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Probe Reports from the NIH Molecular Libraries Program [Internet].
Bethesda (MD): National Center for Biotechnology Information (US); 2010-.
Table of contents
Identification of Selective Agonists of the Transient Receptor Potential Channels 3 (TRPML3).
Saldanha SA, Grimm C, Allais C, et al. 2012 Mar 21 [Updated 2013 Sep 3].
Identification of Inhibitors of Trypanosoma brucei Hexokinases.
Sharlow E, Golden JE, Dodson H, et al. 2010 Dec 15 [Updated 2011 Jun 24].
Identification of a Selective Small-Molecule Inhibitor of Breast Cancer Stem Cells—Probe 2.
Carmody LC, Germain A, Morgan B, et al. 2011 Nov 30 [Updated 2014 May 13].
A potent and selective small molecule Kir2.1 inhibitor.
Wu M, Wang H, Yu H, et al. 2010 Feb 26 [Updated 2010 Oct 20].
Small Molecule Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1).
Rai G, Vyjayanti VN, Dorjsuren D, et al. 2010 Oct 29 [Updated 2013 Feb 28].
Selective GPR35 Antagonists - Probe 3.
Heynen-Genel S, Dahl R, Shi S, et al. 2011 Mar 29 [Updated 2011 Nov 21].
Novel Chemical Inhibitor of TRPC4 Channels.
Miller MR, Shi J, Wu M, et al. 2010 Dec 15 [Updated 2011 May 26].
ML238: An Antimalarial Small Molecule of a Unique Structural Class.
Weiwer M, Mulrooney C, Massi D, et al. 2011 Apr 14 [Updated 2011 Dec 12].
Profiling a Selective Probe for RTG Branch of Yeast TORC1 Signaling Pathway.
Chen J, Young SM, Allen C, et al. 2011 Apr 15 [Updated 2013 Feb 25].
A Cell Based Assay for the Identification of Lead Compounds with Anti-Viral Activity Against West Nile Virus.
Chung DH, Ardecky R, Ganji SR, et al. 2010 Feb 27 [Updated 2010 Oct 4].
Discovery, SAR, and Biological Evaluation of a Non-Inhibitory Chaperone for Acid Alpha Glucosidase.
Marugan JJ, Zheng W, Ferrer M, et al. 2011 Dec 16 [Updated 2013 May 3].
5-(4-(4-Acetylphenyl)piperazin-1-ylsulfonyl)indolin-2-one Analogs as Inhibitors of Acid alpha-Glucosidase for Potential Chaperone Treatment of Pompe Disease or Intervention for Diabetes Mellitus Type 2.
Xiao J, Marugan JJ, Zheng W, et al. 2010 Oct 28 [Updated 2013 May 3].
ML365: Development of Bis-Amides as Selective Inhibitors of the KCNK3/TASK1 Two Pore Potassium Channel.
Zou B, Flaherty DP, Simpson DS, et al. 2013 Apr 15 [Updated 2013 Nov 14].
ML345, A Small-Molecule Inhibitor of the Insulin-Degrading Enzyme (IDE).
Bannister TD, Wang H, Abdul-Hay SO, et al. 2012 Dec 17 [Updated 2014 May 13].
ML311: A Small Molecule that Potently and Selectively Disrupts the Protein-Protein Interaction of Mcl-1 and Bim: A Probe for Studying Lymphoid Tumorigenesis.
Bannister T, Koenig M, He Y, et al. 2012 Apr 16 [Updated 2013 Mar 14].
N-(pyridin-4-yl)benzo[d]thiazole-6-carboxamide inhibits E. coli UT189 bacterial capsule biogenesis.
Noah JW, Ananthan S, Evans CW, et al. 2012 Dec 17 [Updated 2013 Apr 5].
Therapeutic Inhibitors of Phosphomannose Isomerase - Probe 1.
Hedrick M, Brown B, Rascon J, et al. 2009 Apr 21 [Updated 2010 Sep 2].
Selective inhibitors of FAS-TE.
Ardecky R, Hedrick MP, Gosalia P, et al. 2013 Apr 12 [Updated 2014 Jan 13].
Campaign to Identify Agonists of Transient Receptor Potential Channels 3 and 2 (TRPML3 & TRPML2).
Saldanha SA, Grimm C, Mercer BA, et al. 2009 Nov 13 [Updated 2011 May 5].
Discovery, SAR and Biological Evaluation of Aryl-thiazol-piperidines as SMN Modulators.
Xiao J, Marugan JJ, Zheng W, et al. 2010 Mar 19 [Updated 2011 May 5].
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