A Structure−Activity Relationship Study of Novel Phenylacetamides Which Are Sodium Channel Blockers

1996 ◽  
Vol 39 (7) ◽  
pp. 1514-1520 ◽  
Author(s):  
Ioannis Roufos ◽  
Sheryl Hays ◽  
Roy D. Schwarz
Keyword(s):  
Sodium Channel ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Channel Blockers ◽  
Sodium Channel Blockers ◽  
Structure Activity ◽  
Relationship Study

Voltage-dependent sodium channel blocker anticonvulsants: an approach to the structure-activity relationship

2020 ◽  
Vol 16 ◽  
Author(s):  
M. del Carmen Salazar-López ◽  
J. Alberto Guevara-Salazar ◽  
Mónica G. Arellano-Mendoza ◽  
Hugo A. Jiménez-Vázquez ◽  
Adriana Benavides ◽  
...  
Keyword(s):  
Biological Activity ◽  
Sodium Channel ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Channel Blockers ◽  
Experimental Conditions ◽  
Electronic Density ◽  
Relationship Analysis ◽  
Structure Activity ◽  
Voltage Dependent

: Anticonvulsants are drugs used in the treatment of seizures, their pharmacology includes promoters of brain inhibition and inhibitors of brain activity; Of the latter, voltage-dependent sodium channel blockers (VGSCB) are the most widely used in therapeutics. Objective: To propose the structural requirements of VGSC blockers through a quantitative structure-activity relationship analysis of drugs with proven activity. Methods: IC50 values of anticonvulsant drugs on VGSCs were considered under similar experimental conditions; some physicochemical properties of the molecules that were correlated with their biological activity were determined in silico. Results: Relationships were found between the dipole moment, pKa, EHOMO, and MR with the biological activity, which infers that between greater polarity and basicity of the drugs, their activity as blockers will increase. Subsequently, the structural subclassification of the drugs was carried out, based on the urea derivation, the groups of which were: Group 1 (direct and bioisoster derivatives) and Group 2 (homologue and vinylogue derivatives of urea). Conclusion: The biological activity depends on the polarity, basicity, and electronic density of the drugs. The derivation of urea is essential, which is present in its original substituted form or a bioisosteric form. Urea can be in the form of a homologue or a vinylogue at the ends of the molecule. Aromatic substitution to the urea portion is necessary.

Strategic structure-activity relationship study on a follistatin-derived myostatin inhibitory peptide

2021 ◽  
pp. 128163
Author(s):  
Mariko Saitoh ◽  
Kentaro Takayama ◽  
Yoshimi Roppongi ◽  
Takahiro Shimada ◽  
Akihiro Taguchi ◽  
...  
Keyword(s):  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Inhibitory Peptide ◽  
Structure Activity ◽  
Relationship Study

Structure-activity relationship study of vitamin D analogs with oxolane group in their side chain

2017 ◽  
Vol 134 ◽  
pp. 86-96 ◽  
Author(s):  
Anna Y. Belorusova ◽  
Andrea Martínez ◽  
Zoila Gándara ◽  
Generosa Gómez ◽  
Yagamare Fall ◽  
...  
Keyword(s):  
Vitamin D ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Side Chain ◽  
Vitamin D Analogs ◽  
Structure Activity ◽  
Relationship Study
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