A New Method for the Detection and Measurement of Polyaromatic Carcinogens and Related Compounds by DNA Intercalation

Author(s):  
John J. Horvath ◽  
Manana Gueguetchkeri ◽  
Adarsh Gupta ◽  
Devi Penumatchu ◽  
Howard H. Weetall
1976 ◽  
Vol 7 (29) ◽  
pp. no-no
Author(s):  
A. M. OSMAN ◽  
M. A. EL-MAGHRABY ◽  
K. M. HASSAN

1923 ◽  
Vol 45 (5) ◽  
pp. 1303-1307 ◽  
Author(s):  
James B. Conant ◽  
Robert E. Lutz
Keyword(s):  

1976 ◽  
Vol 7 (3) ◽  
pp. no-no
Author(s):  
J. ROBERT ADAMSON ◽  
ROY BYWOOD ◽  
DAVID T. EASTLICK ◽  
GERARD GALLAGHER ◽  
DEREK WALKER ◽  
...  

Author(s):  
J. Robert Adamson ◽  
Roy Bywood ◽  
David T. Eastlick ◽  
Gerard Gallagher ◽  
Derek Walker ◽  
...  

1991 ◽  
Vol 44 (1) ◽  
pp. 1 ◽  
Author(s):  
MG Banwell

The ring expansion of 7-halogenobicyclo[4.1.0] heptenones and related compounds provides a useful new method for the preparation of the seven-membered conjugated carbocyclic compounds known as tropones and tropolones. This methodology has been exploited in the synthesis of various biologically active troponoid natural products including nezukone, the thujaplicins, thujaplicinol, MY3-469 and colchicine.


Marine Drugs ◽  
2019 ◽  
Vol 17 (1) ◽  
pp. 60 ◽  
Author(s):  
Jarmo-Charles Kalinski ◽  
Samantha Waterworth ◽  
Xavier Siwe Noundou ◽  
Meesbah Jiwaji ◽  
Shirley Parker-Nance ◽  
...  

The temperate marine sponge, Tsitsikamma favus, produces pyrroloiminoquinone alkaloids with potential as anticancer drug leads. We profiled the secondary metabolite reservoir of T. favus sponges using HR-ESI-LC-MS/MS-based molecular networking analysis followed by preparative purification efforts to map the diversity of new and known pyrroloiminoquinones and related compounds in extracts of seven specimens. Molecular taxonomic identification confirmed all sponges as T. favus and five specimens (chemotype I) were found to produce mainly discorhabdins and tsitsikammamines. Remarkably, however, two specimens (chemotype II) exhibited distinct morphological and chemical characteristics: the absence of discorhabdins, only trace levels of tsitsikammamines and, instead, an abundance of unbranched and halogenated makaluvamines. Targeted chromatographic isolation provided the new makaluvamine Q, the known makaluvamines A and I, tsitsikammamine B, 14-bromo-7,8-dehydro-3-dihydro-discorhabdin C, and the related pyrrolo-ortho-quinones makaluvamine O and makaluvone. Purified compounds displayed different activity profiles in assays for topoisomerase I inhibition, DNA intercalation and antimetabolic activity against human cell lines. This is the first report of makaluvamines from a Tsitsikamma sponge species, and the first description of distinct chemotypes within a species of the Latrunculiidae family. This study sheds new light on the putative pyrroloiminoquinone biosynthetic pathway of latrunculid sponges.


1988 ◽  
Vol 61 (7) ◽  
pp. 2401-2404 ◽  
Author(s):  
Hirokazu Naora ◽  
Takashi Ohnuki ◽  
Asao Nakamura

Sign in / Sign up

Export Citation Format

Share Document