505 results on '"D'AURIA, MARIA VALERIA"'
Search Results
152. Solomonamides A and B, New Anti-inflammatory Peptides from Theonella swinhoei
153. Towards new ligands of nuclear receptors. Discovery of malaitasterol A, an unique bis-secosterol from marine sponge Theonella swinhoei
154. Solomonsterols A and B from Theonella swinhoei. The First Example of C-24 and C-23 Sulfated Sterols from a Marine Source Endowed with a PXR Agonistic Activity
155. ChemInform Abstract: Crellastatin A: A Cytotoxic Bis-Steroid Sulfate from the Vanuatu Marine Sponge Crella sp.
156. ChemInform Abstract: Isolation and Structural Elucidation of the Crellastatins I-M: Cytotoxic Bis-Steroid Derivatives from the Vanuatu Marine Sponge Crella sp.
157. ChemInform Abstract: Dysidotronic Acid, a New and Selective Human Phospholipase A2 Inhibitor from the Sponge Dysidea sp.
158. ChemInform Abstract: Studies Towards the Synthesis of Superstolide A (I). Synthesis and Stereochemical Assignment of the C(21)-C(26) Fragment (II) of Superstolide A.
159. ChemInform Abstract: Isolation of Callipeltins A-C and of Two New Open-Chain Derivatives of Callipeltin A from the Marine Sponge Latrunculia sp. A Revision of the Stereostructure of Callipeltins.
160. ChemInform Abstract: Coscinolactams A and B: New Nitrogen‐Containing Sesterterpenoids from the Marine Sponge Coscinoderma mathewsi Exerting Antiinflammatory Properties.
161. Synthetic studies on homophymine A: stereoselective synthesis of (2R,3R,4R,6R)-3-hydroxy-2,4,6-trimethyloctanoic acid
162. ChemInform Abstract: Jaspamides M—P: New Tryptophan Modified Jaspamide Derivatives from the Sponge Jaspis splendans
163. Homophymines B–E and A1–E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp.
164. ChemInform Abstract: Homophymine A, an anti-HIV Cyclodepsipeptide from the Sponge Homophymia sp.
165. Homophymine A, an Anti-HIV Cyclodepsipeptide from the Sponge Homophymia sp.
166. ChemInform Abstract: Total Synthesis of Natural Products (2005)
167. New Jaspamide Derivatives with Antimicrofilament Activity from the Sponge Jaspis splendans.
168. Isolation and Structural Elucidation of Callipeltins J—M: Antifungal Peptides from the Marine Sponge Latrunculia sp.
169. Callipeltins F—I: New Antifungal Peptides from the Marine Sponge Latrunculia sp.
170. The Molecular Mechanism of Bee Venom Phospholipase A2 Inactivation by Bolinaquinone
171. Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound.
172. Quantum Mechanical Calculation of Coupling Constants in the Configurational Analysis of Flexible Systems: Determination of the Configuration of Callipeltin A
173. Concise Synthesis of All Stereoisomers of β-Methoxytyrosine and Determination of the Absolute Configuration of the Residue in Callipeltin A
174. Modulatory Effect of Bolinaquinone, a Marine Sesquiterpenoid, on Acute and Chronic Inflammatory Processes
175. Isolation of callipeltins A–C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins
176. Stereoselective synthesis of (2R,3R,4R)-3-hydroxy-2,4,6-trimethylheptanoic acid and determination of the absolute stereochemistry of the natural product from callipeltin A
177. Synthetic studies on callipeltin A: stereoselective synthesis of (2 R ,3 R ,4 S )-3-hydroxy-2,4,6-trimethylheptanoic acid
178. Stereochemistry of Sphinxolides and Reidispongiolides. Asymmetric Synthesis of the C17−C22 Fragment of Reidispongiolide A
179. Cover Picture
180. Studies towards the synthesis of superstolide A. Synthesis and stereochemical assignment of the C(21)C(26) fragment of superstolide A
181. New Sesquiterpene Derivatives from the Sponge Dysidea Species with a Selective Inhibitor Profile against Human Phospholipase A2 and Other Leukocyte Functions
182. ChemInform Abstract: Amphiasterins: A New Family of Cytotoxic Metabolites from the Marine Sponge Plakortis quasiamphiaster
183. Stereochemical Studies on Sphinxolide: Advances in theJ-Based NMR Determination of the Relative Configuration of Flexible Systems
184. New Isomalabaricane Derivatives from a New Species of Jaspis Sponge Collected at the Vanuatu Islands
185. Dysidotronic acid, a new and selective human phospholipase A2 inhibitor from the sponge Dysidea sp.
186. Bioactive Cembrane Derivatives from the Indian Ocean Soft Coral, Sinularia kavarattiensis.
187. Design, Synthesis, and BiologicalEvaluation of PotentDual Agonists of Nuclear and Membrane Bile Acid Receptors.
188. Solomonsterol A, a Marine Pregnane-X-Receptor Agonist, Attenuates Inflammation and Immune Dysfunction in a Mouse Model of Arthritis.
189. New Jaspamide Derivatives from the Marine Sponge Jaspis splendans Collected in Vanuatu
190. On the Composition of Sulfated Polyhydroxysteroids in Some Ophiuroids and the Structure Determination of Six New Constituents
191. HIV-Inhibitory Natural Products. 11. Comparative Studies of Sulfated Sterols from Marine Invertebrates
192. BindingMechanism of the Farnesoid X Receptor Marine Antagonist Suvanine Revealsa Strategy To Forestall Drug Modulation on Nuclear Receptors. Design,Synthesis, and Biological Evaluation of Novel Ligands.
193. Isolation and Structure Characterization of Two Novel Bioactive Sulphated Polyhydroxysteroids from the Antarctic OphiuroidOphioderma longicaudum
194. Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei.
195. Plakilactones from theMarine Sponge Plakinastrellamamillaris. Discovery of a New Class of Marine Ligands ofPeroxisome Proliferator-Activated Receptor γ.
196. Quantitative NMR-Derived Interproton Distances Combined with Quantum Mechanical Calculations of 13C Chemical Shifts in the Stereochemical Determination of Conicasterol F, a Nuclear Receptor Ligand from Theonella swinhoei.
197. Synthesis of 24-methyl-26-hydroxysteroid side-chains: models for stereochemical assignments in polyhydroxylated marine steroids
198. Stereochemical assignment at C-24 and C-25 of marine 24-ethyl-26-hydroxy steroids through comparison with synthetic (24S,25S)-, (24S,25R)-, (24R,25R)-, and (24R,25S)-models
199. Stereochemical Studies on Sphinxolide: Advances in the J-Based NMR Determination of the Relative Configuration of Flexible Systems.
200. Stereoselective synthesis of (2 R,3 R,4 R)-3-hydroxy-2,4,6-trimethylheptanoic acid and determination of the absolute stereochemistry of the natural product from callipeltin A
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.