Design, Synthesis, and Evaluation of Psorospermin/Quinobenzoxazine Hybrids as Structurally Novel Antitumor Agents-Reference-Cited by-同舟云学术

Design, Synthesis, and Evaluation of Psorospermin/Quinobenzoxazine Hybrids as Structurally Novel Antitumor Agents

Published:2003-06-05 Issue:14 Volume:46 Page:2958-2972
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Kim Mu-Yong¹,Na Younghwa¹,Vankayalapati Hariprasad¹,Gleason-Guzman Mary¹,Hurley Laurence H.¹

Affiliation:

1. College of Pharmacy, The University of Arizona, 1703 E. Mabel, Tucson, Arizona 85721, Arizona Cancer Center, 1515 N. Campbell Avenue, Tucson, Arizona 85724, and Department of Chemistry, The University of Arizona, Tucson, Arizona 85721

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm030096i

Reference43 articles.

1. Natural Products as a Source of Potential Cancer Chemotherapeutic and Chemopreventive Agents

2. Psorospermin, A New Antileukemic Xanthone From Psorospermum febrifugum

3. Pluramycins. Old Drugs Having Modern Friends in Structural Biology

4. Hedamycin intercalates the DNA helix and, through carbohydrate-mediated recognition in the minor groove, directs N7-alkylation of guanine in the major groove in a sequence-specific manner

5. On the Mechanism of Asymmetric Nucleophilic Ring-Opening of Epoxides Catalyzed by (Salen)CrIII Complexes

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