639 results on '"Avery Mitchell"'
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102. Two Prenylated and C-Methylated Flavonoids fromTripterygium wilfordii
103. Computational Approaches for the Discovery of Cysteine Protease Inhibitors Against Malaria and SARS
104. Design, Synthesis, and Docking Studies of Novel Benzimidazoles for the Treatment of Metabolic Syndrome
105. In vitro erythrocytic uptake studies of artemisinin and selected derivatives using LC–MS and 2D-QSAR analysis of uptake in parasitized erythrocytes
106. Sipholane Triterpenoids: Chemistry, Reversal of ABCB1/P-Glycoprotein-Mediated Multidrug Resistance, and Pharmacophore Modeling
107. (2S,4aR,6aR,7R,9S,10aS,10bR)-7-Carboxy-2-(3-furyl)-6a,10b-dimethyl-4,10-dioxoperhydrobenzo[f]isochromen-9-yl acetate
108. 5-{[(3R,5aS,6R,8aS,9R,10S,12R,12aR)-3,6,9-Trimethylperhydro-3,12-epoxy-1,2-dioxepino[4,3-i]isochromen-10-yl]oxymethyl}benzene-1,3-diol
109. Convenient Synthesis and Evaluation of Biological Activity of Benzyl (2S)-2-[(R)-1-hydroxy-2-oxo-(1-phenethyl)prop-3-ylcarbamoyl]- 4-oxopiperidine- (or -4-oxopyrrolidine)-1-carboxylate as Novel Histone Deacetylase Inhibitors
110. Cycloartane Glycosides from Sutherlandia frutescens
111. Determination of a novel epothilone D analog (AV‐EPO‐106) in human plasma using ultra‐performance liquid chromatography–tandem mass spectrometry
112. 1,3-Diaxially Substituted trans-Decalins: Potential Nonsteroidal Human Progesterone Receptor Inhibitors
113. ChemInform Abstract: Probing the Structures of Leishmanial Farnesyl Pyrophosphate Synthases: Homology Modeling and Docking Studies.
114. (6aR,10aR)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-yl 4-methylbenzenesulfonate
115. Unusual hemiacetal structure derived from Salvinorin A
116. Mollamides B and C, Cyclic Hexapeptides from the Indonesian Tunicate Didemnum molle
117. Nigellidine-4-O-sulfite, the First Sulfated Indazole-Type Alkaloid from the Seeds of Nigella sativa
118. Probing the Structures of Leishmanial Farnesyl Pyrophosphate Synthases: Homology Modeling and Docking Studies
119. Structure-based virtual screening against SARS-3CLpro to identify novel non-peptidic hits
120. Structural Analysis of Farnesyl Pyrophosphate Synthase from Parasitic Protozoa, a Potential Chemotherapeutic Target
121. A Simple Synthesis of 4-Substituted 2-(3-Hydroxy-2-oxo-1-phenethylpropylcarbamoyl) pyrrolidine-1-carboxylic Acid Benzyl Esters as Novel Cysteine Protease Inhibitors
122. Semisynthetic Studies on the Manzamine Alkaloids
123. 7β-Hydroxyartemisinin
124. Type 2 Diabetes and Oral Antihyperglycemic Drugs
125. The Fight Against Drug-Resistant Malaria: Novel Plasmodial Targets and Antimalarial Drugs
126. Total Synthesis and Absolute Configuration of Laurenditerpenol: A Hypoxia Inducible Factor-1 Activation Inhibitor
127. Synthesis of New β-Lactam Analogs and Evaluation of Their Histone Deacetylase (HDAC) Activity
128. Design, Synthesis, and Biological Evaluation of Plasmodium falciparum Lactate Dehydrogenase Inhibitors
129. Targeting the Methyl Erythritol Phosphate (MEP) Pathway for Novel Antimalarial, Antibacterial and Herbicidal Drug Discovery: Inhibition of 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) Enzyme
130. Generation of Oxamic Acid Libraries: Antimalarials and Inhibitors of Plasmodium falciparum Lactate Dehydrogenase
131. An Efficient Synthesis of Cyclic Urethanes from Boc‐Protected Amino Acids Through a Metal Triflate‐Catalyzed Intramolecular Diazocarbonyl Insertion Reaction.
132. A New Library of C-16 Modified Artemisinin Analogs and Evaluation of Their Anti-Parasitic Activities
133. Recent Developments in the Syntheses of the Epothilones and Related Analogues
134. An efficient synthesis of cyclic urethanes from Boc-protected amino acids through a metal triflate-catalyzed intramolecular diazocarbonyl insertion reaction
135. Ligand-supported homology modeling of the human angiotensin II type 1 (AT1) receptor: Insights into the molecular determinants of telmisartan binding
136. Diastereoselective synthesis of (2S,5S)- and (2S,5R)-N-benzyloxycarbonyl-5-hydroxypipecolic acids from trans-4-hydroxy-l-proline
137. Cover Picture: Recent Developments in the Syntheses of the Epothilones and Related Analogues (Eur. J. Org. Chem. 18/2006)
138. Terpenes from Eunicea laciniata and Plexaurella nutans
139. Use of Raman Spectroscopy to Characterize Hydrogenation Reactions
140. Comparative Protein Modeling of 1‐Deoxy‐D‐xylulose‐5‐phosphate Reductoisomerase Enzyme from Plasmodium falciparum: A Potential Target for Antimalarial Drug Discovery.
141. Design and Synthesis of the First Generation of Dithiolane Thiazolidinedione- and Phenylacetic Acid-Based PPARγ Agonists
142. Homology Modeling of G-Protein-Coupled Receptors and Implications in Drug Design
143. Bioassay for the Identification of Natural Product-Based Activators of Peroxisome Proliferator-Activated Receptor-γ (PPARγ): The Marine Sponge Metabolite Psammaplin A Activates PPARγ and Induces Apoptosis in Human Breast Tumor Cells
144. Identification of Novel Parasitic Cysteine Protease Inhibitors by Use of Virtual Screening. 2. The Available Chemical Directory
145. Microbial transformation of artemisinin to 5-hydroxyartemisinin by Eurotium amstelodami and Aspergillus niger
146. The Trimethylsilyl Xylyl (TIX) Ether: A Useful Protecting Group for Alcohols.
147. Total Syntheses of Epothilones B (I) and D (II).
148. The Epothilones and Related Analogues-A Review of Their Syntheses and Anti-Cancer Activities
149. Synthesis and Cyclization Reaction of Pyrazolin‐5‐one Derivatives.
150. Antimalarial Artemisinin Drugs Induce Cytochrome P450 and MDR1 Expression by Activation of Xenosensors Pregnane X Receptor and Constitutive Androstane Receptor
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