Isothiourea derivatives of 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole with broad-spectrum anthelmintic activity

1987 ◽  
Vol 30 (10) ◽  
pp. 1848-1853 ◽  
Author(s):  
Malcolm D. Brewer ◽  
Roderick J. J. Dorgan ◽  
Brian R. Manger ◽  
Patrick Mamalis ◽  
Richard A. B. Webster
ChemInform ◽  
1988 ◽  
Vol 19 (10) ◽  
Author(s):  
M. D. BREWER ◽  
R. J. J. DORGAN ◽  
B. R. MANGER ◽  
P. MAMALIS ◽  
R. A. B. WEBSTER

2016 ◽  
Vol 7 (36) ◽  
pp. 5709-5718 ◽  
Author(s):  
Huimin Yuan ◽  
Bingran Yu ◽  
Li-Hai Fan ◽  
Meng Wang ◽  
Yiwen Zhu ◽  
...  

A series of hydroxyl-rich quaternized polymers with Ag ions have been proposed for broad-spectrum antibacterial and antifouling coatings.


1966 ◽  
Vol 9 (4) ◽  
pp. 545-551 ◽  
Author(s):  
Alfons H. M. Raeymaekers ◽  
Fernand T. N. Allewijn ◽  
Jan Vandenberk ◽  
Paul J. A. Demoen ◽  
Theo T. T. Van Offenwert ◽  
...  

2006 ◽  
Vol 72 (6) ◽  
pp. 4492-4496 ◽  
Author(s):  
Paul D. Cotter ◽  
Lorraine A. Draper ◽  
Elaine M. Lawton ◽  
Olivia McAuliffe ◽  
Colin Hill ◽  
...  

ABSTRACT Lacticin 3147 is a broad-spectrum two-peptide lantibiotic whose genetic determinants are located on two divergent operons on the lactococcal plasmid pMRC01. Here we introduce each of 14 subclones, containing different combinations of lacticin 3147 genes, into MG1363 (pMRC01) and determine that a number of them can facilitate overproduction of the lantibiotic. Based on these studies it is apparent that while the provision of additional copies of genes encoding the biosynthetic/production machinery and the regulator LtnR is a requirement for high-level overproduction, the presence of additional copies of the structural genes (i.e., ltnA1A2) is not.


2021 ◽  
Vol 14 (1) ◽  
pp. 68-74
Author(s):  
M. V. Filimonova ◽  
A. S. Saburova ◽  
L. I. Shevchenko ◽  
V. M. Makarchuk ◽  
A. A. Lychagin ◽  
...  

According to leading experts, the vast arsenal of radioprotective agents available in the world today does not fully meet modern practical needs, both in the field of radiation protection, and in the prevention and treatment of complications of radiotherapy. The purpose of the study was to evaluate the effect of the salt-forming acids type on the radioprotective activity of NOS inhibitor T1023. The chemical part of this study included methods of chemical synthesis, physicochemical and elemental analysis. Pharmacological part – assessment of acute toxicity using V.B. Prozorovsky express method and the study of radioprotective activity using Till and McCulloch method based on the ability of mice hematopoietic cells to form spleen colonies after irradiation. The number of endogenous hematopoietic spleen colonies were assessed on the 8th day after total exposure to gamma-irradiation at a dose of 6 Gy in six independent experiments. As a result of directed chemical synthesis, six new derivatives of T1023 – salts of N-isobutanoyl-S-isopropylisothiourea have been developed, identified and characterized. The results of studying the safety and radioprotective activity of the synthesized compounds showed that changes in the salt-forming acid don’t significantly influence the toxicity: all studied compounds are in the 3rd class of toxicity and hazard. At the same time, it was found that the replacement of the salt-forming acid significantly influenced the severity of the radioprotective effect. For some of these compounds radioprotective efficacy is comparable to or exceeds the efficacy of the initial compound T1023. It is important to note that these new compounds were used in lower, more save doses than T1023. The results suggest promising further development of NOS inhibitors – isothiourea derivatives as radioprotective agents.


1952 ◽  
Vol 74 (2) ◽  
pp. 498-499 ◽  
Author(s):  
Glenn S. Skinner ◽  
William H. Waitz

2015 ◽  
Vol 7 (18) ◽  
pp. 7690-7696 ◽  
Author(s):  
Changmin Shao ◽  
Jian Zheng ◽  
Bo Fan ◽  
Shaman Luo ◽  
Jixiang Lin ◽  
...  

Both 10-methoxycamptothecin (MCPT) and 10-hydroxycamptothecin (HCPT) are natural derivatives of camptothecin (CPT) isolated from Camptotheca acuminata, possessing broad-spectrum antitumor activity.


1961 ◽  
Vol 6 (11) ◽  
pp. 1061-1068
Author(s):  
J. C. Swartzwelder ◽  
W. W. Frye ◽  
A. Pena Chavarria ◽  
R. Lampert ◽  
J. P. Muhleisen ◽  
...  

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