Tham khảo Camptothecin

  1. . the stem bark of Mappia foetida, a tree native to India, has proved to be another source significant for the isolation of camptothecin.TR Govindachari and N. Viswnathan, Phytochemistry,11(12), 3529-31 (1972).Efferth T, Fu YJ, Zu YG, Schwarz G, Konkimalla VS, Wink M (2007). “Molecular target-guided tumor therapy with natural products derived from traditional Chinese medicine.”. Current Medicinal Chemistry 14 (19): 2024–32. doi:10.2174/092986707781368441
  2. “Curran Synthesis of Camptothecin”. Bản gốc lưu trữ ngày 5 tháng 9 năm 2009. 
  3. “Comins Synthesis of Camptothecin”. Bản gốc lưu trữ ngày 5 tháng 9 năm 2009. 
  4. “Rapaport Synthesis of Camptothecin”. [liên kết hỏng]
  5. Takimoto CH, Calvo E. "Principles of Oncologic Pharmacotherapy" in Pazdur R, Wagman LD, Camphausen KA, Hoskins WJ (Eds) Cancer Management: A Multidisciplinary Approach. 11 ed. 2008.
  6. M.E. Wall; M.C.Wani; C.E. Cook; K.H.Palmer; A.I.McPhail; G.A.Sim (1966). “Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminate”. J. Am. Chem. Soc. 88 (16): 3888–3890. doi:10.1021/ja00968a057
  7. G. Samuelsson (2004). Drugs of Natural Origin: a Textbook of Pharmacognosy (ấn bản 5). Stokkholm: Swedish pharmaceutical press. ISBN 91-974318-4-2
  8. 1 2 3 4 5 6 7 H. Ulukan; P.W. Swaan (2002). “Camptothecins, a review of their chemotherapeutical potential”. Drugs (ấn bản 27) 62 (2): 2039–2057. PMID 12269849. doi:10.2165/00003495-200262140-00004
  9. A. J. Lu; Z. S. Zhang; M. Y. Zheng; H. J. Zou; X. M. Luo; H. L. Jiang (2007). “3D-QSAR study of 20 (S)-camptothecin analogs”. Acta Pharmacologica Sinica 28 (2): 307–314. doi:10.1111/j.1745-7254.2007.00477.x
  10. “Camptothecin”. DrugBank. Truy cập ngày 9 tháng 10 năm 2016. 
  11. 1 2 3 D. J. Adams; M. L. Wahl; J. L. Flowers; B. Sen; M. Colvin; M. W. Dewhirst; G. Manikumar; M. C. Wani (2005). “Camptothecin analogs with enhanced activity against human breast cancer cells. II. Impact of the tumor pH gradient”. Cancer Chemotherapy and Pharmacology 57 (2): 145–154. PMID 16001167. doi:10.1007/s00280-005-0008-5
  12. M. R. Redinbo; L. Stewart; P. Kuhn; J. J. Champoux; W. G. J. Hol (1998). “Crystal structure of human topoisomerase I in covalent and noncovalent complexes with DNA”. Science 279 (5356): 1504–1513. PMID 9488644. doi:10.1126/science.279.5356.1504
  13. Del Bino G, Lassota P, Darzynkiewicz Z. (1991) The S-phase cytotoxicity of camptothecin. Exp Cell Res 193:27-35. PMID 1995300
  14. Y. Pommier; C. Redon; V.A. Rao; J.A. Seiler; O. Sordet; H. Takemura; S. Antony; L. Meng; Z.Liao (2003). “Repair of and checkpoint response to topoisomerase I-mediated DNA damage”. Mutat. Res. 532 (1–2): 173–203. PMID 14643436. doi:10.1016/j.mrfmmm.2003.08.016
  15. 1 2 3 4 5 6 7 8 9 10 F. Zunino; S. Dallavalle; D. Laccabue; G. Beretta; L. Merlini; G. Pratesi (2002). “Current status and perspectives in the Development of Camptothecins”. Current Pharmaceutical Design (ấn bản 27) 8 (27): 2505–2520. PMID 12369944. doi:10.2174/1381612023392801
  16. M. K. Chung; S. S. Han; J. C. Kim (2006). “Evaluation of the toxic potentials of a new camptothecin anticancer agent CKD-602 on fertility and early embryonic development in rats”. Regulatory Toxicology and Pharmacology 45 (3): 273–281. PMID 16814440. doi:10.1016/j.yrtph.2006.05.004
  17. M. Palumbo; C. Sissi; B. Gatto; S. Moro; G. Zagotto (2001). “Quantitation of camptothecin and related compounds”. J. Chromatogr. B 764 (1–2): 121–40. doi:10.1016/S0378-4347(01)00345-0
  18. “Cerulean Raises $24M to Progress Clinical Development of Nanopharmaceuticals”. 15 tháng 11 năm 2010. 

Tài liệu tham khảo

WikiPedia: Camptothecin http://www.drugbank.ca/drugs/DB04690 http://www.cancernetwork.com/cancer-management-11/ http://www.cancernetwork.com/cancer-management-11/... http://www.chemspider.com/Chemical-Structure.22775... http://www.genengnews.com/gen-news-highlights/ceru... http://www.chem.wisc.edu/areas/reich/syntheses/cam... http://www.chem.wisc.edu/areas/reich/syntheses/cam... http://www.chem.wisc.edu/areas/reich/syntheses/cam... //www.ncbi.nlm.nih.gov/pubmed/12269849 //www.ncbi.nlm.nih.gov/pubmed/12369944