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Efforts Towards the Total Synthesis of Abyssomicin C and Its Derivatives- [electronic resource]
Contents Info
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.
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Biosynthesis.
Subject Added Entry-Topical Term  
Chemical reactions.
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Vitamin B.
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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.
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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  
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Control Number  
joongbu:643903
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