» Articles » PMID: 21525397

The NCGC Pharmaceutical Collection: a Comprehensive Resource of Clinically Approved Drugs Enabling Repurposing and Chemical Genomics

Overview
Journal Sci Transl Med
Date 2011 Apr 29
PMID 21525397
Citations 227
Authors
Affiliations
Soon will be listed here.
Abstract

Small-molecule compounds approved for use as drugs may be "repurposed" for new indications and studied to determine the mechanisms of their beneficial and adverse effects. A comprehensive collection of all small-molecule drugs approved for human use would be invaluable for systematic repurposing across human diseases, particularly for rare and neglected diseases, for which the cost and time required for development of a new chemical entity are often prohibitive. Previous efforts to build such a comprehensive collection have been limited by the complexities, redundancies, and semantic inconsistencies of drug naming within and among regulatory agencies worldwide; a lack of clear conceptualization of what constitutes a drug; and a lack of access to physical samples. We report here the creation of a definitive, complete, and nonredundant list of all approved molecular entities as a freely available electronic resource and a physical collection of small molecules amenable to high-throughput screening.

Citing Articles

High-throughput screening identifies Aurora kinase B as a critical therapeutic target for Merkel cell carcinoma.

Gelb T, Garman K, Urban D, Coxon A, Gryder B, Hill N Nat Commun. 2025; 16(1):1583.

PMID: 39939315 PMC: 11822212. DOI: 10.1038/s41467-025-56504-7.


Proteasome Inhibitors Induce Apoptosis in Ex Vivo Cells of T-Cell Prolymphocytic Leukemia.

Gasparini V, Rampazzo E, Barila G, Buratin A, Buson E, Calabretto G Int J Mol Sci. 2025; 25(24.

PMID: 39769335 PMC: 11676081. DOI: 10.3390/ijms252413573.


High-throughput screening for small-molecule stabilizers of misfolded glucocerebrosidase in Gaucher disease and Parkinson's disease.

Williams D, Glasstetter L, Jong T, Chen T, Kapoor A, Zhu S Proc Natl Acad Sci U S A. 2024; 121(42):e2406009121.

PMID: 39388267 PMC: 11494340. DOI: 10.1073/pnas.2406009121.


Prediction of chemical-induced acute toxicity using in vitro assay data and chemical structure.

Luo X, Xu T, Ngan D, Xia M, Zhao J, Sakamuru S Toxicol Appl Pharmacol. 2024; 492:117098.

PMID: 39251042 PMC: 11563913. DOI: 10.1016/j.taap.2024.117098.


Revolutionizing adjuvant development: harnessing AI for next-generation cancer vaccines.

Zhang W, Zheng X, Coghi P, Chen J, Dong B, Fan X Front Immunol. 2024; 15:1438030.

PMID: 39206192 PMC: 11349682. DOI: 10.3389/fimmu.2024.1438030.


References
1.
Feasey N, Wansbrough-Jones M, Mabey D, Solomon A . Neglected tropical diseases. Br Med Bull. 2009; 93:179-200. DOI: 10.1093/bmb/ldp046. View

2.
Chong C, Sullivan Jr D . New uses for old drugs. Nature. 2007; 448(7154):645-6. DOI: 10.1038/448645a. View

3.
Blommel M, Blommel A . Pregabalin: an antiepileptic agent useful for neuropathic pain. Am J Health Syst Pharm. 2007; 64(14):1475-82. DOI: 10.2146/ajhp060371. View

4.
Kola I, Landis J . Can the pharmaceutical industry reduce attrition rates?. Nat Rev Drug Discov. 2004; 3(8):711-5. DOI: 10.1038/nrd1470. View

5.
Jacobson J . Thalidomide: a remarkable comeback. Expert Opin Pharmacother. 2001; 1(4):849-63. DOI: 10.1517/14656566.1.4.849. View