Статті в журналах з теми "Maytansinoids"
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Giles, Francis, Rodica Morariu-Zamfir, John Lambert, Srdan Verstovsek, Deborah Thomas, Farhad Ravandi, and Dan Deangelo. "Phase I Study of AVE9633, an AntiCD33-Maytansinoid Immunoconjugate, Administered as an Intravenous Infusion in Patients with Refractory/Relapsed CD33-Positive Acute Myeloid Leukemia (AML)." Blood 108, no. 11 (November 16, 2006): 4548. http://dx.doi.org/10.1182/blood.v108.11.4548.4548.
Повний текст джерелаPlattner, Ronald D., and Richard G. Powell. "Tandem Mass Spectrometry of Maytansinoids." Journal of Natural Products 49, no. 3 (May 1986): 475–82. http://dx.doi.org/10.1021/np50045a016.
Повний текст джерелаLarson, Gretchen M., Brian T. Schaneberg, and Albert T. Sneden. "Two New Maytansinoids fromMaytenus buchananii." Journal of Natural Products 62, no. 2 (February 1999): 361–63. http://dx.doi.org/10.1021/np9803732.
Повний текст джерелаLo, Chen-Fu, Tai-Yu Chiu, Yu-Tzu Liu, Li-Rung Huang, Teng-Kuang Yeh, Kuan-Hsun Huang, Kuan-Liang Liu, et al. "Synthesis and Evaluation of Small Molecule Drug Conjugates Harnessing Thioester-Linked Maytansinoids." Pharmaceutics 14, no. 7 (June 21, 2022): 1316. http://dx.doi.org/10.3390/pharmaceutics14071316.
Повний текст джерелаNittoli, Thomas, Frank Delfino, Marcus Kelly, Serena Carosso, Thomas Markotan, Arthur Kunz, Zhaoyuan Chen, et al. "Antibody drug conjugates of cleavable amino-benzoyl-maytansinoids." Bioorganic & Medicinal Chemistry 28, no. 23 (December 2020): 115785. http://dx.doi.org/10.1016/j.bmc.2020.115785.
Повний текст джерелаSuchocki, John A., and Albert T. Sneden. "New maytansinoids: reduction products of the C(9)-carbinolamide." Journal of Organic Chemistry 53, no. 17 (August 1988): 4116–18. http://dx.doi.org/10.1021/jo00252a047.
Повний текст джерелаLadino, Cynthia A., Ravi V. J. Chari, Lizabeth A. Bourret, Nancy L. Kedersha, and Victor S. Goldmacher. "Folate-maytansinoids: Target-selective drugs of low molecular weight." International Journal of Cancer 73, no. 6 (December 10, 1997): 859–64. http://dx.doi.org/10.1002/(sici)1097-0215(19971210)73:6<859::aid-ijc16>3.0.co;2-#.
Повний текст джерелаPerrino, Elena, Martina Steiner, Nikolaus Krall, Gonçalo J. L. Bernardes, Francesca Pretto, Giulio Casi, and Dario Neri. "Curative Properties of Noninternalizing Antibody–Drug Conjugates Based on Maytansinoids." Cancer Research 74, no. 9 (February 11, 2014): 2569–78. http://dx.doi.org/10.1158/0008-5472.can-13-2990.
Повний текст джерелаNittoli, Thomas, Marcus P. Kelly, Frank Delfino, John Rudge, Arthur Kunz, Thomas Markotan, Jan Spink, et al. "Antibody drug conjugates of cleavable amino-alkyl and aryl maytansinoids." Bioorganic & Medicinal Chemistry 26, no. 9 (May 2018): 2271–79. http://dx.doi.org/10.1016/j.bmc.2018.02.025.
Повний текст джерелаLiu, C., B. M. Tadayoni, L. A. Bourret, K. M. Mattocks, S. M. Derr, W. C. Widdison, N. L. Kedersha, et al. "Eradication of large colon tumor xenografts by targeted delivery of maytansinoids." Proceedings of the National Academy of Sciences 93, no. 16 (August 6, 1996): 8618–23. http://dx.doi.org/10.1073/pnas.93.16.8618.
Повний текст джерелаBénéchie, Michel, Bernard Delpech, Qui Khuong-Huu, and Françoise Khuong-Huu. "Total synthesis of maytansinoids. Approach to 4,6-bisdemethylmaytansine and 4-demethylmaytansine." Tetrahedron 48, no. 10 (January 1992): 1895–910. http://dx.doi.org/10.1016/s0040-4020(01)88513-6.
Повний текст джерелаLi, Ya-Nan, Jia-Nan Li, Qin Ouyang, Yu-Bo Zhou, Chun Lei, Ming-Jun Cui, Kai-Cong Fu, Jia Li, Jian-Ming Huang, and Ai-Jun Hou. "Determination of maytansinoids in Trewia nudiflora using QuEChERS extraction combined with HPLC." Journal of Pharmaceutical and Biomedical Analysis 198 (May 2021): 113993. http://dx.doi.org/10.1016/j.jpba.2021.113993.
Повний текст джерелаReich, Eike, and Albert T. Sneden. "Normal- and bonded-phase liquid chromatography with photodiode array detection of maytansinoids." Journal of Chromatography A 763, no. 1-2 (February 1997): 213–19. http://dx.doi.org/10.1016/s0021-9673(96)00849-7.
Повний текст джерелаLiu, Changnian, and Ravi VJ Chari. "The development of antibody delivery systems to target cancer with highly potent maytansinoids." Expert Opinion on Investigational Drugs 6, no. 2 (February 1997): 169–72. http://dx.doi.org/10.1517/13543784.6.2.169.
Повний текст джерелаBENECHIE, M., B. DELPECH, Q. KHUONG-HUU, and F. KHUONG-HUU. "ChemInform Abstract: Total Synthesis of Maytansinoids. Approach to 4,6- Bisdemethylmaytansine and 4-Demethylmaytansine." ChemInform 23, no. 26 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199226292.
Повний текст джерелаLi, Wenting, Minhao Huang, Yuyan Li, Anjie Xia, Lun Tan, Zhixiong Zhang, Yuxi Wang, and Jinliang Yang. "C3 ester side chain plays a pivotal role in the antitumor activity of Maytansinoids." Biochemical and Biophysical Research Communications 566 (August 2021): 197–203. http://dx.doi.org/10.1016/j.bbrc.2021.05.071.
Повний текст джерелаDang, Giap van, Bernd M. Rode, and Hermann Stuppner. "Quantitative electronic structure-activity relationship (QESAR) of natural cytotoxic compounds: maytansinoids, quassinoids and cucurbitacins." European Journal of Pharmaceutical Sciences 2, no. 5-6 (December 1994): 331–50. http://dx.doi.org/10.1016/0928-0987(94)00061-1.
Повний текст джерелаLi, Shanren, Chunhua Lu, Xiaoyan Chang, and Yuemao Shen. "Constitutive overexpression of asm18 increases the production and diversity of maytansinoids in Actinosynnema pretiosum." Applied Microbiology and Biotechnology 100, no. 6 (November 17, 2015): 2641–49. http://dx.doi.org/10.1007/s00253-015-7127-7.
Повний текст джерелаPullen, Christian B., Petra Schmitz, Dietmar Hoffmann, Kristina Meurer, Theresa Boettcher, Daniel von Bamberg, Ana Maria Pereira, et al. "Occurrence and non-detectability of maytansinoids in individual plants of the genera Maytenus and Putterlickia." Phytochemistry 62, no. 3 (February 2003): 377–87. http://dx.doi.org/10.1016/s0031-9422(02)00550-2.
Повний текст джерелаEckelmann, Dennis, Souvik Kusari, and Michael Spiteller. "Occurrence and spatial distribution of maytansinoids in Putterlickia pyracantha , an unexplored resource of anticancer compounds." Fitoterapia 113 (September 2016): 175–81. http://dx.doi.org/10.1016/j.fitote.2016.08.006.
Повний текст джерелаHodgson, David M., Philip J. Parsons, and Peter A. Stones. "A short and efficient synthesis of the C-3 to C-10 portion of the maytansinoids." Tetrahedron 47, no. 24 (January 1991): 4133–42. http://dx.doi.org/10.1016/s0040-4020(01)86450-4.
Повний текст джерелаZhu, Na, Peiji Zhao, and Yuemao Shen. "Selective Isolation and Ansamycin-Targeted Screenings of Commensal Actinomycetes from the “Maytansinoids-Producing” Arboreal Trewia nudiflora." Current Microbiology 58, no. 1 (October 25, 2008): 87–94. http://dx.doi.org/10.1007/s00284-008-9284-8.
Повний текст джерелаMadrigal, Richard V., Bruce W. Zilkowski, and Cecil R. Smith. "Structure-activity relationships among maytansinoids in their effect on the European corn borer,Ostrinia nubilalis (Hübner)." Journal of Chemical Ecology 11, no. 4 (April 1985): 501–6. http://dx.doi.org/10.1007/bf00989561.
Повний текст джерелаQi-Tao, Yu, Zhi-Heng Huang, Zhou Yun-Li, and Zhou Qi-Ting. "Mass spectrometry of maytansinoids-A study on the fragmentation mechanism and identification of synthetic analogs of maytansine." Acta Chimica Sinica 4, no. 1 (March 1986): 48–54. http://dx.doi.org/10.1002/cjoc.19860040108.
Повний текст джерелаSakai, Kunikazu, Tetsuya Ichikawa, Kaoru Yamada, Mitsuo Yamashita, Mitsutoshi Tanimoto, Akio Hikita, Yasuharu Ijuin, and Kiyosi Kondo. "Antitumor Principles in Mosses: the First Isolation and Identification of Maytansinoids, Including a Novel 15-Methoxyansamitocin P-3." Journal of Natural Products 51, no. 5 (September 1988): 845–50. http://dx.doi.org/10.1021/np50059a005.
Повний текст джерелаHODGSON, D. M., P. J. PARSONS, and P. A. STONES. "ChemInform Abstract: A Short and Efficient Synthesis of the C-3 to C-10 Portion of the Maytansinoids." ChemInform 22, no. 35 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199135273.
Повний текст джерелаKo, Soo sung, and Pat N. Confalone. "Model studies for the total synthesis of the maytansinoids based on the intramolecular nitrile oxide-olefin [3+2] cycloaddition reaction." Tetrahedron 41, no. 17 (January 1985): 3511–18. http://dx.doi.org/10.1016/s0040-4020(01)96704-3.
Повний текст джерелаIkeda, Hiroshi, Teru Hideshima, Mariateresa Fulciniti, Robert J. Lutz, Hiroshi Yasui, Yutaka Okawa, Tanyel Kiziltepe, et al. "The Monoclonal Antibody nBT062 Conjugated to Cytotoxic Maytansinoids Has Selective Cytotoxicity Against CD138-Positive Multiple Myeloma Cells In vitro and In vivo." Clinical Cancer Research 15, no. 12 (June 9, 2009): 4028–37. http://dx.doi.org/10.1158/1078-0432.ccr-08-2867.
Повний текст джерелаCheng, Hong, Guoqing Xiong, Yi Li, Jiaqi Zhu, Xianghua Xiong, Qingyang Wang, Liancheng Zhang, et al. "Increased yield of AP-3 by inactivation of asm25 in Actinosynnema pretiosum ssp. auranticum ATCC 31565." PLOS ONE 17, no. 3 (March 22, 2022): e0265517. http://dx.doi.org/10.1371/journal.pone.0265517.
Повний текст джерелаIkeda, Hiroshi, Teru Hideshima, Robert J. Lutz, Sonia Vallet, Samantha Pozzi, Loredana Santo, Elisabetta Calabrese, et al. "The Monoclonal Antibody nBT062 Conjugated to Cytotoxic Maytansinoids Has Potent and Selective Cytotoxicity against CD138 Positive Multiple Myeloma Cells in Vitro and in Vivo." Blood 112, no. 11 (November 16, 2008): 1716. http://dx.doi.org/10.1182/blood.v112.11.1716.1716.
Повний текст джерелаErickson, Hans K., and John M. Lambert. "ADME of Antibody–Maytansinoid Conjugates." AAPS Journal 14, no. 4 (August 9, 2012): 799–805. http://dx.doi.org/10.1208/s12248-012-9386-x.
Повний текст джерелаWang, Hangxiang, Jiaping Wu, Li Xu, Ke Xie, Chao Chen, and Yuehan Dong. "Albumin nanoparticle encapsulation of potent cytotoxic therapeutics shows sustained drug release and alleviates cancer drug toxicity." Chemical Communications 53, no. 17 (2017): 2618–21. http://dx.doi.org/10.1039/c6cc08978j.
Повний текст джерелаFishkin, Nathan. "Maytansinoid–BODIPY Conjugates: Application to Microscale Determination of Drug Extinction Coefficients and for Quantification of Maytansinoid Analytes." Molecular Pharmaceutics 12, no. 6 (March 16, 2015): 1745–51. http://dx.doi.org/10.1021/mp500843r.
Повний текст джерелаCassady, John M., Kenneth K. Chan, Heinz G. Floss, and Eckhard Leistner. "Recent Developments in the Maytansinoid Antitumor Agents." Chemical and Pharmaceutical Bulletin 52, no. 1 (2004): 1–26. http://dx.doi.org/10.1248/cpb.52.1.
Повний текст джерелаHenning, Peter. "T-DM1 als Innovation beim HER2-positiven Brustkrebs: Antikörper und Zytostatikum als duale Wirkkombination." Onkologische Welt 03, no. 04 (2012): 172. http://dx.doi.org/10.1055/s-0038-1630203.
Повний текст джерелаKovtun, Yelena V., Charlene A. Audette, Michele F. Mayo, Gregory E. Jones, Heather Doherty, Erin K. Maloney, Hans K. Erickson, et al. "Antibody-Maytansinoid Conjugates Designed to Bypass Multidrug Resistance." Cancer Research 70, no. 6 (March 2, 2010): 2528–37. http://dx.doi.org/10.1158/0008-5472.can-09-3546.
Повний текст джерелаLuo, Quanzhou, Hyo Helen Chung, Christopher Borths, Matthew Janson, Jie Wen, Marisa K. Joubert, and Jette Wypych. "Structural Characterization of a Monoclonal Antibody–Maytansinoid Immunoconjugate." Analytical Chemistry 88, no. 1 (December 14, 2015): 695–702. http://dx.doi.org/10.1021/acs.analchem.5b03709.
Повний текст джерелаLutz, Robert J., and Kathleen R. Whiteman. "Antibody-maytansinoid conjugates for the treatment of myeloma." mAbs 1, no. 6 (November 2009): 548–51. http://dx.doi.org/10.4161/mabs.1.6.10029.
Повний текст джерелаGoodwin, Thomas E., Shari G. Orlicek, N. Renee Adams, Lynn A. Covey-Morrison, J. Steve Jenkins, and Gary L. Templeton. "Preparation of an aromatic synthon for maytansinoid synthesis." Journal of Organic Chemistry 50, no. 26 (December 1985): 5889–92. http://dx.doi.org/10.1021/jo00350a098.
Повний текст джерелаKirschning, Andreas, Kirsten Harmrolfs, and Tobias Knobloch. "The chemistry and biology of the maytansinoid antitumor agents." Comptes Rendus Chimie 11, no. 11-12 (November 2008): 1523–43. http://dx.doi.org/10.1016/j.crci.2008.02.006.
Повний текст джерелаSherman, Igor A., Rebecca J. Boohaker, Karr Stinson, Patricia Griffin, and Wendy Hill. "An alpha-fetoprotein-maytansine conjugate for the treatment of AFP receptor expressing tumors." Journal of Clinical Oncology 40, no. 16_suppl (June 1, 2022): e15056-e15056. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.e15056.
Повний текст джерелаSherman, Igor A., Rebecca J. Boohaker, Karr Stinson, Patricia Griffin, and Wendy Hill. "An alpha-fetoprotein-maytansine conjugate for the treatment of AFP receptor expressing tumors." Journal of Clinical Oncology 40, no. 16_suppl (June 1, 2022): e15056-e15056. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.e15056.
Повний текст джерелаCatcott, Kalli C., Molly A. McShea, Carl Uli Bialucha, Kathy L. Miller, Stuart W. Hicks, Parmita Saxena, Thomas G. Gesner, et al. "Microscale screening of antibody libraries as maytansinoid antibody-drug conjugates." mAbs 8, no. 3 (January 11, 2016): 513–23. http://dx.doi.org/10.1080/19420862.2015.1134408.
Повний текст джерелаGoodwin, Thomas E., Kimberley R. Cousins, Heidi M. Crane, Phyllis O. Eason, Timothy E. Freyaldenhoven, Charles C. Harmon, Brock K. King, et al. "Synthesis of Two New Maytansinoid Model Compounds from Carbohydrate Precursors." Journal of Carbohydrate Chemistry 17, no. 3 (April 1998): 323–39. http://dx.doi.org/10.1080/07328309808002895.
Повний текст джерелаWiddison, Wayne, Sharon Wilhelm, Karen Veale, Juliet Costoplus, Gregory Jones, Charlene Audette, Barbara Leece, Laura Bartle, Yelena Kovtun, and Ravi Chari. "Metabolites of Antibody–Maytansinoid Conjugates: Characteristics and in Vitro Potencies." Molecular Pharmaceutics 12, no. 6 (April 8, 2015): 1762–73. http://dx.doi.org/10.1021/mp5007757.
Повний текст джерелаZhao, Robert Y., Sharon D. Wilhelm, Charlene Audette, Gregory Jones, Barbara A. Leece, Alexandru C. Lazar, Victor S. Goldmacher, et al. "Synthesis and Evaluation of Hydrophilic Linkers for Antibody–Maytansinoid Conjugates." Journal of Medicinal Chemistry 54, no. 10 (May 26, 2011): 3606–23. http://dx.doi.org/10.1021/jm2002958.
Повний текст джерелаReddy, Joseph A., Elaine Westrick, Hari K. R. Santhapuram, Stephen J. Howard, Michael L. Miller, Marilynn Vetzel, Iontcho Vlahov, Ravi V. J. Chari, Victor S. Goldmacher, and Christopher P. Leamon. "Folate Receptor–Specific Antitumor Activity of EC131, a Folate-Maytansinoid Conjugate." Cancer Research 67, no. 13 (July 1, 2007): 6376–82. http://dx.doi.org/10.1158/0008-5472.can-06-3894.
Повний текст джерелаOroudjev, Emin, Manu Lopus, Leslie Wilson, Charlene Audette, Carmela Provenzano, Hans Erickson, Yelena Kovtun, Ravi Chari, and Mary Ann Jordan. "Maytansinoid-Antibody Conjugates Induce Mitotic Arrest by Suppressing Microtubule Dynamic Instability." Molecular Cancer Therapeutics 9, no. 10 (October 2010): 2700–2713. http://dx.doi.org/10.1158/1535-7163.mct-10-0645.
Повний текст джерелаJiang, Zhengyang, Zhen Yang, Feng Li, Zheng Li, Nathan Fishkin, and Kevin Burgess. "Targeted Maytansinoid Conjugate Improves Therapeutic Index for Metastatic Breast Cancer Cells." Bioconjugate Chemistry 29, no. 9 (August 13, 2018): 2920–26. http://dx.doi.org/10.1021/acs.bioconjchem.8b00340.
Повний текст джерелаAb, O., V. S. Goldmacher, L. M. Bartle, D. Tavares, C. N. Carrigan, S. Xu, M. Okamoto, H. Johnson, K. R. Whiteman, and T. Chittenden. "236 Antibody–maytansinoid conjugates targeting folate receptor 1 for cancer therapy." European Journal of Cancer Supplements 8, no. 7 (November 2010): 77. http://dx.doi.org/10.1016/s1359-6349(10)71941-8.
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