Antibody-drug conjugates: linking cytotoxic payloads to monoclonal antibodies.
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[1] W. Denny,et al. Design, synthesis, and in vitro evaluation of dipeptide-based antibody minor groove binder conjugates. , 2005, Journal of medicinal chemistry.
[2] G. Bringmann,et al. Selective treatment of cancer: synthesis, biological evaluation and structural elucidation of novel analogues of the antibiotic CC-1065 and the duocarmycins. , 2007, Chemistry.
[3] A. Mountain,et al. A calicheamicin conjugate with a fully humanized anti-MUC1 antibody shows potent antitumor effects in breast and ovarian tumor xenografts. , 2005, Bioconjugate chemistry.
[4] U. Zangemeister‐Wittke. Antibodies for Targeted Cancer Therapy – Technical Aspects and Clinical Perspectives , 2006, Pathobiology.
[5] S. Horning,et al. Complete remissions with weekly dosing of SGN-35, a novel antibody-drug conjugate (ADC) targeting CD30, in a phase I dose-escalation study in patients with relapsed or refractory Hodgkin lymphoma (HL) or systemic anaplastic large cell lymphoma (sALCL). , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[6] R. Chari. Targeted cancer therapy: conferring specificity to cytotoxic drugs. , 2008, Accounts of chemical research.
[7] P. Trail,et al. Cure of xenografted human carcinomas by BR96-doxorubicin immunoconjugates. , 1993, Science.
[8] Damon L. Meyer,et al. Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: effects of linker technology on efficacy and toxicity. , 2006, Bioconjugate chemistry.
[9] L. Tietze,et al. Synthesis and Biological Evaluation of Novel Analogues and Prodrugs of the Cytotoxic Antibiotic CC-1065 for Selective Cancer Therapy , 2002 .
[10] M. Sliwkowski,et al. Perspectives on Anti-HER Monoclonal Antibodies , 2002, Oncology.
[11] I. Bernstein,et al. Targeting of the CD33-calicheamicin immunoconjugate Mylotarg (CMA-676) in acute myeloid leukemia: in vivo and in vitro saturation and internalization by leukemic and normal myeloid cells. , 2001, Blood.
[12] Damon L. Meyer,et al. cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity. , 2003, Blood.
[13] M. Birkner,et al. A phase II study of trastuzumab-DM1 (T-DM1), a HER2 antibody-drug conjugate (ADC), in patients (pts) with HER2+ metastatic breast cancer (MBC): Final results. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[14] I. Bernstein,et al. An anti-CD33 antibody-calicheamicin conjugate for treatment of acute myeloid leukemia. Choice of linker. , 2002, Bioconjugate chemistry.
[15] Hongsheng Xie,et al. Pharmacokinetics and Biodistribution of the Antitumor Immunoconjugate, Cantuzumab Mertansine (huC242-DM1), and Its Two Components in Mice , 2004, Journal of Pharmacology and Experimental Therapeutics.
[16] Peter D. Senter,et al. Development of potent monoclonal antibody auristatin conjugates for cancer therapy , 2003 .
[17] G. Frantz,et al. Antibody-drug conjugates for the treatment of non-Hodgkin's lymphoma: target and linker-drug selection. , 2009, Cancer research.
[18] P. Trail,et al. Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: model studies of enzymatic drug release and antigen-specific in vitro anticancer activity. , 2002, Bioconjugate chemistry.
[19] N. Damle,et al. Antitumor Efficacy of a Combination of CMC-544 (Inotuzumab Ozogamicin), a CD22-Targeted Cytotoxic Immunoconjugate of Calicheamicin, and Rituximab against Non-Hodgkin's B-Cell Lymphoma , 2006, Clinical Cancer Research.
[20] D. Kroll,et al. Design, synthesis, and biological evaluation of antibody-drug conjugates comprised of potent camptothecin analogues. , 2009, Bioconjugate chemistry.
[21] I. Hollander,et al. Selection of reaction additives used in the preparation of monomeric antibody-calicheamicin conjugates. , 2008, Bioconjugate chemistry.
[22] Irwin Hollander,et al. Gemtuzumab ozogamicin, a potent and selective anti-CD33 antibody-calicheamicin conjugate for treatment of acute myeloid leukemia. , 2002, Bioconjugate chemistry.
[23] Damon L. Meyer,et al. Dipeptide-based highly potent doxorubicin antibody conjugates. , 2006, Bioorganic & medicinal chemistry letters.
[24] Damon L. Meyer,et al. Minor groove binder antibody conjugates employing a water soluble beta-glucuronide linker. , 2007, Bioorganic & medicinal chemistry letters.
[25] Anna M Wu,et al. Arming antibodies: prospects and challenges for immunoconjugates , 2005, Nature Biotechnology.
[26] R. Panchal,et al. Novel therapeutic strategies to selectively kill cancer cells. , 1998, Biochemical pharmacology.
[27] Jennifer B. Webster,et al. Engineered antibody-drug conjugates with defined sites and stoichiometries of drug attachment. , 2006, Protein engineering, design & selection : PEDS.
[28] A. Wahl,et al. In vivo drug-linker stability of an anti-CD30 dipeptide-linked auristatin immunoconjugate. , 2005, Clinical cancer research : an official journal of the American Association for Cancer Research.
[29] K. Khandke,et al. CMC-544 (inotuzumab ozogamicin): A CD22-targeted immunoconjugate of calicheamicin , 2009 .
[30] Yelena Kovtun,et al. Semisynthetic maytansine analogues for the targeted treatment of cancer. , 2006, Journal of medicinal chemistry.
[31] P. Senter,et al. Novel peptide linkers for highly potent antibody-auristatin conjugate. , 2008, Bioconjugate chemistry.
[32] D. Boger,et al. CBI Prodrug Analogs of CC-1065 and the Duocarmycins , 1999 .
[33] J. Larrick,et al. Synthesis and antitumor activity of CBI-bearing ester and carbamate prodrugs of CC-1065 analogue. , 2006, Bioorganic & medicinal chemistry.
[34] S. Winstein,et al. Neighboring Carbon and Hydrogen. Li. Dienones from Ar1[UNK]-3 Participation. Isolation and Behavior of Spiro(2,5)octa-1,4-diene-3-one , 1963 .
[35] Damon L. Meyer,et al. Contribution of linker stability to the activities of anticancer immunoconjugates. , 2008, Bioconjugate chemistry.
[36] A. Wahl,et al. Protease-mediated fragmentation of p-amidobenzyl ethers: a new strategy for the activation of anticancer prodrugs. , 2002, The Journal of organic chemistry.
[37] Bonnie F. Sloane,et al. Unraveling the role of proteases in cancer. , 2000, Clinica chimica acta; international journal of clinical chemistry.
[38] X. Geng,et al. Tumor-specific novel taxoid-monoclonal antibody conjugates. , 2004, Journal of medicinal chemistry.
[39] Prodrug Strategies in Anticancer Chemotherapy , 2008, ChemMedChem.
[40] A. Tolcher,et al. Technology Insight: cytotoxic drug immunoconjugates for cancer therapy , 2007, Nature Clinical Practice Oncology.
[41] R. Lutz,et al. Antibody-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing. , 2006, Cancer research.
[42] T. Chittenden,et al. Antibody-drug conjugates designed to eradicate tumors with homogeneous and heterogeneous expression of the target antigen. , 2006, Cancer research.
[43] K. Gomi,et al. Synthesis and antitumor activity of duocarmycin derivatives. , 1995, Chemical & pharmaceutical bulletin.