Literature DB >> 1589797

Designed enediynes: a new class of DNA-cleaving molecules with potent and selective anticancer activity.

K C Nicolaou1, W M Dai, S C Tsay, V A Estevez, W Wrasidlo.   

Abstract

The rational design and biological actions of a new class of DNA-cleaving molecules with potent and selective anticancer activity are reported. These relatively simple enediyne-type compounds were designed from basic chemical principles to mimic the actions of the rather complex naturally occurring enediyne anticancer antibiotics, particularly dynemicin A. Equipped with locking and triggering devices, these compounds damage DNA in vitro and in vivo on activation by chemical or biological means. Their damaging effects are manifested in potent anticancer activity with remarkable selectivities. Their mechanism of action involves intracellular unlocking and triggering of a Bergman reaction, leading to highly reactive benzenoid diradicals that cause severe DNA damage. The results of these studies demonstrate the potential of these de novo designed molecules as biotechnology tools and anticancer agents.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1589797     DOI: 10.1126/science.256.5060.1172

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  21 in total

1.  Direct comparison of solution and gas-phase reactions of the three distonic isomers of the pyridine radical cation with methanol.

Authors:  Fanny Widjaja; Zhicheng Jin; John J Nash; Hilkka I Kenttämaa
Journal:  J Am Chem Soc       Date:  2012-01-18       Impact factor: 15.419

2.  Prodrugs of dynemicin analogs for selective chemotherapy mediated by an aldolase catalytic Ab.

Authors:  Subhash C Sinha; Lian-Sheng Li; Gregory P Miller; Shantanu Dutta; Christoph Rader; Richard A Lerner
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-23       Impact factor: 11.205

Review 3.  Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.

Authors:  K C Nicolaou; Christopher R H Hale; Christian Nilewski; Heraklidia A Ioannidou
Journal:  Chem Soc Rev       Date:  2012-06-28       Impact factor: 54.564

Review 4.  Recent developments in the design of bioreductive drugs.

Authors:  W A Denny; W R Wilson; M P Hay
Journal:  Br J Cancer Suppl       Date:  1996-07

Review 5.  Mechanisms of target selection by DNA-damaging chemicals: studies with enediyne anticancer drugs.

Authors:  P C Dedon
Journal:  Int Arch Occup Environ Health       Date:  1996       Impact factor: 3.015

Review 6.  Transition metal-catalyzed couplings of alkynes to 1,3-enynes: modern methods and synthetic applications.

Authors:  Barry M Trost; James T Masters
Journal:  Chem Soc Rev       Date:  2016-02-01       Impact factor: 54.564

7.  Reversible Bergman cyclization by atomic manipulation.

Authors:  Bruno Schuler; Shadi Fatayer; Fabian Mohn; Nikolaj Moll; Niko Pavliček; Gerhard Meyer; Diego Peña; Leo Gross
Journal:  Nat Chem       Date:  2016-01-25       Impact factor: 24.427

8.  Synthesis of a 1,3-Bridged Macrobicyclic Enyne via Chemoselective Cycloisomerization Using Palladium-Catalyzed Alkyne-Alkyne Coupling.

Authors:  Barry M Trost; James T Masters; Franck Le Vaillant; Jean-Philip Lumb
Journal:  J Org Chem       Date:  2016-10-13       Impact factor: 4.354

Review 9.  Chemistry and biology of natural and designed enediynes.

Authors:  K C Nicolaou; A L Smith; E W Yue
Journal:  Proc Natl Acad Sci U S A       Date:  1993-07-01       Impact factor: 11.205

10.  Oxygen dependence of the cytotoxicity of the enediyne anti-tumour antibiotic esperamicin A1.

Authors:  R M Batchelder; W R Wilson; M P Hay; W A Denny
Journal:  Br J Cancer Suppl       Date:  1996-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.