(Q39824380)

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Bingchamides A and B, two novel cyclic pentapeptides from the Streptomyces bingchenggensis: fermentation, isolation, structure elucidation and biological properties

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scholarly article

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Europe PubMed Central

14 September 2017

Bingchamides A and B, two novel cyclic pentapeptides from the Streptomyces bingchenggensis: fermentation, isolation, structure elucidation and biological properties (English)

1 reference

Europe PubMed Central

14 September 2017

Streptomyces bingchenggensis

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1 reference

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author name string

Wen-Sheng Xiang

1

1 reference

Europe PubMed Central

14 September 2017

Ji-Dong Wang

2

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Europe PubMed Central

14 September 2017

Xiang-Jing Wang

3

1 reference

Europe PubMed Central

14 September 2017

Ji Zhang

4

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Europe PubMed Central

14 September 2017

publication date

17 July 2009

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Europe PubMed Central

14 September 2017

full work available at URL

https://www.nature.com/articles/ja200960.pdf

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19 March 2024

https://api.unpaywall.org/v2/10.1038/ja.2009.60?email=unpaywall_01@example.com

The Journal of Antibiotics

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Europe PubMed Central

14 September 2017

62

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Europe PubMed Central

14 September 2017

501-505

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Europe PubMed Central

14 September 2017

9

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Europe PubMed Central

14 September 2017

online access status

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19 March 2024

https://api.unpaywall.org/v2/10.1038/ja.2009.60?email=unpaywall_01@example.com

access restriction status

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https://scigraph.springernature.com/pub.10.1038/ja.2009.60

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Two new beta-class milbemycins from streptomyces bingchenggensis: fermentation, isolation, structure elucidation and biological properties.

1 reference

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21 January 2018

Further new milbemycin antibiotics from Streptomyces bingchenggensis. Fermentation, isolation, structural elucidation and biological activities.

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New seco-milbemycins from Streptomyces bingchenggensis: fermentation, isolation and structure elucidation.

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A novel macrolide compound from Streptomyces bingchenggensis: fermentation, isolation, structure elucidation and biological properties

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Rapid, high-yield, solid-phase synthesis of the antitumor antibiotic sansalvamide A using a side-chain-tethered phenylalanine building block

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Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives

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Scaffold targeting drug-resistant colon cancers

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Plant cyclopeptides

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Natural products in drug discovery

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Comprehensive study of sansalvamide A derivatives and their structure-activity relationships against drug-resistant colon cancer cell lines.

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Identification of Sansalvamide a analog potent against pancreatic cancer cell lines

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Synthesis of second-generation sansalvamide A derivatives: novel templates as potential antitumor agents.

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Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-29.

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A novel peptide sansalvamide analogue inhibits pancreatic cancer cell growth through G0/G1 cell-cycle arrest

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Mechanism of inhibition of a poxvirus topoisomerase by the marine natural product sansalvamide A.

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Solid-phase, Pd-catalyzed silicon-aryl carbon bond formation. Synthesis of sansalvamide A peptide

1 reference

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7 January 2021

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Synthesis and cytotoxicity of novel sansalvamide A derivatives

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.60

7 January 2021

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Synthesis and cytotoxicity of a new class of potent decapeptide macrocycles

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Identifiers

10.1038/JA.2009.60

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

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