CAS 1170-76-9
:3-fenil-N-[N-[(fenilmetoxi)carbonil]glicil]-L-alanina
Descripción:
3-fenil-N-[N-[(fenilmetoxi)carbonil]glicil]-L-alanina, con el número CAS 1170-76-9, es un compuesto sintético que pertenece a la clase de aminoácidos y péptidos. Esta sustancia presenta un grupo fenilo, que contribuye a sus características aromáticas, y un moiety glicilo, lo que indica que su estructura incluye un derivado de glicina. La presencia del grupo fenilmetoxicarbonilo sugiere que tiene funcionalidades protectoras o modificadoras, a menudo utilizadas en la síntesis de péptidos para mejorar la estabilidad o solubilidad. El componente L-alanina indica que es un aminoácido ópticamente activo, lo que puede influir en su actividad biológica e interacciones. Este compuesto puede exhibir propiedades típicas de los péptidos, como potencial bioactividad, solubilidad en disolventes polares y la capacidad de formar enlaces de hidrógeno debido a sus grupos funcionales. Sus aplicaciones específicas pueden variar, pero puede ser relevante en la investigación farmacéutica, particularmente en el desarrollo de fármacos basados en péptidos o como un bloque de construcción en la síntesis orgánica.
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
Clave 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
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Encontrado 5 productos.
(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%Forma y color: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




