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:
Z-TRP-OSU
CAS:
50305-28-7
MF:
C23H21N3O6
Structure:
Chemical Name:
BOC-(S)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID
CAS:
500770-83-2
MF:
C14H18N2O6
Structure:
Chemical Name:
H-GLY-OBZL P-TOSYLATE
CAS:
114342-15-3
MF:
C16H19NO5S
Structure:
Chemical Name:
(1-ADAMANTANEACETYL-D-ARG0,HYP3,BETA-(2-THIENYL)-ALA5,8,D-PHE7)-BRADYKININ
CAS:
130942-96-0
MF:
C68H99N19O14S2
Structure:
Chemical Name:
BOC-S-TERT-BUTYLMERCAPTO-L-CYSTEINE
CAS:
30044-61-2
MF:
C12H23NO4S2
Structure:
Chemical Name:
TOS-ALA-OH
CAS:
99076-56-9
MF:
C10H13NO4S
Structure:
Chemical Name:
N-ACETYL-5-METHOXY SERINE
CAS:
98632-99-6
MF:
C6H11NO4
Structure:
Chemical Name:
L-4-THIAZOLYLALANINE
CAS:
136010-41-8
MF:
C6H8N2O2S
Structure:
Chemical Name:
BZ-PHE-NH2
CAS:
72150-35-7
MF:
C16H16N2O2
Structure:
Chemical Name:
(R)-(+)-2-AMINO-1,1,3-TRIPHENYL-1-PROPANOL
CAS:
86906-05-0
MF:
C21H21NO
Structure:
Chemical Name:
(S)-(-)-2-AMINO-1,1,3-TRIPHENYL-1-PROPANOL
CAS:
79868-78-3
MF:
C21H21NO
Structure:
Chemical Name:
3-METHYLAMINO-BENZOIC ACID
CAS:
51524-84-6
MF:
C8H9NO2
Structure:
Chemical Name:
ALPHA-METHYL-DL-PHENYLALANINE METHYL ESTER HYDROCHLORIDE
CAS:
64665-60-7
MF:
C11H16ClNO2
Structure:
Chemical Name:
N-ACETYL-S-(3-HYDROXYPROPYL-1-METHYL)-L-CYSTEINE, DICYCLOHEXYLAMMONIUM SALT
CAS:
33164-70-4
MF:
C21H40N2O4S
Structure:
Chemical Name:
BOC-(R)-3-AMINO-3-(3-BROMO-PHENYL)-PROPIONIC ACID
MF:
C14H18BrNO4
Structure:
Chemical Name:
(2S, 4R)-BOC-GAMMA-MSO-PROLINE METHYL ESTER
CAS:
84520-67-2
MF:
C12H21NO7S
Structure:
Chemical Name:
H-DL-ASP-OME
CAS:
65414-77-9
MF:
C5H9NO4
Structure:
Chemical Name:
FMOC-(R)-2-THIENYLGLYCINE
CAS:
208259-66-9
MF:
C21H17NO4S
Structure:
Chemical Name:
H-PRO-4M-BETANA HCL
CAS:
100930-07-2
MF:
C16H19ClN2O2
Structure:
Chemical Name:
ARG-LYS-GLU-VAL-TYR ACETATE SALT
CAS:
105184-37-0
MF:
C33H55N9O11
Structure:
Chemical Name:
FMOC-ALA(BETA-CYCLOBUTYL)-OH
CAS:
478183-62-9
MF:
C22H23NO4
Structure:
Chemical Name:
FMOC-D-CIT-OH
CAS:
200344-33-8
MF:
C21H23N3O5
Structure:
Chemical Name:
5-METHYL-DL-TRYPTOPHAN
CAS:
951-55-3
MF:
C12H14N2O2
Structure:
Chemical Name:
FMOC-[15N]VAL-OH
CAS:
125700-35-8
MF:
C20H21NO4
Structure:
Chemical Name:
Z-D-CIS-HYP-OH
CAS:
130930-25-5
MF:
C13H15NO5
Structure:
Chemical Name:
MEOSUC-AAPM-PNA
CAS:
70967-91-8
MF:
C27H38N6O9S
Structure:
Chemical Name:
L-Leucine hydrochloride
CAS:
760-84-9
MF:
C6H14ClNO2
Structure:
Chemical Name:
N-Hexadecanoyl-L-valine
CAS:
45287-42-1
MF:
C21H41NO3
Structure:
Chemical Name:
Sodium N-tetradecanoyl-L-phenlyalaninate
CAS:
36577-41-0
MF:
C23H36NNaO3
Structure:
Chemical Name:
N-Palmitoyl-L-serine
CAS:
16417-38-2
MF:
C19H37NO4
Structure:
Chemical Name:
DL-2-ISOPROPYLSERINE
CAS:
7522-43-2
MF:
C6H13NO3
Structure:
Chemical Name:
H-TYR-AMC TFA
CAS:
94099-57-7
MF:
C19H18N2O4
Structure:
Chemical Name:
N-BENZOYL-L-THREONINE
CAS:
27696-01-1
MF:
C11H13NO4
Structure:
Chemical Name:
N-BSMOC-L-ASPARAGINE
CAS:
197245-31-1
MF:
C14H14N2O7S
Structure:
Chemical Name:
BOC-(S)-3-AMINO-3-(3-METHYL-PHENYL)-PROPIONIC ACID
MF:
C15H21NO4
Structure:
Chemical Name:
Z-ASP-OME DCHA
CAS:
19720-12-8
MF:
C25H38N2O6
Structure:
Chemical Name:
BENZOYLGLYCINE METHYL ESTER
CAS:
1205-08-9
MF:
C10H11NO3
Structure:
Chemical Name:
N-Formyl-L-aspartic acid
CAS:
19427-28-2
MF:
C5H7NO5
Structure:
Chemical Name:
(BOC-CYS-OH)2
CAS:
10389-65-8
MF:
C16H28N2O8S2
Structure:
Chemical Name:
CBZL-D-TERT-LEUCINE
CAS:
70874-05-4
MF:
C14H19NO4
Structure:
Chemical Name:
DL-2-BENZYLSERINE
CAS:
4740-47-0
MF:
C10H13NO3
Structure:
Chemical Name:
L-GLUTAMIC-15N ACID
CAS:
21160-87-2
MF:
C5H9NO4
Structure:
Chemical Name:
ARG-ARG BETA-NAPHTHYLAMIDE TRIHYDROCHLORIDE
CAS:
100900-26-3
MF:
C22H36Cl3N9O2
Structure:
Chemical Name:
Ademethionine 1,4-Butanedisulfonate
CAS:
101020-79-5
MF:
C42H74N12O28S8
Structure:
Chemical Name:
methyl 3-phenyl-L-alaninate
CAS:
2577-90-4
MF:
C10H13NO2
Structure:
Chemical Name:
L-Cyclopentyl-gly-methyl ester HCL
CAS:
14328-62-2
MF:
C8H16ClNO2
Structure:
Chemical Name:
3,4,5-Trifluoro-L-phenylalanine
CAS:
646066-73-1
MF:
C9H8F3NO2
Structure:
Chemical Name:
DL-2-Cyanophenylalanine
CAS:
263396-40-3
MF:
C10H10N2O2
Structure:
Chemical Name:
3,4-Difluorophenylglycine
CAS:
225641-94-1
MF:
C8H7F2NO2
Structure:
Chemical Name:
2-Bromo-DL-Phenylalanine
CAS:
30163-16-7
MF:
C9H10BrNO2
Structure:
Chemical Name:
(R)-2-Amino-3-(4-ethylphenyl)propanoic acid
CAS:
721385-17-7
MF:
C11H15NO2
Structure:
Chemical Name:
(S)-(-)-(3-CHLORO-2-HYDROXYPROPYL)TRIMETHYLAMMONIUM CHLORIDE
CAS:
101396-91-2
MF:
C6H15Cl2NO
Structure:
Chemical Name:
(1S,2R)-2-Aminocyclopentanecarboxylic acid
CAS:
64191-14-6
MF:
C6H11NO2
Structure:
Chemical Name:
Benzoic acid, 3-amino-4,5-dichloro- (9CI)
CAS:
50917-30-1
MF:
C7H5Cl2NO2
Structure:
Chemical Name:
METHYL (3S)-3-AMINO-3-PHENYLPROPANOATE
CAS:
37088-66-7
MF:
C10H13NO2
Structure:
Chemical Name:
Citiolone
CAS:
17896-21-8
MF:
C6H9NO2S
Structure:
Chemical Name:
N-ACETYL-5-METHOXY-DL-TRYPTOPHAN MONOHYDRATE
CAS:
43167-40-4
MF:
C14H16N2O4
Structure:
Chemical Name:
BOC-TYR-OBZL
CAS:
19391-35-6
MF:
C21H25NO5
Structure:
Chemical Name:
POLY(GLU, TYR) SODIUM SALT
CAS:
97105-00-5
MF:
C14H21N2NaO7
Structure:
Chemical Name:
3-NITRO-L-TYROSINE ETHYL ESTER HYDROCHLORIDE
CAS:
66737-54-0
MF:
C11H15ClN2O5
Structure:
Chemical Name:
BZ-MET-NH2
CAS:
52811-71-9
MF:
C12H16N2O2S
Structure:
Chemical Name:
N-DICHLOROACETYL-L-SERINE SODIUM SALT
CAS:
80174-64-7
MF:
C5H7Cl2NO4
Structure:
Chemical Name:
FMOC-L-PHE(4-GUANIDINO-BOC2)-OH
CAS:
187283-25-6
MF:
C35H40N4O8
Structure:
Chemical Name:
BOC-ALPHA-ALLYL-ME-DL-PRO-OH
CAS:
203869-80-1
MF:
C11H19NO4
Structure:
Chemical Name:
(1R,2R)-2-AMINO-1,2-DIPHENYLETHANOL, 97
CAS:
88082-66-0
MF:
C14H15NO
Structure:
Chemical Name:
Z-D-PROLINOL, 97
CAS:
72597-18-3
MF:
C13H17NO3
Structure:
Chemical Name:
L-GLUTAMIC ACID MONOPOTASSIUM SALT
CAS:
6382-01-0
MF:
C5H8NO4.K.H2O
Structure:
Chemical Name:
N-Tetradecanoyl-L-alanine
CAS:
71448-29-8
MF:
C17H33NO3
Structure:
Chemical Name:
N-Dodecanoyl-L-proline
CAS:
58725-39-6
MF:
C17H31NO3
Structure:
Chemical Name:
N-Hexadecanoyl-L-alanine
CAS:
56255-31-3
MF:
C19H37NO3
Structure:
Chemical Name:
N-FMOC-3-(triphenylmethyl)-L-histidine
CAS:
128545-09-5
MF:
C40H33N3O4
Structure:
Chemical Name:
1H-Thieno[3,2-c]pyrazole-5-carboxylic acid, 3-amino-, methyl ester
CAS:
648411-35-2
MF:
C7H7N3O2S
Structure:
Chemical Name:
FMOC-(R)-3-AMINO-3-(2-TRIFLUOROMETHYL-PHENYL)-PROPIONIC ACID
CAS:
517905-86-1
MF:
C25H20F3NO4
Structure:
Chemical Name:
2,4-Dichloro-DL-phenylalanine
CAS:
5472-68-4
MF:
C9H9Cl2NO2
Structure:
Chemical Name:
(R)-3-Amino-3-(2-bromo-phenyl)-propionic acid
CAS:
737751-95-0
MF:
C9H10BrNO2
Structure:
Chemical Name:
(S)-N-BOC-(2'-CHLOROPHENYL)GLYCINE
CAS:
225918-60-5
MF:
C13H16ClNO4
Structure:
Chemical Name:
H-[15N]LEU-OH
CAS:
59935-31-8
MF:
C6H13NO2
Structure:
Chemical Name:
Z-ASP(OTBU)-OH DCHA
CAS:
23632-70-4
MF:
C28H44N2O6
Structure:
Chemical Name:
EDTA DIPOTASSIUM MAGNESIUM SALT, DIHYDRATE
CAS:
68015-77-0
MF:
C10H16K2MgN2O10
Structure:
Chemical Name:
H-D-ALA-GLY-OH
CAS:
3997-90-8
MF:
C5H10N2O3
Structure:
Chemical Name:
S-2-Hydroxyethyl-D-cysteine
CAS:
85955-36-8
MF:
C5H11NO3S
Structure:
Chemical Name:
Ethyl 1-Boc-4-iso-propyl-4-piperidinecarboxylate
CAS:
1022128-75-1
MF:
C16H29NO4
Structure:
Chemical Name:
FMOC-THR(TBU)-ODHBT
CAS:
119767-84-9
MF:
C30H30N4O6
Structure:
Chemical Name:
H-D-Glu(Otbu)-OMe.HCL
CAS:
16948-36-0
MF:
C10H19NO4.ClH
Structure:
Chemical Name:
3-Amino-N-Boc-L-alanine methyl ester
CAS:
61040-20-8
MF:
C9H18N2O4
Structure:
Chemical Name:
H-CYS(BZL)-OET HCL
CAS:
52844-67-4
MF:
C12H18ClNO2S
Structure:
Chemical Name:
ALPHA-METHYL-DL-SERINE
CAS:
3398-40-1
MF:
C4H9NO3
Structure:
Chemical Name:
FMOC-MENVA-OH
CAS:
252049-05-1
MF:
C21H23NO4
Structure:
Chemical Name:
(S)-(+)-1-DIMETHYLAMINO-2-PROPANOL
CAS:
53636-17-2
MF:
C5H13NO
Structure:
Chemical Name:
Fmoc-S-Trityl-L-penicillamine
CAS:
201531-88-6
MF:
C39H35NO4S
Structure:
Chemical Name:
L-4-TRIFLUOROMETHYLPHENYLALANINE
CAS:
122839-56-9
MF:
C10H10F3NO2
Structure:
Chemical Name:
FMOC-HOCHA-OH
CAS:
269078-73-1
MF:
C25H29NO4
Structure:
Chemical Name:
L-GLUTAMINE-15N2
CAS:
204451-48-9
MF:
C5H10N2O3
Structure:
Chemical Name:
FMOC-GLU-OBZL
CAS:
122350-52-1
MF:
C27H25NO6
Structure:
Chemical Name:
N-CARBOBENZYLOXY-L-PROLINE METHYL ESTER
CAS:
5211-23-4
MF:
C14H17NO4
Structure:
Chemical Name:
N-FORMYLGLYCINE METHYL ESTER
CAS:
3154-54-9
MF:
C4H7NO3
Structure:
Chemical Name:
GLYCINE N-BUTYL ESTER HYDROCHLORIDE
CAS:
13048-99-2
MF:
C6H14ClNO2
Structure:
Chemical Name:
BOC-(R)-3-AMINO-3-(3-FLUORO-PHENYL)-PROPIONIC ACID
MF:
C14H18FNO4
Structure:
Chemical Name:
FA-GLY-LEU-NH2
CAS:
26400-33-9
MF:
C15H21N3O4
Structure:
Chemical Name:
1-(FMOC-AMINO)CYCLOHEXANECARBOXYLIC ACID
CAS:
162648-54-6
MF:
C22H23NO4