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| [[File:QMPSB_structure.svg|thumb|QMPSB_structure.svg]] {{Short description|Synthetic cannabinoid}}
| | QMPSB |
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| | The term '''[[QMPSB]]''' refers to a class of synthetic compounds known as "Quinolinyl Methyl Piperidinyl Substituted Benzamides." These compounds are of interest in the field of medicinal chemistry due to their potential pharmacological properties. This article provides an overview of the chemical structure, synthesis, pharmacology, and potential applications of QMPSB compounds. |
| | PubChem =
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| | ChemSpiderID =
| | ==Chemical Structure== |
| | UNII =
| | |
| | KEGG =
| | QMPSB compounds are characterized by a core structure that includes a quinoline moiety, a piperidine ring, and a benzamide group. The general chemical formula can be represented as: |
| | ChEBI =
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| | ChEMBL =
| | - '''[[Quinoline]]''': A heterocyclic aromatic organic compound with the formula C₉H₇N. |
| | DrugBank =
| | - '''[[Piperidine]]''': A saturated heterocyclic organic compound with the formula C₅H₁₁N. |
| | ChemBl =
| | - '''[[Benzamide]]''': An organic compound with the formula C₆H₅CONH₂. |
| | synonyms =
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| | IUPHAR_ligand =
| | The specific arrangement and substitution of these groups can vary, leading to different derivatives with unique properties. |
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| | ==Synthesis== |
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| | The synthesis of QMPSB compounds typically involves multi-step organic reactions. A common synthetic route includes: |
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| | Stdinchi =
| | 1. '''[[Formation of the Quinoline Core]]''': This can be achieved through the Skraup synthesis, which involves the reaction of aniline with glycerol and sulfuric acid in the presence of an oxidizing agent. |
| | Stdinchikey =
| | 2. '''[[Piperidine Substitution]]''': The quinoline core is then reacted with a piperidine derivative, often through nucleophilic substitution reactions. |
| | SMILES =
| | 3. '''[[Benzamide Coupling]]''': Finally, the piperidinyl quinoline is coupled with a benzoyl chloride to form the benzamide linkage. |
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| | InChIKey =
| | Each step requires careful control of reaction conditions to ensure high yield and purity of the final product. |
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| | ==Pharmacology== |
| | C=
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| | H=
| | QMPSB compounds have been studied for their potential as therapeutic agents. Some of the pharmacological activities include: |
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| | O=
| | - '''[[Antimicrobial Activity]]''': Certain QMPSB derivatives have shown effectiveness against bacterial and fungal pathogens. |
| | molecular_weight =
| | - '''[[Anticancer Properties]]''': Research has indicated that some QMPSB compounds can inhibit the growth of cancer cells by interfering with specific cellular pathways. |
| | density =
| | - '''[[Neurological Effects]]''': Due to their structural similarity to known psychoactive substances, some QMPSB compounds are being investigated for their effects on the central nervous system. |
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| | ==Potential Applications== |
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| | The potential applications of QMPSB compounds are diverse and include: |
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| | - '''[[Drug Development]]''': As lead compounds in the development of new pharmaceuticals targeting infectious diseases, cancer, and neurological disorders. |
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| | - '''[[Chemical Probes]]''': As tools in biochemical research to study cellular processes and pathways. |
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| | ==Also see== |
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| | - [[Quinoline]] |
| | pregnancy_AU =
| | - [[Piperidine]] |
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| | - [[Benzamide]] |
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| | - [[Medicinal Chemistry]] |
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| | - [[Synthetic Organic Chemistry]] |
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| | [[Category:Medicinal Chemistry]] |
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| | [[Category:Organic Compounds]] |
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| | [[Category:Pharmacology]] |
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QMPSB
The term QMPSB refers to a class of synthetic compounds known as "Quinolinyl Methyl Piperidinyl Substituted Benzamides." These compounds are of interest in the field of medicinal chemistry due to their potential pharmacological properties. This article provides an overview of the chemical structure, synthesis, pharmacology, and potential applications of QMPSB compounds.
Chemical Structure
QMPSB compounds are characterized by a core structure that includes a quinoline moiety, a piperidine ring, and a benzamide group. The general chemical formula can be represented as:
- Quinoline: A heterocyclic aromatic organic compound with the formula C₉H₇N.
- Piperidine: A saturated heterocyclic organic compound with the formula C₅H₁₁N.
- Benzamide: An organic compound with the formula C₆H₅CONH₂.
The specific arrangement and substitution of these groups can vary, leading to different derivatives with unique properties.
Synthesis
The synthesis of QMPSB compounds typically involves multi-step organic reactions. A common synthetic route includes:
1. Formation of the Quinoline Core: This can be achieved through the Skraup synthesis, which involves the reaction of aniline with glycerol and sulfuric acid in the presence of an oxidizing agent.
2. Piperidine Substitution: The quinoline core is then reacted with a piperidine derivative, often through nucleophilic substitution reactions.
3. Benzamide Coupling: Finally, the piperidinyl quinoline is coupled with a benzoyl chloride to form the benzamide linkage.
Each step requires careful control of reaction conditions to ensure high yield and purity of the final product.
Pharmacology
QMPSB compounds have been studied for their potential as therapeutic agents. Some of the pharmacological activities include:
- Antimicrobial Activity: Certain QMPSB derivatives have shown effectiveness against bacterial and fungal pathogens.
- Anticancer Properties: Research has indicated that some QMPSB compounds can inhibit the growth of cancer cells by interfering with specific cellular pathways.
- Neurological Effects: Due to their structural similarity to known psychoactive substances, some QMPSB compounds are being investigated for their effects on the central nervous system.
Potential Applications
The potential applications of QMPSB compounds are diverse and include:
- Drug Development: As lead compounds in the development of new pharmaceuticals targeting infectious diseases, cancer, and neurological disorders.
- Chemical Probes: As tools in biochemical research to study cellular processes and pathways.
Also see
- Quinoline
- Piperidine
- Benzamide
- Medicinal Chemistry
- Synthetic Organic Chemistry