Here you will learn about the latest changes and new features of our platform. We are constantly working on improving the functionality to make your user experience as convenient and efficient as possible
Platform updates
The User Guide has been fully migrated to a new documentation platform, providing:
- More intuitive navigation between sections and easier language switching
- Faster keyword search across the documentation
- Consistent and responsive display across various devices
Updated User Guide
- Improved the registration form by reducing the number of required fields and enhancing error handling — making the process faster and more intuitive.
- Integrated a regular user feedback survey into the product. This will help us continuously gather insights and incorporate them into future updates.
Platform Registration and User Feedback
- Began the transition to TypeScript, increasing the reliability of the frontend and accelerating the debugging process.
- Optimized the logic for dataset type selection, improving context-aware behavior across the platform.
- Refreshed the visual design of the “Spectra prediction” and “Synthesis Cost” sections — data presentation is now cleaner and easier to read.
- In the SMILES2IUPAC converter, users can now draw structures directly using the embedded editor, offering greater flexibility in molecule input.
- Fixed visual glitches when navigating between molecule cards and pages.
Architectural and Interface Enhancements
The tabular analysis module has been significantly upgraded:
- Introduced model applicability threshold settings for predicted properties, allowing users to filter out low-confidence results and ensure data reliability.
- All results are now exportable in CSV and XLSX formats — ready for further analysis or inclusion in scientific reports.
- The interface has been redesigned for better structure and clarity, making it easier and faster to locate relevant compounds across large datasets by property combinations.
Enhanced Tabular Analysis and Data Export
- Added 32,008 new data points for experimentally measured molecular properties.
- Compiled a set of approximately 5,000 trusted molecules — compounds most frequently used by our users. Reliable experimental properties are being collected for this set.
- Over 2 million chemical reactions have been imported into the system.
- Corrected rounding errors and unit inconsistencies in molecular property data.
Expanded Database and Improved Data Quality
19.05.2025
Syntelly Updates: Version 2.4 Improvements to Tabular Analysis, Product Interface, and Database Expansion
11.03.2025
Syntelly 2.3: platform updates
Cintelli is starting to formulate a refinement plan for 2025. If you have any suggestions or comments on the platform, now is the time to share your thoughts. Email us at admin@syntelly.com.
Reaction Search
A new functionality for searching through a database of chemical reactions containing 3 million entries has been implemented. This tool allows:
- Searching for reactions by reagent or product structures using the molecular editor or identifiers (SMILES, IUPAC, CAS number, InChI, trivial name)
- Configuring search parameters by the role of a substance in the reaction and percentage yield
- Obtaining information about reaction conditions (temperature, pressure, catalyst, etc.), as well as viewing data about agents and solvents used
- Finding references to relevant scientific publications and more
Enhanced Literature Search
Boolean operators AND/OR/NOT have been added to the scientific literature search mechanism, significantly improving the accuracy of search queries:
- Construction of complex search queries using multiple conditions
- Application of the "AND" operator to find documents containing all specified terms
- Use of the "OR" operator to broaden the range of results
- Exclusion of irrelevant results using the "NOT" operator
Structure Comparison
The product allows comparing different properties of molecules, with simultaneous comparison of up to 20 structures:
- Ability to select specific characteristics for comparison from the property list
- Comparison by a complex of parameters: physicochemical properties, toxicity, biological activity, etc.
- Visual representation of similarities and differences between compounds This functionality increases the efficiency of analyzing series of compounds, as well as structure-function relationships.
Change Logging in Datasets
A system for documenting all modifications made to datasets has been implemented:
- Recording the date and time of each action
- Tracking the type of operation (addition, deletion, calculation, modification)
- Accounting for the number of structures affected during changes
- Restoring the sequence of actions in chronological order This function is especially relevant for research groups where several researchers work with shared datasets, ensuring transparency and reproducibility of research.
Enhanced Data Export Options
Export options have been updated in all key system modules:
- Improved PDF format for structure cards with all calculated parameters
- Export of spectrum prediction results
- Saving synthesis prediction results in PNG format These improvements simplify the integration of obtained results into further research processes.
Refinements to the SynMap Module
The interface and functionality of the new compound generation module have been improved:
- Informative tooltips for generation parameters have been added
- The ability to return to initial generation conditions has been implemented
- Control elements for adjusting parameter weight coefficients have been improved
- The user interface has been optimized for more intuitive operation These updates aim to increase the efficiency of designing molecules with specified properties.
Expanded Dataset Functionality
The dataset module has been supplemented with the following capabilities:
- Exporting datasets to Excel format
- Personalizing information about molecules according to research tasks:
- Adding personal experimental data to structures in personal datasets
- Adding user notes to structure cards These functions provide more flexible data organization and integration of experimental results with theoretical predictions.
Molecular Editor Update
The Syntelly molecular editor has been updated to a new version that provides a more convenient and functional interface for working with chemical structures.
The Syntelly platform can be used in the pharmaceutical, cosmetic and chemical industries, in intellectual property protection, in education, science and regulatory activities. Version 2.2 contains a number of new features and additions to enhance the ability to search, process and analyze chemical data.
Syntelly has updated its eponymous platform for searching, processing and analyzing chemical information to version 2.3. The new version includes improvements to the Datasets module, SynMap and a number of changes in the product interface that simplify its use.
21.11.2024
Syntelly 2.2: platform updates
Cintelli is starting to formulate a refinement plan for 2025. If you have any suggestions or comments on the platform, now is the time to share your thoughts. Email us at admin@syntelly.com.
- Quick structure transfer to other modules from the structure card has been implemented;
- Improved feedback form: added separate topics of appeals, as well as uploading files and images;
- Fixed rendering errors of structural formulas, and improved the quality and contrast of images;
- Split the synonyms block into “Titles” and “Database IDs” for easy search and browsing;
- SynMap module: added buttons to completely clear the map and stop generation, as well as the ability to view the generator settings after it is started.
Visual and logical refinements:
- Tabular analysis: You can now sort and filter structures within your own datasets by target property values before exporting;
- Datasets can be sorted by number of structures, by creation date and by name;
- The search bar has been integrated into the module: now it is possible to search both datasets and structures within each dataset;
- Added the ability to select an operator when loading a CSV file, which provides more accurate recognition of the structures loaded into personal datasets;
- My Company Datasets: it is now available within the platform for employees from the same organization to work on shared datasets (if you want to see a specific role policy in this vein - let us know);
- It is also now possible to create personal notes/comments on structures within personal datasets.
Improvements to the Datasets module:
The Syntelly platform can be used in the pharmaceutical, cosmetic and chemical industries, in intellectual property protection, in education, science and regulatory activities. Version 2.2 contains a number of new features and additions to enhance the ability to search, process and analyze chemical data.
Syntelly has updated its eponymous platform for searching, processing and analyzing chemical information to version 2.2. The new version includes improvements to the Datasets module, SynMap and a number of changes in the product interface that simplify its use.
01.08.2024
Syntelly 2.1: new platform features
1. Literature search: 160 million literature sources as well as 15 million patents have been added to the Syntelly database. Previously searchable solely by structure, it is now also possible to find related scientific publications and patents, with combined and full-text search, sorting and filtering. Text queries can be entered in Russian and English. This greatly simplifies the process of finding the necessary information among many sources;
2. Search by Markush structures: allows to easily find and analyze complex chemical structures, which saves time and efforts of users. This function is especially relevant in patent search, when the user needs to search for a group of chemical compounds;
3. updated SynMap module: added optimization and additional parameters for generation of new compounds, the quality of the generated array became much higher;
4. updated module for automatic extraction of structural formulas from documents - PDF2SMILES 2.0: the accuracy of the neural network has been improved, now it is possible to recognize Markush structures on any documents, such as patents, scientific articles, test reports and dissertations. This simplifies and speeds up the process of collecting and analyzing data for research, developing new compounds, and writing literature reviews;
5. One of the new integrations is the model applicability indicator. For each prediction, it provides an assessment of its applicability to a specific molecule, which increases the reliability of profiling new compounds and enables informed strategic planning decisions for applications in organic synthesis, medicinal and pharmaceutical chemistry;
6. New thematic datasets: datasets on molecular targets and therapeutic indications have been added to the platform. The datasets compiled by the Syntelly team may be particularly useful for educational applications;
7. Improved usability of the platform: notifications of important events on the platform have been implemented. In addition, it is possible to customize the hint system. The interface has become more intuitive and navigation is smoother;
2. Search by Markush structures: allows to easily find and analyze complex chemical structures, which saves time and efforts of users. This function is especially relevant in patent search, when the user needs to search for a group of chemical compounds;
3. updated SynMap module: added optimization and additional parameters for generation of new compounds, the quality of the generated array became much higher;
4. updated module for automatic extraction of structural formulas from documents - PDF2SMILES 2.0: the accuracy of the neural network has been improved, now it is possible to recognize Markush structures on any documents, such as patents, scientific articles, test reports and dissertations. This simplifies and speeds up the process of collecting and analyzing data for research, developing new compounds, and writing literature reviews;
5. One of the new integrations is the model applicability indicator. For each prediction, it provides an assessment of its applicability to a specific molecule, which increases the reliability of profiling new compounds and enables informed strategic planning decisions for applications in organic synthesis, medicinal and pharmaceutical chemistry;
6. New thematic datasets: datasets on molecular targets and therapeutic indications have been added to the platform. The datasets compiled by the Syntelly team may be particularly useful for educational applications;
7. Improved usability of the platform: notifications of important events on the platform have been implemented. In addition, it is possible to customize the hint system. The interface has become more intuitive and navigation is smoother;
Version 2.1 contains a number of new features and additions to enhance the ability to search and predict chemical compounds:
Syntelly's platform can be applied in the pharmaceutical, cosmetics and chemical industries, intellectual property protection, education and regulatory activities.
Syntelly has updated its eponymous platform for searching, processing and analyzing chemical information to version 2.1. The new version includes full-text literature search, Markush structures, improved modules for generating new compounds and automatic extraction of structural formulas from documents. In addition, a number of changes have been made to the product interface to simplify its use.
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