Location History:
- Pomezia, IT (2009)
- Florence, IT (1985 - 2010)
Company Filing History:
Years Active: 1985-2010
Title: Innovations of Alessandro Giolitti in Pharmaceutical Chemistry
Introduction
Alessandro Giolitti is a notable inventor based in Florence, Italy, recognized for his contributions to pharmaceutical chemistry. With a total of six patents to his name, Giolitti has made significant strides in the development of non-peptide bradykinin antagonists, which have potential applications in treating various medical conditions.
Latest Patents
Giolitti's latest patents include innovative compounds that act as selective antagonists of the bradykinin B2 receptor. One of his key inventions is a non-peptide compound characterized by a specific general formula, where R can be hydrogen or methyl, and W can be a single bond or an oxygen atom. These compounds are designed to treat patients suffering from conditions related to the activation of bradykinin B2 receptors. Another significant patent involves basic non-peptide bradykinin antagonists, which are chemically defined by the presence of an alpha, alpha-disubstituted amino acid. These compounds represent a novel class of medicaments that can be utilized in various disorders linked to bradykinin receptors.
Career Highlights
Throughout his career, Giolitti has worked with prominent companies in the pharmaceutical industry, including A. Menarini S.a.s. and Menarini Ricerche S.p.a. His work has been instrumental in advancing the understanding and treatment of diseases associated with bradykinin receptors.
Collaborations
Giolitti has collaborated with esteemed colleagues such as Carlo Alberto Maggi and Danilo Giannotti, contributing to the collective knowledge and innovation in the field of pharmaceutical research.
Conclusion
Alessandro Giolitti's innovative work in developing non-peptide bradykinin antagonists showcases his significant impact on pharmaceutical chemistry. His contributions continue to pave the way for new treatments and advancements in medical science.