Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12. (Q48319028)

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scientific article published on 5 April 2017

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English	Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12.	scientific article published on 5 April 2017

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scholarly article

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Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/28378450

Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12. (English)

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Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/28378450

Aspergillus flavipes

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Asperflavipine B

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Asperflavipine A

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6

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4 June 2020

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4 June 2020

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4 June 2020

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Jing Yang

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4 June 2020

Guangzheng Wei

5

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4 June 2020

Jianping Wang

7

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4 June 2020

Zengwei Luo

8

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4 June 2020

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5 April 2017

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10 February 2018

http://europepmc.org/abstract/MED/28378450

Angewandte Chemie International Edition

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4 June 2020

5242-5246

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4 June 2020

The chemistry and biology of cytochalasans

1 reference

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Chaetoglobosin A preferentially induces apoptosis in chronic lymphocytic leukemia cells by targeting the cytoskeleton.

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Chaetoglobosin F, a small molecule compound, possesses immunomodulatory properties on bone marrow-derived dendritic cells via TLR9 signaling pathway

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Epicochalasines A and B: Two Bioactive Merocytochalasans Bearing Caged Epicoccine Dimer Units from Aspergillus flavipes.

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Enzymatic catalysis of the Diels-Alder reaction in the biosynthesis of natural products

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Programmed cell death pathways in cancer: a review of apoptosis, autophagy and programmed necrosis

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21 January 2018

Asperchalasine A, a Cytochalasan Dimer with an Unprecedented Decacyclic Ring System, from Aspergillus flavipes

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Pericoannosin A, a Polyketide Synthase–Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.

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Armochaetoglobins K-R, Anti-HIV Pyrrole-Based Cytochalasans fromChaetomium globosumTW1-1

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Chaetoconvosins A and B, alkaloids with new skeleton from fungus Chaetomium convolutum

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Periconiasins A–C, New Cytotoxic Cytochalasans with an Unprecedented 9/6/5 Tricyclic Ring System from Endophytic Fungus Periconia sp.

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Spicarins A–D from acetylated extract of fungus Spicaria elegans KLA03

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Molecular Basis of Cytochalasan Biosynthesis in Fungi: Gene Cluster Analysis and Evidence for the Involvement of a PKS-NRPS Hybrid Synthase by RNA Silencing

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Biomimetic synthesis of the calcineurin phosphatase inhibitor dibefurin

1 reference

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Periconiasin G, a new cytochalasan with unprecedented 7/6/5 tricyclic ring system from the endophytic fungus Periconia sp.

1 reference

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Phomopchalasins A and B, Two Cytochalasans with Polycyclic-Fused Skeletons from the Endophytic Fungus Phomopsis sp. shj2

1 reference

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Identifiers

10.1002/ANIE.201701125

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28378450%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28378450%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

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