D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 40 Citations 5,598 164 World Ranking 14935 National Ranking 1114

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Enzyme
  • Hydrogen

His scientific interests lie mostly in Tautomer, Organic chemistry, Enzyme, Stereochemistry and Xanthine. His Tautomer study combines topics in areas such as Combinatorial chemistry and Prodrug. His work in the fields of Organic chemistry, such as Scientific method, overlaps with other areas such as Benzene derivatives.

His work deals with themes such as Enantiomer, Inhibitory effect and Diastereomer, which intersect with Enzyme. His Stereochemistry research integrates issues from Oral administration and Stereoisomerism. Matthias Eckhardt has included themes like Enzyme assay, Linagliptin and Enzyme inhibitor in his Xanthine study.

His most cited work include:

  • Empagliflozin, a novel selective sodium glucose cotransporter-2 (SGLT-2) inhibitor: characterisation and comparison with other SGLT-2 inhibitors. (361 citations)
  • (R)-8-(3-amino-piperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors. (268 citations)
  • 8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes. (239 citations)

What are the main themes of his work throughout his whole career to date?

Matthias Eckhardt focuses on Tautomer, Stereochemistry, Organic chemistry, Xanthine and Enantiomer. His biological study spans a wide range of topics, including Diastereomer, Enzyme, Prodrug, Combinatorial chemistry and Inhibitory effect. His Enzyme research is multidisciplinary, incorporating elements of Salt and Diabetes mellitus.

In his research, Medicinal chemistry is intimately related to Alkyl, which falls under the overarching field of Stereochemistry. His Scientific method, Imidazole and Benzonitrile study in the realm of Organic chemistry connects with subjects such as Benzene derivatives. His study in Xanthine is interdisciplinary in nature, drawing from both Substituent, Dipeptidylpeptidase iv and Dipeptidyl peptidase.

He most often published in these fields:

  • Tautomer (42.15%)
  • Stereochemistry (37.19%)
  • Organic chemistry (26.45%)

What were the highlights of his more recent work (between 2010-2020)?

  • Combinatorial chemistry (16.53%)
  • Receptor (4.13%)
  • Stereochemistry (37.19%)

In recent papers he was focusing on the following fields of study:

His main research concerns Combinatorial chemistry, Receptor, Stereochemistry, Free fatty acid receptor 1 and Tautomer. His Scientific method research extends to the thematically linked field of Combinatorial chemistry. His Stereochemistry study incorporates themes from Amino acid, Benzene and Enzyme.

His work in the fields of Dehydrogenase overlaps with other areas such as Biological activity. His Tautomer research is multidisciplinary, incorporating perspectives in Prodrug, Enzyme assay, Inhibitory effect and Xanthine. In his research on the topic of Xanthine, Medicinal chemistry is strongly related with Salt.

Between 2010 and 2020, his most popular works were:

  • Empagliflozin, a novel selective sodium glucose cotransporter-2 (SGLT-2) inhibitor: characterisation and comparison with other SGLT-2 inhibitors. (361 citations)
  • Long-term treatment with empagliflozin, a novel, potent and selective SGLT-2 inhibitor, improves glycaemic control and features of metabolic syndrome in diabetic rats. (42 citations)
  • Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor. (19 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Enzyme
  • Diabetes mellitus

His primary areas of investigation include Receptor, Stereochemistry, Diabetes mellitus, Free fatty acid receptor 1 and Organic chemistry. His research on Receptor often connects related topics like Combinatorial chemistry. His studies deal with areas such as Dehydrogenase, Enzyme and Dyslipidemia as well as Stereochemistry.

His work carried out in the field of Diabetes mellitus brings together such families of science as Urinary system and Excretion. His research ties Amino acid and Organic chemistry together. His Salt study combines topics from a wide range of disciplines, such as Organic acid, Prodrug, Enantiomer and Tautomer.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Empagliflozin, a novel selective sodium glucose cotransporter-2 (SGLT-2) inhibitor: characterisation and comparison with other SGLT-2 inhibitors.

R. Grempler;L. Thomas;M. Eckhardt;F. Himmelsbach.
Diabetes, Obesity and Metabolism (2012)

640 Citations

(R)-8-(3-amino-piperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors.

Leo Thomas;Matthias Eckhardt;Elke Langkopf;Moh Tadayyon.
Journal of Pharmacology and Experimental Therapeutics (2008)

423 Citations

8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes.

Matthias Eckhardt;Elke Langkopf;Michael Mark;Moh Tadayyon.
Journal of Medicinal Chemistry (2007)

381 Citations

8-[3-amino-piperidin-1-yl]-xanthines, the production thereof and the use of the same as medicaments

Frank Himmelsbach;Elke Langkopf;Matthias Eckhardt;Michael Mark.
(2003)

231 Citations

Glucopyranosyl-substituted phenyl derivatives, medicaments containing such compounds, their use and process for their manufacture

Matthias Eckhardt;Peter Eickelmann;Frank Himmelsbach;Edward Leon Barsoumian.
(2005)

224 Citations

8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions

Frank Himmelsbach;Elke Langkopf;Matthias Eckhardt;Michael Mark.
(2008)

201 Citations

Novel substituted imidazo-pyridinones and imidazo-pyridazeiones, the production and use thereof as medicaments

Hauel Norbert;Himmelsbach Frank;Langkopf Elke;Eckhardt Mathias.
(2003)

199 Citations

Glucopyranosyl-substituted benzyl-benzene derivatives, medicaments containing such compounds, their use and process for their manufacture

Matthias Eckhardt;Frank Himmelsbach;Peter Eickelmann;Leo Thomas.
(2006)

197 Citations

Glucopyranosyl-substituted benzonitrile derivatives, pharmaceutical compositions containing such compounds, their use and process for their manufacture

Matthias Eckhardt;Frank Himmelsbach;Peter Eickelmann;Achim Sauer.
(2007)

165 Citations

Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions

Frank Himmelsbach;Michael Mark;Matthias Eckhardt;Elke Langkopf.
(2003)

165 Citations

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