CAS 1148-11-4
:Benzyloxi-carbonil-L-prolina
Descripción:
Benzyloxi-carbonil-L-prolina, comúnmente conocido como Z-Prolina, es un derivado del aminoácido prolina, caracterizado por la presencia de un grupo protector benzyloxycarbonilo (Z). Este compuesto se utiliza típicamente en la síntesis de péptidos como un grupo protector para la funcionalidad amino de la prolina, lo que ayuda a prevenir reacciones no deseadas durante el proceso de síntesis. La Z-Prolina es un sólido cristalino blanco a blanco sucio que es soluble en disolventes orgánicos como el metanol y el dimetilsulfóxido, pero tiene una solubilidad limitada en agua. Su estructura molecular incluye un esqueleto de prolina, que contribuye a sus propiedades conformacionales únicas, haciéndola valiosa en el diseño de péptidos y proteínas. El compuesto es estable bajo condiciones normales de laboratorio, pero puede sufrir hidrólisis o desprotección bajo condiciones ácidas o básicas. Debido a su papel en la química de péptidos, la Z-Prolina es significativa en la investigación farmacéutica y el desarrollo de compuestos biológicamente activos. Se deben consultar los datos de seguridad para su manipulación, como con cualquier sustancia química.
Fórmula:C13H15NO4
InChI:InChI=1S/C13H15NO4/c15-12(16)11-7-4-8-14(11)13(17)18-9-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9H2,(H,15,16)/t11-/m0/s1
Clave InChI:InChIKey=JXGVXCZADZNAMJ-NSHDSACASA-N
SMILES:C(OCC1=CC=CC=C1)(=O)N2[C@H](C(O)=O)CCC2
Sinónimos:- (2S)-1,2-Pyrrolidinedicarboxylic acid 1-(phenylmethyl) ester
- (2S)-1-(Benzyloxycarbonyl)pyrrolidine-2-carboxylic acid
- (2S)-1-Phenylmethoxycarbonylpyrrolidine-2-carboxylic acid
- (2S)-1-[(benzyloxy)carbonyl]pyrrolidine-2-carboxylate
- (S)-1-(Benzyloxycarbonyl)pyrrolidine-2-carboxylic acid
- 1,2-Pyrrolidinedicarboxylic acid, 1-(phenylmethyl) ester, (2S)-
- 1,2-Pyrrolidinedicarboxylic acid, 1-(phenylmethyl) ester, (S)-
- 1,2-Pyrrolidinedicarboxylic acid, 1-benzyl ester, <span class="text-smallcaps">L</span>-
- 1,2-Pyrrolidinedicarboxylic acid, 1-benzyl ester, L-
- 1-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-proline
- 1-(Benzyloxycarbonyl)-L-proline
- 1-Carbobenzoxy-<span class="text-smallcaps">L</span>-proline
- 1-Carbobenzoxy-L-proline
- 1-[(Benzyloxy)Carbonyl]Proline
- 1-[(benzyloxy)carbonyl]-D-proline
- 1-[(benzyloxy)carbonyl]-L-proline
- <span class="text-smallcaps">L</span>-Cbz-Proline
- Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-proline
- Benzyloxycarbonyl-L-proline
- Carbobenzoxy-<span class="text-smallcaps">L</span>-proline
- Carbobenzoxy-L-proline
- Carbobenzoxy-S-proline
- Carbobenzyloxy-<span class="text-smallcaps">L</span>-proline
- Carbobenzyloxy-L-proline
- Cbz-<span class="text-smallcaps">L</span>-Pro-OH
- Cbz-L-Pro-OH
- Cbz-L-proline
- N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-proline
- N-(Carbobenzyloxy)-<span class="text-smallcaps">L</span>-proline
- N-Benzyloxycarbonyl-(S)-proline
- N-Benzyloxycarbonyl-L-prolin
- N-Benzyloxycarbonyl-L-proline
- N-CBZ-L-Proline N-Carbobenzyloxy-L-proline
- N-Carbobenzoxy-<span class="text-smallcaps">L</span>-proline
- N-Carbobenzoxy-L-proline
- N-Carbobenzyloxy-(S)-proline
- N-Cbz-<span class="text-smallcaps">L</span>-proline
- N-Cbz-L-Pro-OH
- N-Cbz-L-proline
- N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-proline
- N-[(Phenylmethoxy)carbonyl]-L-proline
- N-benciloxicarbonil-L-prolina
- N-cbz-L-proline crystalline
- Z-L-Proline
- Z-Pro-OH
- N-CARBOBENZYLOXY-L-PROLINE
- N-ALPHA-BENZYLOXYCARBONYL-L-PROLINE
- N-ALPHA-CBZ-L-PROLINE
- (2S)-1-[(BENZYLOXY)CARBONYL]PYRROLIDINE-2-CARBOXYLIC ACID
- CBZ-PRO-OH
- N-ALPHA-CARBOBENZOXY-L-PROLINE
- (S)-N-CBZ-PYRROLIDINE-2-CARBOXYLIC ACID
- N-CBZ-L-PROLINE-OH
- Z-L-PRO-OH
- N-ALPHA-CARBOBENZOXY-L-PYRROLIDINE-2-CARBOXYLIC ACID
- L-CBZ-PROLINE
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Encontrado 13 productos.
N-Benzyloxycarbonyl-L-proline
CAS:Fórmula:C13H15NO4Pureza:>98.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:249.27N-Benzyloxycarbonyl-L-proline, 98+%
CAS:<p>N-(Benzyloxycarbonyl)-L-proline is a potent inhibitor of prolidase; a specific peptidase that cleaves dipeptides with a C-terminal prolyl and hydroxylprolyl residue. It is also used in the synthesis of N-(L-Prolyl)--alanine which is a derivative of the naturally occurring beta amino acid -Alanine. T</p>Fórmula:C13H14NO4Pureza:98+%Forma y color:Powder or crystalline powder or crystals or granules, White to creamPeso molecular:248.26Z-Pro-OH
CAS:<p>Bachem ID: 4001343.</p>Fórmula:C13H15NO4Pureza:99.1%Forma y color:WhitePeso molecular:249.27(2S)-Pyrrolidine-2-carboxylic acid, N-CBZ protected
CAS:<p>(2S)-Pyrrolidine-2-carboxylic acid, N-CBZ protected</p>Fórmula:C13H15NO4Pureza:98%Forma y color: white solidPeso molecular:249.26g/molCarbobenzoxyproline
CAS:<p>Carbobenzoxyproline (Carbobenzoxy-S-proline) is a prolidase inhibitor.</p>Fórmula:C13H15NO4Pureza:99.79%Forma y color:White To Light Yellow Crystal PowderPeso molecular:249.26Z-Pro-OH
CAS:<p>M03066 - Z-Pro-OH</p>Fórmula:C13H15NO4Pureza:98%Forma y color:SolidPeso molecular:249.266N-Benzyloxycarbonyl-L-proline
CAS:<p>N-Benzyloxycarbonyl-L-proline is a cationic polymerization inhibitor that has been shown to inhibit the growth of Pseudomonas aeruginosa. It inhibits bacterial growth by inhibiting the production of collagen, an important component in the cell wall. N-Benzyloxycarbonyl-L-proline is also used as a histological staining agent and has been shown to be effective against breast cancer cells resistant to tamoxifen therapy.</p>Fórmula:C13H15NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:249.26 g/molZ-L-Proline extrapure, 99%
CAS:Fórmula:C13H15NO4Pureza:min. 99%Forma y color:White, Crystalline powderPeso molecular:249.3N-(Benzyloxycarbonyl)-L-proline
CAS:Producto controlado<p>Applications N-(Benzyloxycarbonyl)-L-proline is a potent in vitro and in vivo inhibitor of prolidase; a specific peptidase that cleaves dipeptides with a C-terminal prolyl and hydroxylprolyl residue. N-(Benzyloxycarbonyl)-L-proline is also used in the synthesis of N-(L-Prolyl)-β-alanine (P756190) which is a derivative of the naturally occurring beta amino acid β-Alanine (A637320).<br>References Lupi, A., et al.: BBA-Mol. Cell Res., 1744, 157 (2005)<br></p>Fórmula:C13H15NO4Forma y color:NeatPeso molecular:249.26











