6-Methylthio-IMP

6-Methylthioinosine-5'-monophosphate, Triethylammonium salt

6-Methylmercapto-9-(β-D-ribofuranosyl)purine-5'-monophosphate

Catálogo Nº Apresentação Preço (R$) Comprar
NU-1131S 150 μl (10 mM)Sob demanda Adicionar ao Carrinho
NU-1131L 5 x 150 μl (10 mM)Sob demanda Adicionar ao Carrinho
Structural formula of 6-Methylthio-IMP (6-Methylthioinosine-5'-monophosphate, Triethylammonium salt)
Structural formula of 6-Methylthio-IMP

For general laboratory use.

Envio: shipped on gel packs

Condições de armazenamento: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Validade: 12 months after date of delivery

Fórmula molecular: C11H15N4O7PS (free acid)

Peso molecular: 378.29 g/mol (free acid)

CAS#: 7021-52-5

Pureza: ≥ 95 % (HPLC)

Forma: solution in water

Concentração: 10 mM - 11 mM

pH: 7.5 ±0.5

Propriedades espectroscópicas: λmax 224/292 nm, ε 11.5/19.0 L mmol-1 cm-1 (Tris-HCl pH 7.5)

Formulários:
Catabolism by purine-5'-nucleotidase[1]
Transport by multidrug resistance proteins MRP4 and MRP5[2]
Strong inhibitor of purine synthesis de novo[3]

Referências selecionadas:
[1] Brouwer et al. (2005) Role of 5'-nucleotidase in thiopurine metabolism:Enzyme kinetic profile and association with thio-GMP levels in patients with acute lymphoblastic leukemia during 6-mercaptopurine treatment. Clinica Chemica Acta 361:95.

[2] Wielinga et al. (2002) Thiopurine metabolism and identification of the thiopurine metabolites transported by MRP4 and MRP5 overexpressed in human embryonic kidney cells. Molecular Pharmacology 62:1321.

[3] Stet et al. (1994) Decrease of S-adenosylmethionine synthesis by 6-mercaptopurine ribonucleoside in Molt F4 human malignant lymphoblasts. Biochemical J. 304:163.

Lavi et al. (1985) A rapid and sensitive high-performance liquid chromatographic assay for 6-mercaptopurine metabolites in red blood cells. Anal. Biochem. 144 (2):514.