-
1
-
-
0029891101
-
The structure and function of proteins involved in mammalian pre-mRNA splicing
-
Kramer, A. The structure and function of proteins involved in mammalian pre-mRNA splicing Annu. Rev. Biochem. 1996, 65, 367-409
-
(1996)
Annu. Rev. Biochem.
, vol.65
, pp. 367-409
-
-
Kramer, A.1
-
2
-
-
0038670209
-
Molecular architecture of the multiprotein splicing factor SF3b
-
Golas, M. M.; Sander, B.; Will, C. L.; Luhrmann, R.; Stark, H. Molecular architecture of the multiprotein splicing factor SF3b Science 2003, 300, 980-984
-
(2003)
Science
, vol.300
, pp. 980-984
-
-
Golas, M.M.1
Sander, B.2
Will, C.L.3
Luhrmann, R.4
Stark, H.5
-
3
-
-
0032489021
-
Mechanical devices of the spliceosome: Motors, clocks, springs, and things
-
Staley, J. P.; Guthrie, C. Mechanical devices of the spliceosome: Motors, clocks, springs, and things Cell 1998, 92, 315-326
-
(1998)
Cell
, vol.92
, pp. 315-326
-
-
Staley, J.P.1
Guthrie, C.2
-
4
-
-
84868236149
-
Splicing programs and cancer
-
Germann, S.; Gratadou, L.; Dutertre, M.; Auboeuf, D. Splicing programs and cancer J. Nucleic Acids 2012, 2012, 269570-1-269570-9
-
(2012)
J. Nucleic Acids
, vol.2012
, pp. 2695701-2695709
-
-
Germann, S.1
Gratadou, L.2
Dutertre, M.3
Auboeuf, D.4
-
5
-
-
0030466895
-
New antitumor substances, FR901463, FR901464 and FR901465. II. Activities against experimental tumors in mice and mechanism of action
-
Nakajima, H.; Hori, Y.; Terano, H.; Okuhara, M.; Manda, T.; Matsumoto, S.; Shimomura, K. New antitumor substances, FR901463, FR901464 and FR901465. II. Activities against experimental tumors in mice and mechanism of action J. Antibiot. 1996, 49, 1204-1211
-
(1996)
J. Antibiot.
, vol.49
, pp. 1204-1211
-
-
Nakajima, H.1
Hori, Y.2
Terano, H.3
Okuhara, M.4
Manda, T.5
Matsumoto, S.6
Shimomura, K.7
-
6
-
-
0030461311
-
New antitumor substances, FR901463, FR901464 and FR901465. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities
-
Nakajima, H.; Sato, B.; Fujita, T.; Takase, S.; Terano, H.; Okuhara, M. New antitumor substances, FR901463, FR901464 and FR901465. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities J. Antibiot. 1996, 49, 1196-1203
-
(1996)
J. Antibiot.
, vol.49
, pp. 1196-1203
-
-
Nakajima, H.1
Sato, B.2
Fujita, T.3
Takase, S.4
Terano, H.5
Okuhara, M.6
-
7
-
-
0031054453
-
New antitumor substances, FR901463, FR901464 and FR901465. III. Structures of FR901463, FR901464 and FR901465
-
Nakajima, H.; Takase, S.; Terano, H.; Tanaka, H. New antitumor substances, FR901463, FR901464 and FR901465. III. Structures of FR901463, FR901464 and FR901465 J. Antibiot. 1997, 50, 96-99
-
(1997)
J. Antibiot.
, vol.50
, pp. 96-99
-
-
Nakajima, H.1
Takase, S.2
Terano, H.3
Tanaka, H.4
-
8
-
-
1842865013
-
Pladienolides, new substances from culture of Streptomyces platensis Mer-11107. III. in vitro and in vivo antitumor activities
-
Mizui, Y.; Sakai, T.; Iwata, M.; Uenaka, T.; Okamoto, K.; Shimizu, H.; Yamori, T.; Yoshimatsu, K.; Asada, M. Pladienolides, new substances from culture of Streptomyces platensis Mer-11107. III. In vitro and in vivo antitumor activities J. Antibiot. 2004, 57, 188-196
-
(2004)
J. Antibiot.
, vol.57
, pp. 188-196
-
-
Mizui, Y.1
Sakai, T.2
Iwata, M.3
Uenaka, T.4
Okamoto, K.5
Shimizu, H.6
Yamori, T.7
Yoshimatsu, K.8
Asada, M.9
-
9
-
-
34948868946
-
Stereochemistry of pladienolide B
-
Asai, N.; Kotake, Y.; Niijima, J.; Fukuda, Y.; Uehara, T.; Sakai, T. Stereochemistry of pladienolide B J. Antibiot. 2007, 60, 364-369
-
(2007)
J. Antibiot.
, vol.60
, pp. 364-369
-
-
Asai, N.1
Kotake, Y.2
Niijima, J.3
Fukuda, Y.4
Uehara, T.5
Sakai, T.6
-
10
-
-
34548095157
-
Spliceostatin A targets SF3b and inhibits both splicing and nuclear retention of pre-mRNA
-
Kaida, D.; Motoyoshi, H.; Tashiro, E.; Nojima, T.; Hagiwara, M.; Ishigami, K.; Watanabe, H.; Kitahara, T.; Yoshida, T.; Nakajima, H.; Tani, T.; Horinouchi, S.; Yoshida, M. Spliceostatin A targets SF3b and inhibits both splicing and nuclear retention of pre-mRNA Nat. Chem. Biol. 2007, 3, 576-583
-
(2007)
Nat. Chem. Biol.
, vol.3
, pp. 576-583
-
-
Kaida, D.1
Motoyoshi, H.2
Tashiro, E.3
Nojima, T.4
Hagiwara, M.5
Ishigami, K.6
Watanabe, H.7
Kitahara, T.8
Yoshida, T.9
Nakajima, H.10
Tani, T.11
Horinouchi, S.12
Yoshida, M.13
-
11
-
-
34548104659
-
Splicing factor SF3b as a target of the antitumor natural product pladienolide
-
Kotake, Y.; Sagane, K.; Owa, T.; Mimori-Kiyosue, Y.; Shimizu, H.; Uesugi, M.; Ishihama, Y.; Iwata, M.; Mizui, Y. Splicing factor SF3b as a target of the antitumor natural product pladienolide Nat. Chem. Biol. 2007, 3, 570-575
-
(2007)
Nat. Chem. Biol.
, vol.3
, pp. 570-575
-
-
Kotake, Y.1
Sagane, K.2
Owa, T.3
Mimori-Kiyosue, Y.4
Shimizu, H.5
Uesugi, M.6
Ishihama, Y.7
Iwata, M.8
Mizui, Y.9
-
12
-
-
79955573435
-
Identification of SAP155 as the target of GEX1A (Herboxidiene), an antitumor natural product
-
Hasegawa, M.; Miura, T.; Kuzuya, K.; Inoue, A.; Won, K. S.; Horinouchi, S.; Yoshida, T.; Kunoh, T.; Koseki, K.; Mino, K.; Sasaki, R.; Yoshida, M.; Mizukami, T. Identification of SAP155 as the target of GEX1A (Herboxidiene), an antitumor natural product ACS Chem. Biol. 2011, 6, 229-233
-
(2011)
ACS Chem. Biol.
, vol.6
, pp. 229-233
-
-
Hasegawa, M.1
Miura, T.2
Kuzuya, K.3
Inoue, A.4
Won, K.S.5
Horinouchi, S.6
Yoshida, T.7
Kunoh, T.8
Koseki, K.9
Mino, K.10
Sasaki, R.11
Yoshida, M.12
Mizukami, T.13
-
13
-
-
84876916289
-
Genomics-guided discovery of thailanstatins A, B, and C as pre-mRNA splicing inhibitors and antiproliferative agents from Burkholderia thailandensis MSMB43
-
Liu, X.; Biswas, S.; Berg, M. G.; Antapli, C. M.; Xie, F.; Wang, Q.; Tang, M. C.; Tang, G. L.; Zhang, L.; Dreyfuss, G.; Cheng, Y. Q. Genomics-guided discovery of thailanstatins A, B, and C as pre-mRNA splicing inhibitors and antiproliferative agents from Burkholderia thailandensis MSMB43 J. Nat. Prod. 2013, 76, 685-693
-
(2013)
J. Nat. Prod.
, vol.76
, pp. 685-693
-
-
Liu, X.1
Biswas, S.2
Berg, M.G.3
Antapli, C.M.4
Xie, F.5
Wang, Q.6
Tang, M.C.7
Tang, G.L.8
Zhang, L.9
Dreyfuss, G.10
Cheng, Y.Q.11
-
14
-
-
34547883872
-
A synthetic entry to pladienolide B and FD-895
-
Mandel, A. L.; Jones, B. D.; La Clair, J. J.; Burkart, M. D. A synthetic entry to pladienolide B and FD-895 Bioorg. Med. Chem. Lett. 2007, 17, 5159-5164
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 5159-5164
-
-
Mandel, A.L.1
Jones, B.D.2
La Clair, J.J.3
Burkart, M.D.4
-
15
-
-
84868347442
-
Structure of FD-895 revealed through total synthesis
-
Villa, R.; Mandel, A. L.; Jones, B. D.; La Clair, J. J.; Burkart, M. D. Structure of FD-895 revealed through total synthesis Org. Lett. 2012, 14, 5396-5399
-
(2012)
Org. Lett.
, vol.14
, pp. 5396-5399
-
-
Villa, R.1
Mandel, A.L.2
Jones, B.D.3
La Clair, J.J.4
Burkart, M.D.5
-
16
-
-
0036808433
-
GEX1 compounds, novel antitumor antibiotics related to herboxidiene, produced by Streptomyces sp. II. The effects on cell cycle progression and gene expression
-
Sakai, Y.; Tsujita, T.; Akiyama, T.; Yoshida, T.; Mizukami, T.; Akinaga, S.; Horinouchi, S.; Yoshida, M. GEX1 compounds, novel antitumor antibiotics related to herboxidiene, produced by Streptomyces sp. II. The effects on cell cycle progression and gene expression J. Antibiot. 2002, 55, 863-872
-
(2002)
J. Antibiot.
, vol.55
, pp. 863-872
-
-
Sakai, Y.1
Tsujita, T.2
Akiyama, T.3
Yoshida, T.4
Mizukami, T.5
Akinaga, S.6
Horinouchi, S.7
Yoshida, M.8
-
17
-
-
84871924824
-
The development and application of small molecule modulators of SF3b as therapeutic agents for cancer
-
Webb, T. R.; Joyner, A. S.; Potter, P. M. The development and application of small molecule modulators of SF3b as therapeutic agents for cancer Drug Discovery Today 2013, 18, 43-49
-
(2013)
Drug Discovery Today
, vol.18
, pp. 43-49
-
-
Webb, T.R.1
Joyner, A.S.2
Potter, P.M.3
-
18
-
-
7444220147
-
Aberrant and alternative splicing in cancer
-
Venables, J. P. Aberrant and alternative splicing in cancer Cancer Res. 2004, 64, 7647-7654
-
(2004)
Cancer Res.
, vol.64
, pp. 7647-7654
-
-
Venables, J.P.1
-
19
-
-
13944251747
-
Alterations of pre-mRNA splicing in cancer
-
Kalnina, Z.; Zayakin, P.; Silina, K.; Line, A. Alterations of pre-mRNA splicing in cancer Genes, Chromosomes Cancer 2005, 42, 342-357
-
(2005)
Genes, Chromosomes Cancer
, vol.42
, pp. 342-357
-
-
Kalnina, Z.1
Zayakin, P.2
Silina, K.3
Line, A.4
-
20
-
-
84868355027
-
The spliceosome as a target of novel antitumour drugs
-
Bonnal, S.; Vigevani, L.; Valcarcel, J. The spliceosome as a target of novel antitumour drugs Nat. Rev. Drug Discovery 2012, 11, 847-859
-
(2012)
Nat. Rev. Drug Discovery
, vol.11
, pp. 847-859
-
-
Bonnal, S.1
Vigevani, L.2
Valcarcel, J.3
-
21
-
-
84868148842
-
Splicing factor mutations in myelodysplasia
-
Ogawa, S. Splicing factor mutations in myelodysplasia Int. J. Hematol. 2012, 96, 438-442
-
(2012)
Int. J. Hematol.
, vol.96
, pp. 438-442
-
-
Ogawa, S.1
-
22
-
-
84865861620
-
Spliceosome and other novel mutations in chronic lymphocytic leukemia and myeloid malignancies
-
Damm, F.; Nguyen-Khac, F.; Fontenay, M.; Bernard, O. A. Spliceosome and other novel mutations in chronic lymphocytic leukemia and myeloid malignancies Leukemia 2012, 26, 2027-2031
-
(2012)
Leukemia
, vol.26
, pp. 2027-2031
-
-
Damm, F.1
Nguyen-Khac, F.2
Fontenay, M.3
Bernard, O.A.4
-
23
-
-
84865161055
-
Myeloid malignancies: Mutations, models and management
-
Murati, A.; Brecqueville, M.; Devillier, R.; Mozziconacci, M. J.; Gelsi-Boyer, V.; Birnbaum, D. Myeloid malignancies: Mutations, models and management BMC Cancer 2012, 12, 304
-
(2012)
BMC Cancer
, vol.12
, pp. 304
-
-
Murati, A.1
Brecqueville, M.2
Devillier, R.3
Mozziconacci, M.J.4
Gelsi-Boyer, V.5
Birnbaum, D.6
-
24
-
-
84873086305
-
Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma
-
Harbour, J. W.; Roberson, E. D.; Anbunathan, H.; Onken, M. D.; Worley, L. A.; Bowcock, A. M. Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma Nat. Genet. 2013, 45, 133-135
-
(2013)
Nat. Genet.
, vol.45
, pp. 133-135
-
-
Harbour, J.W.1
Roberson, E.D.2
Anbunathan, H.3
Onken, M.D.4
Worley, L.A.5
Bowcock, A.M.6
-
25
-
-
84877308573
-
Genome-wide RNAi screens in human brain tumor isolates reveal a novel viability requirement for PHF5A
-
Hubert, C. G.; Bradley, R. K.; Ding, Y.; Toledo, C. M.; Herman, J.; Skutt-Kakaria, K.; Girard, E. J.; Davison, J.; Berndt, J.; Corrin, P.; Hardcastle, J.; Basom, R.; Delrow, J. J.; Webb, T.; Pollard, S. M.; Lee, J.; Olson, J. M.; Paddison, P. J. Genome-wide RNAi screens in human brain tumor isolates reveal a novel viability requirement for PHF5A Genes Dev. 2013, 27, 1032-1045
-
(2013)
Genes Dev.
, vol.27
, pp. 1032-1045
-
-
Hubert, C.G.1
Bradley, R.K.2
Ding, Y.3
Toledo, C.M.4
Herman, J.5
Skutt-Kakaria, K.6
Girard, E.J.7
Davison, J.8
Berndt, J.9
Corrin, P.10
Hardcastle, J.11
Basom, R.12
Delrow, J.J.13
Webb, T.14
Pollard, S.M.15
Lee, J.16
Olson, J.M.17
Paddison, P.J.18
-
26
-
-
84878061031
-
Chemical perturbation of Mcl-1 pre-mRNA splicing to induce apoptosis in cancer cells
-
Gao, Y.; Koide, K. Chemical perturbation of Mcl-1 pre-mRNA splicing to induce apoptosis in cancer cells ACS Chem. Biol. 2013, 8, 895-900
-
(2013)
ACS Chem. Biol.
, vol.8
, pp. 895-900
-
-
Gao, Y.1
Koide, K.2
-
27
-
-
78651417715
-
Structural requirements for the antiproliferative activity of pre-mRNA splicing inhibitor FR901464
-
Osman, S.; Albert, B. J.; Wang, Y.; Li, M.; Czaicki, N. L.; Koide, K. Structural requirements for the antiproliferative activity of pre-mRNA splicing inhibitor FR901464 Chem.-Eur. J. 2011, 17, 895-904
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 895-904
-
-
Osman, S.1
Albert, B.J.2
Wang, Y.3
Li, M.4
Czaicki, N.L.5
Koide, K.6
-
28
-
-
0034715459
-
Convergent assembly of chiral components prepared by asymmetric catalysis
-
Thompson, C. F.; Jamison, T. F.; Jacobsen, E. N. Convergent assembly of chiral components prepared by asymmetric catalysis J. Am. Chem. Soc. 2000, 122, 10482-10483
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 10482-10483
-
-
Thompson, C.F.1
Jamison, T.F.2
Jacobsen, E.N.3
-
29
-
-
0035851340
-
A synthesis of FR901464
-
Horigome, M.; Motoyoshi, H.; Watanabe, H.; Kitahara, T. A synthesis of FR901464 Tetrahedron Lett. 2001, 42, 8207-8210
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8207-8210
-
-
Horigome, M.1
Motoyoshi, H.2
Watanabe, H.3
Kitahara, T.4
-
30
-
-
0035904404
-
FR901464: Total synthesis, proof of structure, and evaluation of synthetic analogues
-
Thompson, C. F.; Jamison, T. F.; Jacobsen, E. N. FR901464: Total synthesis, proof of structure, and evaluation of synthetic analogues J. Am. Chem. Soc. 2001, 123, 9974-9983
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 9974-9983
-
-
Thompson, C.F.1
Jamison, T.F.2
Jacobsen, E.N.3
-
31
-
-
33644959352
-
Total synthesis of FR901464, an antitumor agent that regulates the transcription of oncogenes and tumor suppressor genes
-
Albert, B. J.; Sivaramakrishnan, A.; Naka, T.; Koide, K. Total synthesis of FR901464, an antitumor agent that regulates the transcription of oncogenes and tumor suppressor genes J. Am. Chem. Soc. 2006, 128, 2792-2793
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2792-2793
-
-
Albert, B.J.1
Sivaramakrishnan, A.2
Naka, T.3
Koide, K.4
-
32
-
-
33847668813
-
Total syntheses, fragmentation studies, and antitumor/antiproliferative activities of FR901464 and its low picomolar analogue
-
Albert, B. J.; Sivaramakrishnan, A.; Naka, T.; Czaicki, N. L.; Koide, K. Total syntheses, fragmentation studies, and antitumor/antiproliferative activities of FR901464 and its low picomolar analogue J. Am. Chem. Soc. 2007, 129, 2648-2659
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 2648-2659
-
-
Albert, B.J.1
Sivaramakrishnan, A.2
Naka, T.3
Czaicki, N.L.4
Koide, K.5
-
33
-
-
53549135238
-
Antitumor compounds based on a natural product consensus pharmacophore
-
Lagisetti, C.; Pourpak, A.; Jiang, Q.; Cui, X.; Goronga, T.; Morris, S. W.; Webb, T. R. Antitumor compounds based on a natural product consensus pharmacophore J. Med. Chem. 2008, 51, 6220-6224
-
(2008)
J. Med. Chem.
, vol.51
, pp. 6220-6224
-
-
Lagisetti, C.1
Pourpak, A.2
Jiang, Q.3
Cui, X.4
Goronga, T.5
Morris, S.W.6
Webb, T.R.7
-
34
-
-
70949100953
-
Synthetic mRNA splicing modulator compounds with in vivo antitumor activity
-
Lagisetti, C.; Pourpak, A.; Goronga, T.; Jiang, Q.; Cui, X.; Hyle, J.; Lahti, J. M.; Morris, S. W.; Webb, T. R. Synthetic mRNA splicing modulator compounds with in vivo antitumor activity J. Med. Chem. 2009, 52, 6979-6990
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6979-6990
-
-
Lagisetti, C.1
Pourpak, A.2
Goronga, T.3
Jiang, Q.4
Cui, X.5
Hyle, J.6
Lahti, J.M.7
Morris, S.W.8
Webb, T.R.9
-
35
-
-
79961049732
-
Sudemycins, novel small molecule analogues of FR901464, induce alternative gene splicing
-
Fan, L.; Lagisetti, C.; Edwards, C. C.; Webb, T. R.; Potter, P. M. Sudemycins, novel small molecule analogues of FR901464, induce alternative gene splicing ACS Chem. Biol. 2011, 6, 582-589
-
(2011)
ACS Chem. Biol.
, vol.6
, pp. 582-589
-
-
Fan, L.1
Lagisetti, C.2
Edwards, C.C.3
Webb, T.R.4
Potter, P.M.5
-
36
-
-
80052376000
-
Design, synthesis and initial biological evaluation of a novel pladienolide analog scaffold
-
Gundluru, M. K.; Pourpak, A.; Cui, X.; Morris, S. W.; Webb, T. R. Design, synthesis and initial biological evaluation of a novel pladienolide analog scaffold MedChemCommun 2011, 2, 904-908
-
(2011)
MedChemCommun
, vol.2
, pp. 904-908
-
-
Gundluru, M.K.1
Pourpak, A.2
Cui, X.3
Morris, S.W.4
Webb, T.R.5
-
37
-
-
69149091031
-
Predicting outcome in melanoma: Where are we now?
-
Jennings, L.; Murphy, G. M. Predicting outcome in melanoma: where are we now? Br. J. Dermatol. 2009, 161, 496-503
-
(2009)
Br. J. Dermatol.
, vol.161
, pp. 496-503
-
-
Jennings, L.1
Murphy, G.M.2
-
38
-
-
69349091667
-
Total synthesis of (+)-sorangicin A
-
Smith, A. B., 3rd.; Dong, S.; Brenneman, J. B.; Fox, R. J. Total synthesis of (+)-sorangicin A J. Am. Chem. Soc. 2009, 131, 12109-12111
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 12109-12111
-
-
Smith III, A.B.1
Dong, S.2
Brenneman, J.B.3
Fox, R.J.4
-
39
-
-
33746857820
-
Polymethylhydrosiloxane: A versatile reducing agent for organic synthesis
-
Lawrence, N. J.; Drew, M. D.; Bushell, S. M. Polymethylhydrosiloxane: A versatile reducing agent for organic synthesis J. Chem. Soc., Perkin Trans. 1 1999, 0, 3381-3391
-
(1999)
J. Chem. Soc., Perkin Trans. 1
, vol.0
, pp. 3381-3391
-
-
Lawrence, N.J.1
Drew, M.D.2
Bushell, S.M.3
-
40
-
-
34848850746
-
An efficient, inexpensive, and shelf-stable diazotransfer reagent: Imidazole-1-sulfonyl azide hydrochloride
-
Goddard-Borger, E. D.; Stick, R. V. An efficient, inexpensive, and shelf-stable diazotransfer reagent: Imidazole-1-sulfonyl azide hydrochloride Org. Lett. 2007, 9, 3797-3800
-
(2007)
Org. Lett.
, vol.9
, pp. 3797-3800
-
-
Goddard-Borger, E.D.1
Stick, R.V.2
-
41
-
-
84874029122
-
A safe and facile route to imidazole-1-sulfonyl azide as a diazotransfer reagent
-
Ye, H.; Liu, R.; Li, D.; Liu, Y.; Yuan, H.; Guo, W.; Zhou, L.; Cao, X.; Tian, H.; Shen, J.; Wang, P. G. A safe and facile route to imidazole-1-sulfonyl azide as a diazotransfer reagent Org. Lett. 2012, 15, 18-21
-
(2012)
Org. Lett.
, vol.15
, pp. 18-21
-
-
Ye, H.1
Liu, R.2
Li, D.3
Liu, Y.4
Yuan, H.5
Guo, W.6
Zhou, L.7
Cao, X.8
Tian, H.9
Shen, J.10
Wang, P.G.11
-
42
-
-
67650488269
-
Synergistic drug combinations tend to improve therapeutically relevant selectivity
-
Lehar, J.; Krueger, A. S.; Avery, W.; Heilbut, A. M.; Johansen, L. M.; Price, E. R.; Rickles, R. J.; Short, G. F., 3rd.; Staunton, J. E.; Jin, X.; Lee, M. S.; Zimmermann, G. R.; Borisy, A. A. Synergistic drug combinations tend to improve therapeutically relevant selectivity Nat. Biotechnol. 2009, 27, 659-666
-
(2009)
Nat. Biotechnol.
, vol.27
, pp. 659-666
-
-
Lehar, J.1
Krueger, A.S.2
Avery, W.3
Heilbut, A.M.4
Johansen, L.M.5
Price, E.R.6
Rickles, R.J.7
-
43
-
-
51049109033
-
Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity
-
Maira, S. M.; Stauffer, F.; Brueggen, J.; Furet, P.; Schnell, C.; Fritsch, C.; Brachmann, S.; Chene, P.; De Pover, A.; Schoemaker, K.; Fabbro, D.; Gabriel, D.; Simonen, M.; Murphy, L.; Finan, P.; Sellers, W.; Garcia-Echeverria, C. Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity Mol. Cancer Ther. 2008, 7, 1851-1863
-
(2008)
Mol. Cancer Ther.
, vol.7
, pp. 1851-1863
-
-
Maira, S.M.1
Stauffer, F.2
Brueggen, J.3
Furet, P.4
Schnell, C.5
Fritsch, C.6
Brachmann, S.7
Chene, P.8
De Pover, A.9
Schoemaker, K.10
Fabbro, D.11
Gabriel, D.12
Simonen, M.13
Murphy, L.14
Finan, P.15
Sellers, W.16
Garcia-Echeverria, C.17
-
44
-
-
43049131769
-
Targeting the PI3K/Akt/mTOR pathway: Effective combinations and clinical considerations
-
LoPiccolo, J.; Blumenthal, G. M.; Bernstein, W. B.; Dennis, P. A. Targeting the PI3K/Akt/mTOR pathway: Effective combinations and clinical considerations Drug Resist. Updates 2008, 11, 32-50
-
(2008)
Drug Resist. Updates
, vol.11
, pp. 32-50
-
-
Lopiccolo, J.1
Blumenthal, G.M.2
Bernstein, W.B.3
Dennis, P.A.4
-
45
-
-
68849131434
-
Sorafenib has soluble epoxide hydrolase inhibitory activity, which contributes to its effect profile in vivo
-
Liu, J. Y.; Park, S. H.; Morisseau, C.; Hwang, S. H.; Hammock, B. D.; Weiss, R. H. Sorafenib has soluble epoxide hydrolase inhibitory activity, which contributes to its effect profile in vivo Mol. Cancer Ther. 2009, 8, 2193-2203
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 2193-2203
-
-
Liu, J.Y.1
Park, S.H.2
Morisseau, C.3
Hwang, S.H.4
Hammock, B.D.5
Weiss, R.H.6
-
46
-
-
64249112966
-
Mammalian epoxide hydrolases in xenobiotic metabolism and signalling
-
Decker, M.; Arand, M.; Cronin, A. Mammalian epoxide hydrolases in xenobiotic metabolism and signalling Arch. Toxicol. 2009, 83, 297-318
-
(2009)
Arch. Toxicol.
, vol.83
, pp. 297-318
-
-
Decker, M.1
Arand, M.2
Cronin, A.3
-
47
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
-
Chou, T. C.; Talalay, P. Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors Adv. Enzyme Regul. 1984, 22, 27-55
-
(1984)
Adv. Enzyme Regul.
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
48
-
-
84875463958
-
The role of human carboxylesterases in drug metabolism: Have we overlooked their importance?
-
Laizure, S. C.; Herring, V.; Hu, Z.; Witbrodt, K.; Parker, R. B. The role of human carboxylesterases in drug metabolism: Have we overlooked their importance? Pharmacotherapy 2013, 33, 210-222
-
(2013)
Pharmacotherapy
, vol.33
, pp. 210-222
-
-
Laizure, S.C.1
Herring, V.2
Hu, Z.3
Witbrodt, K.4
Parker, R.B.5
-
49
-
-
84857213761
-
Sensitivities of some imidazole-1-sulfonyl azide salts
-
Fischer, N.; Goddard-Borger, E. D.; Greiner, R.; Klapötke, T. M.; Skelton, B. W.; Stierstorfer, J. Sensitivities of some imidazole-1-sulfonyl azide salts J. Org. Chem. 2012, 77, 1760-1764
-
(2012)
J. Org. Chem.
, vol.77
, pp. 1760
-
-
Fischer, N.1
Goddard-Borger, E.D.2
Greiner, R.3
Klapötke, T.M.4
Skelton, B.W.5
Stierstorfer, J.6
|