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Exploring the Conformational and Biological Versatility of β-Turn-Modified Gramicidin S by Using Sugar Amino Acid Homologues that Vary in Ring Size.
Published in:
Chemistry - A European Journal, 2011, v. 17, n. 14, p. 3995, doi. 10.1002/chem.201002895
By:
- Knijnenburg, Annemiek D.;
- Tuin, Adriaan W.;
- Spalburg, Emile;
- de Neeling, Albert J.;
- Mars-Groenendijk, Roos H.;
- Noort, Daan;
- Otero, José M.;
- Llamas-Saiz, Antonio L.;
- van Raaij, Mark J.;
- van der Marel, Gijs A.;
- Overkleeft, Herman S.;
- Overhand, Mark
Publication type:
Article
An Adamantyl Amino Acid Containing Gramicidin S Analogue with Broad Spectrum Antibacterial Activity and Reduced Hemolytic Activity.
Published in:
Chemistry - A European Journal, 2010, v. 16, n. 40, p. 12174, doi. 10.1002/chem.201001686
By:
- Kapoerchan, Varsha V.;
- Knijnenburg, Annemiek D.;
- Niamat, Miquel;
- Spalburg, Emile;
- de Neeling, Albert J.;
- Nibbering, Peter H.;
- Mars-Groenendijk, Roos H.;
- Noort, Daan;
- Otero, José M.;
- Llamas-Saiz, Antonio L.;
- van Raaij, Mark J.;
- van der Marel, Gijs A.;
- Overkleeft, Herman S.;
- Overhand, Mark
Publication type:
Article
Ring-Extended Gramicidin S Analogs Containing cis δ-Sugar Amino Acid Turn Mimetics with Varying Ring Size.
Published in:
Helvetica Chimica Acta, 2012, v. 95, n. 12, p. 2544, doi. 10.1002/hlca.201200497
By:
- Knijnenburg, Annemiek D.;
- Spalburg, Emile;
- de Neeling, Albert J.;
- Mars-Groenendijk, Roos H.;
- Noort, Daan;
- Grotenbreg, Gijsbert M.;
- van der Marel, Gijs A.;
- Overkleeft, Herman S.;
- Overhand, Mark
Publication type:
Article
Ring-Extended Derivatives of Gramicidin S with Furanoid Sugar Amino Acids in the Turn Region Have Enhanced Antimicrobial Activity.
Published in:
ChemMedChem, 2009, v. 4, n. 12, p. 1976, doi. 10.1002/cmdc.200900379
By:
- Knijnenburg, Annemiek D.;
- Spalburg, Emile;
- de Neeling, Albert J.;
- Mars-Groenendijk, Roos H.;
- Noort, Daan;
- Grotenbreg, Gijsbert M.;
- van der Marel, Gijsbert A.;
- Overkleeft, Herman S.;
- Overhand, Mark
Publication type:
Article
Discovery of Selective Luteinizing Hormone Receptor Agonists Using the Bivalent Ligand Method.
Published in:
ChemMedChem, 2009, v. 4, n. 7, p. 1189, doi. 10.1002/cmdc.200900058
By:
- Bonger, Kimberly M.;
- van den Berg, Richard J. B. H. N.;
- Knijnenburg, Annemiek D.;
- Heitman, Laura H.;
- van Koppen, Chris J.;
- Timmers, Cornelis M.;
- Overkleeft, Herman S.;
- van der Marel, Gijsbert A.
Publication type:
Article

Found: 5

Exploring the Conformational and Biological Versatility of β-Turn-Modified Gramicidin S by Using Sugar Amino Acid Homologues that Vary in Ring Size.

An Adamantyl Amino Acid Containing Gramicidin S Analogue with Broad Spectrum Antibacterial Activity and Reduced Hemolytic Activity.

Ring-Extended Gramicidin S Analogs Containing cis δ-Sugar Amino Acid Turn Mimetics with Varying Ring Size.

Ring-Extended Derivatives of Gramicidin S with Furanoid Sugar Amino Acids in the Turn Region Have Enhanced Antimicrobial Activity.

Discovery of Selective Luteinizing Hormone Receptor Agonists Using the Bivalent Ligand Method.