Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tukaram S. Ingole"'
Autor:
Kuruppanthara N. Vijayadas, K. N. Chaitanya, Rajesh G. Gonnade, Tukaram S. Ingole, Amol S. Kotmale, Gangadhar J. Sanjayan, P. R. Rajamohanan, Rupesh L. Gawade
Publikováno v:
European Journal of Organic Chemistry. 2016:1380-1388
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2120270260d6ba180a42502d3efdcff
https://doi.org/10.1002/ejoc.201501558
https://doi.org/10.1002/ejoc.201501558
Autor:
Gangadhar J. Sanjayan, Rajesh G. Gonnade, Pattuparambil R. Rajamohanan, Rupesh L. Gawade, Tukaram S. Ingole, Amol S. Kotmale
Publikováno v:
New Journal of Chemistry. 40:9205-9210
This paper describes the consequences of incorporating a constrained heterocyclic aromatic β-amino acid 3-aminothiophenecarboxylic acid (3-Atc) into peptides containing β-turn forming elements such as Pro-Gly motif and the effect on the secondary s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8020bf670f22d3dcf690561aa837491a
https://doi.org/10.1039/c6nj01667g
https://doi.org/10.1039/c6nj01667g
Publikováno v:
Chem. Commun.. 50:13874-13884
Structural mimicry of peptides has witnessed perceptible progress in the last three decades. Reverse turn and β-hairpin units are the smallest secondary structural motifs that are some of the most scrutinized functional cores of peptides and protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ef9c62efd869b427f921ecd4102c941
https://doi.org/10.1039/c4cc03114h
https://doi.org/10.1039/c4cc03114h
Autor:
Rajesh G. Gonnade, Veera V. E. Ramesh, Vijaykumar H. Thorat, Pattuparambil R. Rajamohanan, Roshna V. Nair, Tukaram S. Ingole, Kuruppanthara N. Vijayadas, Hilda C. Davis, Gangadhar J. Sanjayan, Panchami Prabhakaran, Rupesh L. Gawade, Sangram S. Kale, Vedavati G. Puranik
Publikováno v:
European Journal of Organic Chemistry. 2013:3529-3542
This article details the characteristic conformational features of the Ant-Pro reverse turn ― a folded pseudo β-turn motif that displays a closed nine-membered-ring hydrogen-bonded network involving just two amino acid residues, namely anthranilic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2159aa301363fdb83a5e291fcf5cd5f
https://doi.org/10.1002/ejoc.201201739
https://doi.org/10.1002/ejoc.201201739
Publikováno v:
Chemical communications (Cambridge, England). 52(71)
Molecular self-assembly of nonamphiphilic α,β-hybrid foldamers based on urea-tethered anthranilic acid–proline (Ant–Pro) foldamers is reported. These self-assembled hollow vesicular architectures can take up and release the anticancer hydrophob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4519db7bd9c81d6324eb2be494238de
https://pubmed.ncbi.nlm.nih.gov/27511290
https://pubmed.ncbi.nlm.nih.gov/27511290