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Literature DB >> 16562866

Cyclic semipeptoids: peptoid-organic hybrid macrocycles.

Abstract

[structure: see text] Cyclic semipeptoids 1 and 2 represent constrained, secondary structure mimics where the R(1) and R(2) side chains correspond to those of amino acids. Solid-phase syntheses and conformational analyses of these compounds are described.

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Year: 2006 PMID： 16562866 DOI： 10.1021/ol052867d

Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005

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Cited

8 in total

1. Development of homomultimers and heteromultimers of lung cancer-specific peptoids.

Authors: Jared C Hooks; Jaya P Matharage; D Gomika Udugamasooriya
Journal: Biopolymers Date: 2011 Impact factor: 2.505

2. Microwave-assisted synthesis of macrocycles via intramolecular and/or bimolecular Ullmann coupling.

Authors: Li Shen; Charles J Simmons; Dianqing Sun
Journal: Tetrahedron Lett Date: 2012-06-06 Impact factor: 2.415

Review 3. Structure-function relationships in peptoids: recent advances toward deciphering the structural requirements for biological function.

Authors: Sarah A Fowler; Helen E Blackwell
Journal: Org Biomol Chem Date: 2009-02-11 Impact factor: 3.876

4. Piptides: New, Easily Accessible Chemotypes For Interactions With Biomolecules.

Authors: Maritess Arancillo; Jaru Taechalertpaisarn; Xiaowen Liang; Kevin Burgess
Journal: Angew Chem Int Ed Engl Date: 2021-02-04 Impact factor: 15.336

5. A diversity-oriented synthesis strategy enabling the combinatorial-type variation of macrocyclic peptidomimetic scaffolds.

Authors: Albert Isidro-Llobet; Kathy Hadje Georgiou; Warren R J D Galloway; Elisa Giacomini; Mette R Hansen; Gabriela Méndez-Abt; Yaw Sing Tan; Laura Carro; Hannah F Sore; David R Spring
Journal: Org Biomol Chem Date: 2015-04-21 Impact factor: 3.876

Cyclic semipeptoids: peptoid-organic hybrid macrocycles.

1. Development of homomultimers and heteromultimers of lung cancer-specific peptoids.

2. Microwave-assisted synthesis of macrocycles via intramolecular and/or bimolecular Ullmann coupling.

Review 3. Structure-function relationships in peptoids: recent advances toward deciphering the structural requirements for biological function.

4. Piptides: New, Easily Accessible Chemotypes For Interactions With Biomolecules.

5. A diversity-oriented synthesis strategy enabling the combinatorial-type variation of macrocyclic peptidomimetic scaffolds.

6. Association of a peptoid ligand with the apical loop of pri-miR-21 inhibits cleavage by Drosha.

Review 7. Solid-phase synthesis of N-substituted glycine oligomers (alpha-peptoids) and derivatives.

Review 8. Macrocyclic drugs and synthetic methodologies toward macrocycles.