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KENNETH KLOTZ, M.D.
M.D.
Internal Medicine Physician
NPI: 1326052200IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
01028628A(IN)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
INDIANA UNIVERSITY SCHOOL OF MEDICINE
Class of 1978
Research & Publications (20)
Mechanism of the iron-mediated alkene aziridination reaction: experimental and computational investigations.
PMID 19102690·Inorg Chem·2009
8-other
Clinical and consumer trial performance of a sensitive immunodiagnostic home test that qualitatively detects low concentrations of sperm following vasectomy.
PMID 18930494·J Urol·2008
3-trial
Non-heme iron(II) complexes are efficient olefin aziridination catalysts.
PMID 17713079·Chem Commun (Camb)·2007
8-other
[3H]HEMADO--a novel tritiated agonist selective for the human adenosine A3 receptor.
PMID 17126322·Eur J Pharmacol·2007
7-preclinical
9-Ethyladenine derivatives as adenosine receptor antagonists: 2- and 8-substitution results in distinct selectivities.
PMID 12734636·Naunyn Schmiedebergs Arch Pharmacol·2003
7-preclinical
Adenosine receptors and their ligands.
PMID 11111832·Naunyn Schmiedebergs Arch Pharmacol·2000
6-review
8-Bromo-9-alkyl adenine derivatives as tools for developing new adenosine A2A and A2B receptors ligands.
PMID 19282184·Bioorg Med Chem·2009
7-preclinical
SCF(Fbxw7/hCdc4) targets cyclin E2 for ubiquitin-dependent proteolysis.
PMID 19084516·Exp Cell Res·2009
8-other
Adenosine A2A receptor antagonists: new 8-substituted 9-ethyladenines as tools for in vivo rat models of Parkinson's disease.
PMID 19343763·ChemMedChem·2009
7-preclinical
Combining selectivity and affinity predictions using an integrated Support Vector Machine (SVM) approach: An alternative tool to discriminate between the human adenosine A(2A) and A(3) receptor pyrazolo-triazolo-pyrimidine antagonists binding sites.
PMID 19501513·Bioorg Med Chem·2009
8-other
N6-Cycloalkyl- and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice.
PMID 19317449·J Med Chem·2009
7-preclinical
Linear and nonlinear 3D-QSAR approaches in tandem with ligand-based homology modeling as a computational strategy to depict the pyrazolo-triazolo-pyrimidine antagonists binding site of the human adenosine A2A receptor.
PMID 18215030·J Chem Inf Model·2008
8-other
Respiration in postharvest sugarbeet roots is not limited by respiratory capacity or adenylates.
PMID 18242773·J Plant Physiol·2008
8-other
Wounding, anoxia and cold induce sugarbeet sucrose synthase transcriptional changes that are unrelated to protein expression and activity.
PMID 17395334·J Plant Physiol·2008
8-other
5'-Carbamoyl derivatives of 2'-C-methyl-purine nucleosides as selective A1 adenosine receptor agonists: affinity, efficacy, and selectivity for A1 receptor from different species.
PMID 17933541·Bioorg Med Chem·2008
7-preclinical
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes.
PMID 18368532·Purinergic Signal·2008
8-other
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure-activity profile.
PMID 18404432·Purinergic Signal·2007
8-other
Synthesis and biological activity of trisubstituted adenines as A 2A adenosine receptor antagonists.
PMID 18066802·Nucleosides Nucleotides Nucleic Acids·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 1481 W 10TH ST
INDIANAPOLIS, IN 46202 - Phone
- (317) 988-2160
Quick Facts
- NPI
- 1326052200
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 48
- Publications
- 20
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