SLAS Discovery

Scope & Guideline

Highlighting Pioneering Research for a Healthier Tomorrow

Introduction

Delve into the academic richness of SLAS Discovery with our guidelines, detailing its aims and scope. Our resource identifies emerging and trending topics paving the way for new academic progress. We also provide insights into declining or waning topics, helping you stay informed about changing research landscapes. Evaluate highly cited topics and recent publications within these guidelines to align your work with influential scholarly trends.
LanguageEnglish
ISSN2472-5552
PublisherELSEVIER SCIENCE INC
Support Open AccessYes
CountryUnited States
TypeJournal
Convergefrom 2017 to 2024
AbbreviationSLAS DISCOV / SLAS Discov.
Frequency10 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressSTE 800, 230 PARK AVE, NEW YORK, NY 10169

Aims and Scopes

SLAS Discovery focuses on innovative methodologies and technologies that drive drug discovery and development, particularly emphasizing high-throughput screening (HTS) and its applications across various therapeutic areas.
  1. High-Throughput Screening (HTS):
    The journal extensively covers the development and optimization of high-throughput screening methodologies for drug discovery, enabling rapid evaluation of large compound libraries against biological targets.
  2. Cell-Based Assays and Imaging:
    SLAS Discovery emphasizes the use of cell-based assays, including high-content imaging and 3D cell cultures, to better mimic in vivo conditions and enhance the relevance of screening results.
  3. Target Identification and Validation:
    Research published in the journal often focuses on novel strategies for target identification and validation, including the application of proteomics and genomics to discover new drug targets.
  4. Automation and Robotics in Drug Discovery:
    The journal highlights advancements in automation and robotics that facilitate efficient assay development and compound screening, improving reproducibility and data quality in drug discovery.
  5. Phenotypic Screening:
    SLAS Discovery also explores phenotypic screening approaches that assess biological responses to compounds in cellular models, offering insights into complex drug action mechanisms.
  6. Emerging Technologies:
    The journal is dedicated to showcasing emerging technologies such as artificial intelligence (AI) and machine learning (ML) in drug discovery, aiming to enhance data analysis and predictive capabilities.
The landscape of drug discovery is rapidly changing, and SLAS Discovery reflects this evolution through an increasing focus on several key emerging themes.
  1. COVID-19 Therapeutics:
    A significant number of recent publications are dedicated to discovering and validating therapeutics for COVID-19, reflecting the urgent need for effective treatments and the journal's responsiveness to global health challenges.
  2. 3D Cell Culture and Organoids:
    There is a growing trend towards the use of 3D cell culture systems and organoids, which provide more accurate representations of human tissues, enhancing drug screening and development processes.
  3. Artificial Intelligence and Machine Learning:
    The integration of AI and machine learning techniques into drug discovery processes is on the rise, with studies focusing on data mining, predictive modeling, and automated analysis to streamline hit identification.
  4. Targeted Protein Degradation:
    Research on targeted protein degradation, particularly using PROTACs (Proteolysis Targeting Chimeras), is emerging as a significant area of interest, offering new strategies for drug discovery against challenging targets.
  5. Synergistic Drug Combinations:
    There is an increasing focus on identifying synergistic drug combinations to enhance therapeutic efficacy, particularly in cancer treatment, which reflects a shift towards personalized medicine approaches.

Declining or Waning

While SLAS Discovery continues to evolve, certain themes are becoming less prominent in recent publications, indicating a shift in focus within the field.
  1. Traditional Biochemical Assays:
    There is a noticeable decline in publications focusing solely on traditional biochemical assays, as the field moves towards more complex and physiologically relevant models.
  2. Single-Dimensional Drug Screening:
    Research centered around single-dimensional drug screening methods is waning, with a shift towards more integrated and multi-parametric approaches that provide a broader understanding of drug effects.
  3. Basic Pharmacology Studies:
    Basic pharmacology studies that do not incorporate advanced technologies or high-throughput capabilities appear to be less frequent, as there is a growing emphasis on translational research and clinical relevance.
  4. In Vitro Models Lacking Complexity:
    The use of simplistic in vitro models is decreasing, as researchers prioritize more complex systems that better replicate human physiology, such as organoids and multi-cellular models.
  5. Focus on Established Targets:
    There is a reduction in studies targeting well-characterized pathways or proteins, as the field increasingly seeks novel targets and mechanisms of action to overcome drug resistance.

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