What is he best known for?
The fields of study he is best known for:
- Enzyme
- Organic chemistry
- Catalysis
Stereochemistry, Biochemistry, Enzyme inhibitor, Enzyme and Cyclin-dependent kinase are his primary areas of study.
His Stereochemistry research includes elements of Potency, In vitro, Structure–activity relationship, Mutase and Organic chemistry.
His Structure–activity relationship study combines topics from a wide range of disciplines, such as Binding site and Non-competitive inhibition.
His Enzyme inhibitor research is multidisciplinary, incorporating elements of Benzamide, Chemical synthesis, DNA and Protein kinase A.
His work on Reductase, 2-Methyleneglutarate mutase, Carbon-Oxygen Lyases and Coenzyme B12 is typically connected to Glutamate synthase as part of general Enzyme study, connecting several disciplines of science.
His biological study spans a wide range of topics, including Kinase, Cell biology, Cell growth and Cyclin-dependent kinase 2.
His most cited work include:
- Identification of a highly potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor (NU7441) by screening of chromenone libraries. (304 citations)
- Resistance-modifying agents. 9. Synthesis and biological properties of benzimidazole inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase (247 citations)
- Metagenomic analysis and metabolite profiling of deep-sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill (181 citations)
What are the main themes of his work throughout his whole career to date?
Bernard T. Golding mainly focuses on Stereochemistry, Organic chemistry, Medicinal chemistry, Biochemistry and Enzyme.
His work in Stereochemistry covers topics such as DNA which are related to areas like DNA-Dependent Protein Kinase.
His study in Alkyl, Reagent and Radical falls within the category of Organic chemistry.
Bernard T. Golding has included themes like Intramolecular force and Nucleophile in his Medicinal chemistry study.
His Biochemistry study is mostly concerned with DNA repair and Poly ADP ribose polymerase.
Bernard T. Golding works on Enzyme which deals in particular with Enzyme inhibitor.
He most often published in these fields:
- Stereochemistry (37.66%)
- Organic chemistry (21.55%)
- Medicinal chemistry (17.36%)
What were the highlights of his more recent work (between 2012-2021)?
- Stereochemistry (37.66%)
- Combinatorial chemistry (4.39%)
- Small molecule (3.14%)
In recent papers he was focusing on the following fields of study:
Bernard T. Golding mainly focuses on Stereochemistry, Combinatorial chemistry, Small molecule, Organic chemistry and Biochemistry.
Bernard T. Golding combines subjects such as Acetamide, Structure–activity relationship and Enzyme with his study of Stereochemistry.
His Combinatorial chemistry research incorporates themes from Polymer science and Mdm2 p53.
His study looks at the intersection of Small molecule and topics like Computational biology with Plasma protein binding and Kinase.
In general Organic chemistry, his work in Alkane, Reagent and Alkylbenzenes is often linked to Anaerobic exercise linking many areas of study.
His studies in Biochemistry integrate themes in fields like Microorganism, Methyl group and Anoxic waters.
Between 2012 and 2021, his most popular works were:
- Metagenomic analysis and metabolite profiling of deep-sea sediments from the Gulf of Mexico following the Deepwater Horizon oil spill (181 citations)
- Anaerobic Microbial Degradation of Hydrocarbons : from Enzymatic Reactions to the Environment (126 citations)
- Identification and Characterization of an Irreversible Inhibitor of CDK2. (48 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Organic chemistry
- Catalysis
Bernard T. Golding spends much of his time researching Stereochemistry, Biochemistry, Moiety, Anaerobic bacteria and Structure–activity relationship.
His work deals with themes such as Transferase, Cofactor, Cyclin-dependent kinase 2, Decarboxylation and Reaction mechanism, which intersect with Stereochemistry.
His study deals with a combination of Biochemistry and Benzylsuccinate synthase.
The study incorporates disciplines such as Acetamide, In vitro, Cytotoxicity, Protein kinase A and Morpholine in addition to Moiety.
The concepts of his Anaerobic bacteria study are interwoven with issues in Microorganism, Alkylbenzenes and Anoxic waters.
His Structure–activity relationship research focuses on Binding site and how it relates to Non-competitive inhibition, Ribose and Active site.
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