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Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups?

ChemMedChem, 2014-11, Vol.9 (11), p.2497-2508

2014

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New Hyaluronic Acid from Plant Origin to Improve Joint Protection—An In Vitro Study

International journal of molecular sciences, 2022-08, Vol.23 (15), p.8114

2022

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Inhalation of the prodrug PI3K inhibitor CL27c improves lung function in asthma and fibrosis

Nature communications, 2018-12, Vol.9 (1), p.5232-16, Article 5232

2018

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In vitro metabolism study of combretastatin A-4 in rat and human liver microsomes

Drug metabolism and disposition, 2007-12, Vol.35 (12), p.2252-2261

2007

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Biological effects of combined resveratrol and vitamin D3 on ovarian tissue

Journal of ovarian research, 2017-09, Vol.10 (1), p.61-14, Article 61

2017

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Metabolic Fate of the Isocyanide Moiety: Are Isocyanides Pharmacophore Groups Neglected by Medicinal Chemists?

Chemical research in toxicology, 2020-04, Vol.33 (4), p.955-966

2020

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An Unexpected Deuterium-Induced Metabolic Switch in Doxophylline

ACS medicinal chemistry letters, 2022-08, Vol.13 (8), p.1278-1285

2022

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Identification of the human UDP-glucuronosyltransferases involved in the glucuronidation of combretastatin A-4

Drug metabolism and disposition, 2010-07, Vol.38 (7), p.1141-1146

2010

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Correction to “An Unexpected Deuterium-Induced Metabolic Switch in Doxophylline”

ACS medicinal chemistry letters, 2023-12, Vol.14 (12), p.1891-1892

2023

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Targeting Transient Receptor Potential Vanilloid 1 (TRPV1) Channel Softly: The Discovery of Passerini Adducts as a Topical Treatment for Inflammatory Skin Disorders

Journal of medicinal chemistry, 2018-05, Vol.61 (10), p.4436-4455

2018

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Regioselective Suzuki Coupling of Dihaloheteroaromatic Compounds as a Rapid Strategy To Synthesize Potent Rigid Combretastatin Analogues

Journal of medicinal chemistry, 2011-07, Vol.54 (14), p.4977-4986

2011

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Identification of potent triazolylpyridine nicotinamide phosphoribosyltransferase (NAMPT) inhibitors bearing a 1,2,3-triazole tail group

European journal of medicinal chemistry, 2019-11, Vol.181, p.111576-111576, Article 111576

2019

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Design, Synthesis, and Biological Evaluation of Combretabenzodiazepines: A Novel Class of Anti-Tubulin Agents

Journal of medicinal chemistry, 2015-02, Vol.58 (3), p.1345-1357

2015

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Pyrtriazoles, a Novel Class of Store-Operated Calcium Entry Modulators: Discovery, Biological Profiling, and in Vivo Proof-of-Concept Efficacy in Acute Pancreatitis

Journal of medicinal chemistry, 2018-11, Vol.61 (21), p.9756-9783

2018

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Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs

ChemMedChem, 2017-09, Vol.12 (18), p.1542-1554

2017

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Semicarbazide Hydrochloride as Impurity in Drug Substances: a Validated LC-DAD-UV Method for Its Determination in Carbazochrome and Carbazochrome Sodium Sulfonate

Chromatographia, 2017-10, Vol.80 (10), p.1535-1544

2017

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Data on metabolic stability, aqueous solubility and CYP inhibition of novel triazole-based nicotinamide phosphoribosyltransferase (NAMPT) inhibitors

Data in brief, 2020-02, Vol.28, p.105034-105034, Article 105034

2020

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A Concise Synthesis of Pyrazole Analogues of CombretastatinA1 as Potent Anti-Tubulin Agents

ChemMedChem, 2013-04, Vol.8 (4), p.633

2013

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Inside Cover: Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups? (ChemMedChem 11/2014)

ChemMedChem, 2014-11, Vol.9 (11), p.2394-2394

2014

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The Metabolic Fate of isoCombretastatin A-4 in Human Liver Microsomes: Identification, Synthesis and Biological Evaluation of Metabolites

ChemMedChem, 2011-10, Vol.6 (10), p.1781-1788

2011

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A Concise Synthesis of Pyrazole Analogues of Combretastatin A1 as Potent Anti-Tubulin Agents

ChemMedChem, 2013-04, Vol.8 (4), p.633-643

2013

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The Metabolic Fate of iso Combretastatin A‐4 in Human Liver Microsomes: Identification, Synthesis and Biological Evaluation of Metabolites

ChemMedChem, 2011-10, Vol.6 (10), p.1781-1788

2011

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Lack of in vitro interactions using human liver microsomes between rabeprazole and anticancer drugs

European journal of drug metabolism and pharmacokinetics, 2009, Vol.34 (1), p.19-26

2009

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Lack ofin vitro interactions using human liver micro-somes between rabeprazole and anticancer drugs

European journal of drug metabolism and pharmacokinetics, 2009-03, Vol.34 (1), p.19-26

2009

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Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups?

New Hyaluronic Acid from Plant Origin to Improve Joint Protection—An In Vitro Study

Inhalation of the prodrug PI3K inhibitor CL27c improves lung function in asthma and fibrosis

In vitro metabolism study of combretastatin A-4 in rat and human liver microsomes

Biological effects of combined resveratrol and vitamin D3 on ovarian tissue

Metabolic Fate of the Isocyanide Moiety: Are Isocyanides Pharmacophore Groups Neglected by Medicinal Chemists?

An Unexpected Deuterium-Induced Metabolic Switch in Doxophylline

Identification of the human UDP-glucuronosyltransferases involved in the glucuronidation of combretastatin A-4

Correction to “An Unexpected Deuterium-Induced Metabolic Switch in Doxophylline”

Targeting Transient Receptor Potential Vanilloid 1 (TRPV1) Channel Softly: The Discovery of Passerini Adducts as a Topical Treatment for Inflammatory Skin Disorders

Identification of Novel Triazole-Based Nicotinamide Phosphoribosyltransferase (NAMPT) Inhibitors Endowed with Antiproliferative and Antiinflammatory Activity

Regioselective Suzuki Coupling of Dihaloheteroaromatic Compounds as a Rapid Strategy To Synthesize Potent Rigid Combretastatin Analogues

Identification of potent triazolylpyridine nicotinamide phosphoribosyltransferase (NAMPT) inhibitors bearing a 1,2,3-triazole tail group

Design, Synthesis, and Biological Evaluation of Combretabenzodiazepines: A Novel Class of Anti-Tubulin Agents

Pyrtriazoles, a Novel Class of Store-Operated Calcium Entry Modulators: Discovery, Biological Profiling, and in Vivo Proof-of-Concept Efficacy in Acute Pancreatitis

Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs

Semicarbazide Hydrochloride as Impurity in Drug Substances: a Validated LC-DAD-UV Method for Its Determination in Carbazochrome and Carbazochrome Sodium Sulfonate

Data on metabolic stability, aqueous solubility and CYP inhibition of novel triazole-based nicotinamide phosphoribosyltransferase (NAMPT) inhibitors

A Concise Synthesis of Pyrazole Analogues of CombretastatinA1 as Potent Anti-Tubulin Agents

Inside Cover: Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups? (ChemMedChem 11/2014)

The Metabolic Fate of isoCombretastatin A-4 in Human Liver Microsomes: Identification, Synthesis and Biological Evaluation of Metabolites

A Concise Synthesis of Pyrazole Analogues of Combretastatin A1 as Potent Anti-Tubulin Agents

The Metabolic Fate of iso Combretastatin A‐4 in Human Liver Microsomes: Identification, Synthesis and Biological Evaluation of Metabolites

Lack of in vitro interactions using human liver microsomes between rabeprazole and anticancer drugs

Lack ofin vitro interactions using human liver micro-somes between rabeprazole and anticancer drugs

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