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The Solubility Fragment Library consists of about 957 low molecular fragments with "Rule-of-Three" compliance and assured solubility in both DMSO (200mM) and PBS buffer (1mM). The library design included diversity filtering in order to provide chemical structure variety for your fragment screening program.
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The OTAVA MolGluesLike Compounds Library is a scientifically curated collection of 2750 small molecules designed to enable the discovery and development of molecular glues — a groundbreaking modality in drug discovery that stabilizes or induces protein-protein interactions (PPIs).
These specialized compounds have the potential to redefine therapeutic strategies by targeting previously “undruggable” proteins, offering exciting opportunities in areas such as oncology, immunology, and neurodegenerative disease research.
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The OTAVA GPCR Antagonist Library is a computationally designed collection created to explore GPCR-privileged chemical space with a focus on antagonist and inverse-agonist pharmacology.
The library integrates ligand-based machine learning, Bayesian modeling, and AI-driven scaffold optimization to enable efficient discovery of structurally diverse GPCR antagonists.
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Our company is currently offering about 100 new quaternary ammonium salts that could be of interest to your research. All quaternary ammonium salts are in stock, and a full list of the salts in our catalog is available upon request.
Synthetic experience of Otava chemists allows to carry out custom syntheses of even more complex structures of quaternary ammonium salts at a reasonable price.
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800+ billion ready-to-synthesize virtual compounds for bRo5 drug discovery
ChemInfinita is a steadily expanding make‑on‑demand virtual space built, in collaboration with Alipheron, from commercial and proprietary building blocks and lab‑validated reaction templates—designed to prioritize robust synthetic feasibility at scale.
The space is searchable through Alipheron’s Hyperspace Search and Pharos‑3D platforms, enabling rapid virtual exploration and practical search‑to‑synthesis workflows.
A defining feature is its deliberate emphasis on beyond‑Rule‑of‑5 (bRo5) chemical matter-an increasingly important region of chemical space for discovery programs aimed at “difficult” targets and non‑classical binding sites.
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