Pular para o conteúdo
Merck
Todas as fotos(1)

Key Documents

View All Documentation

47316

Sigma-Aldrich

Fmoc-D-Leu-OH

≥95.0% (TLC)

Sinônimo(s):

Fmoc-D-leucine

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(1)

About This Item

Fórmula empírica (Notação de Hill):
C21H23NO4
Número CAS:
114360-54-2
Peso molecular:
353.41
Beilstein:
4299950
Número MDL:
MFCD00062957
Código UNSPSC:
12352209
eCl@ss:
32160406
ID de substância PubChem:
57650921
NACRES:
NA.26

Nível de qualidade

100

Ensaio

≥95.0% (TLC)

adequação da reação

reaction type: Fmoc solid-phase peptide synthesis

aplicação(ões)

peptide synthesis

grupo funcional

Fmoc

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CC(C)C[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C21H23NO4/c1-13(2)11-19(20(23)24)22-21(25)26-12-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h3-10,13,18-19H,11-12H2,1-2H3,(H,22,25)(H,23,24)/t19-/m1/s1

chave InChI

CBPJQFCAFFNICX-LJQANCHMSA-N

Categorias relacionadas

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCG8780
BCBX4548
BCBS7532V
BCBK1238V
BCBD6293V

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 6

1 of 6

Fmoc-Leu-OH Novabiochem®

Sigma-Aldrich

8.52011

Fmoc-Leu-OH

Fmoc-D-Ser(tBu)-OH ≥98.0% (TLC)

Sigma-Aldrich

47311

Fmoc-D-Ser(tBu)-OH

Fmoc-D-Thr(tBu)-OH ≥98.0% (TLC)

Sigma-Aldrich

47312

Fmoc-D-Thr(tBu)-OH

Fmoc-D-Ala-OH Novabiochem®

Sigma-Aldrich

8.52142

Fmoc-D-Ala-OH

Fmoc-Trp(Boc)-OH ≥97.0% (HPLC)

Sigma-Aldrich

47561

Fmoc-Trp(Boc)-OH

Fmoc-Tyr(tBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47623

Fmoc-Tyr(tBu)-OH

M J Miller et al.
The Journal of pharmacology and experimental therapeutics, 266(1), 468-472 (1993-07-01)
Anti-inflammatory properties have been ascribed to a series of N-(fluorenyl-9-methoxycarbonyl) amino acids called leumedins that inhibit the activity of granulocytes and T-lymphocytes. We evaluated one of these leumedins, N-(fluorenyl-9-methoxycarbonyl) leucine (NPC 15199), in a model of ileitis in guinea pigs.
C R Jan et al.
The Chinese journal of physiology, 43(1), 29-33 (2000-06-17)
This report demonstrates that NPC-15199 [(N-(9-fluorenylmethoxycarbonyl)L-leucine)], a novel anti-inflammatory agent, increases intracellular Ca2+ concentration ([Ca2+]i) in human bladder female transitional cancer (BFTC) cells. Using fura-2 as a Ca2+ probe, NPC-15199 (0.1-2 mM) was found to increase [Ca2+]i concentration-dependently. The response
Zhimou Yang et al.
Chemical communications (Cambridge, England), (35)(35), 4414-4416 (2005-09-02)
Two types of therapeutic agents, which have discrete yet complementary functions, self-assemble into nanofibers in water to formulate a new supramolecular hydrogel as a self-delivery biomaterial to reduce the toxicity of uranyl oxide at the wound sites.
Chung-Ren Jan et al.
The Chinese journal of physiology, 45(3), 117-122 (2003-06-24)
In Madin-Darby canine kidney (MDCK) cells, effect of NPC-15199 on intracellular Ca2+ concentration ([Ca2+]i) was investigated by using fura-2. NPC-15199 (100-1000 microM) caused a rapid and sustained increase of [Ca2+]i in a concentration-dependent manner (EC50=500 microM). NPC-15199-induced [Ca2+]i rise was
G Cheng et al.
Langmuir : the ACS journal of surfaces and colloids, 26(7), 4990-4998 (2010-01-16)
The self-assembly and hydrogelation properties of two Fmoc-tripeptides [Fmoc = N-(fluorenyl-9-methoxycarbonyl)] are investigated, in borate buffer and other basic solutions. A remarkable difference in self-assembly properties is observed comparing Fmoc-VLK(Boc) with Fmoc-K(Boc)LV, both containing K protected by N(epsilon)-tert-butyloxycarbonate (Boc). In
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica