Please use this identifier to cite or link to this item:
http://ri.uaemex.mx/handle20.500.11799/79879| DC Field | Value | Language |
|---|---|---|
| dc.creator | ESVIETA TENORIO BORROTO | - |
| dc.creator | CLAUDIA GIOVANNA PEÑUELAS RIVAS | - |
| dc.creator | JUAN CARLOS VAZQUEZ CHAGOYAN | - |
| dc.creator | Nilo Ramón Castañedo Cancio | - |
| dc.creator | FRANCISCO JAVIER PRADO PRADO | - |
| dc.creator | Xerardo Garcia-Mera | - |
| dc.creator | HUMBERTO GONZALEZ DIAZ | - |
| dc.date | 2014-01-05 | - |
| dc.date.accessioned | 2022-04-21T05:17:57Z | - |
| dc.date.available | 2022-04-21T05:17:57Z | - |
| dc.identifier | http://hdl.handle.net/20.500.11799/79879 | - |
| dc.identifier.uri | http://ri.uaemex.mx/handle20.500.11799/79879 | - |
| dc.description | Modelos matematicos y citometria | - |
| dc.description | Quantitative Structure-Activity (mt-QSAR) techniques may become an important tool for prediction of cytotoxicity and High-throughput Screening (HTS) of drugs to rationalize drug discovery process. In this work, we train and validate by the first time mt-QSAR model using TOPS-MODE approach to calculate drug molecular descriptors and Linear Discriminant Analysis (LDA) function. This model correctly classifies 8,258 out of 9,000 (Accuracy = 91.76%) multiplexing assay endpoints of 7903 drugs (including both train and validation series). Each endpoint correspond to one out of 1418 assays, 36 molecular and cellular targets, 46 standard type measures, in two possible organisms (human and mouse). After that, we determined experimentally, by the first time, the values of EC50 = 21.58 μg/mL and Cytotoxicity = 23.6 % for the anti-microbial / antiparasite drug G1 over Balb/C mouse peritoneal macrophages using flow cytometry. In addition, the model predicts for G1 only 7 positive endpoints out 1,251 cytotoxicity assays (0.56% of probability of cytotoxicity in multiple assays). The results obtained complement the toxicological studies of this important drug. This work adds a new tool to the existing pool of few methods useful for multi-target HTS of ChEMBL and other libraries of compounds towards drug discovery. | - |
| dc.description | Conacyt | - |
| dc.language | eng | - |
| dc.publisher | European Journal of Medicinal Chemistry | - |
| dc.relation | 24; | - |
| dc.rights | info:eu-repo/semantics/openAccess | - |
| dc.rights | http://creativecommons.org/licenses/by-nc-nd/4.0 | - |
| dc.source | 0223-5234 | - |
| dc.subject | Flow cytometry | - |
| dc.subject | High-throughput model | - |
| dc.subject | Drug immunotoxicity | - |
| dc.subject | Multiplex assay endpoints | - |
| dc.subject | info:eu-repo/classification/cti/3 | - |
| dc.title | Model for High-Throughput Screening of drug immunotoxicity - study of the antimicrobial G1 over peritoneal macrophages using flow cytometry | - |
| dc.type | article | - |
| dc.audience | students | - |
| dc.audience | researchers | - |
| item.grantfulltext | none | - |
| item.fulltext | No Fulltext | - |
| Appears in Collections: | Producción | |
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