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Probe Reports from the NIH Molecular Libraries Program [Internet].

Probe Reports from the NIH Molecular Libraries Program [Internet].

Bethesda (MD): National Center for Biotechnology Information (US); 2010-.

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Table of contents

Select item 23764741.

Selective KOP Receptor Antagonists: Probe 1.

Hedrick MP, Gosalia P, Frankowski K, et al. 2010 Feb 28 [Updated 2010 Oct 4].

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Select item 23769842.

Selective KOP Receptor Agonists: Probe 1 & Probe 2.

Hedrick MP, Gosalia P, Frankowski K, et al. 2010 Feb 28 [Updated 2010 Oct 4].

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Select item 26473723.

Antagonist for the Kappa Opioid Receptor.

Hedrick MP, Gosalia P, Li K, et al. 2010 Oct 31 [Updated 2011 May 26].

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Select item 30700124.

Optimization and characterization of an opioid kappa receptor (OPRK1) antagonist.

Guerrero M, Urbano M, Brown SJ, et al. 2013 Apr 15 [Updated 2014 Sep 18].

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Select item 30259765.

Identification of Potent and Selective RORγ Antagonists.

Huang W, Wang H, Johnson RL, et al. 2010 Dec 15 [Updated 2013 Feb 25].

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Select item 23595506.

Inhibitors of Protein Folding: DnaK.

Cellitti J, Zhang Z, Wang S, et al. 2009 Jan 15 [Updated 2010 Sep 2].

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Select item 24121327.

Identification of Small Molecule Antagonists of the Neuropeptide-S Receptor.

Patnaik S, Marugan J, Liu K, et al. 2010 Mar 19 [Updated 2010 Dec 16].

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Select item 30341348.

Identification of Small Molecule Inhibitors of Wee1 Degradation and Mitotic Entry.

Simanski S, Madoux F, Rahaim RJ, et al. 2010 Sep 1 [Updated 2013 Mar 22].

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Select item 30406749.

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].

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Select item 331864810.

Development of the First Potent, Selective and CNS penetrant M5 Negative Allosteric Modulator (NAM).

Gentry PR, Kokubo M, Bridges TM, et al. 2013 Dec 9 [Updated 2014 Sep 18].

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Select item 341214811.

SMN Modulator ML372 Increases SMN Protein Abundance, Body Weight, Lifespan, and Rescues Motor Function in SMNΔ7 SMA Mice.

Burnett BG, Xiao J, Southall N, et al. 2013 Dec 15 [Updated 2015 Feb 11].

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Select item 304646012.

Discovery of Novel General Anesthetics Using Apoferritin as a Surrogate System.

Rai G, Bu W, Lea WA, et al. 2012 Apr 16 [Updated 2013 May 8].

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Select item 258056613.

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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Select item 302544614.

A small molecule activator of KCNQ2 and KCNQ4 channels.

Yu H, Wu M, Hopkins C, et al. 2011 Mar 29 [Updated 2013 Feb 28].

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Select item 305089215.

A Small Molecule Inhibitor of the MITF Molecular Pathway.

Faloon PW, Bennion M, Weiner WS, et al. 2012 Dec 13 [Updated 2014 Sep 18].

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Select item 305095816.

Identification of Selective Inhibitors of Phosphofructokinase as Lead Compounds Against Trypanosomiasis.

Walsh MJ, Brimacombe KR, Vásquez-Valdivieso MG, et al. 2011 Oct 18 [Updated 2013 Feb 25].

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Select item 304621417.

Discovery, optimization, and biological activity of the first potent and selective small-molecule agonist series of human relaxin receptor 1 (RXFP1).

Xiao J, Chen CZ, Huang Z, et al. 2012 Mar 10 [Updated 2013 May 8].

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Select item 306059018.

Discovery of ML324, a JMJD2 demethylase inhibitor with demonstrated antiviral activity.

Rai G, Kawamura A, Tumber A, et al. 2012 Dec 17 [Updated 2013 Sep 16].

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Select item 302524019.

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].

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Select item 304635020.

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].

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Supplemental Content

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1H NMR Spectrum (400 MHz, Acetone-d6) of the Probe CID72199308, KSC-392-065

¹³C NMR (101 MHz, Acetone-d₆) δ 172.82, 160.59, 159.11, 158.03, 151.30, 137.76, 132.82, 132.07, 131.58, 130.67, 128.96, 126.42, 124.48, 119.08, 118.30, 113.52, 100.39, 17.49.

Small Molecules Targeting the Mitochondrial Permeability Transition.

Probe Reports from the NIH Molecular Libraries Program [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2010-.
N-(2-(dibenzylamino)ethyl)-4-((4-methylphenylsulfonamido)methyl)benzamide (SID-87457827)

¹HNMR (CDCl₃) δ 2.48 (s, 3 H), 2.73 (t, J = 6.0 Hz, 2 H), 3.50 (dt, J = 4.8, 6.0 Hz, 2 H), 3.65 (s, 4 H), 4.23 (s, 2 H), 4.89 (br, 1 H), 6.45 (br, 1 H), 7.25–7.38 (m, 14 H), 7.54 (d, J = 8.4 Hz, 2 H), 7.82 (d, J = 8.4 Hz, 2 H);

Selective KOP Receptor Antagonists: Probe 1.

Probe Reports from the NIH Molecular Libraries Program [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2010-.
N-(2-(dibenzylamino)ethyl)-4-((4-ethylphenylsulfonamido)methyl)benzamide (SID-87457838)

¹HNMR (CDCl₃) δ 1.30 (t, J = 7.6 Hz, 3 H), 2.69–2.80 (m, 4 H), 3.50 (dt, J = 4.5, 6.4 Hz, 2 H), 3.65 (s, 4 H), 4.24 (s, 2H), 6.44 (br, 1 H), 7.25–7.35 (m, 13 H), 7.38 (d, J = 7.6 Hz, 2 H), 7.55 (d, J = 7.6 Hz, 2 H), 7.84 (d, J = 7.6 Hz);

Selective KOP Receptor Antagonists: Probe 1.

Probe Reports from the NIH Molecular Libraries Program [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2010-.
N-(2-(benzyl(ethyl)amino)ethyl)-4-((4-methylphenylsulfonamido)methyl)benzamide (SID-87457826)

¹H NMR (CDCl₃) δ 1.13 (t, J = 7.2 Hz, 3 H), 2.47 (s, 3 H), 2.64 (q, J = 7.2 Hz, 2 H), 2.69 (t, J = 6.0, 2 H), 3.46 (dt, J = 5.1, 6.0 Hz 2 H), 3.63 (s, 2 H), 4.21 (s, 2 H), 4.84–4.97 (br, 1 H), 6.62–6.69 (br, 1 H), 7.25–7.37 (m, 9 H), 7.59 (d, J = 8.4 Hz, 2 H), 7.81 (d, J =8.4 Hz, 2 H);

Selective KOP Receptor Antagonists: Probe 1.

Probe Reports from the NIH Molecular Libraries Program [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2010-.

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