Concepedia

Author

Lothar Heinisch

Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI)

Also Known As

L Heinisch, L. HEINISCH, L. Heinisch, LOTHAR HEINISCH, Lothar Heinisch

66

Publications

810

Citations

14

H-Index

28

Concepts

All Affiliations

Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI)Robert Koch InstituteGrünenthal Group (Germany)
LH

About

Lothar Heinisch is an author at Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) specializing in medicine, pharmacology, and biochemistry.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

500

2

Biochemistry

4

4

218

3

Natural Sciences

3

3

188

4

Engineering

1

1

17

5

Biomolecular Engineering

1

1

270

Lothar Heinisch

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15

Publications

632

Citations

12

H-Index

YearCitations

Siderophores as drug delivery agents: application of the “Trojan Horse” strategy

Ute Möllmann, Lothar Heinisch, A. Bauernfeind,

BioMetals

2009

270

The<i>Pseudomonas aeruginosa pirA</i>gene encodes a second receptor for ferrienterobactin and synthetic catecholate analogues

Bart Ghysels, Urs A. Ochsner, Ute Möllman,

FEMS Microbiology Letters

2005

87

Highly Antibacterial Active Aminoacyl Penicillin Conjugates with Acylated Bis-Catecholate Siderophores Based on Secondary Diamino Acids and Related Compounds

Lothar Heinisch, Steffen Wittmann, Thomas Stoiber,

Journal of Medicinal Chemistry

2002

63

Madurahydroxylactone Derivatives as Dual Inhibitors of Human Immunodeficiency Virus Type 1 Integrase and RNase H

Christophe Marchand, John A. Beutler, Antony Wamiru,

Antimicrobial Agents and Chemotherapy

2007

38

A novel type of nonsteroidal estrone sulfatase inhibitors

Peter Jütten, Winfried Schumann, Albert Härtl,

Bioorganic & Medicinal Chemistry Letters

2002

30

Fe(III) Coordination Properties of Two New Saccharide-Based Enterobactin Analogues:  Methyl 2,3,4-Tris-<i>O</i>-{<i>N</i>-[2,3-di(hydroxy)benzoyl-glycyl]-aminopropyl}-α-<scp>d</scp>-glucopyranoside and Methyl 2,3,4-Tris-<i>O</i>-{<i>N</i>-[2,3-di-(hydroxy)-benzoyl]-aminopropyl}-α-<scp>d</scp>-glucopyranoside

Suraj Dhungana, Susanne Heggemann, Lothar Heinisch,

Inorganic Chemistry

2001

20

Semisynthetic Derivatives of Madurahydroxylactone and Their Antibacterial Activities.

Lothar Heinisch, Ernst Roemer, Peter Jütten,

The Journal of Antibiotics

1999

18

Growth promotion of synthetic catecholate derivatives on Gram-negative bacteria

Rolf Reissbrodt, Lothar Heinisch, Ute M�llmann,

BioMetals

1993

17

Synthesis and Biological Activity of Trisand Tetrakiscatecholate Siderophores Based on Poly-aza Alkanoic Acids or Alkylbenzoic Acids and their Conjugates with β-Lactam Antibiotics

Lothar Heinisch, Steffen Wittmann, Thomas Stoiber,

Arzneimittelforschung

2011

16

New synthetic catecholate-type siderophores based on amino acids and dipeptides

Matthias Schnabelrauch, Steffen Wittmann, Kerstin Rahn,

BioMetals

2000

14

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