Theoretical–Cheminformatic Study of Four Indolylphytoquinones, Prospective Anticancer Candidates

<b>Background/Objectives:</b> Breast cancer is a disease with a high mortality rate worldwide; consequently, urgent achievements are required to design new greener drugs, leaving natural products and their derivatives as good options. A constant antineoplastic effect has been observed when the phytoproduct contains an indole fragment. <b>Methods:</b> Therefore, the objective of this work was to carry out a thoughtful computational study to perform an appropriate evaluation of four novel molecules of the class of the 3-indolylquinones as phytodrug candidates for antineoplastic activity: thymoquinone (TQ), 2,6-dimethoxy-1,4-benzoquinone (DMQ), 2,3-dimethoxy-5-methyl-1,4-benzoquinone (DMMQ), and 2,5-dihydroxy-1,4-benzoquinone (DHQ). It is important to highlight that the obtained computational results of the target compounds were compared-correlated with the theoretical and experimental literature data previously reported of several indolylquinones: indolylperezone, indolylisoperezone, indolylmenadione, and indolylplumbagin (IE-IH, respectively). Results: The results revealed that the studied structures possibly presented antineoplastic activity, in addition to the fact that the reactivity parameters showed that two of the evaluated compounds have the option to present IC<sub>50</sub> values lower than or similar to 25 mg/mL, activity like that of indolylisoperezone; moreover, they show molecular coupling to PARP-1. Finally, the prediction of the calculated physicochemical parameters coincides with the Lipinski and Veber rules, indicating that the adsorption, metabolism, and toxicity parameters are acceptable for the studied compounds, obtaining high drug score values. <b>Conclusions:</b> Finally, a comparison between the proposed molecules and others previously synthesized was appropriately performed, establishing that the synthesis of the studied compounds and the determination of their pharmacological properties in an experimental manner are of interest.

Authors

Institutions

Publication Details

Journal
Pharmaceuticals
Published
2024-11-26
DOI
https://doi.org/10.3390/ph17121595
Citations
1
Primary Topic
Bioactive Compounds and Antitumor Agents
Type
article
Field-Weighted Citation Impact
0.35

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Theoretical–Cheminformatic Study of Four Indolylphytoquinones, Prospective Anticancer Candidates

René Miranda, Edgar Daniel Moyers-Montoya, Carlos A. Perez, María Inés Nicolás‐Vázquez et al.
1 citations
Pharmaceuticals
Bioactive Compounds and Antitumor Agents
0.35
article

Theoretical–Cheminformatic Study of Four Indolylphytoquinones, Prospective Anticancer Candidates

René Miranda, Edgar Daniel Moyers-Montoya, Carlos A. Perez, María Inés Nicolás‐Vázquez, Perla E. García‐Casillas, René Gerardo Escobedo-González, Wilber Montejo-López, María Jazmín Castañeda-Muñoz, Daniel Márquez-Olivas
article en
1 citations

Abstract

<b>Background/Objectives:</b> Breast cancer is a disease with a high mortality rate worldwide; consequently, urgent achievements are required to design new greener drugs, leaving natural products and their derivatives as good options. A constant antineoplastic effect has been observed when the phytoproduct contains an indole fragment. <b>Methods:</b> Therefore, the objective of this work was to carry out a thoughtful computational study to perform an appropriate evaluation of four novel molecules of the class of the 3-indolylquinones as phytodrug candidates for antineoplastic activity: thymoquinone (TQ), 2,6-dimethoxy-1,4-benzoquinone (DMQ), 2,3-dimethoxy-5-methyl-1,4-benzoquinone (DMMQ), and 2,5-dihydroxy-1,4-benzoquinone (DHQ). It is important to highlight that the obtained computational results of the target compounds were compared-correlated with the theoretical and experimental literature data previously reported of several indolylquinones: indolylperezone, indolylisoperezone, indolylmenadione, and indolylplumbagin (IE-IH, respectively). Results: The results revealed that the studied structures possibly presented antineoplastic activity, in addition to the fact that the reactivity parameters showed that two of the evaluated compounds have the option to present IC<sub>50</sub> values lower than or similar to 25 mg/mL, activity like that of indolylisoperezone; moreover, they show molecular coupling to PARP-1. Finally, the prediction of the calculated physicochemical parameters coincides with the Lipinski and Veber rules, indicating that the adsorption, metabolism, and toxicity parameters are acceptable for the studied compounds, obtaining high drug score values. <b>Conclusions:</b> Finally, a comparison between the proposed molecules and others previously synthesized was appropriately performed, establishing that the synthesis of the studied compounds and the determination of their pharmacological properties in an experimental manner are of interest.

PharmaceuticalsVol. 17(12)
Universidad Autónoma de Ciudad Juárez (MX), Universidad Autónoma de Coahuila (MX), Universidad de Cuautitlán Izcalli (MX), Hospital de Especialidades (MX), Universidad Autónoma de Chiapas (MX), Instituto Tecnológico de Ciudad Juárez (MX), Universidad Tecnologica de Ciudad Juarez, Universidad Nacional Autónoma de México (MX), Tecnológico de Monterrey (MX)
Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México
Good health and well-being
Openalex Percentile: Top 39%
Bioactive Compounds and Antitumor Agents
0.35
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.