CAS 1170-76-9
:3-phenyl-N-[N-[(phenylmethoxy)carbonyl]glycyl]-L-alanine
Description:
3-phenyl-N-[N-[(phenylmethoxy)carbonyl]glycyl]-L-alanine, with the CAS number 1170-76-9, is a synthetic compound that belongs to the class of amino acids and peptides. This substance features a phenyl group, which contributes to its aromatic characteristics, and a glycyl moiety, indicating its structure includes a glycine derivative. The presence of the phenylmethoxycarbonyl group suggests that it has protective or modifying functionalities, often used in peptide synthesis to enhance stability or solubility. The L-alanine component indicates that it is an optically active amino acid, which can influence its biological activity and interactions. This compound may exhibit properties typical of peptides, such as potential bioactivity, solubility in polar solvents, and the ability to form hydrogen bonds due to its functional groups. Its specific applications can vary, but it may be relevant in pharmaceutical research, particularly in the development of peptide-based drugs or as a building block in organic synthesis.
Formula:C19H20N2O5
InChI:InChI=1/C19H20N2O5/c22-17(12-20-19(25)26-13-15-9-5-2-6-10-15)21-16(18(23)24)11-14-7-3-1-4-8-14/h1-10,16H,11-13H2,(H,20,25)(H,21,22)(H,23,24)/t16-/m0/s1
InChI key:InChIKey=FLGYJBNDDWLTQR-INIZCTEOSA-N
SMILES:C([C@H](NC(CNC(OCC1=CC=CC=C1)=O)=O)C(O)=O)C2=CC=CC=C2
Synonyms:- (2S)-2-[[2-(Benzyloxycarbonylamino)acetyl]amino]-3-phenyl-propanoic acid
- (2S)-3-Phenyl-2-[[2-(phenylmethoxycarbonylamino)acetyl]amino]propanoic acid
- (Carbobenzoxy)glycyl-<span class="text-smallcaps">L</span>-phenylalanine
- (Carbobenzoxy)glycylphenylalanine
- (Carbobenzyloxy)glycyl-<span class="text-smallcaps">L</span>-phenylalanine
- <span class="text-smallcaps">L</span>-Alanine, N-(N-carboxyglycyl)-3-phenyl-, N-benzyl ester
- <span class="text-smallcaps">L</span>-Phenylalanine, N-[(phenylmethoxy)carbonyl]glycyl-
- <span class="text-smallcaps">L</span>-Phenylalanine, N-[N-[(phenylmethoxy)carbonyl]glycyl]-
- Alanine, N-(N-carboxyglycyl)-3-phenyl-, N-benzyl ester, <span class="text-smallcaps">L</span>-
- Carbobenzoxyglycylphenylalanine
- L-Phenylalanine, N-(N-((phenylmethoxy)carbonyl)glycyl)-
- N-(Benzyloxycarbonyl)glycyl-<span class="text-smallcaps">L</span>-phenylalanine
- N-(Benzyloxycarbonyl)glycylphenylalanine
- N-(Carbobenzoxy)glycyl-<span class="text-smallcaps">L</span>-phenylalanine
- N-(Carbobenzyloxy)glycyl-<span class="text-smallcaps">L</span>-phenylalanine
- N-(N-((Phenylmethoxy)carbonyl)glycyl)-L-phenylalanine
- N-[(Phenylmethoxy)carbonyl]glycyl-<span class="text-smallcaps">L</span>-phenylalanine
- N-[(benzyloxy)carbonyl]glycyl-L-phenylalanine
- N-[(benzyloxy)carbonyl]glycylphenylalanine
- Nsc 89642
- Z-Gly-Phe-Oh
- 3-Phenyl-N-(N-((phenylmethoxy)carbonyl)glycyl)-L-alanine
- N-[(Phenylmethoxy)carbonyl]glycyl-L-phenylalanine
- Alanine, N-(N-carboxyglycyl)-3-phenyl-, N-benzyl ester, L-
- L-Phenylalanine, N-[(phenylmethoxy)carbonyl]glycyl-
- L-Alanine, N-(N-carboxyglycyl)-3-phenyl-, N-benzyl ester
- Cbz-Gly-L-Phe-OH
- Z-GLYCYL-L-PHENYLALANINE
- N-[N-[(Phenylmethoxy)carbonyl]glycyl]-L-pherylalanine
- N-CBZGLYCYL-L-PHENYLALANINE
- Cbr-Gly-L-Phe
- CBZ-GLY-L-PHE
- N-BENZYLOXYCARBONYLGLYCYL-L-PHENYLALANINE
- Z-GLY-PHE
- Z-L-GLYCYL-L-PHENYLALANINE
- Z-Gly-L-Phe-OH
- Cbz-Gly-Phe-OH
- N-(Benzyloxycarbonyl)-Gly-Phe-OH
- (Benzyloxycarbonyl)Gly-L-Phe-OH
- N-CBZ-GLY-PHE
- BENZYLOXYCARBONYLGLYCYL-L-PHENYLALANINE
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
(S)-2-(2-(((Benzyloxy)Carbonyl)Amino)Acetamido)-3-Phenylpropanoic Acid
CAS:<p>(S)-2-(2-(((Benzyloxy)Carbonyl)Amino)Acetamido)-3-Phenylpropanoic Acid</p>Purity:99%Molecular weight:356.37g/mol(S)-2-(2-(((Benzyloxy)carbonyl)amino)acetamido)-3-phenylpropanoic acid
CAS:Formula:C19H20N2O5Purity:98%Color and Shape:Liquid, No data available.Molecular weight:356.378Z-Gly-Phe
CAS:<p>Z-Gly-Phe is a peptide that inhibits protein synthesis by binding to the reactive site of a pancreatic enzyme. This site is normally occupied by a hydrogen bond and the compound binds to it by occupying this space, resulting in the inhibition of enzyme activity. Z-Gly-Phe has been shown to inhibit insulin-stimulated glucose uptake in rats, which may be due to its ability to bind with sodium carbonate. The binding constants of Z-Gly-Phe and its inhibitors have been determined using an analytical method that measures changes in pH. The optimum pH for Z-Gly-Phe is 8.5, which corresponds with the optimal pH for human pancreatic enzymes.</p>Formula:C19H20N2O5Purity:Min. 95%Molecular weight:356.37 g/mol




