Quantitative structure–activity relationship study on sulfanilamide Schiff's bases: CA inhibitors

Bioorganic & Medicinal Chemistry ◽

10.1016/s0968-0896(03)00217-7 ◽

2003 ◽

Author(s):

V Agrawal

Keyword(s):

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Schiff’S Bases ◽

Structure Activity ◽

Schiff's Bases ◽

Relationship Study

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Quantitative structure–Activity relationship study on sulfanilamide schiff's bases: carbonic anhydrase (CA) inhibitors

Bioorganic & Medicinal Chemistry ◽

10.1016/j.bmc.2003.09.037 ◽

2003 ◽

Vol 11 (24) ◽

pp. 5353-5362 ◽

Author(s):

Vijay K. Agrawal ◽

Shachi Srivastava ◽

Padmakar V. Khadikar ◽

Claudiu T. Supuran

Keyword(s):

Carbonic Anhydrase ◽

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Schiff’S Bases ◽

Structure Activity ◽

Schiff's Bases ◽

Relationship Study

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Design, Synthesis and Quantitative Structure-Activity Relationship Study of N-(3-Oxo-3,4-dihydro-2H-benzo(1,4)oxazine-7-carbonyl)guanidine Derivatives as Potent Na/H Exchange Inhibitors.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.45.1975 ◽

1997 ◽

Vol 45 (12) ◽

pp. 1975-1983 ◽

Author(s):

Takeshi YAMAMOTO ◽

Manabu HORI ◽

Ikuo WATANABE ◽

Hisayoshi TSUTSUI ◽

Kengo HARADA ◽

...

Keyword(s):

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Design Synthesis ◽

Guanidine Derivatives ◽

Structure Activity ◽

Relationship Study

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A quantitative structure-activity relationship study on a series of 10 para-substituted toluenes binding to cytochrome P4502B4 (CYP2B4), and their hydroxylation rates

Biochemical Pharmacology ◽

10.1016/0006-2952(95)00188-6 ◽

1995 ◽

Vol 50 (5) ◽

pp. 619-625 ◽

Author(s):

David F.V. Lewis ◽

Costas Ioannides ◽

Dennis V. Parke

Keyword(s):

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Substituted Toluenes ◽

Relationship Study

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Acute toxicity of substituted biphenyls todaphnia magnaand quantitative structure‐activity relationship study

Toxicological and Environmental Chemistry ◽

10.1080/02772249909358661 ◽

1999 ◽

Vol 68 (3-4) ◽

pp. 267-273

Author(s):

C. M. Zhu ◽

L. R. Kong ◽

H. Hong ◽

Q. G. Huang ◽

L. S. Wang

Keyword(s):

Acute Toxicity ◽

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Relationship Study

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Three-Dimensional Quantitative Structure-Activity Relationship Study of Antitumor 2-Formylpyridine Thiosemicarbazones Derivatives as Inhibitors of Ribonucleotide Reductase

QSAR & Combinatorial Science ◽

10.1002/qsar.200960057 ◽

2009 ◽

Vol 28 (11-12) ◽

pp. 1334-1345 ◽

Author(s):

Hamilton Mitsugu Ishiki ◽

Antonia T. do Amaral

Keyword(s):

Ribonucleotide Reductase ◽

Three Dimensional ◽

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Relationship Study

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Quantitative structure–activity relationship study on some benzodiazepine derivatives as anti-Alzheimer agents

Journal of Molecular Modeling ◽

10.1007/s00894-004-0199-4 ◽

2004 ◽

Vol 10 (5-6) ◽

pp. 328-334 ◽

Author(s):

Bikash Debnath ◽

Shovanlal Gayen ◽

Anindya Basu ◽

Kolluru Srikanth ◽

Tarun Jha

Keyword(s):

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Benzodiazepine Derivatives ◽

Relationship Study

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Quantitative structure-activity relationship study on the biodegradation of acid dyestuffs

Journal of Environmental Sciences ◽

10.1016/s1001-0742(07)60134-x ◽

2007 ◽

Vol 19 (7) ◽

pp. 800-804 ◽

Author(s):

Yin LI ◽

Dan-li XI

Keyword(s):

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Relationship Study

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Quantitative Structure Activity Relationship Study of 2,4,6-Trisubstituted-s-triazine Derivatives as Antimalarial Inhibitors of Plasmodium Falciparum Dihydrofolate Reductase

Chemical Biology & Drug Design ◽

10.1111/j.1747-0285.2010.01045.x ◽

2010 ◽

Vol 77 (1) ◽

pp. 57-62 ◽

Author(s):

Himanshu Ojha ◽

Pragya Gahlot ◽

Anjani K. Tiwari ◽

Mallika Pathak ◽

Rita Kakkar

Keyword(s):

Plasmodium Falciparum ◽

Dihydrofolate Reductase ◽

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Triazine Derivatives ◽

Relationship Study

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Understanding Tubulin/Microtubule−Taxane Interactions: A Quantitative Structure–Activity Relationship Study

Molecular Pharmaceutics ◽

10.1021/mp700119e ◽

2008 ◽

Vol 5 (1) ◽

pp. 151-161 ◽

Author(s):

Corwin Hansch ◽

Rajeshwar P. Verma

Keyword(s):

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Structure Activity ◽

Relationship Study

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Quantitative Structure-Activity Relationship Study on Some Azidopyridinyl Neonicotinoid Insecticides for Their Selective Affinity Towards the Drosophila Nicotinic Receptor Over Mammalian a4ß2 Receptor Using Electrotopological State Atom Index

Drug Design and Discovery ◽

10.3109/10559610290249557 ◽

2003 ◽

Vol 18 (2-3) ◽

pp. 81-89 ◽

Author(s):

Bikash Debnath ◽

Shovanlal Gayen ◽

Sudip Naskar ◽

Kunal Roy ◽

Tarun Jha

Keyword(s):

Nicotinic Receptor ◽

Quantitative Structure Activity Relationship ◽

Structure Activity Relationship ◽

Activity Relationship ◽

Quantitative Structure ◽

Neonicotinoid Insecticides ◽

Structure Activity ◽

Relationship Study ◽

Electrotopological State

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