CAS 1170-76-9
:3-fenil-N-[N-[(fenilmetoxi)carbonil]glicil]-L-alanina
Descrição:
3-fenil-N-[N-[(fenilmetoxi)carbonil]glicil]-L-alanina, com o número CAS 1170-76-9, é um composto sintético que pertence à classe de aminoácidos e peptídeos. Esta substância apresenta um grupo fenila, que contribui para suas características aromáticas, e um grupo glicila, indicando que sua estrutura inclui um derivado da glicina. A presença do grupo fenilmetoxicarbonila sugere que possui funcionalidades protetoras ou modificadoras, frequentemente utilizadas na síntese de peptídeos para aumentar a estabilidade ou solubilidade. O componente L-alanina indica que é um aminoácido opticamente ativo, o que pode influenciar sua atividade biológica e interações. Este composto pode exibir propriedades típicas de peptídeos, como potencial bioatividade, solubilidade em solventes polares e a capacidade de formar ligações de hidrogênio devido aos seus grupos funcionais. Suas aplicações específicas podem variar, mas pode ser relevante na pesquisa farmacêutica, particularmente no desenvolvimento de medicamentos baseados em peptídeos ou como um bloco de construção na síntese orgânica.
Fórmula: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
Chave InChI:InChIKey=FLGYJBNDDWLTQR-INIZCTEOSA-N
SMILES:C([C@H](NC(CNC(OCC1=CC=CC=C1)=O)=O)C(O)=O)C2=CC=CC=C2
Sinónimos:- (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
- Ver mais sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
5 produtos.
(S)-2-(2-(((Benzyloxy)Carbonyl)Amino)Acetamido)-3-Phenylpropanoic Acid
CAS:(S)-2-(2-(((Benzyloxy)Carbonyl)Amino)Acetamido)-3-Phenylpropanoic AcidPureza:99%Peso molecular:356.37g/mol(S)-2-(2-(((Benzyloxy)carbonyl)amino)acetamido)-3-phenylpropanoic acid
CAS:Fórmula:C19H20N2O5Pureza:98%Cor e Forma:Liquid, No data available.Peso molecular: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>Fórmula:C19H20N2O5Pureza:Min. 95%Peso molecular:356.37 g/mol




