Our in vitro biology team is highly skilled in wide range of therapeutic areas and target classes. De novo assay development for novel target classes or therapeutic indications, as well as assay customization, have added significant value to our Integrated Drug Discovery (IDD) projects. This has also resulted in successful compound progression and clinical candidate nomination. The in vitro team interacts seamlessly with CADD and medicinal chemists for better SAR optimizations.
Our offerings include screening and profiling services or platforms under different therapeutic areas and target classes. We have experience in target classes such as enzymes (of various classes), GPCRs, ion channels, proteases, membrane receptors etc. Aurigene focuses and caters to a wide range of therapeutic areas like asthma and COPD, metabolic disorders, inflammation, oncology, immunology, stem cell biology, osteoporosis, angiogenesis, CNS, fibrosis, and pain. In addition, we have experience in epigenetics and protein-protein Interaction targets. At Aurigene, along with small molecules, we are continuously adding the services for advanced and emerging drug classes like PROTACs, peptides, Oligonucleotide (siRNAs, ASOs), ADC, and mRNA. We offer a complete set of bioassays for PROTAC discovery, right from binary binding assays, ternary complex assays, and associated phenotypic and mechanistic assays.

Complex and specialized assay development
High throughput expression system
Functional, Mechanism of Action (MoA), and Target Engagement Studies
Supported by in-house reagent generation team specialized in making quality reagents like plasmids, cell lines, antibodies, and proteins in small and large scale.
We understand that clear communication is essential to successful collaborations, and that's why we have a dedicated team that is always ready to help you. Whether you have questions about our services, want to discuss a potential partnership, or simply want to learn more about our company, we're here to help.
Our team of experts is dedicated to providing personalised solutions tailored to your unique needs. So, please don't hesitate to reach out to us. We look forward to hearing from you and helping you achieve your business goals.
JUNE 28, 2022
An effective anti-tumor immune response in human is marked by presence of T cells reactive against neoantigens. Neoantigens are HLA-bound unique peptides arise from tumor-specific somatic mutations. Neoantigens are highly immunogenic because they are not present in normal tissues and hence bypass central thymic tolerance. The success of immune checkpoint blockade...
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The global Highly Potent Active Pharmaceutical Ingredients (HPAPI) market is expected to reach USD 26.84 Billion by 2023 from USD 17.72 Billion in 2018, at a CAGR 8.7%....
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Introduction: An orally-available anti-diabetic candidate that simultaneously targets all three key organs of diabetes: Pancreas, Liver and Muscles. This drug targets the two main defects seen in patients with type 2 diabetes: The pancreas by increasing insulin secretion, in a glucose-dependent manner; and the muscles and liver by decreasing the excess production...
Read MoreAugust 28, 2020
A convenient and one-pot synthesis of tetracyclic isoindolo [1,2-a]quinazoline derivatives via Lewis acid mediated sequential C–N bond formation reactions is reported. This protocol provides a simple and rapid strategy for the synthesis of 12-benzylidene-10,12-dihydroisoindolo[1,2-b]quinazoline derivatives. However, a variety of tetracyclo indole fused quinazol...
Read MoreJanuary 31, 2025
Drug Delivery System (DDS) has been used successfully in the past few decades to cure illnesses and enhance health because of its improved systemic circulation and ability to regulate the drug's pharmacological action. As pharmacology and pharmacokinetics advanced, the idea of controlled release emerged, demonstrating the significance of drug release in assessing...
Read MoreJanuary 31, 2025
Proteolysis-targeting chimera (PROTACs) represents a promising modality that has gained significant attention for cancer treatment. Using PROTAC technology, we synthesized novel structurally modified paullone-based PROTACs using Cereblon (CRBN) and Von Hippel–Lindau (VHL) E3 ligands....
Read MoreMarch 13, 2025
Decitabine is an anti-cancer chemotherapy drug. This article describes method development and method verification of Assay of Decitabine in tablet formulation. A new, precise, rapid, accurate RP-HPLC method has been developed for the estimation of Decitabine in pharmaceutical tablets dosage form. After optimization the good chromatographic separation was achieved...
Read MoreIn vitro biology services at Aurigene play a critical role in early drug discovery and development by helping sponsors evaluate target engagement, potency, selectivity, and mechanism of action before moving into animal studies. As an experienced in vitro biology services company, we design fit-for-purpose assays that generate reliable data for hit identification, lead optimization, and candidate selection.
Our in vitro biology CRO services support rapid screening of compound libraries, validation of biological targets, and assessment of functional activity in relevant cell-based systems. By using robust in vitro biology and screening services, sponsors can reduce attrition risk, refine SAR strategies, and make data-driven decisions early in the development cycle.
Aurigene offers a broad range of in vitro biology assay formats to support different therapeutic areas and target classes. These include biochemical assays, enzyme inhibition assays, receptor binding assays, cell-based functional assays, reporter gene assays, cytotoxicity assays, and pathway-based assays.
As part of our in vitro biology and screening services, we also support high-throughput screening (HTS), secondary assays, selectivity profiling, and mechanistic studies. Our in vitro biology CRO services are tailored to sponsor needs, whether for small molecules, peptides, or biologics, and are designed to generate reproducible and actionable biological data.
Quality and reliability are ensured through standardized assay development, validated protocols, trained scientific teams, and controlled laboratory systems. As a trusted in vitro biology services company, Aurigene emphasizes assay optimization, proper controls, statistical validation, and reproducibility testing.
Our in vitro biology services follow SOP-driven execution, detailed documentation, and data review processes to ensure accuracy and traceability. This structured approach allows sponsors to confidently use the data for internal decision-making and regulatory interactions.
The in vitro biology services workflow at Aurigene starts with understanding the biological target, mechanism, and development objective. We then move to assay selection or development, optimization, validation, and pilot testing. Once finalized, the assay is executed with defined controls and statistical parameters.
Data analysis, interpretation, and reporting follow, with clear communication throughout the project. As part of our in vitro biology CRO services, we ensure transparency in timelines, experimental design, and deliverables to support efficient drug discovery progression.
High-throughput screening (HTS) at Aurigene is conducted using automated platforms, validated assay formats, and robust data analysis systems. As part of our in vitro biology and screening services, we screen large compound libraries against defined biological targets using optimized in vitro biology assay systems.
Each screening campaign includes assay validation, Z′ factor assessment, positive and negative controls, and statistical quality checks to ensure reliable hit identification. Our in vitro biology services enable rapid and reproducible screening, helping sponsors identify promising leads for further development.
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October 24th-26th, 2023 | Barcelona, Spain
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