Directed production of aurantizolicin and new members based on a YM-216391 biosynthetic system

Literature Information

Publication Date 2018-11-27
DOI 10.1039/C8OB02665C
Impact Factor 3.876
Authors

Zeng-Fei Pei, Min-Jie Yang, Lei Li, Xiao-Hong Jian, Yue Yin, Dehai Li, Hai-Xue Pan, Yinhua Lu, Weihong Jiang, Gong-Li Tang


View Original

Abstract

Using a highly effective heterologous expression system, the YM-216391 (1) biosynthetic gene cluster was engineered to yield aurantizolicin (2) and the hybrid compound 3. Both of these compounds were isolated and fully structurally characterised and the bioactivity was evaluated. The results indicate that compound 3 exhibits significantly improved antitumor activity.

Related Literature

Self-assembly of a nanotube from a black phosphorus nanoribbon on a string of fullerenes at low temperature

Jiao Shi, Ling-Nan Liu, Qing-Hua Qin

2017-08-10 Paper

DOI: 10.1039/C7CP04427E

Unveiling universal trends for the energy level alignment in organic/oxide interfaces

José I. Martínez, Fernando Flores, José Ortega, Sylvie Rangan, Charles M. Ruggieri, Robert A. Bartynski

2017-08-08 Perspective

DOI: 10.1039/C7CP03853D

A topological study of chemical bonds under pressure: solid hydrogen as a model case

Vanessa Riffet, Vanessa Labet, Julia Contreras-García

2017-09-11 Paper

DOI: 10.1039/C7CP04349J

Contents list

Front/Back Matter

DOI: 10.1039/C7CP90217D

The electronic structure of Ag1−xSn1+xSe2 (x = 0.0, 0.1, 0.2, 0.25 and 1.0)

Takanori Wakita, Eugenio Paris, Kaya Kobayashi, Kensei Terashima, Teppei Ueno, Federica Bondino, Luca Olivi, Jun Akimitsu, Yuji Muraoka, Takayoshi Yokoya, Naurang L. Saini

2017-09-22 Paper

DOI: 10.1039/C7CP05369J

The magnetic and adsorption properties of ZnO1−xSx nanoparticles

Huiyun Zhang, Guixian Liu, Yanqiang Cao, Jing Chen, Kai Shen, Ashwini Kumar, Mingxiang Xu, Qi Li

2017-09-12 Paper

DOI: 10.1039/C7CP03470A

A study on an unusual SN2 mechanism in the methylation of benzyne through nickel-complexation

Makoto Hatakeyama, Koji Ogata, Yuto Sumida, Tomoe Sumida

2017-09-28 Paper

DOI: 10.1039/C7CP04739H

Front cover

Cover

DOI: 10.1039/C7CP90221B

Two coexisting liquid phases in switchable ionic liquids

Juan Yao, David B. Lao, Xiao Sui, Yufan Zhou, Satish K. Nune, Xiang Ma, Tyler P. Troy, Musa Ahmed, Zihua Zhu, David J. Heldebrant, Xiao-Ying Yu

2017-06-23 Communication

DOI: 10.1039/C7CP03754F

You might also like

Compound Q&A

What is 3-Fluoro-2-methylbenzylamine (CAS: 771573-36-5)?

3-Fluoro-2-methylbenzylamine is an organic compound with the CAS number 771573-3...

771573-36-53-Fluoro-2-methylben...
Compound Q&A

Is Tert-butyl 2-(oxetan-3-ylidene)acetate (CAS: 1207175-03-8) safe?

Tert-butyl 2-(oxetan-3-ylidene)acetate is considered safe for its intended uses ...

1207175-03-8Tert-butyl 2-(oxetan...
Compound Q&A

What precautions should be taken when handling 4-Acetyl-2-fluorobenzonitrile (CAS: 214760-18-6)?

Proper personal protective equipment (PPE) such as gloves, goggles, and a lab co...

214760-18-64-Acetyl-2-fluoroben...
Compound Q&A

How is 2-Ethyl-4-methyl-1,3-thiazole (CAS: 15679-12-6) typically synthesized?

2-Ethyl-4-methyl-1,3-thiazole is commonly synthesized via the reaction of thiour...

15679-12-62-Ethyl-4-methyl-1,3...
Compound Q&A

How should 5',5''-([2,2'-Bithiophene]-5,5'-diyl)bis(([1,1':3',1''-terphenyl]-4,4''-dicarboxylic acid)) (CAS: 1227780-71-3) be stored?

This compound should be stored in a cool, dry place away from direct sunlight an...

1227780-71-35',5''''-([2,2'-Bith...
Compound Q&A

What regulatory guidelines apply to L-Lysine Acetate Salt (CAS: 52315-92-1)?

L-Lysine Acetate Salt (CAS: 52315-92-1) is subject to various regulatory guideli...

52315-92-1L-LYSINE ACETATE SAL...
Compound Q&A

Is 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) safe?

6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) is generally conside...

259793-96-96-Fluoro-3-hydroxy-2...
Compound Q&A

What are the physical and chemical properties of 1,1'-Sulfonylbis(1H-imidazole) (CAS: 7189-69-7)?

1,1'-Sulfonylbis(1H-imidazole) is a crystalline solid with a molecular weight of...

7189-69-71,1'-Sulfonylbis(1H-...
Compound Q&A

What industries use 4-methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5)?

4-Methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5) is primarily used i...

289483-82-54-methyl-7-nitro-1H-...
Compound Q&A

How should waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) be handled?

Waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) should be ...

97753-82-75-Bromo-3-indolyl-be...

Source Journal

Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
CiteScore: 3.4
Self-citation Rate: 10.3%
Articles per Year: 1041

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.