ANTINEOPLASTIC ACTIVITY;
ANTIPROLIFERATIVE ACTIVITY;
ARTICLE;
BREAST CANCER;
CANCER CELL CULTURE;
CENTRAL NERVOUS SYSTEM TUMOR;
CHEMICAL MODIFICATION;
COLON CANCER;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG BINDING;
DRUG CYTOTOXICITY;
DRUG DESIGN;
DRUG POTENCY;
DRUG PROTEIN BINDING;
DRUG SOLUBILITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IC 50;
INHIBITION KINETICS;
KIDNEY CANCER;
LEUKEMIA CELL LINE;
LUNG NON SMALL CELL CANCER;
MELANOMA;
MICROTUBULE ASSEMBLY;
PRIORITY JOURNAL;
PROSTATE CANCER;
STRUCTURE ACTIVITY RELATION;
Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance
Gangjee A, Zhao Y, Lin L, Raghavan S, Roberts EG, Risinger AL, et al. Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance. J Med Chem. 2010;53(22):8116-28.
Corrections to synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance
Gangjee A, Zhao Y, Lin L, Raghavan S, Roberts EG, Risinger AL, et al. Corrections to synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance. J Med Chem 2011;54(3):913.
Ferrandina G, Zannoni GF, Martinelli E, Paglia A, Gallotta V, Mozzetti S, et al. Class III β-tubulin overexpression is a marker of poor clinical outcome in advanced ovarian cancer patients. Clin Cancer Res. 2006;12:2774-9.
Class III β-tubulin overexpression is a prominent mechanism of paclitaxel resistance in ovarian cancer patients
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Mozzetti S, Ferlini C, Concolino P, Filippetti F, Raspaglio G, Prislei S, et al. Class III β-tubulin overexpression is a prominent mechanism of paclitaxel resistance in ovarian cancer patients. Clin Cancer Res. 2005;11:298-305.
Rosell R, Scagliotti G, Danenberg KD, Lord RVN, Bepler G, Novello S, et al. Transcripts in pretreatment biopsies from a three-arm randomized trial in metastatic non-small-cell lung cancer. Oncogene. 2003;22:3548-53.
Expression of class III β-tubulin is predictive of patient outcome in patients with non-small cell lung cancer receiving vinorelbine-based chemotherapy
Seve P, Isaac S, Tredan O, Souquet P-J, Pacheco Y, Perol M, et al. Expression of class III β-tubulin is predictive of patient outcome in patients with non-small cell lung cancer receiving vinorelbine-based chemotherapy. Clin Cancer Res. 2005;11:5481-6.
Tommasi S, Mangia A, Lacalamita R, Bellizzi A, Fedele V, Chiriatti A, et al. Cytoskeleton and paclitaxel sensitivity in breast cancer: the role of β-tubulins. Int J Cancer. 2007;120:2078-85.
Design, synthesis, and biological evaluation of classical and nonclassical 2-amino-4-oxo-5-substituted-6-methylpyrrolo[3,2-d]pyrimidines as dual thymidylate synthase and dihydrofolate reductase inhibitors
Gangjee A, Li W, Yang J, Kisliuk RL. Design, synthesis, and biological evaluation of classical and nonclassical 2-amino-4-oxo-5-substituted-6- methylpyrrolo[3,2-d]pyrimidines as dual thymidylate synthase and dihydrofolate reductase inhibitors. J Med Chem. 2008;51(1):68-76.
An access to the β-anomer of 4'-thio-c-ribonucleosides: Hydroboration of 1-C-aryl- or 1-C-heteroaryl-4-thiofuranoid glycals and its regiochemical outcome
Haraguchi K, Horii C, Yoshimura Y, Ariga F, Tadokoro A, Tanaka H. An access to the β-anomer of 4'-thio-c-ribonucleosides: Hydroboration of 1-C-aryl- or 1-C-heteroaryl-4-thiofuranoid glycals and its regiochemical outcome. J Org Chem. 2011;76:8658-69.
Stadlwieser J, Schmidt B, Bernsmann H, Dunkern T, Benediktus E, Pahl A, et al. inventors; Nycomed GmbH, Germany. assignee. Methylpyrrolopyrimidinecarboxamides as phosphodiesterase type 5 inhibitors and their preparation and use in the treatment of diseases. Patent WO2011023693A1. 2011.
Lee L, Robb LM, Lee M, Davis R, Mackay H, Chavda S, et al. Design, synthesis, and biological evaluations of 2,5-diaryl-2,3-dihydro-1,3,4- oxadiazoline analogs of combretastatin-A4. J Med Chem. 2010;53(1):325-34.
Boyd MR, Paull KD. Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen. Drug Develop Res. 1995;34(2):91-109.
Risinger AL, Jackson EM, Polin LA, Helms GL, LeBoeuf DA, Joe PA, et al. The taccalonolides: microtubule stabilizers that circumvent clinically relevant taxane resistance mechanisms. Cancer Res. 2008;68(21):8881-8.
Hamel E. Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin. Cell Biochem Biophys. 2003;38(1):1-21.
Separation of active tubulin and microtubule-associated proteins by ultracentrifugation and isolation of a component causing the formation of microtubule bundles
Hamel E, Lin CM. Separation of active tubulin and microtubule-associated proteins by ultracentrifugation and isolation of a component causing the formation of microtubule bundles. Biochemistry. 1984;23(18):4173-84.
(1984)Biochemistry, vol.23, Issue.18, pp. 4173-4184
Antimitotic natural products combretastatin a-4 and combretastatin a-2: Studies on the mechanism of their inhibition of the binding of colchicine to tubulin
Lin CM, Ho HH, Pettit GR, Hamel E. Antimitotic natural products combretastatin A-4 and combretastatin A-2: Studies on the mechanism of their inhibition of the binding of colchicine to tubulin. Biochemistry. 1989;28(17):6984-91.
(1989)Biochemistry, vol.28, Issue.17, pp. 6984-6991
Structure-activity analysis of the interaction of curacin a, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of mcf-7 breast cancer cells
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Verdier-Pinard P, Lai J-Y, Yoo H-D, Yu J, Marquez B, Nagle DG, et al. Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells. Mol Pharmacol. 1998;53(1):62-76.