Our IDD team comprises medicinal chemists, computational chemists, biologists, pharmacologists, and toxicologists with extensive experience in delivering developmental candidates for clients. The key component of our IDD programs is a focused and dedicated team of experts, well-coordinated to deliver to clients expectations efficiently.
Our IDD platform spans across discovery and development of large and small molecules with the most effective and efficient means to conduct target validation, translational interrogation, therapeutic discovery, and preclinical development for our clients.
We have the capabilities to simultaneously apply multiple modalities for target validation and therapeutic discovery, as per specific target or pathway. With seamless integration into development stages, we offer a hassle-free outsourcing experience that is outcome driven and quality focused.
IDD services
We deliver a wide range of IDD services spanning chemistry, biology, DMPK, and toxicology to global clients based across diverse therapeutic areas. Our services seamlessly span the entire journey from early discovery to IND.
We offer an array of help in terms of project management and logistics. Our seasoned project management and senior scientific advisory services team adds value with insight and guidance for a smooth path to a development candidate.
Mix and Match programs
We provide mix and match services which includes the following service combinations:
- Medicinal chemistry + DMPK
- Medicinal chemistry design and synthesis: iterate design, synthesize and develop SAR
- Chemistry + DMPK + scale up
- Chemistry + DMPK + biology + toxicology
Why Aurigene Integrated Drug Discovery (IDD) Services?
18 years' experience in drug discovery
Various customer models: multi-year contract-based FTE models with big pharma as well as rapid hit
100+ discovery programs
Track record of delivering 8+ IND candidates
Speed: Our average candidate nomination time is 24-28 months
Capabilities to apply multiple modalities
Integrated project management
Various therapeutic modalities like oncology, anti-infectives, CNS & inflammation
Virtual Tour
Hyderabad R and D Center
Bangalore R and D Center
Connect with our scientific experts for your drug discovery, development, and manufacturing needs
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.
Methoxy Polyethylene Glycol (m-PEGs)
Aurigene Pharmaceutical Services is a leader in the synthesis of activated MethoxyPolyethyleneGlycol(m-PEGs), With a comprehensive product range and customized services. ...
Read More
Base mediated spirocyclization of quinazoline: one-step synthesis of spiro-isoindolinone dihydroquinazolinones
2020
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 More-
Ultrasound assisted rapid synthesis of mefenamic acid based indole derivatives under ligand free Cu-catalysis: Their pharmacological evaluation
2005
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 More -
Formal synthesis of Cladospolide C & epi-Cladospolide C using R- (þ)-g-valerolactone as a chiral synthon
2005
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 More -
Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds
2005
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 ...
Read More
You are about to leave Aurigene Pharmaceutical Services and affiliates website. Aurigene Pharmaceutical Services assumes no responsibility for the information presented on the external website or any further links from such sites. These links are presented to you only as a convenience, and the inclusion of any link does not imply endorsement by Aurigene Pharmaceutical Services.
If you wish to continue to this external website, click Proceed.
Leaving already?
Don't forget to join us at
CPHI Worldwide 2023.
October 24th-26th, 2023 | Barcelona, Spain
Get ready to accelerate your drug’s journey to the market