A custom selection of compounds that suits your specific needs could be dispatched in any custom format to you within 1-3 weeks.
To meet a wide range of research needs of small molecules screening projects, ChemDiv has a carefully designed set of diversified Targeted and Focused libraries. Focused and targeted compounds libraries cover over 20 therapeutic areas, target families including GPCR, Ion Channels, Kinases, Proteases, Phosphotases, Nuclear receptors, different mechanism of actions, PPI modulators, various receptors ligands, epigenetic mechanisms and specific structural motives grouped in screening sets like mimetics compounds, macrocylces, spiro compounds, indioles, cyclic compounds, fragments, covalent inhibitors, natural and natural-based small molecules.
There are assembled screening sets for agrochemical, including antifungal compounds, antiparasitic libraries. Small molecules conform to the Generally Recognized as Safe (GRAS) concepts in cosmetics and food industries.
Our computational, structural biology, synthetic and medicinal screening team follows current trends in modern structure-based drug discovery to adds novel diverse and targeted compounds. The latter selections are aimed at tackling multiple targets, protein domains, pathways, cellular processes, etc. Representative examples of these biased screening libraries include modulators of numerous protein-protein interactions, stem cell differentiation, apoptosis, proteasome cascade including diverse ligases, autophagy, epigenetics machinery, cell cycle including quiescent cancer cells, motor proteins, mitochondrial homeostasis and cell energetic, viral targets, bacterial genome, protein folding machinery including scaffolding proteins and chaperones and many others. Our general approach to these sets includes analysis of the available chemical and biological information, identification of key pathway nodules/targets, computational and ‘wet biology’ assessment of target draggability and potential binding domains. The resulting information is analyzed by our synthetic team to design scaffolds for novel chemical libraries production that are likely to interact with the designated targets yielding focused screening compound libraries and Libraries for Hit Identification.
Our compounds screening libraries have a perfect diversity scoring by Tanimoto similarity threshold, by bias against undesirable structural patterns. Structural enrichment is done with the focus on novel chemistry by Markush fragments. The scaffolds are prioritized by structural complexity, by 3D shape diversity and Fsp3 distribution range. All chemical compounds passed REOS and PAINS filters, have high MCE-18 score, optimized solubility, and «target diversity» approach in biological activity.
A list of diversity screening compounds libraries includes 9 compounds libraries prepared using different design approaches.
100,000 maximum diversity preplated screening compounds library represents 1.6m stock available screening compounds collection and 13B virtual space of drug-like and lead-like chemical compounds. The collection has perfect diversity scoring by Tanimoto similarity, includes concentric diversity subsets 20k-30k-50k-100k. Structural enrichment is done with the focus on novel chemistry by Markush fragments. All screening compounds passed REOS and PAINS, have high MCE-18 score optimized solubility and «target diversity» approach in biological activity. Chemical compounds from over 70 targeted and focused libraries are included. Customers can cherry-pick small molecules by plates.
3D-Pharmacophore Based Screening Diversity Library is designed taking into consideration that proteins contain binding sites different in their spatial geometry and potential hot-spots / binding points for small molecule compounds. Following the “Picklock” Concept, a library that contains a minimal number of compounds with high diversity in terms of potential pharmacophore points could be applied for any protein to obtain primary hits during HTS campaigns.
Each molecule has 3D-conformation generated in Corina Software. Three the most different 3-centered pharmacophore hypothesis have been automatically constructed per a conformation mainly focusing on HBA, HBD and HYD/LIPO/ARO points. All the generated pharmacophore hypothesis has been then clustered to obtain a pool of the most divers 3D-models. 13B small molecules have been subsequently screened in silico using this pool. The most divers virtual compounds hits have been then selected from each pharmacophore pool. These screening compounds properly cover the operating chemical space.
Soluble Diversity Screening Library is aimed to improve biophysical properties including solubility and drug-like properties of the screening set while maintain its chemical diversity. We anticipate that this set will address the undesired „supra-molecular‟ phenomena in the in vitro/ex vivo assays associated with aggregation, precipitation or formation of colloidal systems.
‘Soluble diversity” set is designed consistent with key points, namely:
— Predicted high solubility of compounds (logSW > -2.0).
— High diversity of substances. The current set is built around 500 diverse scaffolds to yield a library of 10K compounds.
— Novelty. A special effort has been made to select compounds and scaffolds with good IP potential.
— High chemical quality. The special rules of ChemDiv‟s medchem filters ensure the high quality of selected drug-like molecules. All unwanted chemotypes or compounds bearing reactive groups were removed (e.g. Michael acceptors, redox agents, polyaromatics, epoxides, quinones, etc.).
— Good physico-chemical properties of compounds selected. A variety of criteria was considered for this library selection; among those are:
3D diversity is pivotal because the molecular shape is a crucial factor in molecular recognition by a biomolecule. 3D-Diversity Natural-Product-Like Screening Library contains 1479 clusters based on the pharmacophore 3D-similarity metric and 738 unique heterocycles. The key concepts that the chemical library design is based on are 3D shape, pharmacophore diversity, drug-likeness, and chemical beauty. Natural products (NP) have been widely used for the treatment of diseases and illnesses since antient times. Analysis of natural products over the past 30 years revealed that approximately 40% of the developed therapeutics drugs approved by FDA were NPs, NP derivatives, or synthetic mimetics related to NPs. With their highly and sophisticated biological and chemical diversity, NPs and their derivatives have been used to explore biologically relevant space. The significant impact of NPs on the discovery of therapeutic agents is based on their embedded biosynthetic molecular recognition.
The concept of Targeted Diversity chemical space is intended for the design of high-quality screening libraries of drug-like compounds that have been focused against various biological targets. Targeted diversity signifies the superposition of highly diverse chemical space on the assortment of divergent families or sub-families of targets and unique biomolecules. Targeted Diversity make possible the design of high-quality discovery chemical libraries of drug-like molecules, selectable focused against different biological targets. This concept also uses the superposition of a highly diverse chemical space on a representative assortment of divergent families & sub-families of targets, signaling, and transport molecules. The Targeted Diversity concept is a broadly applicable platform approach, for it can be used to design and/or select high quality screening libraries of drug-like compounds focused in individual therapeutics areas, target families, or control pathways.
A major benefit of Smart Library approach is that it represents a thoughtful and multi-purpose diversity set, incorporated it into one single compound library for different screening goals. Those goals may include: “Difficult” targets (no target/ligand structure(-s) known, study and interrogation of cellular processes (e.g. apoptosis, cell cycle, etc.); Signaling pathways (e.g. WNT, Hh, RTK, Ras, etc.) and “eclectic” biological targets, including cellular processes (e.g. apoptosis and cell cycle); Protein-protein interactions (the most «hot spots», e.g. XIAP, pGPCRs, beta-catenin, etc.); An entire selected therapeutic area that incorporates multiple biological targets;
The paradigm of “drug likeness” dramatically altered the behavior of the medicinal chemistry community for a long time. In recent years, scientists have empirically found a significant increase in key properties of drugs that have moved structures closer to the periphery or the outside of the rule-of-five “cage”. Herein, we show that for the past decade, the number of small molecules claimed in patent records by major pharmaceutical companies has dramatically decreased, which may lead to a “chemical singularity”. New screening compounds containing fragments with increased 3D complexity are generally larger, slightly more lipophilic, and more polar. A core difference between this study and recently published papers is that we consider the nature and quality of sp3-rich frameworks rather than sp3 count. We introduce the original descriptor MCE-18, which stands for Medicinal Chemistry Evolution, 2018. This measure can effectively score molecules by novelty in terms of their cumulative sp3 complexity.
The drug discovery process is long and expensive. Our aim is to shorten this process by producing high-quality, hit-like, lead-like, and drug-like screening compounds that generate valuable data from discovery screening programs.
If you have an existing therapeutic target but no chemical starting point, we can be your partner to find such a lead and accelerate drug discovery.
Chemical arrays as small as 20 and as large as 500 members can be custom-made or picked up from the existing stock reflective of the structure-based assessment of a target or pathway. Notably, all screening compounds are chosen to exhibit a range of drug-like and lead-like properties. Generally, our team requests ca. 2 weeks to generate and propose set of libraries (10-25+) addressing your biological interests. Select it immediately from existing stock of 1.6 M screening compounds.
All chemical libraries for lead discovery are regularly updated at the rate of 100K new screening compounds per year with our novel, IP-defined compounds resulting from the internal development. We are pleased to consider and adopt your custom protocols in order to make focused inhibitors set(s) that suit your specific needs. Our highly diverse molecules are produced using ‘traditional’ synthetic approaches with yields of up to 100-150 mg per compound and average purity greater than 92% as determined by both NMR and LCMS analyses. Complimentary to our proprietary chemotypes, we also offer a selection of custom building blocks.
In addition to producing libraries, we could be your partner of choice for screening. For the list of our in vitro, ex vivo and in vivo assay capabilities, please visit this Biology Services.
ChemDiv ensures resupply, resynthesis, immediate active chemical analogs selection, medchem FTE support for H2L.
Please e-mail us to sb@chemdiv.com or chemdiv@chemdiv.com and we configure the best screening set for your projects and inventory.
Customers are welcome to order selected screening sets in 96- and 384- well formats as dry powders and /or as DMSO solutions frozen. ChemDiv’s chemical compounds are delivered as dry powders or DMSO solution frozen in a convenient predefined custom plate format or vials. Detailed structure files and plate map and spectral data are available via secure FTP. Equimolar weighting is available.
Standard volume per well options for DMSO solutions frozen includes 10ul, 25 ul, 50ul, 100 ul, 200ul and 500 ul @10mM. Samples may be delivered in your labware or in our standard 96 or 384 well screening plates or standard minitubes.
Compounds for small selections (<100 items) are shipped within 1-2 business days. Any larger selection of Compounds will be delivered within 2 weeks after the confirmation of the Customer’s Purchase Order.
Please contact us and send your request to chemdiv@chemdiv.com. We will discuss in details your preferable options for screening compounds selection, screening set design, format requirements and delivery time. After placing Purchase order, we will deliver in 2-6 weeks, depending on the compounds library size. Delivery terms DAP, 30 days payment connection.
ChemDiv, Inc. Standard Terms & Conditions
Title and License to Designs and Compounds.
ChemDiv retains title and reserves all rights to its Discovery Collection ©, Discovery outSource ® and Chemistry on Demand ® and Store.ChemDiv.com ®, Chemdiv.com ®, Compound Designs (Designs and Compounds) except as provided herein.
ChemDiv grants the Purchaser a royalty-free, worldwide license for any commercial use of its Designs and Compounds, except for sale, transfer, or sublicense to Third Parties without prior consent. Purchaser will have the title and unrestricted rights for any derivative design and compound in any field of use.
No Infringement. ChemDiv has no knowledge that the transfer to and use by the Purchaser of any delivered Designs and Compounds will violate any Patents which have been issued, or that other proprietary rights of any Third Party would be infringed by the manufacture, use, sale or distribution of the Designs and Compounds.
Indemnification. Purchaser agrees to indemnify, defend and hold harmless ChemDiv from and against any loss, damage, or liability, including interest and penalties and reasonable attorney's fees, and any claim, complaint, suit, proceeding or cause of action against ChemDiv resulting from or arising out of the Purchaser's use of the Designs and Compounds supplied by the ChemDiv.
No Resale. The resale, grant, gift, transfer or trade of the Designs and Compounds in whole or part, or any associated data, to any Third Party is prohibited without the express written consent of ChemDiv.
The libraries and compounds transferred to customers are provided for convenience, so the customer can verify the chemical structures, assess their physio-chemical and biological characteristics, and determine the suitability of the libraries and compounds for their own research and development purposes.
The purchaser has full rights to make, use, and have made the compounds and libraries. Purchasers hold title and unrestricted rights for any derivative design or derivative compound in any field of use. ChemDiv reserves a right, in advance, to evaluate any proposed transfer, sale or sublicensing of its libraries and compounds to any third party, and provide its consent.
In case the invoice for the completed scope of work or product delivery is not paid in full, then the corresponding research work as well as any resulting compounds and IP remain the property of ChemDiv, Inc. until the bill is paid in full.
Contacts: For any questions concerning these Terms of Use, contact ChemDiv Inc. at chemdiv@chemdiv.com
Delivery policy for screening libraries
Payment policy for screening libraries
ChemDiv conducts rigorous quality control testing on 100% of the chemical Compounds. Customer is provided with all analytical data, including interpreted nuclear magnetic resonance imaging spectra or LC MS spectra for each structure and formatted as a database of .tif or .jpg images on any chemical Compounds shipped to the Customer. Optional C13 or IR spectroscopy is available for dedicated study of cases.
All screening compounds pass quality control with LCMS and/or 1H NMR to meet requirement of >90% purity. The discovery compounds are stored in format of dry powders. All DMSO solutions frozen to be prepared freshly from dry powders.
80% of the compounds in our collection are available in >50 mg stock quantities. A large proportion of our collection is available in gram quantities—this means we can ensure a very high level of re-supply of originally tested compounds from the same batch. We work with most brands of plates and vials but are happy to use those supplied by customers on request.
Please contact us for a price quotation, format options, selections criteria at chemdiv@chemdiv.com or sb@chemdiv.com and we will reply the very day.
