About this item
- Title
- The Synthesis of Aigialomycin D Analogues
- Content partner
- Victoria University of Wellington
- Collection
- Open Access Victoria University of Wellington
- Description
Aigialomycin D is a fungal natural product possessing kinase inhibition properties. It is a member of a class of compounds known as the resorcylic acid lactones, a expansive group containing compounds exhibiting a vast array of biological activities. These include kinase and Hsp90 inhibition, highly desirable properties in the drug development field. This research project sought to capitalise on previous work involving the successful total synthesis of aigialomycin D. By developing the synthe...
- Format
- Research paper
- Research format
- Scholarly text / Thesis
- Thesis level
- Masters
- Date created
- 2010
- Creator
- Ting, Samuel Z.Y.
- URL
- https://figshare.com/articles/thesis/The_Synthesis_of_Aigialomycin_D_Analogues/16973215
- Related subjects
- Organic chemistry not elsewhere classified / Resorcylic acid lactones / Drug development / Lactones / School: School of Chemical and Physical Sciences / Organic Chemistry not elsewhere classified / Marsden: 250301 Organic Chemical Synthesis / Degree Discipline: Chemistry / Degree Level: Masters / Degree Name: Master of Science
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Report this itemDigitalNZ brings together more than 30 million items from institutions so that they are easy to find and use. This information is the best information we could find on this item. This item was added on 15 November 2021, and updated 08 December 2024.
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