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:
DL-METHIONINE SULFONE
CAS:
820-10-0
MF:
C5H11NO4S
Structure:
Chemical Name:
FMOC-ALA-WANG RESIN
MF:
C18H16NO3R
Structure:
Chemical Name:
FMOC-D-HOMOPHENYLALANINE
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135994-09-1
MF:
C8H6ClN6O3P
Structure:
Chemical Name:
S-ADENOSYL-L-METHIONINE
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17176-17-9
MF:
C15H22N6O5S
Structure:
Chemical Name:
CHLOROACETYL-L-VALINE
CAS:
2279-16-5
MF:
C7H12ClNO3
Structure:
Chemical Name:
(1R,4S)-4-Aminocyclopent-2-enecarboxylic acid
CAS:
134003-04-6
MF:
C6H9NO2
Structure:
Chemical Name:
(S)-3-AMINO-4-(4-NITROPHENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
270062-87-8
MF:
C10H12N2O4
Structure:
Chemical Name:
BOC-(R)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID
CAS:
269726-83-2
MF:
C16H20N2O4
Structure:
Chemical Name:
DL-Homocystine
CAS:
870-93-9
MF:
C8H16N2O4S2
Structure:
Chemical Name:
H-TYR(TBU)-OME HCL
CAS:
51482-39-4
MF:
C14H22ClNO3
Structure:
Chemical Name:
2-AMINO-5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER
CAS:
184174-80-9
MF:
C9H11NO2S
Structure:
Chemical Name:
H-SER-OBZL HCL
CAS:
1738-72-3
MF:
C10H13NO3
Structure:
Chemical Name:
BOC-D-TRP(FOR)-OH
CAS:
64905-10-8
MF:
C17H20N2O5
Structure:
Chemical Name:
N-CARBOBENZYLOXY-S-PHENYL-L-CYSTEINE
CAS:
82611-65-2
MF:
C17H17NO4S
Structure:
Chemical Name:
BOC-(S)-3-AMINO-4-(3-CHLORO-PHENYL)-BUTYRIC ACID
CAS:
270596-39-9
MF:
C15H20ClNO4
Structure:
Chemical Name:
FMOC-7-AMINO-HEPTANOIC ACID
CAS:
127582-76-7
MF:
C22H25NO4
Structure:
Chemical Name:
N-Acetyl-DL-aspartic acid
CAS:
2545-40-6
MF:
C6H9NO5
Structure:
Chemical Name:
Brivanib
CAS:
649735-46-6
MF:
C19H19FN4O3
Structure:
Chemical Name:
Z-ALA-OSU
CAS:
3401-36-3
MF:
C15H16N2O6
Structure:
Chemical Name:
3-AMINO-2,4,5-TRIFLUOROBENZOIC ACID
CAS:
119385-80-7
MF:
C7H4F3NO2
Structure:
Chemical Name:
H-PHE-NHNH2
CAS:
52386-52-4
MF:
C9H13N3O
Structure:
Chemical Name:
3-AMINO-4-PYRIDAZINECARBOXYLIC ACID
CAS:
21141-03-7
MF:
C5H5N3O2
Structure:
Chemical Name:
3-AMINO-4-(TRIFLUOROMETHYL)BENZOIC ACID
CAS:
125483-00-3
MF:
C8H6F3NO2
Structure:
Chemical Name:
Thiamphenicol glycinate hydrochloride
CAS:
2611-61-2
MF:
C14H18Cl2N2O6S.ClH
Structure:
Chemical Name:
Methotrexate disodium salt
CAS:
7413-34-5
MF:
C20H23N8NaO5
Structure:
Chemical Name:
N-FORMYL-L-ALANINE
CAS:
10512-86-4
MF:
C4H7NO3
Structure:
Chemical Name:
Fmoc-Lys(Ddiv)-OH
CAS:
204777-78-6
MF:
C34H42N2O6
Structure:
Chemical Name:
ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE
CAS:
174775-48-5
MF:
C11H11NO3
Structure:
Chemical Name:
H-D-TYR(TBU)-OH
CAS:
186698-58-8
MF:
C13H19NO3
Structure:
Chemical Name:
4-BORONO-DL-PHENYLALANINE B10 ENRICHED
CAS:
90580-64-6
MF:
C9H12BNO4
Structure:
Chemical Name:
H-DL-2-NAL-OH
CAS:
14108-60-2
MF:
C13H13NO2
Structure:
Chemical Name:
3-(2-NAPHTHYL)-L-ALANINE HYDROCHLORIDE
CAS:
122745-12-4
MF:
C13H14ClNO2
Structure:
Chemical Name:
FMOC-PRO-OL
CAS:
148625-77-8
MF:
C20H21NO3
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID
CAS:
270065-87-7
MF:
C26H22N2O4
Structure:
Chemical Name:
H-NVA-OME HCL
CAS:
56558-30-6
MF:
C6H14ClNO2
Structure:
Chemical Name:
2-AMINO-2-PHENYLBUTYRIC ACID
CAS:
5438-07-3
MF:
C10H13NO2
Structure:
Chemical Name:
Boc-(R)-3-Amino-3-(4-methylphenyl)propionic acid
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479064-97-6
MF:
C15H21NO4
Structure:
Chemical Name:
3-Cyanophenylalanine
CAS:
63999-80-4
MF:
C10H10N2O2
Structure:
Chemical Name:
N-2-NITROPHENYLSULFENYL-L-ALANINE DICYCLOHEXYLAMMONIUM SALT
CAS:
7675-46-9
MF:
C21H33N3O4S
Structure:
Chemical Name:
Z-PRO-OSU
CAS:
3397-33-9
MF:
C17H18N2O6
Structure:
Chemical Name:
H-D-TYR(BZL)-OH
CAS:
65733-15-5
MF:
C16H17NO3
Structure:
Chemical Name:
(S)-3-AMINO-4-(2-CYANOPHENYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
270065-82-2
MF:
C11H12N2O2
Structure:
Chemical Name:
(R)-(+)-alpha-[(3-Methoxy-1-methyl-3-oxo-1-propenyl)amino]-1,4-cyclohexadiene-1-acetic acid sodium salt
CAS:
26774-89-0
MF:
C13H18NNaO4
Structure:
Chemical Name:
Creatine phosphate disodium salt
CAS:
922-32-7
MF:
C4H11N3NaO5P
Structure:
Chemical Name:
2-(Boc-aminomethyl)phenylacetic acid
CAS:
40851-66-9
MF:
C14H19NO4
Structure:
Chemical Name:
3-FLUORO-DL-VALINE
CAS:
43163-94-6
MF:
C5H10FNO2
Structure:
Chemical Name:
N-Tigloylglycine
CAS:
35842-45-6
MF:
C7H11NO3
Structure:
Chemical Name:
(R)-3-AMINO-4-(2-NAPHTHYL)BUTANOIC ACID HYDROCHLORIDE
CAS:
269398-90-5
MF:
C14H15NO2
Structure:
Chemical Name:
DL-3-(1-NAPHTHYL)ALANINE
CAS:
28095-56-9
MF:
C13H13NO2
Structure:
Chemical Name:
N-Tosyl-L-alanine 3-indoxyl ester
CAS:
75062-54-3
MF:
C18H18N2O4S
Structure:
Chemical Name:
BOC-L-BETA-HOMOTRYPTOPHAN
CAS:
229639-48-9
MF:
C17H22N2O4
Structure:
Chemical Name:
N-(2,4-DINITROPHENYL)-L-SERINE
CAS:
1655-64-7
MF:
C9H9N3O7
Structure:
Chemical Name:
D-Cyclopentylglycine
CAS:
2521-86-0
MF:
C7H13NO2
Structure:
Chemical Name:
3,5-DINITRO-L-TYROSINE MONOHYDRATE
CAS:
17360-11-1
MF:
C9H9N3O7
Structure:
Chemical Name:
N-Acetylcysteine amide
CAS:
38520-57-9
MF:
C5H10N2O2S
Chemical Name:
HexarelinAcetate
Structure:
Chemical Name:
N-ISOBUTYRYLGLYCINE
CAS:
15926-18-8
MF:
C6H11NO3
Structure:
Chemical Name:
Phosphatidylserine
CAS:
51446-62-9
MF:
C42H82NO10P
Structure:
Chemical Name:
BOC-PHG-OSU
CAS:
201152-47-8
MF:
C17H20N2O6
Chemical Name:
Fmoc-Phe(4-Cl)-Wang resin
Structure:
Chemical Name:
3-AZIDO-L-ALANINE
CAS:
105661-40-3
Structure:
Chemical Name:
N-Benzyloxycarbonylglycine N-carboxylic anhydride
CAS:
159396-61-9
MF:
C11H9NO5
Structure:
Chemical Name:
GLYCINE-2-13C
CAS:
20220-62-6
MF:
C2H5NO2
Structure:
Chemical Name:
6-CHLOROBENZO[D]OXAZOL-2-AMINE
CAS:
52112-68-2
MF:
C7H5ClN2O
Structure:
Chemical Name:
3-AMINO-2,2-DIMETHYL-PROPIONIC ACID ETHYL ESTER HYDROCHLORIDE
CAS:
80253-38-9
MF:
C7H15NO2.ClH
Structure:
Chemical Name:
2-AMINOHEPTANOIC ACID
CAS:
1115-90-8
MF:
C7H15NO2
Structure:
Chemical Name:
(R)-2-amino-2-methyl-dec-6-enoic acid
CAS:
1195967-46-4
MF:
C11H21NO2
Structure:
Chemical Name:
(S)-N-Fmoc-2-(4'-pentenyl)glycine
CAS:
856412-22-1
MF:
C22H23NO4
Structure:
Chemical Name:
(S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-3-cyanopropanoic acid
CAS:
127273-06-7
MF:
C19H16N2O4
Structure:
Chemical Name:
(S)- 2-(7'-octenyl) alanine
CAS:
1221256-52-5
MF:
C11H21NO2
Structure:
Chemical Name:
DL-PHENYLALANINE-CARBOXY-13C
CAS:
64193-00-6
MF:
C9H11NO2
Structure:
Chemical Name:
Fmoc-4-trifluoromethyl-D-homophenylalanine
CAS:
1260604-58-7
MF:
C26H22F3NO4
Structure:
Chemical Name:
(R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride
CAS:
103889-79-8
MF:
C9H12ClNO3
Structure:
Chemical Name:
Fmoc-2-trifluoromethyl-L-homophenylalanine
CAS:
1260591-46-5
MF:
C26H22F3NO4
Structure:
Chemical Name:
3,4-Difluoro-D-homophenylalanine
CAS:
1260610-37-4
MF:
C10H11F2NO2
Structure:
Chemical Name:
N-Fmoc-7-methyl-L-tryptophan
CAS:
1808268-53-2
MF:
C27H24N2O4
Structure:
Chemical Name:
Z-GLY-ILE-OH
CAS:
20807-11-8
MF:
C16H22N2O5
Structure:
Chemical Name:
ALPHA-METHYL-L-4-FLUOROPHE
CAS:
130855-57-1
MF:
C10H12FNO2
Structure:
Chemical Name:
H-GLY-GLY-HIS-GLY-OH
CAS:
128114-56-7
MF:
C12H18N6O5
Structure:
Chemical Name:
FMOC-D-MEHIS(TRT)-OH
CAS:
1217608-75-7
MF:
C41H35N3O4
Structure:
Chemical Name:
FMOC-N(HMB)-GLY-OH
CAS:
148515-78-0
MF:
C25H23NO6
Chemical Name:
Novex 10% Tris-Glycine Mini Gels, WedgeWell format, 10-well
Structure:
Chemical Name:
Fmoc-2-trifluoromethyl-D-homophenylalanine
CAS:
1260614-05-8
MF:
C26H22F3NO4
Structure:
Chemical Name:
(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[1-[(2-methylpropan-2-yl)oxycarbonyl]piperidin-4-yl]acetic acid
CAS:
281655-71-8
MF:
C27H32N2O6
Structure:
Chemical Name:
FOR-PHE-OME
CAS:
2311-21-9
MF:
C11H13NO3
Structure:
Chemical Name:
PTH-METHIONINE
CAS:
4370-90-5
MF:
C12H14N2OS2
Structure:
Chemical Name:
BOC-CYS(4-MEBZL)-OL
CAS:
129397-85-9
MF:
C16H25NO3S
Structure:
Chemical Name:
FMOC-(S)-3-AMINO-3-(4-BROMO-PHENYL)-PROPIONIC ACID
CAS:
220497-68-7
MF:
C24H20BrNO4
Structure:
Chemical Name:
N-Cbz-N-methyl-L-leucine
CAS:
33099-08-0
MF:
C15H21NO4
Structure:
Chemical Name:
N-EPSILON-2,4-DNP-L-LYSINE HYDROCHLORIDE
CAS:
14401-10-6
MF:
C12H17ClN4O6
Structure:
Chemical Name:
BOC-D-4-AMINOMETHYLPHENYLALANINE(FMOC)
CAS:
215302-77-5
MF:
C30H32N2O6
Structure:
Chemical Name:
Z-SER-GLY-OET
CAS:
4526-93-6
MF:
C15H20N2O6
Structure:
Chemical Name:
PTH-GLYCINE
CAS:
2010-15-3
MF:
C9H8N2OS
Structure:
Chemical Name:
DL-LYSINE DIHYDROCHLORIDE
CAS:
617-68-5
MF:
C6H16Cl2N2O2
Structure:
Chemical Name:
Z-THR-GLY-OET
CAS:
27482-74-2
MF:
C16H22N2O6
Structure:
Chemical Name:
(S)-2-(3-((2-Isopropylthiazol-4-yl)methyl)-3-methylureido)-3-methylbutanoic acid
CAS:
154212-61-0
MF:
C14H23N3O3S
Structure:
Chemical Name:
Methyl (2R,3S)-3-(tert-butoxycarbonylamino)-2-hydroxy-3-phenylpropionate
CAS:
124605-42-1
MF:
C15H21NO5
Structure:
Chemical Name:
[N,N-bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]cuprate(3-)
CAS:
11065-66-0
MF:
C14H18CuN3O10
Structure:
Chemical Name:
3-Hydroxy-D-phenylalanine
CAS:
32140-49-1
MF:
C9H11NO3
Structure:
Chemical Name:
Boc-L-isoleucine methyl ester
CAS:
17901-01-8
MF:
C12H23NO4