U heeft gezocht op: Nickel+iron+copper+molybdenum

Leverancier: TCI

Omschrijving: 3-Methylxanthine ≥98.0% (by HPLC, titration analysis)

Leverancier: TCI

Omschrijving: 1-Methylxanthine ≥97.0% (by HPLC, titration analysis)

Leverancier: Apollo Scientific

Omschrijving: 3-Methylxanthine

Leverancier: Thermo Fisher Scientific

Omschrijving: 7-Methylxanthine ≥98%

MSDS Certificaten

Leverancier: Cayman Chemical

Omschrijving: 3-Isobutyl-1-methylxanthine

Leverancier: Thermo Fisher Scientific

Omschrijving: 3-Isobutyl-1-methylxanthine 99+%

MSDS

Leverancier: ENZO LIFE SCIENCES

Omschrijving: Potent, non-specific inhibitor of phosphodiesterases (IC₅₀=2-50 µM). More potent than theophylline at adenosine receptors. Accelerates conversion of mouse fibroblast cells into adipose cells.

Leverancier: TCI

Omschrijving: 8-Bromo-7-(2-butyn-1-yl)-3-methylxanthine ≥98.0% (by HPLC, titration analysis)

Leverancier: Thermo Fisher Scientific

Omschrijving: 3-Methylxanthine ≥98%

MSDS Certificaten

Catalogus nummer: (TCIAB4134-1G)

Leverancier: TCI

Omschrijving: 8-Bromo-3-methylxanthine ≥98.0% (by HPLC, titration analysis)

UOM: 1 * 1 g

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Catalogus nummer: (PROOMM0176.05)

Leverancier: LGC Standards PROMOCHEM

Omschrijving: 7-Methylxanthine

UOM: 1 * 100 mg

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Catalogus nummer: (SERA26445.02)

Leverancier: Serva

Omschrijving: 3-Isobutyl-1-methylxanthine

UOM: 1 * 500 mg

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Catalogus nummer: (PROOMM0176.03)

Leverancier: LGC Standards PROMOCHEM

Omschrijving: 3-Methylxanthine

UOM: 1 * 100 mg

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Leverancier: MP Biomedicals

Omschrijving: 3-Methylxanthine, a metabolite of theophylline, was quantitated in rat plasma by a sensitive LC-MS/MS method.

Leverancier: Merck Millipore (Calbiochem‎)

Omschrijving: 3-Isobutyl-1-methylxanthine, Millipore®

Leverancier: MP Biomedicals

Omschrijving: IBMX has been shown to be a potent, non-specific inhibitor of adenosine 3',5'-cyclic monophosphate phosphodiesterase (cAMP PDE)4, significantly more effective than theophylline. Also inhibits cGMP phosphodiesterases. IBMX inhibits cyclic nucleotide PDE with subsequent inhibition of cyclic nucleotide hydrolysis, resulting in accumulation of cyclic AMP and guanosine 3',5'-cyclic monophosphate.