Dipeptide analogues of fluorinated aminophosphonic acid sodium salts as moderate competitive inhibitors of cathepsin C
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Dipeptide analogues of fluorinated aminophosphonic acid sodium salts as moderate competitive inhibitors of cathepsin C ; volume:19 ; year:2023 ; pages:434-439
Beilstein journal of organic chemistry ; 19 (2023), 434-439
- Creator
-
Wątroba, Karolina
Pawełczak, Małgorzata
Kaźmierczak, Marcin
- DOI
-
10.3762/bjoc.19.33
- URN
-
urn:nbn:de:101:1-2409261429009.589090958948
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Wątroba, Karolina
- Pawełczak, Małgorzata
- Kaźmierczak, Marcin
Other Objects (12)
Efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates
Fluorinated Analogues to the Pentuloses of the Pentose Phosphate Pathway
Engineering Enzyme‐Cleavable Oligonucleotides by Automated Solid‐Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers
Engineering Enzyme‐Cleavable Oligonucleotides by Automated Solid‐Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers
Synthesis of Conformationally Restricted and Optically Pure Analogues of Serine-Proline Dipeptide via Aldol Condensation
Untersuchungen zur Selbstassemblierung zyklischer Dipeptide
Fluorinated butatrienes
Dipeptide Synthesis by Two-Component Organocatalysis
Exploration of charge states of balanol analogues acting as ATP-competitive inhibitors in kinases
Solid‐Phase Synthesis of Fluorinated Analogues of Glycosyl 1‐Phosphate Repeating Structures from Leishmania using the Phosphoramidite Method
Verwertung und Resorption eines Gemisches synthetischer Dipeptide
Neue Methoden zur asymmetrischen Synthese nichtproteinogener Dipeptide
Efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates
Fluorinated Analogues to the Pentuloses of the Pentose Phosphate Pathway
Engineering Enzyme‐Cleavable Oligonucleotides by Automated Solid‐Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers
Engineering Enzyme‐Cleavable Oligonucleotides by Automated Solid‐Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers
Synthesis of Conformationally Restricted and Optically Pure Analogues of Serine-Proline Dipeptide via Aldol Condensation
Untersuchungen zur Selbstassemblierung zyklischer Dipeptide
Fluorinated butatrienes
Dipeptide Synthesis by Two-Component Organocatalysis
Exploration of charge states of balanol analogues acting as ATP-competitive inhibitors in kinases
Solid‐Phase Synthesis of Fluorinated Analogues of Glycosyl 1‐Phosphate Repeating Structures from Leishmania using the Phosphoramidite Method
Verwertung und Resorption eines Gemisches synthetischer Dipeptide
Neue Methoden zur asymmetrischen Synthese nichtproteinogener Dipeptide
Efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates
Fluorinated Analogues to the Pentuloses of the Pentose Phosphate Pathway
Engineering Enzyme‐Cleavable Oligonucleotides by Automated Solid‐Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers
Engineering Enzyme‐Cleavable Oligonucleotides by Automated Solid‐Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers
Synthesis of Conformationally Restricted and Optically Pure Analogues of Serine-Proline Dipeptide via Aldol Condensation
Untersuchungen zur Selbstassemblierung zyklischer Dipeptide
Fluorinated butatrienes
Dipeptide Synthesis by Two-Component Organocatalysis
Exploration of charge states of balanol analogues acting as ATP-competitive inhibitors in kinases
Solid‐Phase Synthesis of Fluorinated Analogues of Glycosyl 1‐Phosphate Repeating Structures from Leishmania using the Phosphoramidite Method
Verwertung und Resorption eines Gemisches synthetischer Dipeptide