서브메뉴
검색
Efforts Towards the Total Synthesis of Abyssomicin C and Its Derivatives- [electronic resource]
Efforts Towards the Total Synthesis of Abyssomicin C and Its Derivatives- [electronic resource]
- 자료유형
- 학위논문
- Control Number
- 0016932917
- International Standard Book Number
- 9798379866372
- Dewey Decimal Classification Number
- 589
- Main Entry-Personal Name
- Jones, Thane Robinson.
- Publication, Distribution, etc. (Imprint
- [S.l.] : North Carolina State University., 2023
- Publication, Distribution, etc. (Imprint
- Ann Arbor : ProQuest Dissertations & Theses, 2023
- Physical Description
- 1 online resource(128 p.)
- General Note
- Source: Dissertations Abstracts International, Volume: 85-01, Section: B.
- General Note
- Advisor: Bruno-Barcena, Jose;Pierce, Joshua G.
- Dissertation Note
- Thesis (Ph.D.)--North Carolina State University, 2023.
- Restrictions on Access Note
- This item must not be sold to any third party vendors.
- Summary, Etc.
- 요약There is a recognized need for the constant development of novel antibiotic scaffolds to combat pathogenic drug-resistant bacteria. Abyssomicin C is a marine natural product isolated in 2004 from the Sea of Japan which displays activity against MRSA (MIC = 4 μg/mL) and VRSA (MIC = 14 μg/mL). Abyssomicin C is the first compound known to inhibit p-aminobenzoic acid production in bacterial folate biosynthesis, making it a potential lead for the study of new antibacterial agents targeting drug-resistant bacteria. However, the SAR of the abyssomicin scaffold is limited, largely due to the lack of known structural derivatives despite several published syntheses. Abyssomicin C is an exciting synthetic target due to its complex molecular structure. The CG-terpenoid bears 8 stereogenic centers, 5 of which are contiguous throughout a bicyclic spirotetronate core at the base of a 14-membered medium-sized ring. Herein we describe efforts toward a practical, scalable synthetic route to abyssomicin C and potential derivates in order to probe its exciting potential antibacterial lead.
- Subject Added Entry-Topical Term
- Fungi.
- Subject Added Entry-Topical Term
- Cytotoxicity.
- Subject Added Entry-Topical Term
- Biosynthesis.
- Subject Added Entry-Topical Term
- Chemical reactions.
- Subject Added Entry-Topical Term
- Vitamin B.
- Subject Added Entry-Topical Term
- Bacteria.
- Subject Added Entry-Topical Term
- Staphylococcus infections.
- Subject Added Entry-Topical Term
- Chemistry.
- Subject Added Entry-Topical Term
- Hydration.
- Subject Added Entry-Topical Term
- Biological activity.
- Subject Added Entry-Topical Term
- Lithium.
- Subject Added Entry-Topical Term
- Drug resistance.
- Subject Added Entry-Topical Term
- Aqueous solutions.
- Subject Added Entry-Topical Term
- Construction.
- Subject Added Entry-Topical Term
- Oxidation.
- Subject Added Entry-Topical Term
- Antibiotics.
- Subject Added Entry-Topical Term
- Carbon.
- Subject Added Entry-Topical Term
- Bacterial infections.
- Subject Added Entry-Topical Term
- Design.
- Subject Added Entry-Topical Term
- Alcohol.
- Subject Added Entry-Topical Term
- Natural products.
- Subject Added Entry-Topical Term
- Metabolites.
- Subject Added Entry-Topical Term
- Cellular biology.
- Subject Added Entry-Topical Term
- Civil engineering.
- Subject Added Entry-Topical Term
- Organic chemistry.
- Subject Added Entry-Topical Term
- Pathology.
- Subject Added Entry-Topical Term
- Pharmaceutical sciences.
- Subject Added Entry-Topical Term
- Pharmacology.
- Added Entry-Corporate Name
- North Carolina State University.
- Host Item Entry
- Dissertations Abstracts International. 85-01B.
- Host Item Entry
- Dissertation Abstract International
- Electronic Location and Access
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:643903