9-Me-BC

9-Me-BC

Nombre del producto 9-Me-BC
Número CAS 2521-07-5
Fórmula molecular C10H12N2
Peso molecular 160,22 g/mol
Apariencia Off-white to pale yellow crystalline powder
Ensayo (HPLC) ≥98,01 TP3T
Punto de fusión 118–122 °C
Solubilidad Soluble in DMSO, ethanol; slightly soluble in water
Paquete 1 kg, 5 kg, 25 kg fiber drums

9-Me-BC Structure

Synonyms: 9-Methyl-β-carboline, 9-Me-BC, 9-Methyl-9H-pyrido[3,4-b]indole, 9-Methylnorharman, 9-Methyl-β-carboline

9-Me-BC is a synthetic methylated β-carboline derivative that has become a molecule of interest in neuropharmacology and medicinal chemistry research. Unlike many β-carbolines isolated from natural sources, 9-Me-BC is produced through controlled chemical synthesis, allowing for high purity and consistent supply. Its structure features a methyl group at the indole nitrogen, a modification that significantly influences its interaction with monoamine systems and its metabolic stability compared to norharman and harman.

In the research community, 9-Me-BC is primarily investigated for its potential effects on dopaminergic neurons and neurotrophic signaling. Preclinical studies suggest it may upregulate tyrosine hydroxylase and promote neurite outgrowth, making it a valuable tool for studying Parkinson’s disease models and dopamine-related pathways. Its ability to cross the blood-brain barrier and its relatively favorable pharmacokinetic profile in animal models have further fueled interest.

While not approved for human use, 9-Me-BC is supplied as a reference standard and research chemical for in vitro and in vivo studies. It is available at high purity, typically ≥98% by HPLC, and is characterized by NMR and mass spectrometry to ensure structural integrity. Researchers value it for its selectivity and the reproducibility it brings to neurobiological experiments.

Función

  • Dopaminergic modulation: May enhance tyrosine hydroxylase expression and dopamine synthesis in neuronal cultures.
  • Neurotrophic support: Promotes neurite outgrowth and survival in dopaminergic cell models.
  • MAO inhibition: Exhibits inhibitory activity against monoamine oxidase, contributing to its neuroactive profile.
  • Cognitive enhancement: Investigated for potential pro-cognitive effects in animal studies.
  • Neuroprotección: Shows antioxidant and anti-inflammatory properties in preclinical models.

Source & Standardization

  • Source: Synthetic chemical synthesis
  • Standardization: ≥98.0% (HPLC)
  • Identificación: NMR, MS, IR
  • Forms: Crystalline powder
  • Aplicaciones: Research on Parkinson’s disease, dopamine regulation, neuroprotection, and cognitive function

Especificaciones

Parámetro Especificaciones
Ensayo (HPLC) ≥98,01 TP3T
Identificación Conforms to structure
Pérdida por secado ≤0,51 TP3T
Residuo tras la combustión ≤0,11 TP3T
Metales pesados ≤10 ppm
Límites microbianos Total aerobic count ≤1000 CFU/g

Documentation & Supply

  • Monthly capacity: 5–10 kg
  • Plazo de entrega: 3-5 días laborables (artículos en stock)
  • Documentación: COA, MSDS, TDS, NMR, HPLC
  • Embalaje: 1 kg, 5 kg, 25 kg fiber drums with inner liners

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