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1.
Bioorg Chem ; 93: 103309, 2019 12.
Article in English | MEDLINE | ID: mdl-31585266

ABSTRACT

The antibacterial agents and therapies today are facing serious problems such as drug resistance. Introducing dual inhibiting effect is a valid approach to solve this trouble and bring advantages including wide adaptability, favorable safety and superiority of combination. We started from potential DNA Gyrase inhibitory backbone isatin to develop oxoindolin derivatives as atypical dual Gyrase (major) and FabH (assistant) inhibitors via a two-round screening. Aiming at blocking both duplication (Gyrase) and survival (FabH), most of synthesized compounds indicated potency against Gyrase and some of them inferred favorable inhibitory effect on FabH. The top hit I18 suggested comparable Gyrase inhibitory activity (IC50 = 0.025 µM) and antibacterial effect with the positive control Novobiocin (IC50 = 0.040 µM). FabH inhibitory activity (IC50 = 5.20 µM) was also successfully introduced. Docking simulation hinted possible important interacted residues and binding patterns for both target proteins. Adequate Structure-Activity Relation discussions provide the future orientations of modification. With high potency, low initial toxicity and dual inhibiting strategy, advanced compounds with therapeutic methods will be developed for clinical application.


Subject(s)
Acetyltransferases/antagonists & inhibitors , DNA Gyrase/chemistry , Escherichia coli Proteins/antagonists & inhibitors , Indoles/chemistry , Topoisomerase II Inhibitors/chemistry , 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase , Acetyltransferases/metabolism , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/metabolism , Anti-Bacterial Agents/pharmacology , Binding Sites , DNA Gyrase/metabolism , Drug Evaluation, Preclinical , Escherichia coli/enzymology , Escherichia coli Proteins/metabolism , Fatty Acid Synthase, Type II/antagonists & inhibitors , Fatty Acid Synthase, Type II/metabolism , Indoles/metabolism , Indoles/pharmacology , Microbial Sensitivity Tests , Molecular Docking Simulation , Protein Structure, Tertiary , Structure-Activity Relationship , Topoisomerase II Inhibitors/metabolism , Topoisomerase II Inhibitors/pharmacology
2.
Bioorg Med Chem ; 27(8): 1509-1516, 2019 04 15.
Article in English | MEDLINE | ID: mdl-30846404

ABSTRACT

A series of rhodanine derivatives RB1-RB23 were synthesized through a two-round screening. Their Mycobacterial tuberculosis (Mtb) InhA inhibitory activity and Mtb growth blocking capability were evaluated. The most potent hit compound RB23 indicated comparable InhA inhibiton (IC50 = 2.55 µM) with the positive control Triclosan (IC50 = 6.14 µM) and Isoniazid (IC50 = 8.29 µM). Its improved growth-blocking effect on Mtb and low toxicity were attractive for further development. The docking simulation revealed the possible binding pattern of this series and picked the key interacted residues as Ser20, Phe149, Lys165 and Thr196. The 3D-QSAR model visualized the SAR discussion and hinted new information. Modifying the surroundings near rhodanine moiety might be promising attempts in later investigations.


Subject(s)
Bacterial Proteins/metabolism , Oxidoreductases/metabolism , Rhodanine/chemistry , Antitubercular Agents/pharmacology , Bacterial Proteins/antagonists & inhibitors , Binding Sites , Drug Evaluation, Preclinical , Isoniazid/pharmacology , Microbial Sensitivity Tests , Molecular Docking Simulation , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/metabolism , Oxidoreductases/antagonists & inhibitors , Protein Structure, Tertiary , Quantitative Structure-Activity Relationship , Rhodanine/metabolism , Rhodanine/pharmacology
3.
PLoS One ; 10(3): e0122036, 2015.
Article in English | MEDLINE | ID: mdl-25825911

ABSTRACT

Stearoyl-acyl carrier protein desaturase (SAD), locating in the plastid stroma, is an important fatty acid biosynthetic enzyme in higher plants. SAD catalyzes desaturation of stearoyl-ACP to oleyl-ACP and plays a key role in determining the homeostasis between saturated fatty acids and unsaturated fatty acids, which is an important player in cold acclimation in plants. Here, four new full-length cDNA of SADs (ScoSAD, SaSAD, ScaSAD and StSAD) were cloned from four Solanum species, Solanum commersonii, S. acaule, S. cardiophyllum and S. tuberosum, respectively. The ORF of the four SADs were 1182 bp in length, encoding 393 amino acids. A sequence alignment indicated 13 amino acids varied among the SADs of three wild species. Further analysis showed that the freezing tolerance and cold acclimation capacity of S. commersonii are similar to S. acaule and their SAD amino acid sequences were identical but differed from that of S. cardiophyllum, which is sensitive to freezing. Furthermore, the sequence alignments between StSAD and ScoSAD indicated that only 7 different amino acids at residues were found in SAD of S. tuberosum (Zhongshu8) against the protein sequence of ScoSAD. A phylogenetic analysis showed the three wild potato species had the closest genetic relationship with the SAD of S. lycopersicum and Nicotiana tomentosiformis but not S. tuberosum. The SAD gene from S. commersonii (ScoSAD) was cloned into multiple sites of the pBI121 plant binary vector and transformed into the cultivated potato variety Zhongshu 8. A freeze tolerance analysis showed overexpression of the ScoSAD gene in transgenic plants significantly enhanced freeze tolerance in cv. Zhongshu 8 and increased their linoleic acid content, suggesting that linoleic acid likely plays a key role in improving freeze tolerance in potato plants. This study provided some new insights into how SAD regulates in the freezing tolerance and cold acclimation in potato.


Subject(s)
Genes, Plant , Mixed Function Oxygenases/genetics , Solanum tuberosum/genetics , Adaptation, Physiological/genetics , Amino Acid Sequence , Cloning, Molecular , DNA, Complementary/genetics , Evolution, Molecular , Freezing , Mixed Function Oxygenases/chemistry , Molecular Sequence Data , Plants, Genetically Modified , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid , Solanum tuberosum/enzymology , Solanum tuberosum/physiology
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