Functional Group Mimicry

Functional Group Mimicry is a nonclassical bioisosteric strategy in medicinal chemistry whereby a substituent or moiety functions as a bioisostere by emulating the electronic, steric, or pharmacophoric properties of a reference functional group despite differing in chemical structure.

4

Publications

199

Citations

16

Authors

7

Institutions

Publications per year

2017–2026

0

Authors

16

  1. FE
    Floyd E. Romesberg

    Scripps Research Institute, United States

    1 publications · 51 citations

    1

    h-index

  2. TL
    Thomas Lavergne

    Centre National de la Recherche Scientifique, France

    1 publications · 51 citations

    1

    h-index

  3. JR
    James R. Williamson

    Scripps Research Institute, United States

    1 publications · 51 citations

    1

    h-index

  4. DJ
    D.H. Juers

    Whitman College, United States

    1 publications · 52 citations

    1

    h-index

  5. RL
    Rajan Lamichhane

    Scripps Research Institute, United States

    1 publications · 51 citations

    1

    h-index

1–5 of 16

Venues

  1. ACS Chemical Biology

    1 publications · 51 citations

    1

    h-index

  2. The Journal of Organic Chemistry

    JOC · 1 publications · 67 citations

    1

    h-index

  3. 1

    h-index

  4. Biochemistry

    1 publications · 52 citations

    1

    h-index

  5. Organic Letters

    OL · 1 publications · 18 citations

1–5