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Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O

The synthesis and crystal structure of peptide 6,6′-dimethyl biphenyl hybrid are described. The title compound was synthesized by reaction between 6,6′-dimethyl-[1,1′-biphen­yl]-2,2′-dicarbonyl dichloride in CH(2)Cl(2), amine HN–proline–phenyl­alanine–alanine–COOMe and Et(3)N at 273 K under N(2) atm...

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Autores principales: Nguyen, Xuan Tu, Le, Thuy Quynh, Bui Thi, Tra My, Mac, Dinh Hung, Bui, Thai Thanh Thu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534232/
https://www.ncbi.nlm.nih.gov/pubmed/33117588
http://dx.doi.org/10.1107/S2056989020012931
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author Nguyen, Xuan Tu
Le, Thuy Quynh
Bui Thi, Tra My
Mac, Dinh Hung
Bui, Thai Thanh Thu
author_facet Nguyen, Xuan Tu
Le, Thuy Quynh
Bui Thi, Tra My
Mac, Dinh Hung
Bui, Thai Thanh Thu
author_sort Nguyen, Xuan Tu
collection PubMed
description The synthesis and crystal structure of peptide 6,6′-dimethyl biphenyl hybrid are described. The title compound was synthesized by reaction between 6,6′-dimethyl-[1,1′-biphen­yl]-2,2′-dicarbonyl dichloride in CH(2)Cl(2), amine HN–proline–phenyl­alanine–alanine–COOMe and Et(3)N at 273 K under N(2) atmosphere and characterized by single-crystal X-ray diffraction. The asymmetric unit contains one peptide mol­ecule and a quarter of a water mol­ecule. A disorder of a methyl and meth­oxy­carbonyl group of one alanine residue is observed with occupancy ratio 0.502 (6):0.498 (6). The structure is consolidated by intra- and inter­molecular hydrogen bonds.
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spelling pubmed-75342322020-10-27 Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O Nguyen, Xuan Tu Le, Thuy Quynh Bui Thi, Tra My Mac, Dinh Hung Bui, Thai Thanh Thu Acta Crystallogr E Crystallogr Commun Research Communications The synthesis and crystal structure of peptide 6,6′-dimethyl biphenyl hybrid are described. The title compound was synthesized by reaction between 6,6′-dimethyl-[1,1′-biphen­yl]-2,2′-dicarbonyl dichloride in CH(2)Cl(2), amine HN–proline–phenyl­alanine–alanine–COOMe and Et(3)N at 273 K under N(2) atmosphere and characterized by single-crystal X-ray diffraction. The asymmetric unit contains one peptide mol­ecule and a quarter of a water mol­ecule. A disorder of a methyl and meth­oxy­carbonyl group of one alanine residue is observed with occupancy ratio 0.502 (6):0.498 (6). The structure is consolidated by intra- and inter­molecular hydrogen bonds. International Union of Crystallography 2020-09-25 /pmc/articles/PMC7534232/ /pubmed/33117588 http://dx.doi.org/10.1107/S2056989020012931 Text en © Nguyen et al. 2020 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Communications
Nguyen, Xuan Tu
Le, Thuy Quynh
Bui Thi, Tra My
Mac, Dinh Hung
Bui, Thai Thanh Thu
Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O
title Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O
title_full Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O
title_fullStr Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O
title_full_unstemmed Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O
title_short Synthesis and crystal structure of peptide dimethyl biphenyl hybrid C(52)H(60)N(6)O(10)·0.25H(2)O
title_sort synthesis and crystal structure of peptide dimethyl biphenyl hybrid c(52)h(60)n(6)o(10)·0.25h(2)o
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534232/
https://www.ncbi.nlm.nih.gov/pubmed/33117588
http://dx.doi.org/10.1107/S2056989020012931
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