-
1
-
-
0036489886
-
Mother nature's combinatorial libraries; their influence on the synthesis of drugs
-
Kingston DG, Newman DJ: Mother nature's combinatorial libraries; their influence on the synthesis of drugs. Curr Opin Drug Discovery Dev (2002) 5(2):304-316.
-
(2002)
Curr Opin Drug Discovery Dev
, vol.5
, Issue.2
, pp. 304-316
-
-
Kingston, D.G.1
Newman, D.J.2
-
2
-
-
33646748133
-
Novel and diverse assemblage of actinomycetes in marine sponges: A resource for drug discovery
-
Anaheim, CA, USA
-
Peraud O, Mohamed N, Montalvo N, Enticknap JJ, Hill RT, Hamann MT: Novel and diverse assemblage of actinomycetes in marine sponges: A resource for drug discovery. Annual Meeting of the Society for Industrial Microbiology, Anaheim, CA, USA (2004).
-
(2004)
Annual Meeting of the Society for Industrial Microbiology
-
-
Peraud, O.1
Mohamed, N.2
Montalvo, N.3
Enticknap, J.J.4
Hill, R.T.5
Hamann, M.T.6
-
3
-
-
14844286088
-
The manzamines, progress toward kilogram-scale production and application as a control for malaria
-
Anaheim, CA, USA
-
Kasanah N, Rao KV, Peng JN, Donla M, Peraud O, Anderson M, Hill RT, Hamann MT: The manzamines, progress toward kilogram-scale production and application as a control for malaria. Annual Meeting of the Society for Industrial Microbiology, Anaheim, CA, USA (2004). Provides the first definitive report of a compound isolated from a marine invertebrate that was produced fermentatively from a microbe isolated from the same sponge specimen.
-
(2004)
Annual Meeting of the Society for Industrial Microbiology
-
-
Kasanah, N.1
Rao, K.V.2
Peng, J.N.3
Donla, M.4
Peraud, O.5
Anderson, M.6
Hill, R.T.7
Hamann, M.T.8
-
4
-
-
0036009127
-
Molecular identification of an endosymbiotic bacterium associated with pederin biosynthesis in Paederus sabaeus (Colsoptera: Staphylinidae)
-
Kellner RL: Molecular identification of an endosymbiotic bacterium associated with pederin biosynthesis in Paederus sabaeus (Colsoptera: Staphylinidae). Insect Biochem Mol Biol (2002) 32(4):389-395.
-
(2002)
Insect Biochem Mol Biol
, vol.32
, Issue.4
, pp. 389-395
-
-
Kellner, R.L.1
-
5
-
-
10744231115
-
Evidence for a symbiosis island involved in horizontal acquisition of pederin biosynthetic capabilities by the bacterial symbiont of Paederus fuscipes beetles
-
Piel J, Hofer I, Hui D: Evidence for a symbiosis island involved in horizontal acquisition of pederin biosynthetic capabilities by the bacterial symbiont of Paederus fuscipes beetles. J Bacteriol (2004) 186(5):1280-1286. Presents the first genetic proof that the active principle of the blister beetle was made by a commensal microbe.
-
(2004)
J Bacteriol
, vol.186
, Issue.5
, pp. 1280-1286
-
-
Piel, J.1
Hofer, I.2
Hui, D.3
-
6
-
-
9244230571
-
Antitumor polyketide biosynthesis by an uncultivated bacterial symbiont of the marine sponge Theonella swinhoei
-
Piel J, Hui D, Wen G, Butzke D, Platzer M, Fusetani N, Matsunaga S: Antitumor polyketide biosynthesis by an uncultivated bacterial symbiont of the marine sponge Theonella swinhoei. Proc Natl Acad Sci USA (2004) 101(46):16222-16227. Discusses isolation of the genes producing the pederin-like marine metabolite directly from the producing sponge.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, Issue.46
, pp. 16222-16227
-
-
Piel, J.1
Hui, D.2
Wen, G.3
Butzke, D.4
Platzer, M.5
Fusetani, N.6
Matsunaga, S.7
-
7
-
-
1242296319
-
Antineoplastic agents. 520. Isolation and structure of irciniastatins A and B from the Indo-Pacific marine sponge Ircinia ramosa
-
Pettit GR, Xu JP, Chapuis JC, Pettit RK, Tackett LP, Doubek DL, Hooper JN, Schmidt JM: Antineoplastic agents. 520. Isolation and structure of irciniastatins A and B from the Indo-Pacific marine sponge Ircinia ramosa. J Med Chem (2004) 47(5):1149-1152.
-
(2004)
J Med Chem
, vol.47
, Issue.5
, pp. 1149-1152
-
-
Pettit, G.R.1
Xu, J.P.2
Chapuis, J.C.3
Pettit, R.K.4
Tackett, L.P.5
Doubek, D.L.6
Hooper, J.N.7
Schmidt, J.M.8
-
8
-
-
3042706094
-
Psymberin, a potent sponge-derived cytotoxin from Psammocinia distantly related to the pederin family
-
Cichewicz RH, Valeriote FA, Crews P: Psymberin, a potent sponge-derived cytotoxin from Psammocinia distantly related to the pederin family. Org Lett (2004) 6(12):1951-1954.
-
(2004)
Org Lett
, vol.6
, Issue.12
, pp. 1951-1954
-
-
Cichewicz, R.H.1
Valeriote, F.A.2
Crews, P.3
-
9
-
-
1442310087
-
A tale of two tumor targets: Topoisomerase I and tubulin. The Wall and Wani contribution to cancer chemotherapy
-
Cragg GM, Newman DJ: A tale of two tumor targets: Topoisomerase I and tubulin. The Wall and Wani contribution to cancer chemotherapy. J Nat Prod (2004) 67(2):232-244.
-
(2004)
J Nat Prod
, vol.67
, Issue.2
, pp. 232-244
-
-
Cragg, G.M.1
Newman, D.J.2
-
10
-
-
0344653657
-
Cell cycle arrest and antitumor activity of pironetin and its derivatives
-
Kondoh M, Usui T, Kobayashi S, Tsuchiya K, Nishikawa K, Nishikiori T, Mayumi T, Osada H: Cell cycle arrest and antitumor activity of pironetin and its derivatives. Cancer Lett (1998) 126(1):29-32.
-
(1998)
Cancer Lett
, vol.126
, Issue.1
, pp. 29-32
-
-
Kondoh, M.1
Usui, T.2
Kobayashi, S.3
Tsuchiya, K.4
Nishikawa, K.5
Nishikiori, T.6
Mayumi, T.7
Osada, H.8
-
11
-
-
3042686764
-
352 of α-tubulin
-
352 of α-tubulin. Chem Biol (2004) 11(6):799-806. Presents direct evidence for the covalent binding of α-tubulin.
-
(2004)
Chem Biol
, vol.11
, Issue.6
, pp. 799-806
-
-
Usui, T.1
Watanabe, H.2
Nakayama, H.3
Tada, Y.4
Kanoh, N.5
Kondoh, M.6
Asao, T.7
Takio, K.8
Watanabe, H.9
Nishikawa, K.10
Kitahara, T.11
-
12
-
-
2642517177
-
Emerging topoisomerase inhibitors as anticancer drugs
-
Denny WA: Emerging topoisomerase inhibitors as anticancer drugs. Expert Opin Emerg Drugs (2004) 9(1):105-133. Provides good coverage of the current state-of-the-art of topoisomerase inhibitors.
-
(2004)
Expert Opin Emerg Drugs
, vol.9
, Issue.1
, pp. 105-133
-
-
Denny, W.A.1
-
13
-
-
8344262388
-
AK37: The first pyridoacridine described capable of stabilizing the topoisomerase I cleavable complex
-
Marshall KM, Holden JA, Koller A, Kashman Y, Copp BR, Barrows LR: AK37: The first pyridoacridine described capable of stabilizing the topoisomerase I cleavable complex. Anticancer Drugs (2004) 15(9):907-913.
-
(2004)
Anticancer Drugs
, vol.15
, Issue.9
, pp. 907-913
-
-
Marshall, K.M.1
Holden, J.A.2
Koller, A.3
Kashman, Y.4
Copp, B.R.5
Barrows, L.R.6
-
14
-
-
11144339340
-
Biological activities of pyridoacridines
-
Marshall KM, Barrows LR: Biological activities of pyridoacridines. Nat Prod Rep (2004) 21(6):731-751. An excellent review of the biochemistry of these marine-derived compounds.
-
(2004)
Nat Prod Rep
, vol.21
, Issue.6
, pp. 731-751
-
-
Marshall, K.M.1
Barrows, L.R.2
-
15
-
-
0344406759
-
Selective killing of cancer cells by β-lapachone: Direct checkpoint activation as a strategy against cancer
-
Li Y, Sun X, LaMont JT, Pardee AB, Li CJ: Selective killing of cancer cells by β-lapachone: Direct checkpoint activation as a strategy against cancer. Proc Natl Acad Sci USA (2003) 100(5):2674-2678.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.5
, pp. 2674-2678
-
-
Li, Y.1
Sun, X.2
Lamont, J.T.3
Pardee, A.B.4
Li, C.J.5
-
16
-
-
1542405235
-
β-lapachone-induced apoptosis is associated with activation of caspase-3 and inactivation of NF-κB in human colon cancer HCT-116 cells
-
Choi BT, Cheong J, Choi YH: β-Lapachone-induced apoptosis is associated with activation of caspase-3 and inactivation of NF-κB in human colon cancer HCT-116 cells. Anticancer Drugs (2003) 14(10):845-850.
-
(2003)
Anticancer Drugs
, vol.14
, Issue.10
, pp. 845-850
-
-
Choi, B.T.1
Cheong, J.2
Choi, Y.H.3
-
17
-
-
3042518847
-
Recent studies on natural products as anticancer agents
-
Ravelo AG, Estevez-Braun A, Chavez-Orellana H, Perez-Sacau E, Mesa-Siverio D: Recent studies on natural products as anticancer agents. Curr Top Med Chem (2004) 4(2):241-265.
-
(2004)
Curr Top Med Chem
, vol.4
, Issue.2
, pp. 241-265
-
-
Ravelo, A.G.1
Estevez-Braun, A.2
Chavez-Orellana, H.3
Perez-Sacau, E.4
Mesa-Siverio, D.5
-
18
-
-
0034864799
-
Proteasome inhibitors: From research tools to drug candidates
-
Kisselev AF, Goldberg AL: Proteasome inhibitors: From research tools to drug candidates. Chem Biol (2001) 8(8):739-758.
-
(2001)
Chem Biol
, vol.8
, Issue.8
, pp. 739-758
-
-
Kisselev, A.F.1
Goldberg, A.L.2
-
19
-
-
6944235003
-
Multiple myeloma
-
Kyle RA, Rajkumar SV: Multiple myeloma. N Engl J Med (2004) 351(18):1860-1873.
-
(2004)
N Engl J Med
, vol.351
, Issue.18
, pp. 1860-1873
-
-
Kyle, R.A.1
Rajkumar, S.V.2
-
20
-
-
0042844744
-
Natural products as sources of new drugs over the period 1981-2002
-
Newman DJ, Cragg GM, Snader KM: Natural products as sources of new drugs over the period 1981-2002. J Nat Prod (2003) 66(7):1022-1037.
-
(2003)
J Nat Prod
, vol.66
, Issue.7
, pp. 1022-1037
-
-
Newman, D.J.1
Cragg, G.M.2
Snader, K.M.3
-
21
-
-
2342667387
-
The development of proteasome inhibitors as anticancer drugs
-
Adams J: The development of proteasome inhibitors as anticancer drugs. Cancer Cell (2004) 5(5):417-421. Discussion of the development of PS-341 (bortezomib) by its inventor.
-
(2004)
Cancer Cell
, vol.5
, Issue.5
, pp. 417-421
-
-
Adams, J.1
-
22
-
-
0028972449
-
A protein catalytic framework with an N-terminal nucleophile is capable of self-activation
-
Brannigan JA, Dodson G, Duggleby HJ, Moody PC, Smith JL, Tomchick DR, Murzin AG: A protein catalytic framework with an N-terminal nucleophile is capable of self-activation. Nature (1995) 378(6555):416-419.
-
(1995)
Nature
, vol.378
, Issue.6555
, pp. 416-419
-
-
Brannigan, J.A.1
Dodson, G.2
Duggleby, H.J.3
Moody, P.C.4
Smith, J.L.5
Tomchick, D.R.6
Murzin, A.G.7
-
23
-
-
0026065338
-
Lactacystin, a novel microbial metabolite, induces neuritogenesis of neuroblastoma cells
-
Omura S, Fujimoto T, Otoguro K, Matsuzaki K, Moriguchi R, Tanaka H, Sasaki Y: Lactacystin, a novel microbial metabolite, induces neuritogenesis of neuroblastoma cells. J Antibiot (Tokyo) (1991) 44(1):113-116.
-
(1991)
J Antibiot (Tokyo)
, vol.44
, Issue.1
, pp. 113-116
-
-
Omura, S.1
Fujimoto, T.2
Otoguro, K.3
Matsuzaki, K.4
Moriguchi, R.5
Tanaka, H.6
Sasaki, Y.7
-
24
-
-
0029033981
-
Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin
-
Fenteany G, Standaert RF, Lane WS, Choi S, Corey EJ, Schreiber SL: Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin. Science (1995) 268(5211):726-731.
-
(1995)
Science
, vol.268
, Issue.5211
, pp. 726-731
-
-
Fenteany, G.1
Standaert, R.F.2
Lane, W.S.3
Choi, S.4
Corey, E.J.5
Schreiber, S.L.6
-
25
-
-
0030926777
-
Lactacystin and clasto-lactacystin β-lactone modify multiple proteasome β-subunits and inhibit intracellular protein degradation and major histocompatibility complex class I antigen presentation
-
Craiu A, Gaczynska M, Akopian T, Gramm CF, Fenteany G, Goldberg AL, Rock KL: Lactacystin and clasto-lactacystin β-lactone modify multiple proteasome β-subunits and inhibit intracellular protein degradation and major histocompatibility complex class I antigen presentation. J Biol Chem (1997) 272(20):13437-13445.
-
(1997)
J Biol Chem
, vol.272
, Issue.20
, pp. 13437-13445
-
-
Craiu, A.1
Gaczynska, M.2
Akopian, T.3
Gramm, C.F.4
Fenteany, G.5
Goldberg, A.L.6
Rock, K.L.7
-
26
-
-
0029937677
-
Mechanistic studies on the inactivation of the proleosome by lactacystin - A central role for clasto-lactacystin β-lactone
-
Dick LR, Cruikshank AA, Grenier L, Melandri FD, Nunes SL, Stein RL: Mechanistic studies on the inactivation of the proleosome by lactacystin - a central role for clasto-lactacystin β-lactone. J Biol Chem (1996) 271(13):7273-7276.
-
(1996)
J Biol Chem
, vol.271
, Issue.13
, pp. 7273-7276
-
-
Dick, L.R.1
Cruikshank, A.A.2
Grenier, L.3
Melandri, F.D.4
Nunes, S.L.5
Stein, R.L.6
-
27
-
-
15644363581
-
Mechanistic studies on the inactivation of the proteasome by lactacystin in cultured cells
-
Dick LR, Cruikshank AA, Destree AT, Grenier L, McCormack TA, Melandri FD, Nunes SL, Palombella VJ, Parent LA, Plamodon L, Stein RL: Mechanistic studies on the inactivation of the proteasome by lactacystin in cultured cells. J Biol Chem (1997) 272(1):182-188.
-
(1997)
J Biol Chem
, vol.272
, Issue.1
, pp. 182-188
-
-
Dick, L.R.1
Cruikshank, A.A.2
Destree, A.T.3
Grenier, L.4
McCormack, T.A.5
Melandri, F.D.6
Nunes, S.L.7
Palombella, V.J.8
Parent, L.A.9
Plamodon, L.10
Stein, R.L.11
-
28
-
-
0033022744
-
Total synthesis and biological activity of lactacystin, omuralide and analogs
-
Corey EJ, Li WD: Total synthesis and biological activity of lactacystin, omuralide and analogs. Chem Pharm Bull (Tokyo) (1999) 47(1):1-10.
-
(1999)
Chem Pharm Bull (Tokyo)
, vol.47
, Issue.1
, pp. 1-10
-
-
Corey, E.J.1
Li, W.D.2
-
29
-
-
0037455147
-
Salinosporamide A: A highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus Salinospora
-
Feling RH, Buchanan GO, Mincer TJ, Kauffman CA, Jensen PR, Fenical W: Salinosporamide A: A highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus Salinospora. Angew Chem Int Ed (2003) 42(3):355-357. A novel proteasome inhibitor produced by fermentation of an obligate marine microbe.
-
(2003)
Angew Chem Int Ed
, vol.42
, Issue.3
, pp. 355-357
-
-
Feling, R.H.1
Buchanan, G.O.2
Mincer, T.J.3
Kauffman, C.A.4
Jensen, P.R.5
Fenical, W.6
-
30
-
-
2442720189
-
A simple stereocontrolled synthesis of Salinosporamide A
-
Reddy LR, Saravan P, Corey EJ: A simple stereocontrolled synthesis of Salinosporamide A. J Am Chem Soc (2004) 126(20):6230-6231.
-
(2004)
J Am Chem Soc
, vol.126
, Issue.20
, pp. 6230-6231
-
-
Reddy, L.R.1
Saravan, P.2
Corey, E.J.3
-
31
-
-
0033104464
-
The structural requirements for inhibition of proteasome function by the lactacystin-derived β-lactone and synthetic analogs
-
Corey EJ, Li WZ, Nagamitsu T, Fenteany G: The structural requirements for inhibition of proteasome function by the lactacystin-derived β-lactone and synthetic analogs. Tetrahedron (1999) 55:3305-3316.
-
(1999)
Tetrahedron
, vol.55
, pp. 3305-3316
-
-
Corey, E.J.1
Li, W.Z.2
Nagamitsu, T.3
Fenteany, G.4
-
32
-
-
0033520753
-
A novel and efficient synthesis of a highly active analogue of clasto-lactacystin β-lactone
-
Soucy F, Grenier L, Behnke ML, Destree AT, McCormack TA, Adams J, Plamodon L: A novel and efficient synthesis of a highly active analogue of clasto-lactacystin β-lactone. J Am Chem Soc (1999) 121(43):9967-9976.
-
(1999)
J Am Chem Soc
, vol.121
, Issue.43
, pp. 9967-9976
-
-
Soucy, F.1
Grenier, L.2
Behnke, M.L.3
Destree, A.T.4
McCormack, T.A.5
Adams, J.6
Plamodon, L.7
-
33
-
-
0032844108
-
Proteasome inhibition: A novel mechanism to combat asthma
-
Elliott PJ, Pien CS, McCormack TA, Chapman ID, Adams J: Proteasome inhibition: A novel mechanism to combat asthma. J Allergy Clin Immunol (1999) 104(2 Pt 1):294-300.
-
(1999)
J Allergy Clin Immunol
, vol.104
, Issue.2 PART 1
, pp. 294-300
-
-
Elliott, P.J.1
Pien, C.S.2
McCormack, T.A.3
Chapman, I.D.4
Adams, J.5
-
34
-
-
0033083426
-
Cardioprotective effects of a novel proteasome inhibitor following ischemia and reperfusion in the isolated perfused rat heart
-
Campbell B, Adams J, Shin YK, Lefer AM: Cardioprotective effects of a novel proteasome inhibitor following ischemia and reperfusion in the isolated perfused rat heart. J Mol Cell Cardiol (1999) 31(2):467-476.
-
(1999)
J Mol Cell Cardiol
, vol.31
, Issue.2
, pp. 467-476
-
-
Campbell, B.1
Adams, J.2
Shin, Y.K.3
Lefer, A.M.4
-
35
-
-
0033918122
-
Proteasome inhibitor PS519 reduces infarction and attenuates leukocyte infiltration in a rat modal of focal cerebral ischemia
-
Phillips JB, Williams AJ, Adams J, Elliott PJ, Tortella FC: Proteasome inhibitor PS519 reduces infarction and attenuates leukocyte infiltration in a rat modal of focal cerebral ischemia. Stroke (2000) 31(7):1686-1693.
-
(2000)
Stroke
, vol.31
, Issue.7
, pp. 1686-1693
-
-
Phillips, J.B.1
Williams, A.J.2
Adams, J.3
Elliott, P.J.4
Tortella, F.C.5
-
36
-
-
0037215550
-
Delayed treatment with MLN519 reduces infarction and associated neurologic deficit caused by focal ischemic brain injury in rats via antiinflammatory mechanisms involving nuclear factor-κB activation, gliosls and leukocyte infiltration
-
Williams AJ, Hale SL, Moffett JR, Dave JR, Elliott PJ, Adams J, Tortella FC: Delayed treatment with MLN519 reduces infarction and associated neurologic deficit caused by focal ischemic brain injury in rats via antiinflammatory mechanisms involving nuclear factor-κB activation, gliosls and leukocyte infiltration. J Cereb Blood Flow Metab (2003) 23(1):75-87.
-
(2003)
J Cereb Blood Flow Metab
, vol.23
, Issue.1
, pp. 75-87
-
-
Williams, A.J.1
Hale, S.L.2
Moffett, J.R.3
Dave, J.R.4
Elliott, P.J.5
Adams, J.6
Tortella, F.C.7
-
37
-
-
0033621047
-
Epoxomicin, a potent and selective proteasome inhibitor, exhibits in vivo antiinflammatory activity
-
Meng L, Mohan R, Kwok BH, Elofsson M, Sin N, Crews CM: Epoxomicin, a potent and selective proteasome inhibitor, exhibits in vivo antiinflammatory activity. Proc Natl Acad Sci USA (1999) 96(18):10403-10408.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, Issue.18
, pp. 10403-10408
-
-
Meng, L.1
Mohan, R.2
Kwok, B.H.3
Elofsson, M.4
Sin, N.5
Crews, C.M.6
-
38
-
-
0033564512
-
Eponemycin exerts its antitumor effect through the inhibition of proteasome function
-
Meng L, Kwok BH, Sin N, Crews CM: Eponemycin exerts its antitumor effect through the inhibition of proteasome function. Cancer Res (1999) 59(12):2798-2801.
-
(1999)
Cancer Res
, vol.59
, Issue.12
, pp. 2798-2801
-
-
Meng, L.1
Kwok, B.H.2
Sin, N.3
Crews, C.M.4
-
39
-
-
0343262654
-
Crystal structure of epoxomicin: 20S proteasome reveals a molecular basis for selectivity of α',β'-epoxyketone proteasome inhibitors
-
Groll M, Kim KB, Kairies N, Huber R, Crews CM: Crystal structure of epoxomicin: 20S proteasome reveals a molecular basis for selectivity of α',β'-epoxyketone proteasome inhibitors. J Am Chem Soc (2000) 122:1237-1238. Presents direct evidence for the mechanism of action of the epoxy-containing inhibitors.
-
(2000)
J Am Chem Soc
, vol.122
, pp. 1237-1238
-
-
Groll, M.1
Kim, K.B.2
Kairies, N.3
Huber, R.4
Crews, C.M.5
-
40
-
-
0034105791
-
TMC-95A, B, C and D, novel proteasome inhibitors produced by Apiospora montegnai Sacc. TC 1093. Taxonomy, production, isolation and biological activities
-
Koguchi Y, Kohno J, Nishio M, Takahashi K, Okuda T, Ohnuki T, Komatsubara S: TMC-95A, B, C and D, novel proteasome inhibitors produced by Apiospora montegnai Sacc. TC 1093. Taxonomy, production, isolation and biological activities. J Antibiot (2000) 53(2):105-109.
-
(2000)
J Antibiot
, vol.53
, Issue.2
, pp. 105-109
-
-
Koguchi, Y.1
Kohno, J.2
Nishio, M.3
Takahashi, K.4
Okuda, T.5
Ohnuki, T.6
Komatsubara, S.7
-
41
-
-
0035902778
-
Crystal structure of the 20S proteasome: TMC-95A complex: A non-covalent proteasome inhibitor
-
Groll M, Koguchi Y, Huber R, Kohno J: Crystal structure of the 20S proteasome: TMC-95A complex: A non-covalent proteasome inhibitor. J Mol Biol (2001) 311(3):543-548.
-
(2001)
J Mol Biol
, vol.311
, Issue.3
, pp. 543-548
-
-
Groll, M.1
Koguchi, Y.2
Huber, R.3
Kohno, J.4
-
42
-
-
0035918278
-
Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo
-
Nam S, Smith DM, Dou QP: Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo. J Biol Chem (2001) 276(16):13322-13330.
-
(2001)
J Biol Chem
, vol.276
, Issue.16
, pp. 13322-13330
-
-
Nam, S.1
Smith, D.M.2
Dou, Q.P.3
-
43
-
-
0036527775
-
Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
-
Johnstone RW: Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer. Nat Rev Drug Disc (2002) 1(4):287-299. Provides an excellent review of the field of HDAC inhibitors.
-
(2002)
Nat Rev Drug Disc
, vol.1
, Issue.4
, pp. 287-299
-
-
Johnstone, R.W.1
-
44
-
-
2642525295
-
Histone modification enzymes: Novel targets for cancer drugs
-
Kristeleit R, Stimson L, Workman P, Aheme W: Histone modification enzymes: Novel targets for cancer drugs. Expert Opin Emerg Drugs (2004)9(1):135-154.
-
(2004)
Expert Opin Emerg Drugs
, vol.9
, Issue.1
, pp. 135-154
-
-
Kristeleit, R.1
Stimson, L.2
Workman, P.3
Aheme, W.4
-
45
-
-
0037444803
-
Histone deacetylases: Characterization of the classical HDAC family
-
De Ruijter AJ, Van Gennip AH, Caron HN, Kemp S, Van Kuilenburg AB: Histone deacetylases: Characterization of the classical HDAC family. Biochem J (2003) 370(Pt 3):737-749.
-
(2003)
Biochem J
, vol.370
, Issue.PART 3
, pp. 737-749
-
-
De Ruijter, A.J.1
Van Gennip, A.H.2
Caron, H.N.3
Kemp, S.4
Van Kuilenburg, A.B.5
-
46
-
-
0030747725
-
Identification of positively and negatively acting elements regulating expression of the E2F2 gene in response to cell growth signals
-
Sears R, Ohtani K, Nevins JR: Identification of positively and negatively acting elements regulating expression of the E2F2 gene in response to cell growth signals. Mol Cell Biol (1997) 17(9):5227-5235.
-
(1997)
Mol Cell Biol
, vol.17
, Issue.9
, pp. 5227-5235
-
-
Sears, R.1
Ohtani, K.2
Nevins, J.R.3
-
47
-
-
0032905924
-
c-Myc target genes involved in cell growth, apoptosis and metabolism
-
Dang CV: c-Myc target genes involved in cell growth, apoptosis and metabolism. Mol Cell Biol (1999) 19(1):1-11.
-
(1999)
Mol Cell Biol
, vol.19
, Issue.1
, pp. 1-11
-
-
Dang, C.V.1
-
48
-
-
0033557497
-
Ski is a component of the histone deacetylase complex required for franscriptional repression by Mad and thyroid hormone receptor
-
Nomura T, Khan MM, Kaul SC, Dong HD, Wadhwa R, Colmenares C, Kohno I, Ishii S: Ski is a component of the histone deacetylase complex required for franscriptional repression by Mad and thyroid hormone receptor. Genes Dev (1999) 13(4):412-423.
-
(1999)
Genes Dev
, vol.13
, Issue.4
, pp. 412-423
-
-
Nomura, T.1
Khan, M.M.2
Kaul, S.C.3
Dong, H.D.4
Wadhwa, R.5
Colmenares, C.6
Kohno, I.7
Ishii, S.8
-
49
-
-
0032484904
-
Retinoblastoma protein represses transcription by recruiting a histone deacetylase
-
Magnaghi-Jaulin L, Groisman R, Naguibneva I, Robin P, Lorain S, Le Villain JP, Troalen F, Trouche D, Harel-Bellan A: Retinoblastoma protein represses transcription by recruiting a histone deacetylase. Nature (1998) 391(6667):601-605.
-
(1998)
Nature
, vol.391
, Issue.6667
, pp. 601-605
-
-
Magnaghi-Jaulin, L.1
Groisman, R.2
Naguibneva, I.3
Robin, P.4
Lorain, S.5
Le Villain, J.P.6
Troalen, F.7
Trouche, D.8
Harel-Bellan, A.9
-
50
-
-
0032484989
-
Retinoblatoma protein recruits histone deacetylase to repress transcription
-
Brehm A, Miska EA, McCance DJ, Reid JL, Bannister AJ, Kouzarides T: Retinoblatoma protein recruits histone deacetylase to repress transcription. Nature (1998) 391(6667):597-601.
-
(1998)
Nature
, vol.391
, Issue.6667
, pp. 597-601
-
-
Brehm, A.1
Miska, E.A.2
McCance, D.J.3
Reid, J.L.4
Bannister, A.J.5
Kouzarides, T.6
-
51
-
-
0034045040
-
Histone deacetylases, transcriptional control and cancer
-
Cress WD, Seto E: Histone deacetylases, transcriptional control and cancer. J Cell Physiol (2000) 184(1):1-16.
-
(2000)
J Cell Physiol
, vol.184
, Issue.1
, pp. 1-16
-
-
Cress, W.D.1
Seto, E.2
-
52
-
-
0030678627
-
Role of the retinoblastoma protein in the pathogenesis of human cancer
-
Sellers WR, Kaelin WG Jr: Role of the retinoblastoma protein in the pathogenesis of human cancer. J Clin Oncol (1997) 15(11):3301-3312.
-
(1997)
J Clin Oncol
, vol.15
, Issue.11
, pp. 3301-3312
-
-
Sellers, W.R.1
Kaelin Jr., W.G.2
-
53
-
-
0034891385
-
The emerging role of class II histone deacetylases
-
Fischle W, Kiermer V, Dequiedt F, Verdin E: The emerging role of class II histone deacetylases. Biochem Cell Biol (2001) 79(3):337-348.
-
(2001)
Biochem Cell Biol
, vol.79
, Issue.3
, pp. 337-348
-
-
Fischle, W.1
Kiermer, V.2
Dequiedt, F.3
Verdin, E.4
-
54
-
-
0035048449
-
Histone deacetylases induce angiogenesis by negative regulation of tumour suppressor genes
-
Kim MS, Kwon HJ, Lee YM, Baek JH, Jang JE, Lee SW, Moon EJ, Kim HS, Lee SK, Chung HY, Kim CW et al: Histone deacetylases induce angiogenesis by negative regulation of tumour suppressor genes. Nat Med (2001) 7(4):437-443.
-
(2001)
Nat Med
, vol.7
, Issue.4
, pp. 437-443
-
-
Kim, M.S.1
Kwon, H.J.2
Lee, Y.M.3
Baek, J.H.4
Jang, J.E.5
Lee, S.W.6
Moon, E.J.7
Kim, H.S.8
Lee, S.K.9
Chung, H.Y.10
Kim, C.W.11
-
55
-
-
85047699941
-
Histone deacetylase inhibitors as antiangiogenic agents altering vascular endothelial growth factor signalling
-
Deroanne CF, Bonjean K, Servotte S, Devy L, Colige A, Clausse N, Blacher S, Verdin E, Foidart JM, Nusgens BV, Castronovo V: Histone deacetylase inhibitors as antiangiogenic agents altering vascular endothelial growth factor signalling. Oncogene (2002) 21(3):427-436.
-
(2002)
Oncogene
, vol.21
, Issue.3
, pp. 427-436
-
-
Deroanne, C.F.1
Bonjean, K.2
Servotte, S.3
Devy, L.4
Colige, A.5
Clausse, N.6
Blacher, S.7
Verdin, E.8
Foidart, J.M.9
Nusgens, B.V.10
Castronovo, V.11
-
56
-
-
0036651788
-
Recent advances in the discovery of small molecule histone deacetylase inhibitors
-
Remiszewski SW: Recent advances in the discovery of small molecule histone deacetylase inhibitors. Curr Opin Drug Discovery Dev (2002) 5(4):487-499.
-
(2002)
Curr Opin Drug Discovery Dev
, vol.5
, Issue.4
, pp. 487-499
-
-
Remiszewski, S.W.1
-
57
-
-
0001811191
-
Histone deacetylase as a new target of cancer chemotherapy
-
Yoshida M, Furumai R, Nishiyama M, Komatsu Y, Nishino N, Horinouchi S: Histone deacetylase as a new target of cancer chemotherapy. Cancer Chemother Pharmacol (2001) 48(Suppl 1):S20-S26.
-
(2001)
Cancer Chemother Pharmacol
, vol.48
, Issue.SUPPL. 1
-
-
Yoshida, M.1
Furumai, R.2
Nishiyama, M.3
Komatsu, Y.4
Nishino, N.5
Horinouchi, S.6
-
58
-
-
0141885037
-
From discovery to the coming generation of histone deacetylase inhibitors
-
Yoshida M, Matsuyama A, Komatsu Y, Nishino N: From discovery to the coming generation of histone deacetylase inhibitors. Curr Med Chem (2003) 10(22):2351-2358.
-
(2003)
Curr Med Chem
, vol.10
, Issue.22
, pp. 2351-2358
-
-
Yoshida, M.1
Matsuyama, A.2
Komatsu, Y.3
Nishino, N.4
-
59
-
-
0017284850
-
A new antifungal antibiotic, trichostatin
-
Tsuji N, Kobayashi N, Nagashima K, Wakisaka Y, Koizumi K: A new antifungal antibiotic, trichostatin. J Antibiot (1976) 29(1):1-6.
-
(1976)
J Antibiot
, vol.29
, Issue.1
, pp. 1-6
-
-
Tsuji, N.1
Kobayashi, N.2
Nagashima, K.3
Wakisaka, Y.4
Koizumi, K.5
-
60
-
-
2942532642
-
Trichostatin A-like hydroxamate histone deacetylase inhibitors as therapeutic agents: Toxicological point of view
-
Vanhaecke T, Papeleu P, Elaut G, Rogiers V: Trichostatin A-like hydroxamate histone deacetylase inhibitors as therapeutic agents: Toxicological point of view. Curr Med Chem (2004) 11(12):1629-1643.
-
(2004)
Curr Med Chem
, vol.11
, Issue.12
, pp. 1629-1643
-
-
Vanhaecke, T.1
Papeleu, P.2
Elaut, G.3
Rogiers, V.4
-
61
-
-
0029693220
-
The expression of a small fraction of cellular genes is changed in response to histone hyperacetylation
-
Van Lint C, Emiliani S, Verdin E: The expression of a small fraction of cellular genes is changed in response to histone hyperacetylation. Gene Expr (1996) 5(4-5):245-253.
-
(1996)
Gene Expr
, vol.5
, Issue.4-5
, pp. 245-253
-
-
Van Lint, C.1
Emiliani, S.2
Verdin, E.3
-
62
-
-
0034662614
-
Genetic reprogramming in pathways of colonic cell maturation induced by short chain fatty acids: Comparison with trichostatin A, sulindac and curcumin and implications for prevention of colon cancer
-
Mariadason JM, Comer GA, Augenlicht LH: Genetic reprogramming in pathways of colonic cell maturation induced by short chain fatty acids: Comparison with trichostatin A, sulindac and curcumin and implications for prevention of colon cancer. Cancer Res (2000) 60(16):4561-4572.
-
(2000)
Cancer Res
, vol.60
, Issue.16
, pp. 4561-4572
-
-
Mariadason, J.M.1
Comer, G.A.2
Augenlicht, L.H.3
-
63
-
-
0035933731
-
Histone hyperacetylation induced by histone deacetylase inhibitors is not sufficient to cause growth inhibition in human dermal fibroblasts
-
Brinkmann H, Dahler AL, Popa C, Sereweko MM, Parsons PG, Gabrielli BG, Burgess AJ, Saunders NA: Histone hyperacetylation induced by histone deacetylase inhibitors is not sufficient to cause growth inhibition in human dermal fibroblasts. J Biol Chem (2001) 276(25):22491-22499.
-
(2001)
J Biol Chem
, vol.276
, Issue.25
, pp. 22491-22499
-
-
Brinkmann, H.1
Dahler, A.L.2
Popa, C.3
Sereweko, M.M.4
Parsons, P.G.5
Gabrielli, B.G.6
Burgess, A.J.7
Saunders, N.A.8
-
64
-
-
0026446246
-
Hexamethylene bisacetamide in myelodysplastic syndrome and acute myelogenous leukemia - A phase II clinical trial with a differentiation-inducing agent
-
Andreeff M, Stone R, Michaeli J, Young CW, Tong W, Sogoloff H, Ervin T, Kufe D, Rifkind RA, Marks PA: Hexamethylene bisacetamide in myelodysplastic syndrome and acute myelogenous leukemia - a phase II clinical trial with a differentiation-inducing agent. Blood (1992) 80(10):2604-2609.
-
(1992)
Blood
, vol.80
, Issue.10
, pp. 2604-2609
-
-
Andreeff, M.1
Stone, R.2
Michaeli, J.3
Young, C.W.4
Tong, W.5
Sogoloff, H.6
Ervin, T.7
Kufe, D.8
Rifkind, R.A.9
Marks, P.A.10
-
65
-
-
12444321545
-
Phase I clinical trial of histone deacetylase inhibitor: Suberoylanilide hydroxamic acid administered intravenously
-
Kelly WK, Richon VM, O'Connor O, Curley T, MacGregor-Curtelli B, Tong W, Klang M, Schwartz L, Richardson S, Rosa E, Drobnjak M et al: Phase I clinical trial of histone deacetylase inhibitor: Suberoylanilide hydroxamic acid administered intravenously. Clin Cancer Res (2003) 9(10 Pt 1):3578-3588.
-
(2003)
Clin Cancer Res
, vol.9
, Issue.10 PART 1
, pp. 3578-3588
-
-
Kelly, W.K.1
Richon, V.M.2
O'Connor, O.3
Curley, T.4
MacGregor-Curtelli, B.5
Tong, W.6
Klang, M.7
Schwartz, L.8
Richardson, S.9
Rosa, E.10
Drobnjak, M.11
-
66
-
-
1642556738
-
HDAC inhibitors for the treatment of cancer
-
Secrist JP, Zhou X, Richon VM: HDAC inhibitors for the treatment of cancer. Curr Opin Invest Drugs (2003) 4(12):1422-1427. Discusses the clinical aspects of HDAC inhibitors.
-
(2003)
Curr Opin Invest Drugs
, vol.4
, Issue.12
, pp. 1422-1427
-
-
Secrist, J.P.1
Zhou, X.2
Richon, V.M.3
-
67
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks PA, Rifkind RA, Richon VM, Breslow R, Miller T, Kelly WK: Histone deacetylases and cancer: Causes and therapies. Nat Rev Cancer(2001) 1(3):194-202.
-
(2001)
Nat Rev Cancer
, vol.1
, Issue.3
, pp. 194-202
-
-
Marks, P.A.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
68
-
-
0034905872
-
Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase
-
Butler LM, Webb Y, Agus DB, Higgins B, Tolentino TR, Kutko MC, LaQuaglia MP, Drobnjak M, Cordon-Cardo C, Scher HI, Breslow R et al: Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase. Clin Cancer Res (2001) 7(4):962-970.
-
(2001)
Clin Cancer Res
, vol.7
, Issue.4
, pp. 962-970
-
-
Butler, L.M.1
Webb, Y.2
Agus, D.B.3
Higgins, B.4
Tolentino, T.R.5
Kutko, M.C.6
Laquaglia, M.P.7
Drobnjak, M.8
Cordon-Cardo, C.9
Scher, H.I.10
Breslow, R.11
-
69
-
-
0033523895
-
Amide analogues of frichostatin a as inhibitors of histone deacetylase and inducers of terminal cell differentiation
-
Jung M, Brosch G, Kolle D, Scherf H, Gerhauser C, Loidl P: Amide analogues of frichostatin A as inhibitors of histone deacetylase and inducers of terminal cell differentiation. J Med Chem (1999) 42(22):4669-4679.
-
(1999)
J Med Chem
, vol.42
, Issue.22
, pp. 4669-4679
-
-
Jung, M.1
Brosch, G.2
Kolle, D.3
Scherf, H.4
Gerhauser, C.5
Loidl, P.6
-
70
-
-
0037075081
-
Inhibitors of human histone deacetylases: Synthesis and enzyme and cellular activity of straight chain hydroxamates
-
Remiszewski SW, Sambucetti LC, Atadja P, Bair KW, Cornell WD, Green MA, Howell KL, Jung M, Kwon P, Trogani N, Walker H: Inhibitors of human histone deacetylases: Synthesis and enzyme and cellular activity of straight chain hydroxamates. J Med Chem (2002) 45(4):753-757.
-
(2002)
J Med Chem
, vol.45
, Issue.4
, pp. 753-757
-
-
Remiszewski, S.W.1
Sambucetti, L.C.2
Atadja, P.3
Bair, K.W.4
Cornell, W.D.5
Green, M.A.6
Howell, K.L.7
Jung, M.8
Kwon, P.9
Trogani, N.10
Walker, H.11
-
71
-
-
0027378351
-
Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase
-
Kijima M, Yoshida M, Sugita K, Horinouchi S, Beppu T: Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase. J Biol Chem (1993) 268(30):22429-22435.
-
(1993)
J Biol Chem
, vol.268
, Issue.30
, pp. 22429-22435
-
-
Kijima, M.1
Yoshida, M.2
Sugita, K.3
Horinouchi, S.4
Beppu, T.5
-
72
-
-
0033520944
-
Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects
-
Sambucetti LC, Fischer DD, Zabludoff S, Kwon PO, Chamberlin H, Trogani N, Xu H, Cohen D: Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects. J Biol Chem (1999) 274(49):34940-34947.
-
(1999)
J Biol Chem
, vol.274
, Issue.49
, pp. 34940-34947
-
-
Sambucetti, L.C.1
Fischer, D.D.2
Zabludoff, S.3
Kwon, P.O.4
Chamberlin, H.5
Trogani, N.6
Xu, H.7
Cohen, D.8
-
73
-
-
0035793107
-
Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptides including trapoxin
-
Furumai R, Komatsu Y, Nishino N, Khochbin S, Yoshida M, Horinouchi S: Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptides including trapoxin. Proc Natl Acad Sci USA (2001) 98(1):87-92.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, Issue.1
, pp. 87-92
-
-
Furumai, R.1
Komatsu, Y.2
Nishino, N.3
Khochbin, S.4
Yoshida, M.5
Horinouchi, S.6
-
74
-
-
0035361402
-
Cyclic hydroxamic acid-containing peptide 31, a potent synthetic histone deacetylase inhibitor with antitumor activity
-
Komatsu Y, Tomizaki KY, Tsukamoto M, Kato T, Nishino N, Sato S, Yamori T, Tsuruo T, Furumai R, Yoshida M, Horinouchi S et al: Cyclic hydroxamic acid-containing peptide 31, a potent synthetic histone deacetylase inhibitor with antitumor activity. Cancer Res (2001) 61(11):4459-4466.
-
(2001)
Cancer Res
, vol.61
, Issue.11
, pp. 4459-4466
-
-
Komatsu, Y.1
Tomizaki, K.Y.2
Tsukamoto, M.3
Kato, T.4
Nishino, N.5
Sato, S.6
Yamori, T.7
Tsuruo, T.8
Furumai, R.9
Yoshida, M.10
Horinouchi, S.11
-
75
-
-
0028267278
-
FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No 968. III. Antitumor activities on experimental tumors in mice
-
Ueda H, Manda T, Matsumoto S, Mukumoto S, Nishigaki F, Kawamura I, Shimomura K: FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No 968. III. antitumor activities on experimental tumors in mice. J Antibiot (1994) 47(3):315-323.
-
(1994)
J Antibiot
, vol.47
, Issue.3
, pp. 315-323
-
-
Ueda, H.1
Manda, T.2
Matsumoto, S.3
Mukumoto, S.4
Nishigaki, F.5
Kawamura, I.6
Shimomura, K.7
-
76
-
-
0033822112
-
1 arrest with downregulation of cyclin D1 with upregulation of cyclin E by the histone deacetylase inhibitor FR901228
-
1 arrest with downregulation of cyclin D1 with upregulation of cyclin E by the histone deacetylase inhibitor FR901228. Br J Cancer (2000) 83(6):817-825.
-
(2000)
Br J Cancer
, vol.83
, Issue.6
, pp. 817-825
-
-
Sandor, V.1
Senderowicz, A.2
Mertins, S.3
Sackett, D.4
Sausville, E.5
Blagosklonny, M.V.6
Bates, S.E.7
-
77
-
-
0023236004
-
Brominated tyrosine metabolites from an unidentified sponge
-
Arabshahi L, Schmitz FJ: Brominated tyrosine metabolites from an unidentified sponge. J Org Chem (1987) 52:3584-3586.
-
(1987)
J Org Chem
, vol.52
, pp. 3584-3586
-
-
Arabshahi, L.1
Schmitz, F.J.2
-
78
-
-
0000055673
-
Phenolic constituents of Psammaplysilla
-
Quinoa E, Crews P: Phenolic constituents of Psammaplysilla. Tetrahedron Lett (1987) 28(28):3229-3232.
-
(1987)
Tetrahedron Lett
, vol.28
, Issue.28
, pp. 3229-3232
-
-
Quinoa, E.1
Crews, P.2
-
79
-
-
0038627550
-
Psammaplins from the sponge Pseudoceritina purpurea: Inhibition of both histone deacetylase and DMA methyltransferase
-
Pina IC, Gautschi JT, Wang GY, Sanders ML, Schmitz FJ, France D, Cornell-Kennon S, Sarabucetti LC, Remiszewski SW, Perez LB, Bair KW et al: Psammaplins from the sponge Pseudoceritina purpurea: Inhibition of both histone deacetylase and DMA methyltransferase. J Org Chem (2003) 68(10):3866-3873.
-
(2003)
J Org Chem
, vol.68
, Issue.10
, pp. 3866-3873
-
-
Pina, I.C.1
Gautschi, J.T.2
Wang, G.Y.3
Sanders, M.L.4
Schmitz, F.J.5
France, D.6
Cornell-Kennon, S.7
Sarabucetti, L.C.8
Remiszewski, S.W.9
Perez, L.B.10
Bair, K.W.11
-
80
-
-
10744229917
-
N-Hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: Discovery of (2E)-N-hydroxy-3-[4- [[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824)
-
Remiszewski SW, Sambucetti LC, Bair KW, Bontempo J, Cesarz D, Chandramouli N, Chen R, Cheung M, Cornell-Kennon S, Dean K, Diamantidis G et al: N-Hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: Discovery of (2E)-N-hydroxy-3-[4- [[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824). J Med Chem (2003) 46(21):4609-4624.
-
(2003)
J Med Chem
, vol.46
, Issue.21
, pp. 4609-4624
-
-
Remiszewski, S.W.1
Sambucetti, L.C.2
Bair, K.W.3
Bontempo, J.4
Cesarz, D.5
Chandramouli, N.6
Chen, R.7
Cheung, M.8
Cornell-Kennon, S.9
Dean, K.10
Diamantidis, G.11
-
81
-
-
0141953928
-
The discovery of NVP-LAQ824: From concept to clinic
-
Remiszewski SW: The discovery of NVP-LAQ824: From concept to clinic. Curr Med Chem (2003) 10(22):2393-2402. Describes the genesis and ultimate synthesis of this compound, based upon three natural product inhibitors.
-
(2003)
Curr Med Chem
, vol.10
, Issue.22
, pp. 2393-2402
-
-
Remiszewski, S.W.1
-
82
-
-
0141593496
-
NVP-LAQ824 is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma
-
Catley L, Weisberg E, Tai YT, Atadja P, Remiszewski SW, Hideshima T, Mitsiades N, Shringarpure R, LeBlanc R, Chauhan D, Munshi NC et al: NVP-LAQ824 is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma. Blood (2003) 102(7):2615-2622.
-
(2003)
Blood
, vol.102
, Issue.7
, pp. 2615-2622
-
-
Catley, L.1
Weisberg, E.2
Tai, Y.T.3
Atadja, P.4
Remiszewski, S.W.5
Hideshima, T.6
Mitsiades, N.7
Shringarpure, R.8
Leblanc, R.9
Chauhan, D.10
Munshi, N.C.11
-
83
-
-
0141484615
-
A high affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
-
Kamal A, Thao L, Sensintaffar J, Zhang L, Boehm MF, Fritz LC, Burrows FJ: A high affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors. Nature (2003) 425(6956):407-410.
-
(2003)
Nature
, vol.425
, Issue.6956
, pp. 407-410
-
-
Kamal, A.1
Thao, L.2
Sensintaffar, J.3
Zhang, L.4
Boehm, M.F.5
Fritz, L.C.6
Burrows, F.J.7
-
84
-
-
3242893125
-
Quantum chemical calculations and mutational analysis suggest heat shock protein 90 catalyzes transcis isomerization of geldanamycin
-
Lee YS, Marcu MG, Neckers L: Quantum chemical calculations and mutational analysis suggest heat shock protein 90 catalyzes transcis isomerization of geldanamycin. Chem Biol(2004) 11(7):991-998.
-
(2004)
Chem Biol
, vol.11
, Issue.7
, pp. 991-998
-
-
Lee, Y.S.1
Marcu, M.G.2
Neckers, L.3
-
85
-
-
0344511727
-
Crystal structure and molecular modeling of 17-DMAG in complex with human Hsp90
-
Jez JM, Chen JC, Rastelli G, Stroud RM, Santi DV: Crystal structure and molecular modeling of 17-DMAG in complex with human Hsp90. Chem Biol (2003) 10(4):361-368.
-
(2003)
Chem Biol
, vol.10
, Issue.4
, pp. 361-368
-
-
Jez, J.M.1
Chen, J.C.2
Rastelli, G.3
Stroud, R.M.4
Santi, D.V.5
-
86
-
-
3142545683
-
Synthesis and biological evaluation of a new class of geldanamycin derivatives as potent inhibitors of Hsp90
-
Le Brazidec JY, Kamal A, Busch D, Thao L, Zhang L, Timony G, Grecko R, Trent K, Lough R, Salazar T, Khan S et al: Synthesis and biological evaluation of a new class of geldanamycin derivatives as potent inhibitors of Hsp90. J Med Chem (2004) 47(15):3865-3873.
-
(2004)
J Med Chem
, vol.47
, Issue.15
, pp. 3865-3873
-
-
Le Brazidec, J.Y.1
Kamal, A.2
Busch, D.3
Thao, L.4
Zhang, L.5
Timony, G.6
Grecko, R.7
Trent, K.8
Lough, R.9
Salazar, T.10
Khan, S.11
-
87
-
-
4544337503
-
Synthesis and biological activities of novel 17-aminogeldanamycin derivatives
-
Tian ZQ, Liu Y, Zhang D, Wang Z, Dong SD, Carreras CW, Zhou Y, Rastelli G, Santi DV, Myles DC: Synthesis and biological activities of novel 17-aminogeldanamycin derivatives. Bioorg Med Chem (2004) 12(20):5317-5329.
-
(2004)
Bioorg Med Chem
, vol.12
, Issue.20
, pp. 5317-5329
-
-
Tian, Z.Q.1
Liu, Y.2
Zhang, D.3
Wang, Z.4
Dong, S.D.5
Carreras, C.W.6
Zhou, Y.7
Rastelli, G.8
Santi, D.V.9
Myles, D.C.10
-
88
-
-
14844338071
-
17-Dimethylaminoethylamino-17-desmethoxy-geldanamycin (17-DMAG), a potent Hsp90 inhibitor with improved pharmaceutical and antitumor properties
-
Amsterdam, the Netherlands Abs P044
-
Snader KM et al: 17-Dimethylaminoethylamino-17-desmethoxy-geldanamycin (17-DMAG), a potent Hsp90 inhibitor with improved pharmaceutical and antitumor properties. Signal Transduction Modulators in Cancer Therapy - First International Symposium, Amsterdam, the Netherlands (2002):Abs P044.
-
(2002)
Signal Transduction Modulators in Cancer Therapy - First International Symposium
-
-
Snader, K.M.1
-
89
-
-
33646053096
-
Benzoquinone ansamycins
-
Cragg GM, Kingston DGI, Newman DJ (Eds), CRC Press/Taylor and Francis, Boca Raton, FL, USA in press
-
Snader KM: Benzoquinone ansamycins. In: Anticancer Agents from Natural Sources, Cragg GM, Kingston DGI, Newman DJ (Eds), CRC Press/Taylor and Francis, Boca Raton, FL, USA (2005): in press.
-
(2005)
Anticancer Agents from Natural Sources
-
-
Snader, K.M.1
-
90
-
-
0035071607
-
A small molecule designed to bind to the adenine nucleotide pocket of Hsp90 causes HER2 degradation and the growth arrest and differentiation of breast cancer cells
-
Chiosis G, Timaul MN, Lucas B, Munster PN, Zheng FF, Sepp-Lorenzino L, Rosen N: A small molecule designed to bind to the adenine nucleotide pocket of Hsp90 causes HER2 degradation and the growth arrest and differentiation of breast cancer cells. Chem Biol (2001) 8(3):289-299.
-
(2001)
Chem Biol
, vol.8
, Issue.3
, pp. 289-299
-
-
Chiosis, G.1
Timaul, M.N.2
Lucas, B.3
Munster, P.N.4
Zheng, F.F.5
Sepp-Lorenzino, L.6
Rosen, N.7
-
91
-
-
0141485327
-
Development of purine-scaffold small molecule inhibitors of Hsp90
-
Chiosis G, Lucas B, Huezo H, Solit D, Basso A, Rosen N: Development of purine-scaffold small molecule inhibitors of Hsp90. Curr Cancer Drug Targets (2003) 3(5):371-376.
-
(2003)
Curr Cancer Drug Targets
, vol.3
, Issue.5
, pp. 371-376
-
-
Chiosis, G.1
Lucas, B.2
Huezo, H.3
Solit, D.4
Basso, A.5
Rosen, N.6
-
92
-
-
0036836964
-
Development of a purine-scaffold novel class of Hsp90 binders that inhibit the proliferation of cancer cells and induce the degradation of HER2 tyrosine kinase
-
Chiosis G, Lucas B, Shtil A, Huezo H, Rosen N: Development of a purine-scaffold novel class of Hsp90 binders that inhibit the proliferation of cancer cells and induce the degradation of HER2 tyrosine kinase. Bioorg Med Chem (2002) 10(11):3555-3564.
-
(2002)
Bioorg Med Chem
, vol.10
, Issue.11
, pp. 3555-3564
-
-
Chiosis, G.1
Lucas, B.2
Shtil, A.3
Huezo, H.4
Rosen, N.5
-
93
-
-
3042553538
-
Targeting wide-range oncogenic transformation via PU24FCI, a specific inhibitor of tumor Hsp90
-
Vilenchik M, Solit D, Basso A, Huezo H, Lucas B, He H, Rosen N, Spampinato C, Modrich P, Chiosis G: Targeting wide-range oncogenic transformation via PU24FCI, a specific inhibitor of tumor Hsp90. Chem Biol (2004) 11(6):787-797. A 'tour-de-force' providing examples of drug discovery using chemical intuition rather than in silico modeling.
-
(2004)
Chem Biol
, vol.11
, Issue.6
, pp. 787-797
-
-
Vilenchik, M.1
Solit, D.2
Basso, A.3
Huezo, H.4
Lucas, B.5
He, H.6
Rosen, N.7
Spampinato, C.8
Modrich, P.9
Chiosis, G.10
-
94
-
-
0042855994
-
17AAG: Low target binding affinity and potent cell activity - Finding an explanation
-
Chiosis G, Huezo H, Rosen N, Mimnaugh E, Whitesell L, Neckers L: 17AAG: Low target binding affinity and potent cell activity - finding an explanation. Mol Cancer Ther (2003) 2(2):123-129.
-
(2003)
Mol Cancer Ther
, vol.2
, Issue.2
, pp. 123-129
-
-
Chiosis, G.1
Huezo, H.2
Rosen, N.3
Mimnaugh, E.4
Whitesell, L.5
Neckers, L.6
-
95
-
-
3042637928
-
Structure-activity relationships in purine-based inhibitor binding to Hsp90 isoforms
-
Wright L, Barril X, Dymock B, Sheridan L, Surgenor A, Beswick M, Drysdale M, Collier A, Massey M, Davies N, Fink A et al: Structure-activity relationships in purine-based inhibitor binding to Hsp90 isoforms. Chem Biol (2004) 11(6):775-785.
-
(2004)
Chem Biol
, vol.11
, Issue.6
, pp. 775-785
-
-
Wright, L.1
Barril, X.2
Dymock, B.3
Sheridan, L.4
Surgenor, A.5
Beswick, M.6
Drysdale, M.7
Collier, A.8
Massey, M.9
Davies, N.10
Fink, A.11
-
96
-
-
0037665145
-
Roscovitine and other purines as kinase inhibitors. From starfish oocytes to clinical trials
-
Meijer L, Raymond E: Roscovitine and other purines as kinase inhibitors. From starfish oocytes to clinical trials. Acc Chem Res (2003) 36(6):417-425. Describes the evolution of the purine-based CDK inhibitors.
-
(2003)
Acc Chem Res
, vol.36
, Issue.6
, pp. 417-425
-
-
Meijer, L.1
Raymond, E.2
-
97
-
-
0001052186
-
Inhibitors of two enzymes which metabolize cytokinins
-
Parker CW, Entsch B, Letham DS: Inhibitors of two enzymes which metabolize cytokinins. Phytochemistry (1986) 25:303-310.
-
(1986)
Phytochemistry
, vol.25
, pp. 303-310
-
-
Parker, C.W.1
Entsch, B.2
Letham, D.S.3
-
98
-
-
0033150476
-
Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors
-
Chang YT, Gray NS, Rosania GR, Sutherlin DP, Kwon S, Norman TC, Sarohia R, Leost M, Meijer L, Schultz PG: Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors. Chem Biol (1999) 6(6):361-375.
-
(1999)
Chem Biol
, vol.6
, Issue.6
, pp. 361-375
-
-
Chang, Y.T.1
Gray, N.S.2
Rosania, G.R.3
Sutherlin, D.P.4
Kwon, S.5
Norman, T.C.6
Sarohia, R.7
Leost, M.8
Meijer, L.9
Schultz, P.G.10
-
99
-
-
0035940873
-
Identification of an indigo precursor from leaves of Isatis tinctoria (Woad)
-
Maugard T, Enaud E, Choisy P, Legoy MD: Identification of an indigo precursor from leaves of Isatis tinctoria (Woad). Phytochemistry (2001) 58(6):897-904.
-
(2001)
Phytochemistry
, vol.58
, Issue.6
, pp. 897-904
-
-
Maugard, T.1
Enaud, E.2
Choisy, P.3
Legoy, M.D.4
-
100
-
-
0042894451
-
Tyrian purple: 6,6′-Dibromoindigo and related compounds
-
Cooksey CJ: Tyrian purple: 6,6′-Dibromoindigo and related compounds. Molecules (2001) 6:736-769.
-
(2001)
Molecules
, vol.6
, pp. 736-769
-
-
Cooksey, C.J.1
-
101
-
-
0035079979
-
Expression and isolation of antimicrobial small molecules from soil DNA libraries
-
MacNeil IA, Tiong CL, Minor C, August PR, Grossman TH, Loiacono KA, Lynch BA, Phillips T, Narula S, Sundaramoorthi R, Tyler A et al: Expression and isolation of antimicrobial small molecules from soil DNA libraries. J Mol Microbiol Biotechnol (2001) 3(2):301-308.
-
(2001)
J Mol Microbiol Biotechnol
, vol.3
, Issue.2
, pp. 301-308
-
-
MacNeil, I.A.1
Tiong, C.L.2
Minor, C.3
August, P.R.4
Grossman, T.H.5
Loiacono, K.A.6
Lynch, B.A.7
Phillips, T.8
Narula, S.9
Sundaramoorthi, R.10
Tyler, A.11
-
102
-
-
0035943634
-
Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine
-
Adachi J, Mori Y, Matsui S, Takigam H, Fujino J, Kitagawa H, Miller CA III, Kato T, Saeki K, Matsuda T: Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine. J Biol Chem (2001) 276(34):31475-31478.
-
(2001)
J Biol Chem
, vol.276
, Issue.34
, pp. 31475-31478
-
-
Adachi, J.1
Mori, Y.2
Matsui, S.3
Takigam, H.4
Fujino, J.5
Kitagawa, H.6
Miller III, C.A.7
Kato, T.8
Saeki, K.9
Matsuda, T.10
-
103
-
-
0002345418
-
Chemical constituents of a traditional Chinese medicine Ging Dai
-
Chen DH, Xie JX: Chemical constituents of a traditional Chinese medicine Ging Dai. Zhongcaoyao (1984) 15:6-8.
-
(1984)
Zhongcaoyao
, vol.15
, pp. 6-8
-
-
Chen, D.H.1
Xie, J.X.2
-
104
-
-
0036332286
-
Indirubin and mesoindigo in the treatment of chronic myelogenous leukemia in China
-
Xiao Z, Hao Y, Liu B, Qian L: Indirubin and mesoindigo in the treatment of chronic myelogenous leukemia in China. Leuk Lymphoma (2002) 43(9):1763-1768.
-
(2002)
Leuk Lymphoma
, vol.43
, Issue.9
, pp. 1763-1768
-
-
Xiao, Z.1
Hao, Y.2
Liu, B.3
Qian, L.4
-
105
-
-
0346875916
-
GSK-3-selective inhibitors derived from Tyrian purple indirubins
-
Meijer L, Skaltsounis AL, Magiatis P, Polychronopoulos P, Knockaert M, Leost M, Ryan XP, Vonica CA, Brivanlou A, Dajani R, Crovace C et al: GSK-3-selective inhibitors derived from Tyrian purple indirubins. Chem Biol (2003) 10(12):1255-1266. An excellent review of the research involved in the discovery of the multiple activities of simple indirubins and their derivatives.
-
(2003)
Chem Biol
, vol.10
, Issue.12
, pp. 1255-1266
-
-
Meijer, L.1
Skaltsounis, A.L.2
Magiatis, P.3
Polychronopoulos, P.4
Knockaert, M.5
Leost, M.6
Ryan, X.P.7
Vonica, C.A.8
Brivanlou, A.9
Dajani, R.10
Crovace, C.11
-
106
-
-
2442589341
-
Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases
-
Polychronopoulos P, Magiatis P, Skaltsounis AL, Myrianthopoulos V, Mikros E, Tarricone A, Musacchio A, Roe SM, Pearl L, Leost M, Greengard P et al: Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases. J Med Chem (2004) 47(4):935-946.
-
(2004)
J Med Chem
, vol.47
, Issue.4
, pp. 935-946
-
-
Polychronopoulos, P.1
Magiatis, P.2
Skaltsounis, A.L.3
Myrianthopoulos, V.4
Mikros, E.5
Tarricone, A.6
Musacchio, A.7
Roe, S.M.8
Pearl, L.9
Leost, M.10
Greengard, P.11
-
107
-
-
2542635063
-
Generation of new protein kinase inhibitors utilizing cytochrome P450 mutant enzymes for indigoid synthesis
-
Guengerich FP, Sorrells JL, Schmitt S, Krauser JA, Aryal P, Meijer L: Generation of new protein kinase inhibitors utilizing cytochrome P450 mutant enzymes for indigoid synthesis. J Med Chem (2004) 47(12):3236-3241. Provides evidence that cytochrome P450s can be expressed in surrogate hosts and can convert indoles to indirubins.
-
(2004)
J Med Chem
, vol.47
, Issue.12
, pp. 3236-3241
-
-
Guengerich, F.P.1
Sorrells, J.L.2
Schmitt, S.3
Krauser, J.A.4
Aryal, P.5
Meijer, L.6
-
108
-
-
0034595354
-
Directed evolution of the fatty-acid hydroxylase P450 BM-3 into an indole-hydroxylating catalyst
-
Li QS, Schwaneberg U, Fischer P, Schmid RD: Directed evolution of the fatty-acid hydroxylase P450 BM-3 into an indole-hydroxylating catalyst. Chemistry (2000) 6(9):1531-1536.
-
(2000)
Chemistry
, vol.6
, Issue.9
, pp. 1531-1536
-
-
Li, Q.S.1
Schwaneberg, U.2
Fischer, P.3
Schmid, R.D.4
-
109
-
-
0034649422
-
Oxidation of indole by cytochrome P450 enzymes
-
Gillam EM, Notley LM, Cai H, DeVoss JJ, Guengerich FP: Oxidation of indole by cytochrome P450 enzymes. Biochemistry (2000) 39(45):13817-13824.
-
(2000)
Biochemistry
, vol.39
, Issue.45
, pp. 13817-13824
-
-
Gillam, E.M.1
Notley, L.M.2
Cai, H.3
Devoss, J.J.4
Guengerich, F.P.5
-
110
-
-
3042629590
-
Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediates the antiproliferative effects of indirubins
-
Knockaert M, Blondel M, Bach S, Leost M, Elbi C, Hager GL, Nagy SR, Han D, Denison M, Ffrenoh M, Meijer L et al: Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediates the antiproliferative effects of indirubins. Oncogene (2004) 23(25):4400-4412.
-
(2004)
Oncogene
, vol.23
, Issue.25
, pp. 4400-4412
-
-
Knockaert, M.1
Blondel, M.2
Bach, S.3
Leost, M.4
Elbi, C.5
Hager, G.L.6
Nagy, S.R.7
Han, D.8
Denison, M.9
Ffrenoh, M.10
Meijer, L.11
-
111
-
-
0038768712
-
Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals
-
Denison MS, Nagy SR: Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals. Annu Rev Pharmacol Toxicol (2003) 43:309-334.
-
(2003)
Annu Rev Pharmacol Toxicol
, vol.43
, pp. 309-334
-
-
Denison, M.S.1
Nagy, S.R.2
-
112
-
-
3042635178
-
GSK3 inhibitors: Development and therapeutic potential
-
Cohen P, Goedert M: GSK3 inhibitors: Development and therapeutic potential. Nat Rev Drug Disc (2004) 3(6):479-487. A thorough review of the roles of GSK-3 kinase in biology.
-
(2004)
Nat Rev Drug Disc
, vol.3
, Issue.6
, pp. 479-487
-
-
Cohen, P.1
Goedert, M.2
-
113
-
-
1542509425
-
Meridianins, a new family of protein kinase inhibitors isolated from the ascidian Aplidium meridianum
-
Gompel M, Leost M, De Kier Joffe EB, Puricelli L, Franco LH, Palermo J, Meijer L: Meridianins, a new family of protein kinase inhibitors isolated from the ascidian Aplidium meridianum. Bioorg Med Chem Lett (2004) 14(7):1703-1707.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, Issue.7
, pp. 1703-1707
-
-
Gompel, M.1
Leost, M.2
De Kier Joffe, E.B.3
Puricelli, L.4
Franco, L.H.5
Palermo, J.6
Meijer, L.7
-
114
-
-
2942597981
-
The design of drug candidate molecules as selective inhibitors of therapeutically relevant protein kinases
-
Fischer PM: The design of drug candidate molecules as selective inhibitors of therapeutically relevant protein kinases. Curr Med Chem (2004) 11(12):1563-1583. A thorough review of the design of protein kinase inhibitors by one of the leading medicinal chemists in the field.
-
(2004)
Curr Med Chem
, vol.11
, Issue.12
, pp. 1563-1583
-
-
Fischer, P.M.1
-
115
-
-
0037119336
-
From protein domains to drug candidates - Natural products as guiding principles in compound library design and synthesis of compound libraries
-
Breinbauer R, Vetter IR, Waldmann H: From protein domains to drug candidates - natural products as guiding principles in compound library design and synthesis of compound libraries. Angew Chem Int Ed (2002) 41(16):2878-2890. Describes how to devise new inhibitors from older natural products by utilizing topological information from proteins.
-
(2002)
Angew Chem Int Ed
, vol.41
, Issue.16
, pp. 2878-2890
-
-
Breinbauer, R.1
Vetter, I.R.2
Waldmann, H.3
-
116
-
-
0037126836
-
Natural products are biologically validated starting points in structural space for compound library development: Solid-phase synthesis of dysidiolide-derived phosphatase inhibitors
-
Brohm D, Metzger S, Bhargava A, Muller O, Lieb F, Waldmann H: Natural products are biologically validated starting points in structural space for compound library development: Solid-phase synthesis of dysidiolide-derived phosphatase inhibitors. Angew Chem Int Ed (2002) 41(2):307-311.
-
(2002)
Angew Chem Int Ed
, vol.41
, Issue.2
, pp. 307-311
-
-
Brohm, D.1
Metzger, S.2
Bhargava, A.3
Muller, O.4
Lieb, F.5
Waldmann, H.6
-
117
-
-
0037079014
-
The structure of the protein universe and genome evolution
-
Koonin EV, Wolf YI, Karev GP: The structure of the protein universe and genome evolution. Nature (2002) 420(6912):218-223.
-
(2002)
Nature
, vol.420
, Issue.6912
, pp. 218-223
-
-
Koonin, E.V.1
Wolf, Y.I.2
Karev, G.P.3
-
118
-
-
0024239320
-
Methods for drug discovery: Development of potent, selective, orally effective cholecystokinin antagonists
-
Evans BE, Riffle KE, Bock MG, DiPardo RM, Fredinger RM, Whitter WL, Lundell GF, Veber DF, Anderson PS, Chang RSL, Lotti VJ et al: Methods for drug discovery: Development of potent, selective, orally effective cholecystokinin antagonists. J Med Chem (1988) 31(12):2235-2246.
-
(1988)
J Med Chem
, vol.31
, Issue.12
, pp. 2235-2246
-
-
Evans, B.E.1
Riffle, K.E.2
Bock, M.G.3
Dipardo, R.M.4
Fredinger, R.M.5
Whitter, W.L.6
Lundell, G.F.7
Veber, D.F.8
Anderson, P.S.9
Rsl, C.10
Lotti, V.J.11
-
119
-
-
0034684250
-
Natural product-like combinatorial libraries based on privileged structures. 1. General principles and solid-phase synthesis of benzopyrans
-
Nicolaou KC, Pfefferkorn JA, Roecker AJ, Cao G-Q, Barluenga S, Mitchell HJ: Natural product-like combinatorial libraries based on privileged structures. 1. General principles and solid-phase synthesis of benzopyrans. J Am Chem Soc (2000) 122(41):9939-9953.
-
(2000)
J Am Chem Soc
, vol.122
, Issue.41
, pp. 9939-9953
-
-
Nicolaou, K.C.1
Pfefferkorn, J.A.2
Roecker, A.J.3
Cao, G.-Q.4
Barluenga, S.5
Mitchell, H.J.6
-
120
-
-
0034684225
-
Natural product-like combinatorial libraries based on privileged structures. 2. Construction of a 10,000-membered benzopyran library by directed split-and-pool chemistry using nanokans and optical encoding
-
Nicolaou KC, Pfefferkorn JA, Mitchell HJ, Roecker AJ, Barluenga S, Cao GQ, Affleck RL, Lillig JE: Natural product-like combinatorial libraries based on privileged structures. 2. Construction of a 10,000-membered benzopyran library by directed split-and-pool chemistry using nanokans and optical encoding. J Am Chem Soc (2000) 122(41):9954-9967.
-
(2000)
J Am Chem Soc
, vol.122
, Issue.41
, pp. 9954-9967
-
-
Nicolaou, K.C.1
Pfefferkorn, J.A.2
Mitchell, H.J.3
Roecker, A.J.4
Barluenga, S.5
Cao, G.Q.6
Affleck, R.L.7
Lillig, J.E.8
-
121
-
-
0034684186
-
Natural product-like combinatorial libraries based on privileged structures. 3. The 'libraries from libraries' principle for diversity enhancement of benzopyran libraries
-
Nicolaou KC, Pfefferkorn JA, Barluenga S, Mitchell HJ, Roecker AJ, Cao GQ: Natural product-like combinatorial libraries based on privileged structures. 3. The 'libraries from libraries' principle for diversity enhancement of benzopyran libraries. J Am Chem Soc (2000) 122(41):9968-9976.
-
(2000)
J Am Chem Soc
, vol.122
, Issue.41
, pp. 9968-9976
-
-
Nicolaou, K.C.1
Pfefferkorn, J.A.2
Barluenga, S.3
Mitchell, H.J.4
Roecker, A.J.5
Cao, G.Q.6
-
122
-
-
0029142486
-
Nakijiquinones C and D, new sesquiterpenoid quinones with a hydroxy amino acid residue from a marine sponge inhibiting c-Erb2 kinase
-
Kobayashi J, Madono T, Shigemori H: Nakijiquinones C and D, new sesquiterpenoid quinones with a hydroxy amino acid residue from a marine sponge inhibiting c-Erb2 kinase. Tetrahedron (1995) 51(40):10867-10974.
-
(1995)
Tetrahedron
, vol.51
, Issue.40
, pp. 10867-10974
-
-
Kobayashi, J.1
Madono, T.2
Shigemori, H.3
-
123
-
-
0035856967
-
The first naturally occurring Tie2 kinase inhibitor
-
Zhou BN, Johnson RK, Mattern MR, Fisher PW, Kingston DG: The first naturally occurring Tie2 kinase inhibitor. Org Lett (2001) 3(25):4047-4049.
-
(2001)
Org Lett
, vol.3
, Issue.25
, pp. 4047-4049
-
-
Zhou, B.N.1
Johnson, R.K.2
Mattern, M.R.3
Fisher, P.W.4
Kingston, D.G.5
-
124
-
-
0034597072
-
Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective Inhibitors of lck-I
-
Arnold LD, Calderwood DJ. Dixon RW, Johnston DN, Kamens JS, Munschauer R, Rafferty P, Ratnofsky SE: Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective Inhibitors of lck-I. Bioorg Med Chem Lett (2000) 10(19):2167-2170.
-
(2000)
Bioorg Med Chem Lett
, vol.10
, Issue.19
, pp. 2167-2170
-
-
Arnold, L.D.1
Calderwood, D.J.2
Dixon, R.W.3
Johnston, D.N.4
Kamens, J.S.5
Munschauer, R.6
Rafferty, P.7
Ratnofsky, S.E.8
-
125
-
-
0034597116
-
Johnston DN, Munschauer R, Rafferty P, Tometzki GB: Pyrrolo[2,3-d] pyrimidines containing an extended 5-substituent as potent and selective inhibitors of lck-II
-
Burchat AF, Calderwood DJ, Hirst GC, Holman NJ. Johnston DN, Munschauer R, Rafferty P, Tometzki GB: Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective inhibitors of lck-II. Bioorg Med Chem Lett (2000) 10(19):2171-2174.
-
(2000)
Bioorg Med Chem Lett
, vol.10
, Issue.19
, pp. 2171-2174
-
-
Burchat, A.F.1
Calderwood, D.J.2
Hirst, G.C.3
Holman, N.J.4
-
126
-
-
0037124205
-
Pyrrolo[2,3-d]pyrimidines containing diverse N-7 substituents as potent inhibitors of lck
-
Calderwood DJ, Johnston DN, Munschauer R, Rafferty P: Pyrrolo[2,3-d]pyrimidines containing diverse N-7 substituents as potent inhibitors of lck. Bioorg Med Chem Lett (2002) 12(12):1683-1686.
-
(2002)
Bioorg Med Chem Lett
, vol.12
, Issue.12
, pp. 1683-1686
-
-
Calderwood, D.J.1
Johnston, D.N.2
Munschauer, R.3
Rafferty, P.4
-
127
-
-
0037124207
-
Pyrazolo[3,4-d]pyrimidines containing an extended 3-substituent as potent inhibitors of lck - A selective insight
-
Burchat AF, Calderwood DJ, Friedman MM, Hirst GC, Li B, Rafferty P, Ritter K, Skinner BS: Pyrazolo[3,4-d]pyrimidines containing an extended 3-substituent as potent inhibitors of lck - a selective insight. Bioorg Med Chem Lett (2002) 12(12):1687-1690.
-
(2002)
Bioorg Med Chem Lett
, vol.12
, Issue.12
, pp. 1687-1690
-
-
Burchat, A.F.1
Calderwood, D.J.2
Friedman, M.M.3
Hirst, G.C.4
Li, B.5
Rafferty, P.6
Ritter, K.7
Skinner, B.S.8
-
128
-
-
0038798615
-
Development of natural product-derived receptor tyrosine kinase inhibitors based on conservation of protein domain fold
-
Kissau L, Stahl P, Mazitschek R, Giannis A, Waldmann H: Development of natural product-derived receptor tyrosine kinase inhibitors based on conservation of protein domain fold. J Med Chem (2003) 48(14):2917-2931.
-
(2003)
J Med Chem
, vol.48
, Issue.14
, pp. 2917-2931
-
-
Kissau, L.1
Stahl, P.2
Mazitschek, R.3
Giannis, A.4
Waldmann, H.5
-
129
-
-
0141828504
-
Protein structure similarity as guiding principle for combinatorial library design
-
Koch MA, Breinbauer R, Waldmann H: Protein structure similarity as guiding principle for combinatorial library design. Biol Chem (2003) 384(9):1265-1272. Describes research with 'protein-directed' syntheses.
-
(2003)
Biol Chem
, vol.384
, Issue.9
, pp. 1265-1272
-
-
Koch, M.A.1
Breinbauer, R.2
Waldmann, H.3
-
131
-
-
0030975362
-
4 hydrolase: A new target for antiinflammatory intervention
-
4 hydrolase: A new target for antiinflammatory intervention. Curr Med Chem (1997) 4(1):67-78.
-
(1997)
Curr Med Chem
, vol.4
, Issue.1
, pp. 67-78
-
-
Zhang, M.Q.1
-
132
-
-
12244284906
-
Purine-based inhibitors of inositol-1,4,5-trisphosphate-3-kinase
-
Chang YT, Choi S, Bae YS, Burdett M, Moon HS, Lee JW, Gray NS, Schultz PG, Meijer L, Chung SK, Choi KY et al: Purine-based inhibitors of inositol-1,4,5-trisphosphate-3-kinase. ChemBioChem (2002)3(9):897-901.
-
(2002)
ChemBioChem
, vol.3
, Issue.9
, pp. 897-901
-
-
Chang, Y.T.1
Choi, S.2
Bae, Y.S.3
Burdett, M.4
Moon, H.S.5
Lee, J.W.6
Gray, N.S.7
Schultz, P.G.8
Meijer, L.9
Chung, S.K.10
Choi, K.Y.11
-
133
-
-
0034599655
-
Discovery of carbohydrate sulfotransferase inhibitors from a kinase-directed library
-
Armstrong JI, Portley AR, Chang YT, Nierengarten DM, Cook BN, Bowman KG, Bishop A, Gray NS, Shokat KM, Schultz PG, Bertozzi CR: Discovery of carbohydrate sulfotransferase inhibitors from a kinase-directed library. Angew Chem Int Ed (2000) 39(7):1303-1306.
-
(2000)
Angew Chem Int Ed
, vol.39
, Issue.7
, pp. 1303-1306
-
-
Armstrong, J.I.1
Portley, A.R.2
Chang, Y.T.3
Nierengarten, D.M.4
Cook, B.N.5
Bowman, K.G.6
Bishop, A.7
Gray, N.S.8
Shokat, K.M.9
Schultz, P.G.10
Bertozzi, C.R.11
-
134
-
-
0035899193
-
Discovery of estrogen sulfotransferase inhibitors from a purine library screen
-
Verdugo DE, Cancilla MT, Ge X, Gray NS, Chang YT, Schultz PG, Negishi M, Leary JA, Bertozzi CR: Discovery of estrogen sulfotransferase inhibitors from a purine library screen. J Med Chem (2001) 44(17):2683-2686.
-
(2001)
J Med Chem
, vol.44
, Issue.17
, pp. 2683-2686
-
-
Verdugo, D.E.1
Cancilla, M.T.2
Ge, X.3
Gray, N.S.4
Chang, Y.T.5
Schultz, P.G.6
Negishi, M.7
Leary, J.A.8
Bertozzi, C.R.9
-
135
-
-
0037065313
-
A potent and highly selective sulfotransferase inhibitor
-
Chapman E, Ding S, Schultz PG, Wong CH: A potent and highly selective sulfotransferase inhibitor. J Am Chem Soc (2002) 124(49):14524-14525.
-
(2002)
J Am Chem Soc
, vol.124
, Issue.49
, pp. 14524-14525
-
-
Chapman, E.1
Ding, S.2
Schultz, P.G.3
Wong, C.H.4
-
137
-
-
0031466528
-
Cell-line directed screening assay for inhibitors of thioredoxin reductase signaling as potential anti-cancer drugs
-
Kunkel MW, Kirkpatrick DL, Johnson JI, Powis G: Cell-line directed screening assay for inhibitors of thioredoxin reductase signaling as potential anti-cancer drugs. Anticancer Drug Des (1997) 12(8):659-670.
-
(1997)
Anticancer Drug des
, vol.12
, Issue.8
, pp. 659-670
-
-
Kunkel, M.W.1
Kirkpatrick, D.L.2
Johnson, J.I.3
Powis, G.4
-
138
-
-
0035147618
-
1
-
1. J Pharmacol Exp Ther (2001) 296(2):364-371.
-
(2001)
J Pharmacol Exp Ther
, vol.296
, Issue.2
, pp. 364-371
-
-
Lazo, J.S.1
Tamura, K.2
Vogt, A.3
Jung, J.-K.4
Rodriguez, S.5
Balachandran, R.6
Day, B.W.7
Wipf, P.8
-
139
-
-
0035829182
-
New inhibitors of the thioredoxin-thioredoxin reductase system based on a naphthoquinone spiroketal natural product lead
-
Wipf P, Hopkins TD, Jung J-K, Rodriguez S, Birmingham A, Southwick EC, Lazo JS, Powis G: New inhibitors of the thioredoxin-thioredoxin reductase system based on a naphthoquinone spiroketal natural product lead. Bioorg Med Chem Letts (2001) 11(19)2637-2641.
-
(2001)
Bioorg Med Chem Letts
, vol.11
, Issue.19
, pp. 2637-2641
-
-
Wipf, P.1
Hopkins, T.D.2
Jung, J.-K.3
Rodriguez, S.4
Birmingham, A.5
Southwick, E.C.6
Lazo, J.S.7
Powis, G.8
-
140
-
-
0142144338
-
The thioredoxin redox inhibitors 1-methylpropyl 2-imidazoyl disulfide and pleurotin inhibit hypoxia-induced factor 1-α and vascular endothelial growth factor formation
-
Welsh SJ, Williams RR, Birmingham A, Newman DJ, Kirkpatrick DL, Powis G: The thioredoxin redox inhibitors 1-methylpropyl 2-imidazoyl disulfide and pleurotin inhibit hypoxia-induced factor 1-α and vascular endothelial growth factor formation. Mol Cancer Ther (2003) 2(3):235-243.
-
(2003)
Mol Cancer Ther
, vol.2
, Issue.3
, pp. 235-243
-
-
Welsh, S.J.1
Williams, R.R.2
Birmingham, A.3
Newman, D.J.4
Kirkpatrick, D.L.5
Powis, G.6
-
141
-
-
2942700238
-
Natural product based inhibitors of the thioredoxin-thioredoxin reductase system
-
Wipf P, Lynch SM, Birmingham A, Tamayo G, Jimenez A, Campos N, Powis G: Natural product based inhibitors of the thioredoxin-thioredoxin reductase system. Org Biomol Chem (2004) 2(11):1651-1658. Discusses the further utilization of natural products to develop an existing structure-function relationship.
-
(2004)
Org Biomol Chem
, vol.2
, Issue.11
, pp. 1651-1658
-
-
Wipf, P.1
Lynch, S.M.2
Birmingham, A.3
Tamayo, G.4
Jimenez, A.5
Campos, N.6
Powis, G.7
-
142
-
-
6344226681
-
Rescuing combichem
-
Borman S: Rescuing combichem. Chem Eng News (2004) 82(40):32-40. 'Classical' combinatorial chemists begin to recognize the value of natural product scaffolds.
-
(2004)
Chem Eng News
, vol.82
, Issue.40
, pp. 32-40
-
-
Borman, S.1
-
143
-
-
9244238653
-
Natural products as a hunting ground for combinatorial chemistry
-
Ganesan A: Natural products as a hunting ground for combinatorial chemistry. Curr Opin Biotech (2004) 15(6):584-590.
-
(2004)
Curr Opin Biotech
, vol.15
, Issue.6
, pp. 584-590
-
-
Ganesan, A.1
-
144
-
-
2942565810
-
Natural products and combinatorial chemistry: Back to the future
-
Ortholand JY, Ganesan A: Natural products and combinatorial chemistry: Back to the future. Curr Opin Chem Biol (2004) 8(3):271-280.
-
(2004)
Curr Opin Chem Biol
, vol.8
, Issue.3
, pp. 271-280
-
-
Ortholand, J.Y.1
Ganesan, A.2
-
145
-
-
2942590399
-
Libraries from natural product-like scaffolds
-
Boldi AM: Libraries from natural product-like scaffolds. Curr Opin Chem Biol (2004) 8(3):281-286. Covers the role of natural product scaffolds.
-
(2004)
Curr Opin Chem Biol
, vol.8
, Issue.3
, pp. 281-286
-
-
Boldi, A.M.1
-
146
-
-
8844262660
-
Principles for modulation of the nuclear receptor superfamily
-
Gronemeyer H, Gustaffson JA, Laudet V: Principles for modulation of the nuclear receptor superfamily. Nat Rev Drug Disc (2004) 3(11):950-964.
-
(2004)
Nat Rev Drug Disc
, vol.3
, Issue.11
, pp. 950-964
-
-
Gronemeyer, H.1
Gustaffson, J.A.2
Laudet, V.3
-
147
-
-
5644244403
-
Systems biology and the molecular circuits of cancer
-
Alberghina L, Chiaradonna F, Vanoni M: Systems biology and the molecular circuits of cancer. ChemBioChem (2004) 5(10):1322-1333.
-
(2004)
ChemBioChem
, vol.5
, Issue.10
, pp. 1322-1333
-
-
Alberghina, L.1
Chiaradonna, F.2
Vanoni, M.3
-
148
-
-
0242582505
-
Le cycle de division cellulaire et sa regulation
-
Meijer L: Le cycle de division cellulaire et sa regulation. Oncologie (2003) 5:311-326. Provides superb cell cycle figures.
-
(2003)
Oncologie
, vol.5
, pp. 311-326
-
-
Meijer, L.1
-
149
-
-
0037015443
-
Total synthesis of (+)-geldanamycin and (-)-o-quinogeldanamycin with use of asymmetric anti- and syn-glycolate aldol reactions
-
Andrus MB, Meredith EL, Simmons BL, Sekhar BB, Hicken EJ: Total synthesis of (+)-geldanamycin and (-)-o-quinogeldanamycin with use of asymmetric anti- and syn-glycolate aldol reactions. Org Lett (2002) 4(20):3549-3552.
-
(2002)
Org Lett
, vol.4
, Issue.20
, pp. 3549-3552
-
-
Andrus, M.B.1
Meredith, E.L.2
Simmons, B.L.3
Sekhar, B.B.4
Hicken, E.J.5
-
151
-
-
0032490092
-
Chiral crotylsilane-based approach to benzoquinoid ansamycins: Total synthesis of (+)-macbecin I
-
Panek JS, Xu F, Rondon AC: Chiral crotylsilane-based approach to benzoquinoid ansamycins: Total synthesis of (+)-macbecin I. J Am Chem Soc (1998) 120(17):4113-4122.
-
(1998)
J Am Chem Soc
, vol.120
, Issue.17
, pp. 4113-4122
-
-
Panek, J.S.1
Xu, F.2
Rondon, A.C.3
-
153
-
-
0030062803
-
Novel approach to the ansamycin antibiotics macbecin I and herbimycin A. A formal total synthesis of (+)-macbecin I
-
Martin SF, Dodge JA, Burgess LE, Limberakis C, Hartmann M: Novel approach to the ansamycin antibiotics macbecin I and herbimycin A. A formal total synthesis of (+)-macbecin I. Tetrahedron (1996) 52(9):3229-3246.
-
(1996)
Tetrahedron
, vol.52
, Issue.9
, pp. 3229-3246
-
-
Martin, S.F.1
Dodge, J.A.2
Burgess, L.E.3
Limberakis, C.4
Hartmann, M.5
|