make receptor program (OpenEye Scientific Software Inc)
90
Structured Review
OpenEye Scientific Software Inc
make receptor program
Make Receptor Program, supplied by OpenEye Scientific Software Inc, 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/make_receptor+program/make+receptor+program/pmc12152950-162-24-24
Average 90 stars, based on 1 article reviews
Make Receptor Program, supplied by OpenEye Scientific Software Inc, 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/make_receptor+program/make+receptor+program/pmc12152950-162-24-24
Average 90 stars, based on 1 article reviews
make receptor program - by Bioz Stars,
2026-09
90/100 stars
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Docking Assay:Article Title: New inhibitors of cathepsin V impair tumor cell proliferation and elastin degradation and increase immune cell cytotoxicity Article Snippet: .. The docking receptor structure was created using the software package OEDocking 3.2.0.2, Make Software:Article Title: New inhibitors of cathepsin V impair tumor cell proliferation and elastin degradation and increase immune cell cytotoxicity Article Snippet: .. The docking receptor structure was created using the software package OEDocking 3.2.0.2, Make Article Title: Inhibition of MurA Enzyme from Escherichia coli and Staphylococcus aureus by Diterpenes from Lepechinia meyenii and Their Synthetic Analogs Article Snippet: .. The Article Title: Indoles and 1-(3-(benzyloxy)benzyl)piperazines: Reversible and selective monoamine oxidase B inhibitors identified by screening an in-house compound library. Article Snippet: The therapeutic indications for monoamine oxidases A and B (MAO-A and MAO-B) inhibitors that have emerged from biological studies on animal and cellular models of neurological and oncological diseases have focused drug discovery projects upon identifying reversible MAO inhibitors.. Screening of our in-house academic compound library identified two hit compounds that inhibit MAO-B with IC50 values in micromolar range.. Two series of indole (23 analogues) and 3-(benzyloxy)benzyl)piperazine (16 analogues) MAO-B inhibitors were derived from hits, and screened for their structure-activity relationships. Article Title: Thiadiazine-thiones as inhibitors of leishmania pteridine reductase (PTR1) target: investigations and in silico approach. Article Snippet: .. After binding site selection, default parameters of FRED were used to predict the binding affinities of the natural compound against Leishmania-PTR1, a grid map was prepared with a grid box size of 50 50 50Å using Make other:Article Title: Virtual Screening and Experimental Validation Identify Novel Inhibitors of the Plasmodium falciparum Atg8–Atg3 Protein–Protein Interaction Article Snippet: The Binding Assay:Article Title: Thiadiazine-thiones as inhibitors of leishmania pteridine reductase (PTR1) target: investigations and in silico approach. Article Snippet: .. After binding site selection, default parameters of FRED were used to predict the binding affinities of the natural compound against Leishmania-PTR1, a grid map was prepared with a grid box size of 50 50 50Å using Make Selection:Article Title: Thiadiazine-thiones as inhibitors of leishmania pteridine reductase (PTR1) target: investigations and in silico approach. Article Snippet: .. After binding site selection, default parameters of FRED were used to predict the binding affinities of the natural compound against Leishmania-PTR1, a grid map was prepared with a grid box size of 50 50 50Å using Make |