Hochschulschrift
Preparation, properties and pharmacological testing of sulfonic acid nitrophenyl esters : towards the development of sulfonic acid prodrugs of P1 and P2 receptor antagonists with potential peroral bioavailability
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Language
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Englisch
- Notes
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Bonn, Univ., Diss., 2002
- Creator
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Luo, Yan
- URN
-
urn:nbn:de:hbz:5n-01083
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:36 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Luo, Yan
Other Objects (12)
Preparation, properties and pharmacological testing of sulfonic acid nitrophenyl esters : towards the development of sulfonic acid prodrugs of P1 and P2 receptor antagonists with potential peroral bioavailability
Phthalidyl Ester Prodrugs by Catalytic Asymmetric Acetalization of Carboxylic Acids
Einfluss von Cyclodextrinen auf die enzymatische Spaltung peroral applizierter Prodrugs
Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs
Nucleic Acids as a Nature‐Inspired Scaffold for Macromolecular Prodrugs of Nucleoside Analogues
Investigation of Carboxylic Acid Isosteres and Prodrugs for Inhibition of the Human SIRT5 Lysine Deacylase Enzyme **
Investigation of Carboxylic Acid Isosteres and Prodrugs for Inhibition of the Human SIRT5 Lysine Deacylase Enzyme **
Deprotection of 2,2-Dimethyl-2-(o-nitrophenyl) acetyl (DMNA) Group in Amino Acids and Peptides
Dipeptide Synthesis from S-2-Formyl-4-Nitrophenyl Thioesters and Amino Acid Salts
Sustained release of 5-aminosalicylic acid from azoreductase-responsive polymeric prodrugs for prolonged colon-targeted colitis therapy
Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs
Modified peroral pyloromyotomy and placement of a covered stent for refractory gastric outlet obstruction following ingestion of sulfuric acid
Preparation, properties and pharmacological testing of sulfonic acid nitrophenyl esters : towards the development of sulfonic acid prodrugs of P1 and P2 receptor antagonists with potential peroral bioavailability
Phthalidyl Ester Prodrugs by Catalytic Asymmetric Acetalization of Carboxylic Acids
Einfluss von Cyclodextrinen auf die enzymatische Spaltung peroral applizierter Prodrugs
Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs
Nucleic Acids as a Nature‐Inspired Scaffold for Macromolecular Prodrugs of Nucleoside Analogues
Investigation of Carboxylic Acid Isosteres and Prodrugs for Inhibition of the Human SIRT5 Lysine Deacylase Enzyme **
Investigation of Carboxylic Acid Isosteres and Prodrugs for Inhibition of the Human SIRT5 Lysine Deacylase Enzyme **
Deprotection of 2,2-Dimethyl-2-(o-nitrophenyl) acetyl (DMNA) Group in Amino Acids and Peptides
Dipeptide Synthesis from S-2-Formyl-4-Nitrophenyl Thioesters and Amino Acid Salts
Sustained release of 5-aminosalicylic acid from azoreductase-responsive polymeric prodrugs for prolonged colon-targeted colitis therapy
Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs
Modified peroral pyloromyotomy and placement of a covered stent for refractory gastric outlet obstruction following ingestion of sulfuric acid
Preparation, properties and pharmacological testing of sulfonic acid nitrophenyl esters : towards the development of sulfonic acid prodrugs of P1 and P2 receptor antagonists with potential peroral bioavailability
Phthalidyl Ester Prodrugs by Catalytic Asymmetric Acetalization of Carboxylic Acids
Einfluss von Cyclodextrinen auf die enzymatische Spaltung peroral applizierter Prodrugs
Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs
Nucleic Acids as a Nature‐Inspired Scaffold for Macromolecular Prodrugs of Nucleoside Analogues
Investigation of Carboxylic Acid Isosteres and Prodrugs for Inhibition of the Human SIRT5 Lysine Deacylase Enzyme **
Investigation of Carboxylic Acid Isosteres and Prodrugs for Inhibition of the Human SIRT5 Lysine Deacylase Enzyme **
Deprotection of 2,2-Dimethyl-2-(o-nitrophenyl) acetyl (DMNA) Group in Amino Acids and Peptides
Dipeptide Synthesis from S-2-Formyl-4-Nitrophenyl Thioesters and Amino Acid Salts
Sustained release of 5-aminosalicylic acid from azoreductase-responsive polymeric prodrugs for prolonged colon-targeted colitis therapy
Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs