Somerville, MA, United States of America

Alan R Jacobson


Average Co-Inventor Count = 1.6

ph-index = 3

Forward Citations = 55(Granted Patents)


Location History:

  • Edmonds, WA (US) (1987)
  • Somerville, MA (US) (1997)

Company Filing History:


Years Active: 1987-1997

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3 patents (USPTO):Explore Patents

Title: Alan R Jacobson: Innovator in Medicinal Chemistry

Introduction

Alan R Jacobson is a notable inventor based in Somerville, MA (US). He has made significant contributions to the field of medicinal chemistry, particularly in the development of compounds that target matrix metalloproteinases. With a total of 3 patents, his work has implications for treating various diseases, including osteoarthritis and rheumatoid arthritis.

Latest Patents

Jacobson's latest patents include innovative compounds such as amino acid amides of 1,3,4-thiadiazoles, which are designed to inhibit matrix metalloproteinase enzymes and prevent cartilage degradation. These compounds offer methods for treating diseases caused by the over-activity of these enzymes. Another significant patent involves bile acid inhibitors of metalloproteinase enzymes, which describes a bile acid derivative that can inhibit metalloproteinase activity. This invention also outlines methods for therapeutically treating diseases that can be ameliorated by inhibiting these enzymes.

Career Highlights

Throughout his career, Jacobson has worked with various companies, including Osteoarthritis Sciences, Inc. and Proscript, Inc. His expertise in medicinal chemistry has allowed him to develop groundbreaking solutions for complex health issues.

Collaborations

Jacobson has collaborated with notable professionals in his field, including Jozef Oleksyszyn and Douglas G Gabler. These partnerships have contributed to the advancement of his research and the successful development of his patented inventions.

Conclusion

Alan R Jacobson's contributions to medicinal chemistry through his innovative patents highlight his role as a key inventor in the field. His work continues to influence the development of treatments for diseases related to matrix metalloproteinases.

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