✦ LIBER ✦

Relationship between structure and intestinal absorption of bile acids with a steroid or side-chain modification

✍ Scribed by Rita Aldini; Aldo Roda; Marco Montagnani; Carolina Cerre; Roberto Pellicciari; Enrico Roda

Book ID: 117213771
Publisher: Elsevier Science
Year: 1996
Tongue: English
Weight: 837 KB
Volume: 61
Category: Article
ISSN: 0039-128X
DOI: 10.1016/s0039-128x(96)00119-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of the Analogues of Lurlenic A

Synthesis of the Analogues of Lurlenic Acid with Modification in the Side-Chain or in the Aromatic Nucleus: Summary of the Structure−Activity Relationships

✍ Shin-ichi Takanashi; Kenji Mori 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 834 KB

Nine analogues of lurlenic acid {(4E,8E,12E)-14-[2Ј-hydroxy-nate (7), butyl lurlenate (8), the bisdemethyl analogue 9, and the 2Ј-deoxy-2Ј-methyl analogue 10. Structural requirements 3Ј,4Ј-dimethyl-5Ј-(1Љ-β-D-xylopyranosyloxy)phenyl]-4,8,12trimethyltetradeca-4,8,12-trienoic acid (1)}, a component of

Relationship between Faecal Bile Acids,

Relationship between Faecal Bile Acids, Absorption of Fat and Vitamin B12, and Serum Lipids in Patients with Ileal Resections

✍ T. A. Miettinen 📂 Article 📅 1971 🏛 John Wiley and Sons 🌐 English ⚖ 918 KB

Bile Acid Derivatives as Ligands of the

Bile Acid Derivatives as Ligands of the Farnesoid X Receptor. Synthesis, Evaluation, and Structure−Activity Relationship of a Series of Body and Side Chain Modified Analogues of Chenodeoxycholic Acid

✍ Pellicciari, Roberto; Costantino, Gabriele; Camaioni, Emidio; Sadeghpour, Bahman 📂 Article 📅 2004 🏛 American Chemical Society 🌐 English ⚖ 217 KB

ChemInform Abstract: Pheromone Synthesis

ChemInform Abstract: Pheromone Synthesis. Part 187. Synthesis of the Analogues of Lurlenic Acid with Modification in the Side-Chain or in the Aromatic Nucleus: Summary of the Structure—Activity Relationships.

✍ S. TAKANASHI; K. MORI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

In order to clarify structure-activity relationships, nine analogues of the title pheromone (I), which are modified in the side-chain or in the aromatic nucleus, are prepared. The structural requirements for the expression of the pheromonal activity is briefly discussed. The work confirms the import