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Results: 17

Cited In for PubMed (Select 15212527)

1.

Rabeprazole exhibits antiproliferative effects on human gastric cancer cell lines.

Gu M, Zhang Y, Zhou X, Ma H, Yao H, Ji F.

Oncol Lett. 2014 Oct;8(4):1739-1744. Epub 2014 Jul 16.

2.

Evaluation of [(11)C]N-Methyl Lansoprazole as a Radiopharmaceutical for PET Imaging of Tau Neurofibrillary Tangles.

Shao X, Carpenter GM, Desmond TJ, Sherman P, Quesada CA, Fawaz M, Brooks AF, Kilbourn MR, Albin RL, Frey KA, Scott PJ.

ACS Med Chem Lett. 2012 Sep 25;3(11):936-41. doi: 10.1021/ml300216t. eCollection 2012 Nov 8.

3.

High affinity radiopharmaceuticals based upon lansoprazole for PET imaging of aggregated tau in Alzheimer's disease and progressive supranuclear palsy: synthesis, preclinical evaluation, and lead selection.

Fawaz MV, Brooks AF, Rodnick ME, Carpenter GM, Shao X, Desmond TJ, Sherman P, Quesada CA, Hockley BG, Kilbourn MR, Albin RL, Frey KA, Scott PJ.

ACS Chem Neurosci. 2014 Aug 20;5(8):718-30. doi: 10.1021/cn500103u. Epub 2014 Jun 16.

PMID:
24896980
4.

Molecular mechanism of inhibition of the mitochondrial carnitine/acylcarnitine transporter by omeprazole revealed by proteoliposome assay, mutagenesis and bioinformatics.

Tonazzi A, Eberini I, Indiveri C.

PLoS One. 2013 Dec 9;8(12):e82286. doi: 10.1371/journal.pone.0082286. eCollection 2013.

5.

Proteoliposomes as tool for assaying membrane transporter functions and interactions with xenobiotics.

Scalise M, Pochini L, Giangregorio N, Tonazzi A, Indiveri C.

Pharmaceutics. 2013 Sep 18;5(3):472-97. doi: 10.3390/pharmaceutics5030472.

6.

High-throughput identification of promiscuous inhibitors from screening libraries with the use of a thiol-containing fluorescent probe.

McCallum MM, Nandhikonda P, Temmer JJ, Eyermann C, Simeonov A, Jadhav A, Yasgar A, Maloney D, Arnold AL.

J Biomol Screen. 2013 Jul;18(6):705-13. doi: 10.1177/1087057113476090. Epub 2013 Feb 27.

7.

Pharmacokinetics and pharmacodynamics of the proton pump inhibitors.

Shin JM, Kim N.

J Neurogastroenterol Motil. 2013 Jan;19(1):25-35. doi: 10.5056/jnm.2013.19.1.25. Epub 2013 Jan 8.

8.

Characterization of a novel potassium-competitive acid blocker of the gastric H,K-ATPase, 1-[5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamine monofumarate (TAK-438).

Shin JM, Inatomi N, Munson K, Strugatsky D, Tokhtaeva E, Vagin O, Sachs G.

J Pharmacol Exp Ther. 2011 Nov;339(2):412-20. doi: 10.1124/jpet.111.185314. Epub 2011 Aug 9.

9.

Novel approaches to inhibition of gastric acid secretion.

Sachs G, Shin JM, Hunt R.

Curr Gastroenterol Rep. 2010 Dec;12(6):437-47. doi: 10.1007/s11894-010-0149-5. Erratum in: Curr Gastroenterol Rep. 2011 Feb;13(1):110.

10.

Strategies for discovering and derisking covalent, irreversible enzyme inhibitors.

Johnson DS, Weerapana E, Cravatt BF.

Future Med Chem. 2010 Jun;2(6):949-64.

11.

1-Arylsulfonyl-2-(pyridylmethylsulfinyl) benzimidazoles as new proton pump inhibitor prodrugs.

Shin JM, Sachs G, Cho YM, Garst M.

Molecules. 2009 Dec 15;14(12):5247-80. doi: 10.3390/molecules14125247.

12.

The gastric HK-ATPase: structure, function, and inhibition.

Shin JM, Munson K, Vagin O, Sachs G.

Pflugers Arch. 2009 Jan;457(3):609-22. doi: 10.1007/s00424-008-0495-4. Epub 2008 Jun 6. Review. Erratum in: Pflugers Arch. 2011 Mar;461(3):399.

13.

Molecular mechanisms in therapy of acid-related diseases.

Shin JM, Vagin O, Munson K, Kidd M, Modlin IM, Sachs G.

Cell Mol Life Sci. 2008 Jan;65(2):264-81. Review. Erratum in: Cell Mol Life Sci. 2011 Mar;68(5):921.

14.

The gastric H,K ATPase as a drug target: past, present, and future.

Sachs G, Shin JM, Vagin O, Lambrecht N, Yakubov I, Munson K.

J Clin Gastroenterol. 2007 Jul;41 Suppl 2:S226-42. Review.

15.

Analysis of the gastric H,K ATPase for ion pathways and inhibitor binding sites.

Munson K, Law RJ, Sachs G.

Biochemistry. 2007 May 8;46(18):5398-417. Epub 2007 Apr 11.

16.
17.

The chemically elegant proton pump inhibitors.

Roche VF.

Am J Pharm Educ. 2006 Oct 15;70(5):101.

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