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SyntellyApp
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
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Прогноз растворимости
Новый модуль позволяет прогнозировать растворимость органических соединений в 18 растворителях при различных температурах. Вы можете задать температурный диапазон от -30°C до +130°C и получить детализированный график зависимости растворимости от температуры с указанием доверительного интервала.
Поддерживаемые растворители: этанол, метанол, изопропанол, этилацетат, ацетон, н-пропанол, н-бутанол, ацетонитрил, толуол, ДМФА, ДМСО, хлороформ, ТГФ, диоксан, четыреххлористый углерод, циклогексан, гексан, диэтиловый эфир.
Для каждого расчета отображается область применимости модели (Applicability Domain) и стандартное отклонение, что позволяет оценить надежность прогноза.
Улучшения интерфейса и повышение удобства
Пошаговое обучение – во всех модулях платформы реализован онбординг, который помогает новым пользователям быстро освоить функционал. Интерактивные подсказки проведут вас по основным возможностям каждого инструмента.
История поиска — поддержка текстовых подсказок и синонимов в дополнение к SMILES.
Молекулярный редактор — добавлены:
  • Всплывающие подсказки (tooltips) для всех кнопок и инструментов
  • Pop-up с полным списком горячих клавиш
  • Контекстная помощь при работе со сложными функциями
Контекстное меню — оптимизировано для удобства: основные кнопки (обратная связь, уведомления, наверх) оставлены на виду, остальные перемещены в меню «Дополнительно».
SynMap — отображение количества выделенных структур в реальном времени позволяет отслеживать лимит в 1000 структур непосредственно в процессе работы.
Расширение базы данных
Соединения и литература
Интегрированы в платформу:
  • 11.6 млн научных статей
  • 1.6 млн названий ИЮПАК
  • 4.4 млн синонимов (ID ChemDiv, CAS и другие идентификаторы)
Экспериментальные данные
Добавлены новые записи по следующим физико-химическим свойствам:
  • Температура кипения (Boiling point)
  • Температура вспышки (Flash point)
  • Температура плавления (Melting point)
  • Давление пара (Vapor Pressure)
  • Растворимость в воде (Water Solubility)
  • Плотность (Density)
  • Показатель преломления (Refractive Index)
И токсикологические и экологические данные:
  • Guinea pig oral LD50
  • Mouse oral LD50
  • Rat oral LD50
  • Проницаемость гематоэнцефалического барьера (LogBB)
  • Daphnia Magna LC50
  • Tetrahymena Pyriformis IGC50
Датасеты
Интегрированы 25 тематических датасетов по комплексам металлов, которые могут быть полезны для образовательных целей и специализированных исследований.
Добавлено 3 тематических датасета с молекулами из ChemDiv.
Избранное: персональные коллекции данных
Новый раздел "Избранное" позволяет создавать собственные коллекции для быстрого доступа к нужным материалам. Вы можете добавлять в избранное:
  • Химические структуры
  • Научные статьи или патенты
  • Реакции
  • Спектры
Система уведомлений информирует об успешном добавлении или удалении объектов. Все избранные материалы доступны в одном месте, что ускоряет работу с часто используемыми данными.
PDF2SMILES: повышенная точность распознавания
Модуль автоматического извлечения структур из документов получил значительные улучшения:
  • Повышена точность детекции молекул до 90% с минимальными ложными срабатываниями.
  • Улучшена корректность распознавания.
  • Добавлены фильтры, которые удаляют неправильно распознанные молекулы с грубыми ошибками и корректируют некоторые дефекты распознавания.
Улучшен интерфейс – добавлены автоматическая подсветка карточек при клике на молекулу в тексте, новые иконки с подсказками для более удобной работы.
Стоимость синтеза: интеграция российских поставщиков и новых реакций
Ключевое нововведение — интеграция крупнейших российских поставщиков химии. Это критически важно для работы в условиях ограниченного доступа к международным каталогам. Теперь вы можете:
  • Построить дерево реакций с учетом доступности реагентов в России
  • Увидеть стоимость всего синтеза и отдельных стадий у российских поставщиков
  • Перейти напрямую на сайт поставщика для оформления заказа
Это значительно упрощает планирование синтеза для российских фармацевтических компаний, научных институтов и химических предприятий — от прогноза до закупки.
Модуль расчета стоимости синтеза получил масштабное обновление. Теперь в базе данных в 4 раз больше известных реакций, что существенно расширяет возможности планирования синтеза.
В версии 2.6 мы расширили возможности платформы, добавив новые инструменты для прогнозирования свойств и планирования синтеза. Интеграция модуля прогноза растворимости, обновленная стоимость синтеза с российскими поставщиками и значительное расширение базы данных помогут ускорить ваши исследования и повысить точность прогнозов. Интерфейс стал ещё удобнее благодаря новым возможностям работы с данными и пошаговому обучению.
Если вы уже работаете с Синтелли — проверьте, как изменилась функциональность. Если ещё не знакомы с платформой — сейчас самое удобное время начать с помощью нового онбординга.
20.11.2025
Синтелли 2.6: новые инструменты для эффективной работы
In version 2.5, we expanded the scope and depth of data, improved the interface, and carried out a major technical upgrade. These changes make the platform even more stable, accurate, and user-friendly.
Data Coverage and Management
  • Added 682 new entries on DMSO solubility — more experimental properties are now available.
  • The “Full Text” button now takes you directly to the source article or patent.
  • Increased dataset upload limits in trial access: 5,000 structures per operation within a single dataset and 50,000 structures per month — speeding up work with large data collections.
Literature Search
Added connections between structures and 7 million scientific articles. When viewing a molecule card, you can now see even more publications where it is mentioned and described.
Reaction Search
Expanded dropdown suggestions — now, as in structure search, both SMILES and synonyms are recognized. This makes search more convenient and consistent.
Tabular Analysis
  • Improved information displaying and added filtering by model applicability.
  • Experimental values are now visually highlighted and displayed as the most significant.
  • The SMILES column is now fixed and always visible.
Interface
  • Added error alerts in retrosynthesis and synthesis cost modules. The system now flags invalid SMILES or incorrect formats.
  • Enabled molecule highlighting via the context menu in Search and Datasets — a clearer and more visible way to select substances.
  • Optimized molecule pages for small screens — making it comfortable to work on compact devices.
  • Enabled direct navigation from structure comparison to a molecule card to view details.
  • Added cross-module navigation from the molecular editor via the context menu — making switching between different tasks faster.
  • Introduced a toggle to show or hide reaction conditions in bulk, saving screen space.
  • Switching between languages on the platformis now more intuitive and user-friendly.
User Feedback and Data Accuracy
Users can now report experimental data errors directly through the interface. In molecule cards, you can flag incorrect data, suggest corrections, and add source links, which helps improve data accuracy more quickly.
Already using Syntelly? Check out the new interface and features.
New to the platform? Now’s the perfect time to start — it’s faster and smarter than ever.
If you have any suggestions or comments on the platform, now is the time to share your thoughts. Email us at admin@syntelly.com.
Expanded Database and Improved Data Quality
  • 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.
Enhanced Tabular Analysis and Data Export
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.
Architectural and Interface Enhancements
  • 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.
Platform Registration and User Feedback
  • 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.
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.
Updated User Guide
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
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.
  1. Quick structure transfer to other modules from the structure card has been implemented;
  2. Improved feedback form: added separate topics of appeals, as well as uploading files and images;
  3. Fixed rendering errors of structural formulas, and improved the quality and contrast of images;
  4. Split the synonyms block into “Titles” and “Database IDs” for easy search and browsing;
  5. 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:
  1. Tabular analysis: You can now sort and filter structures within your own datasets by target property values before exporting;
  2. Datasets can be sorted by number of structures, by creation date and by name;
  3. The search bar has been integrated into the module: now it is possible to search both datasets and structures within each dataset;
  4. Added the ability to select an operator when loading a CSV file, which provides more accurate recognition of the structures loaded into personal datasets;
  5. 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);
  6. 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.
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.
  1. Quick structure transfer to other modules from the structure card has been implemented;
  2. Improved feedback form: added separate topics of appeals, as well as uploading files and images;
  3. Fixed rendering errors of structural formulas, and improved the quality and contrast of images;
  4. Split the synonyms block into “Titles” and “Database IDs” for easy search and browsing;
  5. 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:
  1. Tabular analysis: You can now sort and filter structures within your own datasets by target property values before exporting;
  2. Datasets can be sorted by number of structures, by creation date and by name;
  3. The search bar has been integrated into the module: now it is possible to search both datasets and structures within each dataset;
  4. Added the ability to select an operator when loading a CSV file, which provides more accurate recognition of the structures loaded into personal datasets;
  5. 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);
  6. 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.
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;
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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