Triggering the Antitumor Activity of Acyclic Enediyne through Maleimide-Assisted Rearrangement and Cycloaromatization-Reference-Cited by-同舟云学术

Triggering the Antitumor Activity of Acyclic Enediyne through Maleimide-Assisted Rearrangement and Cycloaromatization

Published:2020-07-13 Issue:15 Volume:85 Page:9808-9819
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhang Mengsi¹,Li Baojun¹,Chen Huimin¹,Lu Haotian¹,Ma Hailong¹,Cheng Xiaoyu¹,Wang Wenbo¹,Wang Yue¹,Ding Yun¹,Hu Aiguo¹^ORCID

Affiliation:

1. Shanghai Key Laboratory of Advanced Polymeric Materials, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China

Funder

Ministry of Education of the People's Republic of China

Shanghai Municipal Education Commission

National Natural Science Foundation of China

Shanghai Municipal Government

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01124

Reference76 articles.

1. Resistance to Enediyne Antitumor Antibiotics by Sequestration

2. Chemistry and Biology of the Enediyne Anticancer Antibiotics

3. CD20-specific antibody-targeted chemotherapy of non-Hodgkin’s B-cell lymphoma using calicheamicin-conjugated rituximab

4. Antibody-targeted chemotherapy with CMC-544: a CD22-targeted immunoconjugate of calicheamicin for the treatment of B-lymphoid malignancies

5. An Anti-CD33 Antibody−Calicheamicin Conjugate for Treatment of Acute Myeloid Leukemia. Choice of Linker

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