(S)-MK-26
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Drug class | Atypical dopamine reuptake inhibitor |
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Chemical and physical data | |
Formula | C17H13Cl2NOS2 |
Molar mass | 382.32 g·mol−1 |
3D model (JSmol) | |
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(S)-MK-26 is an atypical dopamine reuptake inhibitor (DRI) that was derived from modafinil.[1][2][3] It is closely related to two other modafinil analogues, (S,S)-CE-158 and (S)-CE-123.[2][3]
(S)-MK-26 has markedly improved potency and selectivity as a blocker of the dopamine transporter (DAT) compared to modafinil (IC50 = 49 nM vs. 6,400 nΜ; 130-fold difference).[3]
It has pro-motivational effects in animals and reverses tetrabenazine-induced motivational deficits and depression-like behavior.[1][3] The drug dose-dependently increases extracellular dopamine levels in the nucleus accumbens and prefrontal cortex, does not modify locomotor activity (a measure of psychostimulant-like effect), and slightly enhances spatial memory in animals.[2][3]
There has been interest in (S)-MK-26 as a potential treatment for depression, psychostimulant use disorder (PSUD), Alzheimer's disease, and aging-related disorders.[2][4][3] It was first described by 2022.[3]
See also
[edit]References
[edit]- ^ a b Salamone JD, Correa M (January 2024). "The Neurobiology of Activational Aspects of Motivation: Exertion of Effort, Effort-Based Decision Making, and the Role of Dopamine". Annu Rev Psychol. 75: 1–32. doi:10.1146/annurev-psych-020223-012208. PMID 37788571.
- ^ a b c d Hersey M, Bartole MK, Jones CS, Newman AH, Tanda G (July 2023). "Are There Prevalent Sex Differences in Psychostimulant Use Disorder? A Focus on the Potential Therapeutic Efficacy of Atypical Dopamine Uptake Inhibitors". Molecules. 28 (13): 5270. doi:10.3390/molecules28135270. PMC 10343811. PMID 37446929.
- ^ Shaikh A, Ahmad F, Teoh SL, Kumar J, Yahaya MF (2023). "Targeting dopamine transporter to ameliorate cognitive deficits in Alzheimer's disease". Front Cell Neurosci. 17: 1292858. doi:10.3389/fncel.2023.1292858. PMC 10679733. PMID 38026688.