Our in vitro biology team has in-depth knowledge of different therapeutic areas and target classes. De novo assay development without any literature precedence for novel target classes or therapeutic indications along with assay customization has added significant value to our Integrated Drug Discovery (IDD) projects and driven compound progression and clinical candidate nomination successfully.
Our offerings include screening and profiling services/platforms under different therapeutic areas and target classes.

A platform for screening of NCEs and NBEs against major therapeutic target classes: GPCRs, ion channels, proteases, other hydrolytic enzymes, and membrane receptors are a few examples of our experience in target classes.
APSL focuses and caters to a wide range of therapeutic areas like asthma and COPD, metabolic disorders (diabetes, NASH & obesity), inflammation, oncology, immunology, stem cell biology, osteoporosis, angiogenesis, CNS, and pain. We also have experience in epigenetics and Protein-Protein Interaction (PPI) targets. At APSL, we are continuously adding the experience of advanced and emerging drug classes. Examples include PROTAC, Oligonucleotide, ADC, and mRNA. We offer a complete set of bioassays for PROTAC discovery.
Complex and specialized assay development
High throughput expression system
Functional, Mechanism of Action (MoA) and target engagement studies
Expertise to support Integrated Drug Discovery programs
Deep therapeutic insights and state-of-the-art facilities
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.
Aurigene Pharmaceutical Services is a leader in the synthesis of activated MethoxyPolyethyleneGlycol(m-PEGs), With a comprehensive product range and customized services. ...
Read More2020
A novel approach for the spiro-isoindolinone dihydroquinazolinones has been demonstrated from 2- aminobenzamide and 2-cyanomethyl benzoate in the presence of KHMDS as a base to get moderate yields. The reaction has been screened in various bases followed by solvents and a gram scale reaction has also been executed under the given conditions. Based on the controll...
Read More2005
An improved and rapid synthesis of mefenamic acid based indole derivatives has been achieved via the ligand free Cu-catalyzed coupling-cyclization method under ultrasound irradiation. This simple, straightforward and inexpensive one-pot method involved the reaction of a terminal alkyne derived from mefenamic acid with 2- iodosulfanilides in the presence of CuI ...
Read More2005
The formal synthesis of Cladospolide-C and its analog is achieved by using enantiopure (R)-g evalerolactone 10. The significant points of this synthesis are the stereoselective dihydroxylation of a, bunsaturated ester 16 using Sharpless protocol, Wittig olefination of g evalerolactol 6 with triphenylphosphonium iodide salt 7, one pot selective oxidation ...
Read More2005
A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a catalyst, giving good to moderate yields. In this reaction the substrate scope for amines and aldehydes was also investigated. The reaction has been checked on a large scale ...
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