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Empirical Analysis of Drug Targets for Nervous System Disorders.
Mueller, Louis G; Slusher, Barbara S; Tsukamoto, Takashi.
Affiliation
  • Mueller LG; Division of Geriatric Medicine and Gerontology, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
  • Slusher BS; Johns Hopkins Drug Discovery, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, United States.
  • Tsukamoto T; Johns Hopkins Drug Discovery, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, United States.
ACS Chem Neurosci ; 15(3): 394-399, 2024 02 07.
Article in En | MEDLINE | ID: mdl-38237559
ABSTRACT
The discovery and development of drugs to treat diseases of the nervous system remains challenging. There is a higher attrition rate in the clinical stage for nervous system experimental drugs compared to other disease areas. In the preclinical stage, additional challenges arise from the considerable effort required to find molecules that penetrate the blood-brain barrier (BBB) coupled with the poor predictive value of many preclinical models of nervous system diseases. In the era of target-based drug discovery, the critical first step of drug discovery projects is the selection of a therapeutic target which is largely driven by its presumed pathogenic involvement. For nervous system diseases, however, the feasibility of identifying potent molecules within the stringent range of molecular properties necessary for BBB penetration should represent another important factor in target selection. To address the latter, the present review analyzes the distribution of human protein targets of FDA-approved drugs for nervous system disorders and compares it with drugs for other disease areas. We observed a substantial difference in the distribution of therapeutic targets across the two clusters. We expanded on this finding by analyzing the physicochemical properties of nervous and non-nervous system drugs in each target class by using the central nervous system multiparameter optimization (CNS MPO) algorithm. These data may serve as useful guidance in making more informed decisions when selecting therapeutic targets for nervous system disorders.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Central Nervous System Diseases / Nervous System Diseases Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: ACS Chem Neurosci Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Central Nervous System Diseases / Nervous System Diseases Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: ACS Chem Neurosci Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States