical Name:
(R)-3-AMINO-4-(3-FLUOROPHENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
331763-65-6
MF:
C10H13ClFNO2