What is he best known for?
The fields of study he is best known for:
José Neptuno Rodríguez-López mainly investigates Tyrosinase, Stereochemistry, Biochemistry, Horseradish peroxidase and Peroxidase.
His Tyrosinase study incorporates themes from Steady state, Enzyme kinetics and Hydroxylation.
He combines subjects such as Catalytic cycle and Active site with his study of Stereochemistry.
His work deals with themes such as Molecular biology and Food science, which intersect with Biochemistry.
The Horseradish peroxidase study combines topics in areas such as Ferric and Hydrogen peroxide.
His work on Cytochrome c peroxidase as part of his general Peroxidase study is frequently connected to ABTS, thereby bridging the divide between different branches of science.
His most cited work include:
- Tyrosinase: a comprehensive review of its mechanism. (899 citations)
- Mechanism of Reaction of Hydrogen Peroxide with Horseradish Peroxidase: Identification of Intermediates in the Catalytic Cycle (203 citations)
- Analysis of a kinetic model for melanin biosynthesis pathway. (185 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Tyrosinase, Stereochemistry, Enzyme, Biochemistry and Substrate.
Tyrosinase is a subfield of Organic chemistry that José Neptuno Rodríguez-López studies.
His Stereochemistry research is multidisciplinary, incorporating perspectives in Active site, Reaction rate constant, Horseradish peroxidase, Oxygen and Histidine.
His work on Tetrahydrobiopterin and Biosynthesis as part of general Enzyme study is frequently linked to Anaerobic exercise, therefore connecting diverse disciplines of science.
His study looks at the relationship between Biochemistry and fields such as Food science, as well as how they intersect with chemical problems.
His Substrate research incorporates elements of Steady state, Partition coefficient and Hydroxylation.
He most often published in these fields:
- Tyrosinase (34.37%)
- Stereochemistry (29.37%)
- Enzyme (27.50%)
What were the highlights of his more recent work (between 2014-2021)?
- Cancer research (11.25%)
- Tyrosinase (34.37%)
- Melanoma (10.00%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Cancer research, Tyrosinase, Melanoma, Cancer and Enzyme.
His Tyrosinase research is multidisciplinary, relying on both Docking, Catalysis, Active site and Substrate, Michaelis–Menten kinetics.
José Neptuno Rodríguez-López works mostly in the field of Docking, limiting it down to topics relating to Chemical shift and, in certain cases, Stereochemistry.
His study looks at the relationship between Substrate and topics such as Electrophilic substitution, which overlap with Hydroxylation, Catalytic cycle and Combinatorial chemistry.
His Michaelis–Menten kinetics research includes themes of Medicinal chemistry and Hydrogen peroxide.
His Enzyme study results in a more complete grasp of Organic chemistry.
Between 2014 and 2021, his most popular works were:
- Targeting the epigenetic machinery of cancer cells. (36 citations)
- Action of tyrosinase on alpha and beta-arbutin: A kinetic study. (30 citations)
- Cinnamate of inulin as a vehicle for delivery of colonic drugs (21 citations)
In his most recent research, the most cited papers focused on:
His primary areas of investigation include Cancer research, Cancer, Tyrosinase, Bioinformatics and Carcinogenesis.
José Neptuno Rodríguez-López interconnects Acetylcholinesterase, Surgical oncology, Cholinergic and Butyrylcholinesterase in the investigation of issues within Cancer research.
The study incorporates disciplines such as Carcinoma, Pathology and Nicotinic agonist in addition to Cancer.
His Tyrosinase research incorporates themes from Docking, Stereochemistry, Cinnamic acid, Catalysis and Chemical shift.
In his work, Cell growth is strongly intertwined with Epigenetics, which is a subfield of Bioinformatics.
The concepts of his Carcinogenesis study are interwoven with issues in Methylation, DNA damage, Cancer cell, Transcription factor and Histone.
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