Quantitative Structure−Activity Analysis of the Algae Toxicity of Nitroaromatic Compounds

2000 ◽  
Vol 13 (6) ◽  
pp. 441-450 ◽  
Author(s):  
Heike Schmitt ◽  
Rolf Altenburger ◽  
Bernd Jastorff ◽  
Gerrit Schüürmann
Keyword(s):  
Activity Analysis ◽  
Nitroaromatic Compounds ◽  
Quantitative Structure ◽  
Structure Activity

Three-Dimensional Quantitative Structure—Activity Analysis of Steroidal and Dibenzoylhydrazine-Type Ecdysone Agonists

1995 ◽  
pp. 288-301 ◽  
Author(s):  
Yoshiaki Nakagawa ◽  
Bun-ichi Shimizu ◽  
Nobuhiro Oikawa ◽  
Miki Akamatsu ◽  
Keiichiro Nishimura ◽  
...  
Keyword(s):  
Three Dimensional ◽  
Activity Analysis ◽  
Quantitative Structure ◽  
Structure Activity

scholarly journals Quantitative Structure-Activity Relationship (QSAR) Studies on the Toxic Effects of Nitroaromatic Compounds (NACs): A Systematic Review

2021 ◽  
Vol 22 (16) ◽  
pp. 8557
Author(s):  
Tao Huang ◽  
Guohui Sun ◽  
Lijiao Zhao ◽  
Na Zhang ◽  
Rugang Zhong ◽  
...  
Keyword(s):  
Quantitative Structure Activity Relationship ◽  
Structure Activity Relationship ◽  
Nitroaromatic Compounds ◽  
Toxic Effects ◽  
Activity Relationship ◽  
Quantitative Structure ◽  
Qsar Modeling ◽  
Toxic Response ◽  
Qsar Studies ◽  
Structure Activity

Nitroaromatic compounds (NACs) are ubiquitous in the environment due to their extensive industrial applications. The recalcitrance of NACs causes their arduous degradation, subsequently bringing about potential threats to human health and environmental safety. The problem of how to effectively predict the toxicity of NACs has drawn public concern over time. Quantitative structure–activity relationship (QSAR) is introduced as a cost-effective tool to quantitatively predict the toxicity of toxicants. Both OECD (Organization for Economic Co-operation and Development) and REACH (Registration, Evaluation and Authorization of Chemicals) legislation have promoted the use of QSAR as it can significantly reduce living animal testing. Although numerous QSAR studies have been conducted to evaluate the toxicity of NACs, systematic reviews related to the QSAR modeling of NACs toxicity are less reported. The purpose of this review is to provide a thorough summary of recent QSAR studies on the toxic effects of NACs according to the corresponding classes of toxic response endpoints.

Antifeedant effect of polygodial and drimenol derivatives againstSpodoptera frugiperdaandEpilachna paenulataand quantitative structure-activity analysis

2018 ◽  
Vol 74 (7) ◽  
pp. 1623-1629 ◽  
Author(s):  
Iván J Montenegro ◽  
Soledad del Corral ◽  
Georgina N Diaz Napal ◽  
María C Carpinella ◽  
Marco Mellado ◽  
...  
Keyword(s):  
Activity Analysis ◽  
Quantitative Structure ◽  
Antifeedant Effect ◽  
Structure Activity

Quantitative structure–activity analysis of 5-arylidene-2,4-thiazolidinediones as aldose reductase inhibitors

2006 ◽  
Vol 16 (3) ◽  
pp. 512-520 ◽  
Author(s):  
S.V. Sambasivarao ◽  
Love K. Soni ◽  
Arun K. Gupta ◽  
P. Hanumantharao ◽  
S.G. Kaskhedikar
Keyword(s):  
Aldose Reductase ◽  
Activity Analysis ◽  
Quantitative Structure ◽  
Aldose Reductase Inhibitors ◽  
Reductase Inhibitors ◽  
Structure Activity

scholarly journals Novel phenoxyalkylamine derivatives. V. Synthesis, .ALPHA.-blocking activity and quantitative structure-activity analysis of .ALPHA.-((phenoxyethylamino)propyl)-.ALPHA.-phenylacetonitrile derivatives.

1988 ◽  
Vol 36 (10) ◽  
pp. 4121-4135 ◽  
Author(s):  
KAZUYA MITANI ◽  
SHUNICHIRO SAKURAI ◽  
TOSHIHIRO SUZUKI ◽  
KOJI MORIKAWA ◽  
EIICHI KOSHINAKA ◽  
...  
Keyword(s):  
Activity Analysis ◽  
Quantitative Structure ◽  
Structure Activity ◽  
Alpha Blocking ◽  
Blocking Activity

Quantitative structure-activity analysis of larvicidal 1-(substituted benzoyl)-2-benzoyl-1-tert-butylhydrazines againstChilo suppressalis

1994 ◽  
Vol 41 (2) ◽  
pp. 139-147 ◽  
Author(s):  
Nobuhiro Oikawa ◽  
Yoshiaki Nakagawa ◽  
Keiichiro Nishimura ◽  
Tamio Ueno ◽  
Toshio Fujita
Keyword(s):  
Activity Analysis ◽  
Quantitative Structure ◽  
Structure Activity
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