E-LIB Suche - Ergebnisse für: Kirchhoff, Paul D.

1

Discovery of ARD-2051 as a Potent and Orally Efficacious Pr..:

Han, Xin ; Zhao, Lijie ; Xiang, Weiguo...
Journal of Medicinal Chemistry. 66 (2023) 13 - p. 8822-8843 , 2023

Link: https://doi.org/10.1021/..

2

A selective small-molecule STAT5 PROTAC degrader capable of..:

Kaneshige, Atsunori ; Bai, Longchuan ; Wang, Mi...
Nature Chemical Biology. , 2023

Link: https://doi.org/10.1038/..

3

Discovery of a Potent and Selective STAT5 PROTAC Degrader w..:

Kaneshige, Atsunori ; Bai, Longchuan ; Wang, Mi...
Journal of Medicinal Chemistry. 66 (2023) 4 - p. 2717-2743 , 2023

Link: https://doi.org/10.1021/..

4

Discovery of ARD-1676 as a Highly Potent and Orally Efficac..:

Xiang, Weiguo ; Zhao, Lijie ; Han, Xin...
Journal of Medicinal Chemistry. 66 (2023) 18 - p. 13280-13303 , 2023

Link: https://doi.org/10.1021/..

5

Beiträge zur Völkerforschung

[Textband] Veröffentlichungen des Museums für Völkerkunde zu Leipzig ; 11

Anell, Bengt ; Baldus, Herbebt ; Barthel, Thomas... - Reprint 2021 . , [2022]

Link: https://doi.org/10.1515/..

6

Discovery of ARD-2585 as an Exceptionally Potent and Orally..:

Xiang, Weiguo ; Zhao, Lijie ; Han, Xin...
Journal of Medicinal Chemistry. 64 (2021) 18 - p. 13487-13509 , 2021

Link: https://doi.org/10.1021/..

7

Discovery of M-1121 as an Orally Active Covalent Inhibitor ..:

Zhang, Meng ; Aguilar, Angelo ; Xu, Shilin...
Journal of Medicinal Chemistry. 64 (2021) 14 - p. 10333-10349 , 2021

Link: https://doi.org/10.1021/..

8

Optimization of dipeptidic inhibitors of cathepsin L for im..:

Zwicker, Jeffery D. ; Diaz, Nicolas A. ; Guerra, Alfredo J....
Bioorganic & Medicinal Chemistry Letters. 28 (2018) 10 - p. 1972-1980 , 2018

Link: https://doi.org/10.1016/..

9

Utilizing a structure-based docking approach to develop pot..:

Waldschmidt, Helen V. ; Bouley, Renee ; Kirchhoff, Paul D....
Bioorganic & Medicinal Chemistry Letters. 28 (2018) 9 - p. 1507-1515 , 2018

Link: https://doi.org/10.1016/..

10

Structure-Based Design, Synthesis, and Biological Evaluatio..:

Waldschmidt, Helen V. ; Homan, Kristoff T. ; Cruz-Rodríguez, Osvaldo...
Journal of Medicinal Chemistry. 59 (2016) 8 - p. 3793-3807 , 2016

Link: https://doi.org/10.1021/..

11

Inhibitors of TonB Function Identified by a High-Throughput..:

Yep, Alejandra ; McQuade, Thomas ; Kirchhoff, Paul...
mBio. 5 (2014) 2 - p. , 2014

Link: https://doi.org/10.1128/..

12

Optimization of novel nipecotic bis(amide) inhibitors of th..:

Bell, Jessica L. ; Haak, Andrew J. ; Wade, Susan M....
Bioorganic & Medicinal Chemistry Letters. 23 (2013) 13 - p. 3826-3832 , 2013

Link: https://doi.org/10.1016/..

13

X-ray Crystal Structures of the Escherichia coli RNA Polyme..:

Molodtsov, Vadim ; Nawarathne, Irosha N. ; Scharf, Nathan T....
Journal of Medicinal Chemistry. 56 (2013) 11 - p. 4758-4763 , 2013

Link: https://doi.org/10.1021/..

14

Structure-Based Design of Novel Benzoxazinorifamycins with ..:

Gill, Sumandeep K. ; Xu, Hao ; Kirchhoff, Paul D....
Journal of Medicinal Chemistry. 55 (2012) 8 - p. 3814-3826 , 2012

Link: https://doi.org/10.1021/..

15

Property-based design of a glucosylceramide synthase inhibi..:

Larsen, Scott D. ; Wilson, Michael W. ; Abe, Akira...
Journal of Lipid Research. 53 (2012) 2 - p. 282-291 , 2012

Link: https://doi.org/10.1194/..