Structural characterization of naphthalene sulfonamides and a sulfonate ester and their in vitro efficacy against Leishmania tarentolae promastigotes

2021 ◽  
Vol 45 (10) ◽  
pp. 4791-4801
Author(s):  
Edward W. Li ◽  
Jade Katinas ◽  
Marjorie A. Jones ◽  
Christopher G. Hamaker

Structural and biological activity analyses of two naphthalene sulfonamides and a naphthalene sulfonate ester.

LWT ◽  
2019 ◽  
Vol 108 ◽  
pp. 326-331 ◽  
Author(s):  
Weilin Liu ◽  
Hanghang Lou ◽  
Christos Ritzoulis ◽  
Xiaoze Chen ◽  
Ping Shen ◽  
...  

2019 ◽  
Vol 133 ◽  
pp. 110778 ◽  
Author(s):  
Peilin Chen ◽  
Yan Lin ◽  
Yueyu Chen ◽  
Qing Chang ◽  
Baodong Zheng ◽  
...  

2014 ◽  
Vol 38 (10) ◽  
pp. 4760-4773 ◽  
Author(s):  
Nesrin Korkmaz ◽  
Ahmet Karadağ ◽  
Ali Aydın ◽  
Yusuf Yanar ◽  
İsa Karaman ◽  
...  

Two novel cyanido-complexes having very significant antibacterial, antifungal and anticancer activities in vitro were synthesized and characterized using various techniques.


2013 ◽  
Vol 405 (23) ◽  
pp. 7181-7193 ◽  
Author(s):  
Robert Jirásko ◽  
Tomáš Mikysek ◽  
Vitaliy Chagovets ◽  
Ivan Vokřál ◽  
Michal Holčapek

1994 ◽  
Vol 17 (3) ◽  
pp. 386-390 ◽  
Author(s):  
Chikaku DOGASAKI ◽  
Hajime MURAKAMI ◽  
Motohiro NISHIJIMA ◽  
Naohito OHNO ◽  
Toshiro YADOMAE ◽  
...  

2011 ◽  
Vol 152 (3) ◽  
pp. 108-112 ◽  
Author(s):  
Gerd Lindner ◽  
Reyk Horland ◽  
Ilka Wagner ◽  
Beren Ataç ◽  
Roland Lauster

1988 ◽  
Vol 118 (1) ◽  
pp. 14-21 ◽  
Author(s):  
A. Skottner ◽  
A. Forsman ◽  
B. Skoog ◽  
J. L. Kostyo ◽  
C. M. Cameron ◽  
...  

Abstract. Since deamidation of the human GH molecule may alter the manner and extent to which the hormone is cleaved by proteases, and since it has been repeatedly suggested that proteolytic processing is required for the expression of certain of the activities of GH, the present study was conducted to determine whether the biological activity profiles of more acidic forms of human GH are altered. Three charge isomers, GH-b, GH-c and GH-d, representing primarily deamidated forms, were isolated from a native human GH preparation (Crescormon®) in amounts adequate for characterization of their biological activities. All three were essentially equipotent in a radioimmunoassay for human GH. When assessed for growth-promoting activity in the hypophysectomized rat, the isomers were again equipotent with each other and with the GH preparation from which they were derived. The charge isomers also had significant in vitro insulin-like activity on isolated rat adipose tissue and diabetogenic activity in the ob/ob mouse. Thus, the biological activity profiles of these charge isomers of human GH do not differ greatly from one another.


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