-
1
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
(a) Jordan, M. A.; Wilson L. Microtubules as a Target for Anticancer Drugs. Nat. Rev. Cancer 2004, 4, 253-265.
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
2
-
-
0029360519
-
Microtubule dynamics: Taking aim at a moving target
-
(b) Wilson, L.; Jordan, M. A. Microtubule Dynamics: Taking Aim at a Moving Target. Chem. Biol. 1995, 2, 569-573.
-
(1995)
Chem. Biol.
, vol.2
, pp. 569-573
-
-
Wilson, L.1
Jordan, M.A.2
-
3
-
-
0036850914
-
Discovery and development of antimitotic agents that inhibit tubulin polymerization for the treatment of cancer
-
Li, Q.; Sham, H. L. Discovery and Development of Antimitotic Agents That Inhibit Tubulin Polymerization for the Treatment of Cancer. Expert Opin. Ther. Pat. 2002, 12 (11), 1663-1702.
-
(2002)
Expert Opin. Ther. Pat.
, vol.12
, Issue.11
, pp. 1663-1702
-
-
Li, Q.1
Sham, H.L.2
-
4
-
-
0035493789
-
A therapeutic area review of oncology products and players
-
Fleming, S.; Lucas, F.; Schofield, M. A Therapeutic Area Review of Oncology Products and Players. Expert Opin. Emerging Drugs 2001, 6 (2), 317-329.
-
(2001)
Expert Opin. Emerging Drugs
, vol.6
, Issue.2
, pp. 317-329
-
-
Fleming, S.1
Lucas, F.2
Schofield, M.3
-
5
-
-
0028224534
-
Cell biological mechanisms of multidrug resistance in tumors
-
Simon, S. M.; Schindler, M. Cell Biological Mechanisms of Multidrug Resistance in Tumors. Proc. Natl. Acad. Sci U.S.A. 1994, 91, 3497-3504.
-
(1994)
Proc. Natl. Acad. Sci U.S.A.
, vol.91
, pp. 3497-3504
-
-
Simon, S.M.1
Schindler, M.2
-
6
-
-
0035003021
-
Role of formulation vehicles in taxane pharmacology
-
Van Zuylen, L.; Verweij, J.; Sparreboom, A. Role of Formulation Vehicles in Taxane Pharmacology. Invest. New Drugs 2001, 19, 125-141.
-
(2001)
Invest. New Drugs
, vol.19
, pp. 125-141
-
-
Van Zuylen, L.1
Verweij, J.2
Sparreboom, A.3
-
7
-
-
0019991766
-
Pharmakokinetic properties of noscapine
-
Dahlstrom, B.; Mellstrand, T.; Lofdahl, C.-G.; Johansson, M. Pharmakokinetic Properties of Noscapine. Eur. J. Clin. Pharmacol. 1982, 22, 535-539.
-
(1982)
Eur. J. Clin. Pharmacol.
, vol.22
, pp. 535-539
-
-
Dahlstrom, B.1
Mellstrand, T.2
Lofdahl, C.-G.3
Johansson, M.4
-
8
-
-
17444429486
-
Synergists and antagonists of mitotic poisons
-
(a) Lettre, H. Synergists and Antagonists of Mitotic Poisons. Ann. N. Y. Acad. Sci. 1954, 58, 1264-1275.
-
(1954)
Ann. N. Y. Acad. Sci.
, vol.58
, pp. 1264-1275
-
-
Lettre, H.1
-
9
-
-
0006164865
-
Narcotin, ein Mitosegift (narcotine, a mitotic poison)
-
(b) Lettre, H.; Albrecht, M. Narcotin, ein Mitosegift (Narcotine, a Mitotic Poison). Naturwissenschaften 1942, 30, 184-185.
-
(1942)
Naturwissenschaften
, vol.30
, pp. 184-185
-
-
Lettre, H.1
Albrecht, M.2
-
10
-
-
0032539565
-
Opium alkaloid noscapine is an antitumor agent that arrests metaphase and induces apoptosis in dividing cells
-
(a) Ye, K.; Ke, Y.; Keshava, N.; Shanks, J.; Kapp, J. A.; Tekmal, R. R.; Petros, J.; Joshi, H. C. Opium Alkaloid Noscapine Is an Antitumor Agent That Arrests Metaphase and Induces Apoptosis in Dividing Cells. Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 1601-1606.
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 1601-1606
-
-
Ye, K.1
Ke, Y.2
Keshava, N.3
Shanks, J.4
Kapp, J.A.5
Tekmal, R.R.6
Petros, J.7
Joshi, H.C.8
-
11
-
-
0034491250
-
Noscapine and analogues as potential chemotherapeutic agents
-
(b) Joshi, H. C.; Zhou, J. Noscapine and Analogues as Potential Chemotherapeutic Agents. Drug News Perspect. 2000, 13 (9), 543-546.
-
(2000)
Drug News Perspect.
, vol.13
, Issue.9
, pp. 543-546
-
-
Joshi, H.C.1
Zhou, J.2
-
12
-
-
0033928547
-
Noscapine inhibits tumor growth with little toxicity to normal tissues or inhibition of immune responses
-
Ke, Y.; Ye, K.; Grossniklaus, H. E.; Archer, D. R.; Joshi, H. C.; Kapp, J. A. Noscapine Inhibits Tumor Growth with Little Toxicity to Normal Tissues or Inhibition of Immune Responses. Cancer Immunol. Immunother. 2000, 49, 217-225
-
(2000)
Cancer Immunol. Immunother.
, vol.49
, pp. 217-225
-
-
Ke, Y.1
Ye, K.2
Grossniklaus, H.E.3
Archer, D.R.4
Joshi, H.C.5
Kapp, J.A.6
-
13
-
-
0037099621
-
Noscapine alters microtubule dynamics in living cells and inhibits the progression of melanoma
-
Landen, J. W.; Lang, R.; McMahon, S. J.; Rusan, N. M.; Yvon, A.-M.; Adams, A. W.; Sorcinelli, M. D.; Campbell, R.; Bonaccorsi, P.; Ansel, J. C.; Archer, D. R.; Wadsworth, P.; Armstrong, C. A.; Joshi, H. C. Noscapine Alters Microtubule Dynamics in Living Cells and Inhibits the Progression of Melanoma. Cancer Res. 2002, 62, 4109-4114.
-
(2002)
Cancer Res.
, vol.62
, pp. 4109-4114
-
-
Landen, J.W.1
Lang, R.2
McMahon, S.J.3
Rusan, N.M.4
Yvon, A.-M.5
Adams, A.W.6
Sorcinelli, M.D.7
Campbell, R.8
Bonaccorsi, P.9
Ansel, J.C.10
Archer, D.R.11
Wadsworth, P.12
Armstrong, C.A.13
Joshi, H.C.14
-
14
-
-
20944431721
-
Discovery of S-phase arresting agents derived from noscapine
-
Anderson, J. T.; Ting, A. E.; Boozer, S.; Brunden, K. R.; Danzig, J.; Dent, T.; Harrington, J. J.; Murphy, S. M.; Perry, R.; Raber, A.; Rundlett, S. E.; Wang, J.; Wang, N.; Bennani, Y. L. Discovery of S-Phase Arresting Agents Derived from Noscapine. J. Med. Chem. 2005, 48, 2756-2758.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2756-2758
-
-
Anderson, J.T.1
Ting, A.E.2
Boozer, S.3
Brunden, K.R.4
Danzig, J.5
Dent, T.6
Harrington, J.J.7
Murphy, S.M.8
Perry, R.9
Raber, A.10
Rundlett, S.E.11
Wang, J.12
Wang, N.13
Bennani, Y.L.14
-
15
-
-
10644234537
-
The identification and optimization of a N-hydroxy urea series of flap endonuclease 1 inhibitors
-
Tumey, L. N.; Bom, D.; Huck, B.; Gleason, E.; Wang, J.; Silver, D.; Brunden, K.; Boozer, S.; Rundlett, S.; Sherf, B.; Murphy, S.; Dent, T.; Leventhal, C.; Bailey, A.; Harrington, J.; Bennani, Y. L. The Identification and Optimization of a N-Hydroxy Urea Series of Flap Endonuclease 1 Inhibitors. Bioorg. Med. Chem. Lett. 2005, 15, 277-281.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 277-281
-
-
Tumey, L.N.1
Bom, D.2
Huck, B.3
Gleason, E.4
Wang, J.5
Silver, D.6
Brunden, K.7
Boozer, S.8
Rundlett, S.9
Sherf, B.10
Murphy, S.11
Dent, T.12
Leventhal, C.13
Bailey, A.14
Harrington, J.15
Bennani, Y.L.16
-
16
-
-
0000418343
-
Palladium-catalyzed amination of aryl triflates
-
Louie, J.; Driver, M. S.; Hamann, B. C. Personal communication
-
(a) Wolfe, J. P.; Buchwald, S. L. Palladium-Catalyzed Amination of Aryl Triflates. J. Org. Chem. 1997, 62, 1264-1267. Louie, J.; Driver, M. S.; Hamann, B. C. Personal communication.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1264-1267
-
-
Wolfe, J.P.1
Buchwald, S.L.2
-
17
-
-
0000777908
-
Palladium-catalyzed amination of aryl triflates and importance of triflate addition rate
-
(b) Hartwig, J. F. Palladium-Catalyzed Amination of Aryl Triflates and Importance of Triflate Addition Rate. J. Org. Chem. 1997, 62, 1268-1273.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1268-1273
-
-
Hartwig, J.F.1
-
18
-
-
0032560932
-
A highly active catalyst for palladium-catalyzed cross-coupling reactions: Room-temperature suzuki couplings and amination of unactivated aryl chlorides
-
Old, D. W.; Wolfe, J. P.; Buchwald, S. L. A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides. J. Am. Chem. Soc. 1998, 120, 9722-9723.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 9722-9723
-
-
Old, D.W.1
Wolfe, J.P.2
Buchwald, S.L.3
-
19
-
-
0018198927
-
Neue Reaktionen an Phthalidisochinolinalkaloiden. Alkoxytauschreaktionen und Isomerisierungen an α- Und β-Narcotin
-
Schmidhammer, H.; Klotzer, W. Neue Reaktionen an Phthalidisochinolinalkaloiden. Alkoxytauschreaktionen und Isomerisierungen an α- und β-Narcotin (New Reactions of Phthalidoisoquinoline Alkaloids. Alkoxy Exchange Reactions and Isomerizations of α- and β-Narcotine).Arch. Pharm. (Weinheim, Ger.) 1978, 311, 664-671.
-
(1978)
Arch. Pharm. (Weinheim, Ger.)
, vol.311
, pp. 664-671
-
-
Schmidhammer, H.1
Klotzer, W.2
-
21
-
-
28544436984
-
-
note
-
2O in large-scale reactions.
-
-
-
-
22
-
-
0037031625
-
Aqueous hydroxide as a base for palladium-catalyzed animation of aryl chlorides and bromides
-
Kuwano, R.; Utsunomiya, M.; Hartwig, J. F. Aqueous Hydroxide as a Base for Palladium-Catalyzed Animation of Aryl Chlorides and Bromides. J. Org. Chem. 2002, 67, 6479-6486.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 6479-6486
-
-
Kuwano, R.1
Utsunomiya, M.2
Hartwig, J.F.3
-
23
-
-
0034712156
-
Simple, efficient catalyst system for the palladium-catalyzed amination of aryl chlorides, bromides, and triflates
-
Wolfe, J. P.; Tomori, H.; Sadighi, J. P.; Yin, J.; Buchwald, S. L. Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates. J. Org. Chem. 2000, 65, 1158-1174.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 1158-1174
-
-
Wolfe, J.P.1
Tomori, H.2
Sadighi, J.P.3
Yin, J.4
Buchwald, S.L.5
-
24
-
-
0042704188
-
Palladium-catalyzed synthesis of arylamines from aryl halides and lithium bis(trimethylsilyl)amide as an ammonia equivalent
-
Lee, S.; Jorgensen, M.; Hartwig, J. F. Palladium-Catalyzed Synthesis of Arylamines from Aryl Halides and Lithium Bis(trimethylsilyl)amide as an Ammonia Equivalent. Org. Lett. 2001, 3, 2729-2732.
-
(2001)
Org. Lett.
, vol.3
, pp. 2729-2732
-
-
Lee, S.1
Jorgensen, M.2
Hartwig, J.F.3
-
25
-
-
0033597748
-
Room-temperature palladium-catalyzed amination of aryl bromides and chlorides and extended scope of aromatic C-N bond formation with a commercial ligand
-
Hartwig, J. F.; Kawatsura, M.; Hauck, S. I.; Shaughnessy, K. H.; Alcazar-Roman, L. M. Room-Temperature Palladium-Catalyzed Amination of Aryl Bromides and Chlorides and Extended Scope of Aromatic C-N Bond Formation with a Commercial Ligand. J. Org. Chem. 1999, 64, 5575-5580.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 5575-5580
-
-
Hartwig, J.F.1
Kawatsura, M.2
Hauck, S.I.3
Shaughnessy, K.H.4
Alcazar-Roman, L.M.5
-
26
-
-
0041996505
-
An air and thermally stable one-component catalyst for the amination of aryl chlorides
-
Zim, D.; Buchwald, S. L. An Air and Thermally Stable One-Component Catalyst for the Amination of Aryl Chlorides. Org. Lett. 2003, 5, 2413-2415.
-
(2003)
Org. Lett.
, vol.5
, pp. 2413-2415
-
-
Zim, D.1
Buchwald, S.L.2
-
27
-
-
0037379660
-
Brominated derivatives of noscapine are potent microtubule-interfering agents that perturb mitosis and inhibit cell proliferation
-
Zhou, J.; Gupta, K; Aggarwal, A. R.; Chandra, R.; Panda, D.; Joshi, H. C. Brominated Derivatives of Noscapine Are Potent Microtubule-Interfering Agents That Perturb Mitosis and Inhibit Cell Proliferation. Mol. Pharmacol. 2003, 63, 799-807.
-
(2003)
Mol. Pharmacol.
, vol.63
, pp. 799-807
-
-
Zhou, J.1
Gupta, K.2
Aggarwal, A.R.3
Chandra, R.4
Panda, D.5
Joshi, H.C.6
-
28
-
-
0025317385
-
Deoxygenation of highly hindered phenols
-
Saa, J. M.; Dopico, M.; Martorell, G.; Garcia-Raso, A. Deoxygenation of Highly Hindered Phenols. J. Org. Chem. 1990, 55, 991-995.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 991-995
-
-
Saa, J.M.1
Dopico, M.2
Martorell, G.3
Garcia-Raso, A.4
|