molconvert software (ChemAxon LLC)
90
Structured Review
ChemAxon LLC
molconvert software
Molconvert Software, supplied by ChemAxon LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software-molconvert/software+molconvert/pmc11673719-41-21-20
Average 90 stars, based on 1 article reviews
Molconvert Software, supplied by ChemAxon LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software-molconvert/software+molconvert/pmc11673719-41-21-20
Average 90 stars, based on 1 article reviews
molconvert software - by Bioz Stars,
2026-10
90/100 stars
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In this study, involved 2D Similarity, Molecular docking, and Molecular Simulation for the commercially available ZINC database compounds to overcome this resistance mechanism and find out a proper potent inhibitor for the target L2b-Lactamase, which would not get cleaved by the hydrolytic activity of the L2-b-Lactamase natural enzyme. Article Title: In silico screening of FDA approved drugs against ACE2 receptor: potential therapeutics to inhibit the entry of SARS-CoV-2 to human cells. Article Snippet: An unknown coronavirus that emerged sometime at the end of 2019 in China, the novel SARS-CoV-2, now called COVID-19, has spread all over the world.. Several efforts have been made to prevent or treat this disease, though not with success.. The initiation of COVID-19 viral infection involves specific binding of SARSCoV-2 to the host surface of the receptor, ACE2. Article Title: Potential inhibitors for FKBP51: an in silico study using virtual screening, molecular docking and molecular dynamics simulation. Article Snippet: Over the years, FK506-binding proteins have been targeted for different pharmaceutical interests.. The FK506-binding protein, encoded by the FKBP5 gene, is responsible for stress and metabolic-related disorders, including cancer.. In addition, the FKBD-I domain of the protein is a potential target for endocrine-related physiological diseases. Article Title: Virtual high-throughput screening: potential inhibitors for the mycobacterial α-subunit of tryptophan synthase Article Snippet: Mycobacterium tuberculosis (Mtb), which causes tuberculosis (TB), is the world’s most successful pathogen.. If it is to survive in phagosomes, the tryptophan biosynthetic pathway is essential.. The αsubunit of tryptophan synthase (TRPS) executes the irreversible catalysis of indole-3-glyceral-3phosphate to generate indole. Article Title: Identification of Therapeutic Drug Target of Stenotrophomonas maltophilia Through Subtractive Genomic Approach and in-silico Screening Based on 2D Similarity Filtration and Molecular Dynamic Simulation. Article Snippet: Background: Stenotrophomonas maltophilia is a multi-drug resistant, gram-negative bacterium that causes opportunistic infections and is associated with high morbidity and mortality in severely immunocompromised individuals.. Aim: The study aimed to find out the drug target and a novel inhibitor for Stenotrophomonas Software:Article Title: Structural and functional analysis of Chitinase-IV of Brassica juncea : molecular modeling and dynamic simulation study. Article Snippet: Brassica juncea is an important oil seed crop.. The productivity of this plant, however, is known to be low due to the attack of plant pathogens.. 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Article Title: IN SILICO ON STUDY CHITINASE AND CHITIN COMPLEX Article Snippet: In 3D structure of the chitin, hydrogen was added by employing ( Article Title: In-silico virtual screening for identification of potent inhibitor for L2-β-lactamase from Stenotrophomonas maltophilia through molecular docking, molecular dynamics analysis study. Article Snippet: Stenotrophomonas maltophilia, a Multiple-Drug-Resistant proteobacterium found in healthy normal flora and fauna with an aerobic and non-fermentative respiratory process, is majorly involved in Healthcare-Associated Infections (HAI).. The Multiple-Drug-Resistance takes place by secretion of the b-Lactamase enzyme, which hydrolyzes the b-Lactam antibiotics and currently serving as a significant clinical challenge by substantially effecting the mortality rate.. In this study, involved 2D Similarity, Molecular docking, and Molecular Simulation for the commercially available ZINC database compounds to overcome this resistance mechanism and find out a proper potent inhibitor for the target L2b-Lactamase, which would not get cleaved by the hydrolytic activity of the L2-b-Lactamase natural enzyme. Article Title: In silico screening of FDA approved drugs against ACE2 receptor: potential therapeutics to inhibit the entry of SARS-CoV-2 to human cells. Article Snippet: An unknown coronavirus that emerged sometime at the end of 2019 in China, the novel SARS-CoV-2, now called COVID-19, has spread all over the world.. Several efforts have been made to prevent or treat this disease, though not with success.. The initiation of COVID-19 viral infection involves specific binding of SARSCoV-2 to the host surface of the receptor, ACE2. Article Title: Potential inhibitors for FKBP51: an in silico study using virtual screening, molecular docking and molecular dynamics simulation. Article Snippet: Over the years, FK506-binding proteins have been targeted for different pharmaceutical interests.. The FK506-binding protein, encoded by the FKBP5 gene, is responsible for stress and metabolic-related disorders, including cancer.. In addition, the FKBD-I domain of the protein is a potential target for endocrine-related physiological diseases. Article Title: Virtual high-throughput screening: potential inhibitors for the mycobacterial α-subunit of tryptophan synthase Article Snippet: Mycobacterium tuberculosis (Mtb), which causes tuberculosis (TB), is the world’s most successful pathogen.. If it is to survive in phagosomes, the tryptophan biosynthetic pathway is essential.. The αsubunit of tryptophan synthase (TRPS) executes the irreversible catalysis of indole-3-glyceral-3phosphate to generate indole. Article Title: Identification of Therapeutic Drug Target of Stenotrophomonas maltophilia Through Subtractive Genomic Approach and in-silico Screening Based on 2D Similarity Filtration and Molecular Dynamic Simulation. Article Snippet: Background: Stenotrophomonas maltophilia is a multi-drug resistant, gram-negative bacterium that causes opportunistic infections and is associated with high morbidity and mortality in severely immunocompromised individuals.. Aim: The study aimed to find out the drug target and a novel inhibitor for Stenotrophomonas |