Pular para o conteúdo
Merck
Todas as fotos(4)

Key Documents

K3250

Sigma-Aldrich

Kynuramine dihydrobromide

monoamine oxidase substrate, fluorogenic, ≥97% (TLC), crystalline

Sinônimo(s):

3-(2-Aminophenyl)-3-oxopropanamine

Faça loginpara ver os preços organizacionais e de contrato


About This Item

Fórmula empírica (Notação de Hill):
C9H12N2O · 2HBr
Número CAS:
Peso molecular:
326.03
Número MDL:
Código UNSPSC:
12352204
ID de substância PubChem:
NACRES:
NA.32

product name

Kynuramine dihydrobromide, crystalline

Ensaio

≥97% (TLC)

forma

crystalline

solubilidade

water: 50 mg/mL, clear to slightly hazy

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

Br.NCCC(=O)c1ccccc1N

InChI

1S/C9H12N2O.BrH/c10-6-5-9(12)7-3-1-2-4-8(7)11;/h1-4H,5-6,10-11H2;1H

chave InChI

YUPVVZSYBUIDQR-UHFFFAOYSA-N

Aplicação

Kynuramine dihydrobromide has been used as a substrate for monoamine oxidase.

Ações bioquímicas/fisiológicas

Kynuramine dihydrobromide is a substrate for the enzyme monoamine oxidase. The end product is the formation of fluorescence detectable 4-hydroxyquinoline (4-HOQ) measured in a fluorescence spectrophotometer at 380 nm.

Substratos

Substrate for monoamine oxidase

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)


Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

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

Visite a Biblioteca de Documentos

Evidence for the involvement of the noradrenergic system, dopaminergic and imidazoline receptors in the antidepressant-like effect of tramadol in mice
Jesse CR, et al.
Pharmacology, Biochemistry, and Behavior, 95(3), 344-350 (2010)
Zhanna V Chirkova et al.
Drug development research, 79(2), 81-93 (2018-03-24)
Hit, Lead & Candidate Discovery In recent studies, we have shown that pyrrolo[3,4-f]indole-5,7-dione and indole-5,6-dicarbonitrile derivatives act as good potency in vitro inhibitors of the monoamine oxidase (MAO) enzymes. To expand on these series and to further derive structure-activity relationships
Chronic dietary mercury exposure causes oxidative stress, brain lesions, and altered behaviour in Atlantic salmon (Salmo salar) parr
Berntssen MHG, et al.
Aquatic Toxicology (Amsterdam, Netherlands), 65(1), 55-72 (2003)
Magdalena S Nel et al.
Bioorganic chemistry, 69, 20-28 (2016-09-24)
In the present study a series of fifteen 2-heteroarylidene-1-indanone derivatives were synthesised and evaluated as inhibitors of recombinant human monoamine oxidase (MAO) A and B. These compounds are structurally related to series of heterocyclic chalcone derivatives which have previously been
Synergistic antidepressant-like effect of ferulic acid in combination with piperine: involvement of monoaminergic system
Li G, et al.
Metabolic Brain Disease, 30(6), 1505-1514 (2015)

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