Design Synthesis and Bioevaluation of Novel Bile Acid Conjugate

dc.contributor.guideDr.Satyendra Mishra
dc.coverage.spatial
dc.creator.researcherPatel Sejal Bipinchandra
dc.date.accessioned2023-02-21T05:10:08Z
dc.date.available2023-02-21T05:10:08Z
dc.date.awarded2022
dc.date.completed2022
dc.date.registered2018
dc.description.abstractnewline This thesis briefly introduces bile acid conjugates and their therapeutic applications. Nature continues to be the main source of motivation for synthetic chemists in their expedition to prepare novel conjugates, which can have different physical, biological and medicinal properties. newlineChapter 1 describes the literature report available on bile acid and bile acid-based conjugates with their therapeutic importance in the development of drug. In recent years, steroid structures have gradually become important in various fields, such as pharmacology, bio-mimetic and supramolecular chemistry, and nanotechnology. The administration of bile acids has received a lot of attention. The drug absorption enhancer ability of bile acid helps to dissolve the drug and penetrate the drug molecule. Therefore, bile acids can increase the bioavailability of drugs with poor water solubility or poor membrane permeability. In addition, the hydroxyl and carboxyl functional groups of bile acids can be used for covalent bonding of biologically active molecules, thereby changing the physicochemical and pharmacokinetic properties of biologically active molecules. Syntheses of hybrid molecules via the combination of two bioactive moieties have appeared as a successful strategy in the development of novel therapeutic agents with excellent potency and lower side effects. With this in mind and fetching an advantage from the prevailing bile acid-based conjugates, we planned to synthesize bile acid-chiral amino alcohols/chalcones/thiadiazoles conjugate. newline newlineChapter 2 describes the synthesis, characterization and antibacterial evaluation of deoxycholic acid-chiral amino alcohol conjugates. Various amino alcohols moieties were appended to the C24 position of deoxycholic acid to yield deoxycholic acid-amino alcohol conjugates. The entire synthesized deoxycholic acid-amino alcohol conjugates were evaluated for their antibacterial activity against . coli and S. aureus using the broth dilution method.
dc.description.note
dc.format.accompanyingmaterialNone
dc.format.dimensions
dc.format.extentX, 206
dc.identifier.urihttp://hdl.handle.net/10603/465232
dc.languageEnglish
dc.publisher.institutionDepartment of Biotechnology and Bioengineering
dc.publisher.placeGandhinagar
dc.publisher.universityInstitute of Advanced Research, Gandhinagar
dc.relation
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordChemistry
dc.subject.keywordChemistry Organic
dc.subject.keywordPhysical Sciences
dc.titleDesign Synthesis and Bioevaluation of Novel Bile Acid Conjugate
dc.title.alternative
dc.type.degreePh.D.

Files

Original bundle

Now showing 1 - 5 of 10
Loading...
Thumbnail Image
Name:
01_title.pdf
Size:
71.11 KB
Format:
Adobe Portable Document Format
Description:
Attached File
Loading...
Thumbnail Image
Name:
05_table of contents.pdf
Size:
132.73 KB
Format:
Adobe Portable Document Format
Loading...
Thumbnail Image
Name:
09_abstract.pdf
Size:
569.13 KB
Format:
Adobe Portable Document Format
Loading...
Thumbnail Image
Name:
10_chapter_1.pdf
Size:
5.95 MB
Format:
Adobe Portable Document Format
Loading...
Thumbnail Image
Name:
11_chapter_2.pdf
Size:
7.51 MB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.79 KB
Format:
Plain Text
Description: