What is he best known for?
The fields of study he is best known for:
- Enzyme
- Organic chemistry
- Gene
His main research concerns Stereochemistry, Chemical synthesis, Structure–activity relationship, Adenosine receptor and Biochemistry.
His Stereochemistry research is multidisciplinary, incorporating elements of Tubulin and Biological activity.
His research in Chemical synthesis intersects with topics in Bicyclic molecule, Aryl and Moiety.
His work deals with themes such as Purinergic receptor, Combretastatin A-4, Piperazine, Phenylpiperazine and Cytotoxicity, which intersect with Structure–activity relationship.
His study in Adenosine receptor is interdisciplinary in nature, drawing from both Ligand binding assay, Adenosine and Carboxamide.
The various areas that Romeo Romagnoli examines in his Biochemistry study include Molecule and Combretastatin.
His most cited work include:
- DNA minor groove binders as potential antitumor and antimicrobial agents (295 citations)
- MASTERING BETA -KETO ESTERS (171 citations)
- [(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors. (135 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Stereochemistry, Adenosine receptor, Biochemistry, Chemical synthesis and Structure–activity relationship.
His biological study spans a wide range of topics, including Thiophene, Biological activity, In vitro and Tubulin.
His Tubulin research is multidisciplinary, relying on both Cell cycle and Cell growth.
The concepts of his Adenosine receptor study are interwoven with issues in Allosteric regulation, Adenosine and Pharmacology.
He interconnects Amidine, Cytotoxicity, Pyrazole, Bicyclic molecule and Carboxamide in the investigation of issues within Chemical synthesis.
His work carried out in the field of Structure–activity relationship brings together such families of science as Indole test, HeLa, Thiazole and Antimitotic Agent.
He most often published in these fields:
- Stereochemistry (59.45%)
- Adenosine receptor (24.02%)
- Biochemistry (20.87%)
What were the highlights of his more recent work (between 2012-2021)?
- Stereochemistry (59.45%)
- Structure–activity relationship (18.50%)
- Tubulin (14.17%)
In recent papers he was focusing on the following fields of study:
Romeo Romagnoli mainly focuses on Stereochemistry, Structure–activity relationship, Tubulin, Combretastatin and Thiophene.
He has researched Stereochemistry in several fields, including Apoptosis, Aryl and In vitro.
His Structure–activity relationship study combines topics from a wide range of disciplines, such as Function, HeLa, Receptor, Pyrazole and Thiazole.
His Tubulin study incorporates themes from Cell cycle and Cell growth.
His Combretastatin research incorporates themes from Tubulin Modulators, Chorioallantoic membrane, Tubulin Binding Agent, Pharmacology and Colchicine.
Romeo Romagnoli studied Thiophene and Allosteric regulation that intersect with Enhancer.
Between 2012 and 2021, his most popular works were:
- A3 Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy. (67 citations)
- Synthesis and biological evaluation of 2-(alkoxycarbonyl)-3-anilinobenzo[b]thiophenes and thieno[2,3-b]pyridines as new potent anticancer agents (62 citations)
- TRR469, a potent A1 adenosine receptor allosteric modulator, exhibits anti-nociceptive properties in acute and neuropathic pain models in mice (38 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Organic chemistry
- Gene
Romeo Romagnoli mainly focuses on Stereochemistry, Tubulin, Structure–activity relationship, In vitro and Moiety.
He merges many fields, such as Stereochemistry and Selectivity, in his writings.
In his study, Stereoisomerism, Antimitotic Agent and Propidium iodide is strongly linked to Cell growth, which falls under the umbrella field of Tubulin.
The Structure–activity relationship study combines topics in areas such as Apoptosis and Cytochrome c.
His In vitro study is focused on Biochemistry in general.
His work is dedicated to discovering how Moiety, Aryl are connected with Tubulin Modulators, Syngenic and Biological activity and other disciplines.
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