9-Me-BC (9mbc), (15mg/capsule) 60 Capsules
$62.99
9-Me-BC (9-Methyl-β-carboline) is a synthetic compound demonstrating monoamine oxidase interaction properties in experimental models. Laboratory research indicates specific modulation of amine-related molecular CAS: 2521-07-5 | Formula: C12H10N2 | Content: 900 mg (15 mg per capsule) | Research use only | Third-party lab tested.
Buy 9-Me-BC (9mbc), (15mg/capsule) 60 Capsules – Swiss Chems USA
9-Me-BC (9mbc), (15mg/capsule) 60 Capsules — Research Overview
9-Me-BC (9-Methyl-β-carboline) is a synthetic compound demonstrating monoamine oxidase interaction properties in experimental models. Laboratory research indicates specific modulation of amine-related molecular pathways.
- High Purity – 99% Purity Guaranteed
- Independently Lab Tested
- Research Grade Quality
- For Laboratory Research Use Only
Intended use: This material is supplied for laboratory and in-vitro research only. It is not a drug, food, or cosmetic and is not intended for human or animal consumption.
9-Me-BC (9mbc), (15mg/capsule) 60 Capsules Chemical Properties
| Property | Specification |
|---|---|
| Chemical Formula | C12H10N2 |
| Synonyms | 9-Methyl-beta-carboline, 9-Methyl-norharman, 9-methylpyrido[3,4-b]indole |
| Molar Mass | 182.22 g/mol |
| CAS Number | 2521-07-5 |
| PubChem CID | 164979 |
| Total Compound Content | 900 mg (15 mg per capsule) |
| Shelf Life | 36 months |
9-Me-BC (9mbc), (15mg/capsule) 60 Capsules Research Applications
9-Me-BC (C12H10N2; 9-methyl-9H-pyrido[3,4-b]indole) is a synthetic N-methylated β-carboline compound. Its primary characterized mechanism is selective monoamine oxidase A (MAO-A) inhibition, with the 9-methyl substitution influencing the compound’s interaction profile within the β-carboline class. Experimental investigations have examined its effects on monoamine-associated signaling pathways, transcriptional regulation mechanisms, neurotrophin-associated regulatory networks, and intracellular signaling processes. Studies have also explored its interactions with molecular communication systems, pathway-specific regulatory mechanisms, and structure-function relationships relevant to β-carboline pharmacology. Its combination of MAO-A inhibitory activity and broader signaling pathway interactions makes 9-Me-BC a useful research tool for investigating monoamine pharmacology, molecular regulation, and mechanistic aspects of β-carboline-derived compounds. Supplied in 15 mg capsules. Independently third-party HPLC-tested; COA available per batch.
9-Me-BC (9mbc), (15mg/capsule) 60 Capsules Frequently Asked Questions
How does 9-Me-BC’s mechanism differ from classical MAO inhibitors used in research?
9-Me-BC is a β-carboline-derived compound with selective MAO-A inhibitory activity and a broader molecular interaction profile than many classical MAO inhibitors. Experimental investigations have examined its effects on monoamine-associated signaling pathways, transcriptional regulation mechanisms, and intracellular regulatory networks. This combination of MAO-A inhibition and pathway-modulating activity makes it a useful research tool for studies investigating molecular signaling processes beyond monoamine oxidase inhibition alone.
What regulatory pathways have been investigated in studies of 9-Me-BC?
Experimental studies have examined 9-Me-BC in relation to neurotrophin-associated regulatory networks, gene expression mechanisms, and intracellular signaling pathways. Investigations have explored its interactions with transcriptional control systems, molecular communication pathways, and regulatory processes involved in cellular signaling. These characteristics have contributed to its use in studies of molecular regulation, signal transduction, and β-carboline pharmacology.
Why is 9-Me-BC useful as a research tool in monoamine pharmacology?
9-Me-BC combines selective MAO-A inhibitory activity with documented interactions across multiple signaling and regulatory pathways. This profile makes it useful for investigating monoamine-associated mechanisms, transcriptional regulation, intracellular signaling processes, and structure-function relationships within the β-carboline class. Its well-characterized molecular pharmacology has established it as a valuable tool for mechanistic studies of regulatory pathway interactions and monoamine-related signaling systems.
Research Use Disclaimer
All product information is provided for educational and laboratory research reference only. Any form of introduction into humans or animals is prohibited. Handle only in licensed research settings in accordance with applicable laws and institutional protocols.
| Weight | 3 lbs |
|---|
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