CAS 71989-31-6
:Fmoc-Pro-OH
Descrição:
Fmoc-Pro-OH, ou 9-fluorenilmetoxicarbonila-prolina, é um aminoácido protegido comumente utilizado na síntese de peptídeos. Apresenta um grupo fluorenilmetoxicarbonila (Fmoc), que serve como um grupo protetor para a funcionalidade amino da prolina, permitindo reações seletivas durante a montagem de peptídeos. O grupo Fmoc é estável em condições básicas, mas pode ser removido em condições ácidas suaves, facilitando a etapa de desproteção na síntese de peptídeos. Fmoc-Pro-OH é caracterizado por sua relativamente alta solubilidade em solventes orgânicos, como dimetilformamida (DMF) e diclorometano, enquanto é menos solúvel em água. Este composto é crucial na síntese de peptídeos em fase sólida, onde ajuda na adição sequencial de aminoácidos para formar peptídeos. Sua estrutura inclui um esqueleto de prolina, que introduz propriedades conformacionais únicas devido à sua estrutura cíclica, influenciando a estrutura secundária geral do peptídeo. O número CAS 71989-31-6 identifica de forma única este composto, garantindo comunicação precisa na literatura científica e bancos de dados.
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
Chave 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 mais sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
16 produtos.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-proline
CAS:Fórmula:C20H19NO4Pureza:>98.0%(T)(HPLC)Cor e Forma: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%Cor e Forma: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%Cor e Forma:Solid, Crystalline or PowderPeso molecular:337.375Fmoc-Pro-OH
CAS:<p>Bachem ID: 4003150.</p>Fórmula:C20H19NO4Pureza:99.8%Cor e Forma: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%Cor e Forma: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%Cor e Forma:White to off-white or pale yellow crystalline powderPeso molecular:337.38FMOC-Pro-OH
CAS:FMOC-Pro-OHFórmula:C20H19NO4Pureza:98%Cor e Forma: 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-%Cor e Forma: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%Cor e Forma:White to Off white, Crystalline powderPeso molecular:337.38L-Proline-N-Fmoc
CAS:Produto 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:C20H19NO4Cor e Forma:NeatPeso molecular:337.37L-Proline-d3-N-Fmoc
CAS:Produto 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:C20D3H16NO4Cor e Forma:NeatPeso molecular:340.39












