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References
|
Black TH (1983). The Preparation and reactions of diazomethane. Aldrichimica 16(1):3-4. |
|
|
Duprat RC, Anholeti MC, Sousa BP, Pacheco JPF, Figueiredo MR, Kaplan MAC, Santos MG, Gonzalez MS, Ratcliffe NA, Mello CB, Paiva SR, Feder D (2017). Laboratory evaluation of Clusia fluminensis extracts and their isolated compounds against Dysdercus peruvianus and Oncopeltus fasciatus. Revista Brasileira Farmacognosia 27(1):59-66. |
|
|
Fernandes J, Castilho RO, Costa MR, Wagner-Souza K, Kaplan MAC, Gattass CR (2003). Pentacyclic triterpenes from Chrysobalanaceae species: cytotoxicity on multidrug resistant and sensitive leukemia cell lines. Cancer Letters 190(2):165-169. |
|
|
Giampazolias E, Zunino B, Dhayade S, Bock F, Cloix C, Cao K, Roca A, Lopez J, Ichim G, Proïcs E, Rubio-Patiño C, Fort L, Yatim N, Woodham E, Orozco S, Taraborrelli L, Peltzer N, Lecis D, Machesky L, Walczak H, Albert ML, Milling S, Oberst A, Ricci JE, Ryan KM, Blyth K, Tait SWG (2017). Mitochondrial permeabilization engages NF-κB-dependent anti-tumor activity under caspase deficiency. Nature Cell Biology 19(9):1116-1129. |
|
|
Gill BS, Kumar S (2016). Triterpenes in cancer: significance and their influence. Molecular Biology Reports 43(9):881-896. |
|
|
Huang D, Ding Y, Li Y, Zhang W, Fang W, Chen X (2006). Anti-tumor activity of a 3-oxo derivative of oleanolic acid. Cancer Letters 233(2):289-296. |
|
|
Iqbal J, Abbasi BA, Ahmad R, Mahmood T, Kanwal S, Ali B, Khalil AT, Shah SA, Alam MM, Badshah H (2018). Ursolic acid a promising candidate in the therapeutics of breast cancer: Current status and future implications. Biomedicine and Pharmacotherapy 108:752-756. |
|
|
Jamila N, Khairuddean M, Yeong KK, Osman H, Vikneswaran M (2015). Cholinesterase inhibitory triterpenoids from the bark of Garcinia hombroniana, Journal of Enzyme Inhibition and Medicinal Chemistry 30(1):133-139. |
|
|
Kamble SM, Goyal SN, Patil CR (2014). Multifunctional pentacyclic triterpenoids as adjuvants in cancer chemotherapy: A review. RSC Advances 4(63):33370-33382. |
|
|
Kotraswamy KM, Shaikh IN, Ankalgi RF, Ankalgi SR, Shaikh IN, Bagwan UF (2016). Studies on industrially important Guttiferae and Palmae family. Journal of Pharmacognosy and Phytochemistry 5(6):194-198. |
|
|
Kumar P, Bhadauria AS, Singh AK, Saha S. (2018) Betulinic acid as apoptosis activator: Molecular mechanisms, mathematical modeling and chemical modifications. Life Science 209:24-33. |
|
|
Kumar A, Jaitak V (2019) Natural products as multidrug resistance modulators in cancer. European Journal of Medicinal Chemistry 176:268-291. |
|
|
Li YZ, Li ZL, Yin SL, Shi G, Liu MS, Jing YK, Hua HM. (2010). Triterpenoids from Calophyllum inophyllum and their growth inhibitory effects on human leukemia HL-60 cells. Fitoterapia 81(6):586-589. |
|
|
Liu DL, Li YJ, Yang DH, Wang CR, Xu J, Yao N, Zhang XQ, Chen ZS, Ye WC, Zhang DM (2015). Ganoderma lucidum derived ganoderenic acid B reverses ABCB1-mediated multidrug resistance in HepG2/ADM cells. International Journal of Oncology 46:2029-2038. |
|
|
Mahdizadeh S, Karimi G, Behravan J, Arabzadeh S, Lage H, Kalalinia F (2016). Crocin suppresses multidrug resistance in MRP overexpressing ovarian cancer cell line. DARU Journal of Pharmaceutical Science 24(1):17. |
|
|
Maia RC, Wagner K, Cabral RH, Rumjanek VM (1996). Heparin reverses Rhodamine 123 extrusion by multidrug resistant cells. Cancer Letters 106(1):101-108. |
|
|
Melo MS, Quintans JSS, Araújo AAS, Duarte MC, Bonjardim LR, Nogueira PCL, Moraes VRS, Araújo-Júnior JX, Ribeiro EAN, Quintans-Júnior LJ (2014). A systematic review for anti-inflammatory property of Clusiaceae family: a preclinical approach. Evidence-Based Complementary and Alternative Medicine, Article ID 960258, 10 pages. |
|
|
Mosmann T (1983). Rapid colorimetric assay for cellular growth and survival:application to proliferation and cytotoxicity assays. Journal of Immunology Methods 65(1-2):55-63. |
|
|
Peron G, Marzaro G, Dall'Acqua S (2018). Known triterpenes and their derivatives as scaffolds for the development of new therapeutic agents for cancer. Current Medicinal Chemistry 25(10):1259-1269. |
|
|
Queiroga CL, Silva GF, Dias PC, Possenti A, de Carvalho JE (2000). Evaluation of antiulcerogenic activity of friedelan-3-β-ol and friedelin isolated from Maytenus ilicifolia (Celastraceae). Journal of Etnopharmacology 72(3):465-468. |
|
|
Raghuvar GDV, Narkar AA, Badrinath Y, Mishra KP, Joshi DS. (2005). Betulinic acid induces apoptosis in human chronic myelogenous leukemia (CML) cell line K-562 without altering the levels of Bcr-Abl. Toxicological Letters 155(3):343-351. |
|
|
Ren Y, Kinghorn AD (2019) Natural Product Triterpenoids and Their Semi-Synthetic Derivatives with Potential Anticancer Activity. Planta Medica 85(11/12):802-814. |
|
|
Ribeiro PR, Ferraz CG, Cruz FG (2019). New steroid and other compounds from non-polar extracts of Clusia burle-marxii and their chemotaxonomic significance. Biochemical Systematics and Ecology 82:31-34. |
|
|
Robey RW, Pluchino KM, Hall MD, Fojo AT, Bates SE, Gottesman MM (2018). Revisiting the role of ABC transporters in multidrug-resistant cancer. Nature Reviews Cancer 18:452-464. |
|
|
Salvador JAR, Leal AS, Valdeira AS, Gonçalves BMF, Alho DPS, Figueiredo SAC, Silvestre SM, Mendes VIS (2017). Oleanane-, ursane-, and quinone methide friedelane-type triterpenoid derivatives: Recent advances in cancer treatment. European Journal of Medicinal Chemistry 142:95-130. |
|
|
Shoemaker RH (2006). The NCI60 human tumour cell line anticancer drug screen. Nature Reviews Cancer 6(10):813-823. |
|
|
Souza IGB, Souza VAB, Lima PSC (2013). Molecular characterization of Platonia insignis Mart. ("bacurizeiro") using inter simple sequence repeat (ISSR) markers. Molecular Biology Reports 40(5):3835-3845. |
|
|
Spinner DM. (2001). MTT growth assays in ovarian cancer. Methods Molecular Medicine 39:175-177 |
|
|
Stevens PF (2007 onwards). Angiosperm Phylogeny Website. Version 14, July 2017. |
|
|
Subash-Babu P, Li DK, Alshatwi AA. (2017). In vitro cytotoxic potential of friedelin in human MCF-7 breast cancer cell: Regulate early expression of Cdkn2a and pRb1, neutralize mdm2-p53 amalgamation and functional stabilization of p53. Experimental and Toxicological Pathology 69(8):630-636. |
|
|
Ye K, Liu K, Shen Q, Li Q, Hao J, Han F, Jiang R (2019) Reversal of Multidrug Resistance in Cancer by Multi-Functional Flavonoids Frontiers in Oncology 9:1-16. |
|
|
Zhang W, Men X, Lei P (2014). Review on anti-tumor effect of triterpene acid compounds. Journal of Cancer Research and Therapeutics 10(5):14-19. |
|
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