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A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation

Pasireotide is a multi-receptor ligand somatostatin analogue approved for medical treatment of Cushing’s disease and acromegaly. The liquid-phase total synthesis of pasireotide-a 18-membered cyclic hexapeptide-was achieved by the 3 + 2 + 1 strategy, and the Pro(1)-Phe(6) peptide bond was selected as...

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Autores principales: Ma, Chunying, Chen, Miao, Chu, Weiming, Tao, Jiayi, Kong, Delong, Zhang, Mengmeng, Feng, Wenhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600510/
https://www.ncbi.nlm.nih.gov/pubmed/31212595
http://dx.doi.org/10.3390/molecules24112185
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author Ma, Chunying
Chen, Miao
Chu, Weiming
Tao, Jiayi
Kong, Delong
Zhang, Mengmeng
Feng, Wenhua
author_facet Ma, Chunying
Chen, Miao
Chu, Weiming
Tao, Jiayi
Kong, Delong
Zhang, Mengmeng
Feng, Wenhua
author_sort Ma, Chunying
collection PubMed
description Pasireotide is a multi-receptor ligand somatostatin analogue approved for medical treatment of Cushing’s disease and acromegaly. The liquid-phase total synthesis of pasireotide-a 18-membered cyclic hexapeptide-was achieved by the 3 + 2 + 1 strategy, and the Pro(1)-Phe(6) peptide bond was selected as the final cyclization position. Two key fragments were simply synthesized using N,O-bis(trimethylsilyl)acetamide/N-hydroxysuccinimide ester (BSA/NHS) as coupling agents, and processes of the two key fragments were simple without any chromatographic purification. The current synthesis method is easily scalable and produces the target peptide with an overall yield of 15%.
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spelling pubmed-66005102019-07-16 A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation Ma, Chunying Chen, Miao Chu, Weiming Tao, Jiayi Kong, Delong Zhang, Mengmeng Feng, Wenhua Molecules Article Pasireotide is a multi-receptor ligand somatostatin analogue approved for medical treatment of Cushing’s disease and acromegaly. The liquid-phase total synthesis of pasireotide-a 18-membered cyclic hexapeptide-was achieved by the 3 + 2 + 1 strategy, and the Pro(1)-Phe(6) peptide bond was selected as the final cyclization position. Two key fragments were simply synthesized using N,O-bis(trimethylsilyl)acetamide/N-hydroxysuccinimide ester (BSA/NHS) as coupling agents, and processes of the two key fragments were simple without any chromatographic purification. The current synthesis method is easily scalable and produces the target peptide with an overall yield of 15%. MDPI 2019-06-11 /pmc/articles/PMC6600510/ /pubmed/31212595 http://dx.doi.org/10.3390/molecules24112185 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ma, Chunying
Chen, Miao
Chu, Weiming
Tao, Jiayi
Kong, Delong
Zhang, Mengmeng
Feng, Wenhua
A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation
title A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation
title_full A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation
title_fullStr A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation
title_full_unstemmed A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation
title_short A Practical and Total Synthesis of Pasireotide: Synthesis of Cyclic Hexapeptide via a Three-Component Condensation
title_sort practical and total synthesis of pasireotide: synthesis of cyclic hexapeptide via a three-component condensation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600510/
https://www.ncbi.nlm.nih.gov/pubmed/31212595
http://dx.doi.org/10.3390/molecules24112185
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