9-Me-BC

9-Me-BC

Nom du produit 9-Me-BC
Numéro CAS 2521-07-5
Formule moléculaire C10H12N2
Poids moléculaire 160.22 g/mol
Apparence Off-white to pale yellow crystalline powder
Essai (HPLC) ≥98,01 TP3T
Point de fusion 118–122 °C
Solubilité Soluble in DMSO, ethanol; slightly soluble in water
Colis 1 kg, 5 kg, 25 kg fiber drums

Besoin d'aide ? Contacter notre équipe

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.

Fonction

  • 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.
  • Neuroprotection: Shows antioxidant and anti-inflammatory properties in preclinical models.

Source et normalisation

  • Source: Synthetic chemical synthesis
  • Normalisation: ≥98.0% (HPLC)
  • Identification: NMR, MS, IR
  • Formulaires: Crystalline powder
  • Applications: Research on Parkinson’s disease, dopamine regulation, neuroprotection, and cognitive function

Caractéristiques techniques

Paramètre Spécifications
Essai (HPLC) ≥98,01 TP3T
Identification Conforms to structure
Perte au séchage ≤ 0,51 TP3T
Résidu au feu ≤ 0,11 TP3T
Métaux lourds ≤ 10 ppm
Limites microbiologiques Total aerobic count ≤1000 CFU/g

Documentation et approvisionnement

  • Capacité mensuelle: 5–10 kg
  • Délai de livraison: 3 à 5 jours ouvrés (articles en stock)
  • Documentation: COA, MSDS, TDS, NMR, HPLC
  • Emballage: 1 kg, 5 kg, 25 kg fiber drums with inner liners

Demande de devis

RESTEZ EN CONTACT

Demande de devis

Notre adresse

Room,5-0203, Unit 5, Beiyuanmen Street,Xi'an,Shaanxi,China

✅ ×