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Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone
Pseudo‐natural products (pseudo‐NPs) are de novo combinations of natural product (NP) fragments that define novel bioactive chemotypes. For their discovery, new design principles are being sought. Previously, pseudo‐NPs were synthesized by the combination of fragments originating from biosynthetical...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091983/ https://www.ncbi.nlm.nih.gov/pubmed/36083197 http://dx.doi.org/10.1002/chem.202202164 |
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author | Grigalunas, Michael Patil, Sohan Krzyzanowski, Adrian Pahl, Axel Flegel, Jana Schölermann, Beate Xie, Jianing Sievers, Sonja Ziegler, Slava Waldmann, Herbert |
author_facet | Grigalunas, Michael Patil, Sohan Krzyzanowski, Adrian Pahl, Axel Flegel, Jana Schölermann, Beate Xie, Jianing Sievers, Sonja Ziegler, Slava Waldmann, Herbert |
author_sort | Grigalunas, Michael |
collection | PubMed |
description | Pseudo‐natural products (pseudo‐NPs) are de novo combinations of natural product (NP) fragments that define novel bioactive chemotypes. For their discovery, new design principles are being sought. Previously, pseudo‐NPs were synthesized by the combination of fragments originating from biosynthetically unrelated NPs to guarantee structural novelty and novel bioactivity. We report the combination of fragments from biosynthetically related NPs in novel arrangements to yield a novel chemotype with activity not shared by the guiding fragments. We describe the synthesis of the polyketide pseudo‐NP grismonone and identify it as a structurally novel and potent inhibitor of Hedgehog signaling. The insight that the de novo combination of fragments derived from biosynthetically related NPs may also yield new biologically relevant compound classes with unexpected bioactivity may be considered a chemical extension or diversion of existing biosynthetic pathways and greatly expands the opportunities for exploration of biologically relevant chemical space by means of the pseudo‐NP principle. |
format | Online Article Text |
id | pubmed-10091983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100919832023-04-13 Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone Grigalunas, Michael Patil, Sohan Krzyzanowski, Adrian Pahl, Axel Flegel, Jana Schölermann, Beate Xie, Jianing Sievers, Sonja Ziegler, Slava Waldmann, Herbert Chemistry Research Articles Pseudo‐natural products (pseudo‐NPs) are de novo combinations of natural product (NP) fragments that define novel bioactive chemotypes. For their discovery, new design principles are being sought. Previously, pseudo‐NPs were synthesized by the combination of fragments originating from biosynthetically unrelated NPs to guarantee structural novelty and novel bioactivity. We report the combination of fragments from biosynthetically related NPs in novel arrangements to yield a novel chemotype with activity not shared by the guiding fragments. We describe the synthesis of the polyketide pseudo‐NP grismonone and identify it as a structurally novel and potent inhibitor of Hedgehog signaling. The insight that the de novo combination of fragments derived from biosynthetically related NPs may also yield new biologically relevant compound classes with unexpected bioactivity may be considered a chemical extension or diversion of existing biosynthetic pathways and greatly expands the opportunities for exploration of biologically relevant chemical space by means of the pseudo‐NP principle. John Wiley and Sons Inc. 2022-10-13 2022-12-01 /pmc/articles/PMC10091983/ /pubmed/36083197 http://dx.doi.org/10.1002/chem.202202164 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Grigalunas, Michael Patil, Sohan Krzyzanowski, Adrian Pahl, Axel Flegel, Jana Schölermann, Beate Xie, Jianing Sievers, Sonja Ziegler, Slava Waldmann, Herbert Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone |
title | Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone |
title_full | Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone |
title_fullStr | Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone |
title_full_unstemmed | Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone |
title_short | Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone |
title_sort | unprecedented combination of polyketide natural product fragments identifies the new hedgehog signaling pathway inhibitor grismonone |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091983/ https://www.ncbi.nlm.nih.gov/pubmed/36083197 http://dx.doi.org/10.1002/chem.202202164 |
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