Rapid advancing computational technologies have greatly speeded up the development of computer-aided drug design (CADD). Recently, pharmaceutical companies have increasingly shifted their attentions toward traditional Chinese medicine (TCM) for novel lead compounds. Despite the growing number of studies on TCM, there is no free 3D small molecular structure database of TCM available for virtual screening or molecular simulation. To address this shortcoming, we have constructed TCM Database@Taiwan (http://tcm.cmu.edu.tw/) based on information collected from Chinese medical texts and scientific publications. TCM Database@Taiwan is currently the world's largest non-commercial TCM database. This web-based database contains more than 20,000 pure compounds isolated from 453 TCM ingredients. Both cdx (2D) and Tripos mol2 (3D) formats of each pure compound in the database are available for download and virtual screening. The TCM database includes both simple and advanced web-based query options that can specify search clauses, such as molecular properties, substructures, TCM ingredients, and TCM classification, based on intended drug actions. The TCM database can be easily accessed by all researchers conducting CADD. Over the last eight years, numerous volunteers have devoted their time to analyze TCM ingredients from Chinese medical texts as well as to construct structure files for each isolated compound. We believe that TCM Database@Taiwan will be a milestone on the path towards modernizing traditional Chinese medicine.
Citation: Chen CY-C (2011) TCM Database@Taiwan: The World's Largest Traditional Chinese Medicine Database for Drug Screening In Silico. PLoS ONE 6(1): e15939. doi:10.1371/journal.pone.0015939
Editor: Andreas Hofmann, Griffith University, Australia
Received: October 25, 2010; Accepted: November 30, 2010; Published: January 6, 2011
Copyright: © 2011 Calvin Yu-Chian Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The research was supported by grants from the National Science Council of Taiwan (NSC 99-2221-E-039-013-), China Medical University (CMU99-S-02) and Asia University (CMU98-ASIA-09). This study is also supported in part by Taiwan Department of Health Clinical Trial and Research Center of Excellence (DOH99-TD-B-111-004) and Taiwan Department of Health Cancer Research Center of Excellence (DOH99-TD-C-111-005). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The author has declared that no competing interests exist.
For thousands of years, traditional Chinese medicine (TCM) holds an important role in medical diagnosis and treatments in Eastern Asia. However, due to lack of systematic investigation and poor understanding of TCM regimens, TCM is less recognized in the Western society. Recently, increasing effort has been devoted to study TCM, from which a large number of bioactive compounds have been isolated and studied. Hence, there is a need to establish a database to organize the enormous amounts of TCM data and make the virtual screening of TCM ingredients easily accessible.
Although there are many websites detailing information for TCM sources, traditional usage from ancient material medica texts, and processing and storage procedures, these databases, such as The Chinese medicine sampler (http://www.chinesemedicinesampler.com) and Dictionary of Chinese Herbs (http://alternativehealing.org), contain little information of TCM ingredients at molecular level. The TCMGeneDIT database  is an effective search engine for TCM-related literature, but the information on the TCM constituents is not well organized. Other databases, including TCMD , Chinese Traditional Medicinal Herbs Database , and TCM-ID , provide general TCM information and 3D structures of TCM ingredients. However, these databases are either inaccessible or highly restricted for information sharing. To date, the ZINC database  is currently the largest free 3D molecule database. However, there is no TCM related database similar to the scale of ZINC yet. In the hope of building a complete TCM ingredient library, we construct the TCM Database@Taiwan (http://tcm.cmu.edu.tw/).
In the past, our laboratory has performed screening for multiple TCM components and has successfully discovered novel lead compounds, such as anti-viral, anti-inflammation, anti-cancer, stroke prevention compounds, and hypnotic medications –. By constructing TCM Database@Taiwan, we can further facilitate the virtual screening process in the experiment design for the TCM lead drug discovery. We firmly believe that the constituents from TCM are the sources to derive novel pharmaceutical compounds.
Results and Discussion
TCM Database@Taiwan (http://tcm.cmu.edu.tw) is currently the largest non-commercial TCM database available for download. This web database is designed in both English and traditional Chinese languages. All 3D structures are constructed in mol2 format and are readily used for virtual screening.
Right now, the database contains 20,000 ingredients from 453 different herbs, animal products, and minerals TCM regimens. In the near future, the database will further record folk herb ingredients. The TCM database is organized by proposed actions of Chinese medicines (Table S1). There are a total of twenty-two different drug classes and some are further divided into subclasses based on clinical applications recorded in TCM monographs. It should be noted that our TCM classification is based on traditional Chinese theories including the Yin-yang, the human Meridan/Channel system, the Five Elements theory, and the Zang Fu organ theory. It should also be noted that TCM listed under certain classes, such as parasites elimination, dampness reduction and itchiness relief medicinal, and topical application medicinal, contain toxic ingredients and are no longer prescribed in clinics. These ingredients are present in the TCM database for the completeness of TCM records. These data do not imply endorsement for any clinical or private use of the toxic TCM compounds nor for any animal products present in the database.
Search and Display
An overview of available search options and download options is shown in Figure 1. TCM Database@Taiwan can be browsed by simple and advanced search options. The simple search option enables users to browse the website either by TCM medicine or by TCM ingredients (Figure 2). The search-by-TCM-medicine option allows users to select the intended drug action group and then the desired TCM medicine. The search-by-TCM-chemical-composition option allows users to find possible TCM sources of the given molecule. This search result is directly linked to the TCM compound webpage without the need to specifying TCM action group.
(a) search by TCM category and (b) search by chemical composition.
For each search options, the result is organized in a “TCM profile” that provides the identified TCM compound(s) and the associated references. Clicking on a TCM compound in the profile will display the compound's 2D and 3D structures, as well as its molecular properties in a new page. Users can download the structure of the molecule in cdx (2D) or mol2 (3D) format at the bottom of the TCM compound webpage. In addition, users can also click on the links to browse other Chinese medicines that contains the selected TCM compound.
The advanced search option incorporates a molecular drawing interface (ChemAxon) for structure search (Figure 3). Users can also specify structure types, including exact search and substructure search, whichever best describes users' needs. Moreover, users can perform searches by specifying the molecular properties, such as molecular weight and ALogP. Both of the advanced search options can be used alone or in conjunction. The result will return molecule(s) that satisfy the input specification in a tabular format with name and 2D representation. For users who prefer search by Chinese medicine names and other TCM information, a website search engine is available at top of every page.
The TCM ingredients are organized by their drug action classes and their original sources. Users can download a specific drug class or a specific TCM or the whole TCM database on Download page.
Sharing TCM Constituents
As technology advances, new TCM ingredients have been isolated and studied each day. Therefore, we implemented an upload function for scientists who are interested in sharing their findings on Chinese medicines. Users may upload their own molecules to the TCM database server in mol2 format. The uploaded molecules will be reviewed and incorporated into the TCM database.
Overall, TCM Database@Taiwan is constructed in the hope to create the most complete TCM library and to strengthen the TCM research network to date. In addition, this web-based database is implemented with virtual screening and molecular simulation functions. For both biochemists studying TCM and medicinal chemists designing novel lead compounds, this database serves as a useful resource for virtual screening as well as for the references in biochemical assays. In the future, we will incorporate genetic algorithm (GA) and support vector machine (SVM) for further TCM classifications based on molecular properties. We expect the construction of TCM Database@Taiwan to become a milestone for modern TCM researches.
The TCM herbs, animal products and minerals listed in the TCM Database @Taiwan were originated from Chinese medical texts and dictionaries –. In addition, the TCM constituents were collected manually from published results available on Medline  and ISI Web of Knowledge (http://apps.isiknowledge.com). The data were organized into twenty-two major classes based on their proposed therapeutic actions recorded in Chinese medical texts –. The 2D and 3D structures of TCM constituents were built by ChemBioOffice 2008 (CambridgeSoft, Cambridge, MA). The 3D structures were energy minimized in MM2 force field. Physicochemical properties, including ALogP and polar surface area, were calculated using ChemBioOffice.
With efficiency and stability as our main concern, we implemented our database on a Linux server, then use MySQL5.0, Apache, and hypertext preprocessor (PHP) for database and web server development. For friendly user interfaces, we used ChemAxon MarvinView applet (https://www.chemaxon.com) for 2D and 3D representation. In addition, we applied MarvinSketch tool from ChemAxon for structure drawing in the advanced search option.
In the advanced search section, the search engine was developed based on the Norbert Haider's MolDB5R package . The infrastructure of the advanced search engine is shown in Figure 4. For search-by-specifying-molecular-properties, a search script written in PHP is used to search and retrieve TCM compounds that satisfied all the input properties. Two programs, checkmol and matchmol, are used to perform the background structure searching and matching process. The queried structure is read by the checkmol program to generate molecular descriptors, which is then used in the preliminary search in the TCM database. The matchmol program is responsible for full structure comparison of the input structures from checkmol. For additional structure search options, such as substructure search, the matchmol program treat one compound as “needle” and other molecule(s) as “haystack” to determine the best-fit substructure of another structure. All the search options in the advanced search section can be used in conjunction. By specifying both molecular properties and query structure scaffold, an additional data screening process is performed to ensure that all the input criteria are met.
Summary of medicines present in each TCM class. The English translation of each class is taken from WHO publication.
I am grateful to hundreds of student volunteers who devoted their time checking the TCM compounds from the references and drawing these compounds for more than eight years and National Center of High-performance Computing for computer time and facilities. I also thank the professional suggestion by Drs. Chung Y Hsu, Kun-Lung Chang, Fuu-Jen Tsai of China Medical University, Nobel Laureate Ferid Murad, and professor Marc of Harvard University.
Conceived and designed the experiments: CYCC. Performed the experiments: CYCC. Analyzed the data: CYCC. Contributed reagents/materials/analysis tools: CYCC. Wrote the paper: CYCC.
- 1. Fang YC, Huang HC, Chen HH, Juan HF (2008) TCMGeneDIT: a database for associated traditional Chinese medicine, gene and disease information using text mining. BMC Complement Altern Med 8: 58.
- 2. He M, Yan XJ, Zhou JJ, Xie GR (2001) Traditional Chinese medicine database and application on the Web. J Chem Inf Comput Sci 41: 273–277.
- 3. Qiao XB, Hou TJ, Zhang W, Guo SL, Xu SJ (2002) A 3D structure database of components from Chinese traditional medicinal herbs. J Chem Inf Comput Sci 42: 481–489.
- 4. Chen X, Zhou H, Liu YB, Wang JF, Li H, et al. (2006) Database of traditional Chinese medicine and its application to studies of mechanism and to prescription validation. Br J Pharmacol 149: 1092–1103.
- 5. Irwin JJ, Shoichet BK (2005) ZINC - A free database of commercially available compounds for virtual screening. J Chem Inf Model 45: 177–182.
- 6. Huang HJ, Lee KJ, Yu HW, Chen CY, Hsu CH, et al. (2010) Structure-Based and Ligand-Based Drug Design for HER 2 Receptor. J Biomol Struct Dyn 28: 23–37.
- 7. Chen CY, Chen CYC (2010) Insights into designing the dual-targeted HER2/HSP90 inhibitors. J Mol Graph Model 29: 21–31.
- 8. Huang HJ, Chen CY, Chen HY, Tsai FJ, Chen CYC (2010) Computational screening and QSAR analysis for design of AMP-activated protein kinase agonist. J Taiwan Inst Chem Eng 41: 352–359.
- 9. Chen CYC (2010) Virtual Screening and Drug Design for PDE-5 Receptor from Traditional Chinese Medicine Database. J Biomol Struct Dyn 27: 627–640.
- 10. Chen CYC (2010) Bioinformatics, chemoinformatics, and pharmainformatics analysis of HER2/HSP90 dual-targeted inhibitors. J Taiwan Inst Chem Eng 41: 143–149.
- 11. Chen CY, Huang HJ, Tsai FJ, Chen CYC (2010) Drug design for Influenza A virus subtype H1N1. J Taiwan Inst Chem Eng 41: 8–15.
- 12. Chen CYC (2009) Computational screening and design of traditional Chinese medicine (TCM) to block phosphodiesterase-5. J Mol Graph Model 28: 261–269.
- 13. Chen CY, Chang YH, Bau DT, Huang HJ, Tsai FJ, et al. (2009) Ligand-Based Dual Target Drug Design for H1N1: Swine Flu- A Preliminary First Study. J Biomol Struct Dyn 27: 171–178.
- 14. Huang HJ, Yu HW, Chen CY, Hsu CH, Chen HY, et al. (2010) Current developments of computer-aided drug design. J Taiwan Inst Chem Eng 41: 623–635.
- 15. Chen CYC (2009) Pharmacoinformatics approach for mPGES-1 in anti-inflammation by 3D-QSAR pharmacophore mapping. J Taiwan Inst Chem Eng 40: 155–161.
- 16. Chen CYC (2009) De novo design of novel selective COX-2 inhibitors: From virtual screening to pharmacophore analysis. J Taiwan Inst Chem Eng 40: 55–69.
- 17. Chen CYC (2009) Chemoinformatics and pharmacoinformatics approach for exploring the GABA-A agonist from Chinese herb suanzaoren. J Taiwan Inst Chem Eng 40: 36–47.
- 18. Chen G, Li S (1992) Ben cao gang mu tong shi = General explanation of Compendium of materia medica. Beijing Shi: Xue yuan chu ban she .
- 19. Zhong N, Zhao G, Dai S, Chen R (2006) Zhong yao da ci dian. Shanghai: Shanghai ke xue ji shu chu ban she .
- 20. Miao X, Zheng J (2002) Shennong ben cao jing shu. Beijing: Zhong yi gu ji chu ban she . 777 p.
- 21. Lü X (2002) Zhong yao jian bie da quan. Changsha Shi: Hunan ke xue ji shu chu ban she.
- 22. Fang Y, Zhang Z, Miao X (1991) Shang han lun tiao bian. Shanghai: Shanghai gu ji chu ban she: Xin hua shu dian Shanghai fa xing suo fa xing.
- 23. Sayers EW, Barrett T, Benson DA, Bolton E, Bryant SH, et al. (2010) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 38: D5–D16.
- 24. Shen L, Li S (1998) Ben cao gang mu cai se tu pu. Beijing Shi: Hua xia chu ban she.
- 25. Yang S (1998) The divine farmer's materia medica: a translation of the Shen Nong Ben Cao Jing. Boulder, CO: Blue Poppy Press.
- 26. Yao D, Zhang J, Zhonghua RG (1996) Guangzhou Shi: Guangdong ke ji chu ban she: Jing xiao Guangdong sheng xin hua shu dian.
- 27. Haider N (2010) Functionality Pattern Matching as an Efficient Complementary Structure/Reaction Search Tool: an Open-Source Approach. Molecules 15: 5079–5092.