CAS 71989-31-6
:Fmoc-Pro-OH
Descripción:
Fmoc-Pro-OH, o 9-fluorenilmetoxicarbonilo-prolina, es un aminoácido protegido comúnmente utilizado en la síntesis de péptidos. Presenta un grupo fluorenilmetoxicarbonilo (Fmoc), que actúa como un grupo protector para la funcionalidad amino de la prolina, permitiendo reacciones selectivas durante el ensamblaje de péptidos. El grupo Fmoc es estable en condiciones básicas, pero puede ser eliminado en condiciones ácidas suaves, facilitando el paso de desprotección en la síntesis de péptidos. Fmoc-Pro-OH se caracteriza por su relativamente alta solubilidad en disolventes orgánicos, como el dimetilformamida (DMF) y el diclorometano, mientras que es menos soluble en agua. Este compuesto es crucial en la síntesis de péptidos en fase sólida, donde ayuda en la adición secuencial de aminoácidos para formar péptidos. Su estructura incluye un esqueleto de prolina, que introduce propiedades conformacionales únicas debido a su estructura cíclica, influyendo en la estructura secundaria general del péptido. El número CAS 71989-31-6 identifica de manera única este compuesto, asegurando una comunicación precisa en la literatura científica y bases de datos.
Fórmula:C20H19NO4
InChI:InChI=1S/C20H19NO4/c22-19(23)18-10-5-11-21(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,22,23)/t18-/m0/s1
Clave InChI:InChIKey=ZPGDWQNBZYOZTI-SFHVURJKSA-N
SMILES:C(OC(=O)N1[C@H](C(O)=O)CCC1)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Sinónimos:- (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid
- (2S)-1-[[(9H-Fluoren-9-yl)methoxy]carbonyl]pyrrolidine-2-carboxylic acid
- (S)-N-(9-Fluorenylmethoxycarbonyl)proline
- (S)-hidrogenopirrolidina-1,2-dicarboxilato de 1-(9H-fluoren-9-ilmetilo)
- (S)-hydrogenopyrrolidine-1,2-dicarboxylate de 1-(9H-fluorene-9-ylmethyle)
- 1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester, (S)-
- 1-(9H-fluoren-9-ylmethyl) hydrogen (S)-pyrrolidine-1,2-dicarboxylate
- 1-(9H-fluoren-9-ylmethyl)-(S)-hydrogenpyrrolidin-1,2-dicarboxylat
- Fluorenylmethoxycarbonylproline
- Fmoc-<span class="text-smallcaps">L</span>-Pro-OH
- Fmoc-<span class="text-smallcaps">L</span>-proline
- Fmoc-L-proline
- Fmoc-Pro-OH
- N-(9-Fluorenylmethoxycarbonyl)-<span class="text-smallcaps">L</span>-proline
- N-(9-Fluorenylmethoxycarbonyl)-L-proline
- N-(9-Fluorenylmethoxycarbonyl)proline
- N-FMOC-<span class="text-smallcaps">L</span>-proline
- N-FMOC-L-proline
- Nsc 334294
- Ver más sinónimos
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Encontrado 16 productos.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-proline
CAS:Fórmula:C20H19NO4Pureza:>98.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:337.38N-Fmoc-L-proline, 98%
CAS:<p>It is used as pharmaceutical intermediate. Fmoc method is used for the synthesis of the new polymeric support for the preparation of C-terminal peptide amides. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label inform</p>Fórmula:C20H19NO4Pureza:98%Forma y color:Crystals or powder or crystalline powder, White to pale creamPeso molecular:337.38Fmoc-Pro-OH
CAS:<p>M03372 - Fmoc-Pro-OH</p>Fórmula:C20H19NO4Pureza:98%Forma y color:Solid, Crystalline or PowderPeso molecular:337.375Fmoc-Pro-OH
CAS:<p>Bachem ID: 4003150.</p>Fórmula:C20H19NO4Pureza:99.8%Forma y color:WhitePeso molecular:337.38Ref: IN-DA003QO0
5g21,00€10g25,00€1kg224,00€25g27,00€50g41,00€5kgA consultar100g57,00€250g113,00€500g168,00€Fmoc-L-Proline
CAS:<p>Fmoc-L-Proline (Fmoc-Pro-OH) is a proline derivative.</p>Fórmula:C20H19NO4Pureza:99.22%Forma y color:SolidPeso molecular:337.37Fmoc-L-Proline, 10mM (in DMSO)
CAS:Fmoc-L-Proline, 10mM (in DMSO)Pureza:≥98%Peso molecular:337.37g/molFmoc-Pro-OH
CAS:Fórmula:C20H19NO4Pureza:≥ 99.0%Forma y color:White to off-white or pale yellow crystalline powderPeso molecular:337.38FMOC-Pro-OH
CAS:FMOC-Pro-OHFórmula:C20H19NO4Pureza:98%Forma y color: white to off white powderPeso molecular:337.37g/molFmoc-Pro-OH
CAS:<p>Fmoc-Pro-OH is a synthetic cyclic peptide with the amino acid sequence (Fmoc-Lys-Lys-Ala-Glu)n. Fmoc-Pro-OH binds to the androgen receptor and can be used as a research tool to identify other molecules that bind to the same receptor. It has been shown to inhibit the activity of ester hydrochloride, trifluoroacetic acid, and superparamagnetic iron in coordination complexes.</p>Fórmula:C20H19NO4Pureza:Min. 95 Area-%Forma y color:White Off-White PowderPeso molecular:337.37 g/molFmoc-Pro-OH
CAS:<p>Fmoc-Pro-OH is a peptide that contains the Fmoc protecting group. It is used in the synthesis of peptides and has been shown to be effective against microbial infections with marine sponges. The synthesis of this compound can be carried out on an on-line automated peptide synthesizer. The Fmoc protecting group is removed by treatment with trifluoroacetic acid (TFA) in dichloromethane, which leaves the side chain unprotected. This compound has a high binding affinity for the receptor site of fibrinogen and can potentially inhibit the growth of bacteria that cause bacterial infection, such as Staphylococcus aureus and Pseudomonas aeruginosa.<br>Fmoc-Pro-OH can also be used to synthesize other functional groups such as sulfamoyl groups or acetonitrile groups, depending on the desired outcome.</p>Fórmula:C20H19NO4Pureza:Min. 98 Area-%Peso molecular:337.38 g/molFMOC-L-Proline extrapure, 99%
CAS:Fórmula:C20H19NO4Pureza:min. 99%Forma y color:White to Off white, Crystalline powderPeso molecular:337.38L-Proline-N-Fmoc
CAS:Producto controlado<p>Applications L-Proline-N-Fmoc is N-Fmoc protected L-Proline (P755995) which is an amino acid and precursor (with vitamin C) for collagen, the building block of the structure of tendons, ligaments, arteries, veins and muscles. It is important in wound healing.<br>References Bondarenko, L.B., et al.: Int. J. Peptides., 2, 1687 (2012); Rimer, T., et al.: Biomacromolecules, 13, 2110 (2012);<br></p>Fórmula:C20H19NO4Forma y color:NeatPeso molecular:337.37L-Proline-d3-N-Fmoc
CAS:Producto controlado<p>Applications L-Proline-d3-N-Fmoc was used to prepare potent bombesin-like peptides for GRP-receptor targeting of tumors. It was also used to synthesize tetrapeptide aldehyde inhibitors of dengue virus NS3 protease.<br>References Nock, B., et al.: J. Med. Chem., 48, 100 (2005); Yin, Z., et al.: Bioorg. Med. Chem. Lett., 16, 40 (2006)<br></p>Fórmula:C20D3H16NO4Forma y color:NeatPeso molecular:340.39












