-
1
-
-
84855855321
-
The HDAC inhibitor depsipeptide transactivates the p53/p21 pathway by inducing DNA damage
-
Wang, H.; Zhou, W.; Zheng, Z.; Zhang, P.; Tu, B.; He, Q.; Zhu, W.-G. The HDAC inhibitor depsipeptide transactivates the p53/p21 pathway by inducing DNA damage. DNA. Repair, 2012, 11(2), 146-156.
-
(2012)
DNA. Repair
, vol.11
, Issue.2
, pp. 146-156
-
-
Wang, H.1
Zhou, W.2
Zheng, Z.3
Zhang, P.4
Tu, B.5
He, Q.6
Zhu, W.-G.7
-
2
-
-
79955678223
-
Developing histone deacetylase inhibitors as anti-cancer therapeutics
-
Venugopal, B.; Evans, T.R.J. Developing histone deacetylase inhibitors as anti-cancer therapeutics. Curr. Med. Chem., 2011, 18, 1658-1671.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 1658-1671
-
-
Venugopal, B.1
Evans, T.R.J.2
-
3
-
-
0034610814
-
The language of covalent histone modifications
-
DOI 10.1038/47412
-
Strahl, B.D.; Allis, C.D. The language of covalent histone modifications. Nature, 2000, 403, 41-45. (Pubitemid 30038513)
-
(2000)
Nature
, vol.403
, Issue.6765
, pp. 41-45
-
-
Strahl, B.D.1
Allis, C.D.2
-
4
-
-
0035313803
-
Histone acetyltransferases: Function, structure, and catalysis
-
DOI 10.1016/S0959-437X(00)00173-8
-
Marmorstein, R.; Roth, S.Y. Histone acetyltransferases: Function, structure, and catalysis. Curr. Opin. Genet. Dev., 2001, 11, 155-161. (Pubitemid 32209199)
-
(2001)
Current Opinion in Genetics and Development
, vol.11
, Issue.2
, pp. 155-161
-
-
Marmorstein, R.1
Roth, S.Y.2
-
5
-
-
57749170458
-
The many roles of histone deacetylases in development and physiology: Implications for disease and therapy
-
Haberland, M.; Montgomery, R.L.; Olson, E.N. The many roles of histone deacetylases in development and physiology: Implications for disease and therapy. Nat. Rev. Genet., 2009, 10, 32-42.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 32-42
-
-
Haberland, M.1
Montgomery, R.L.2
Olson, E.N.3
-
6
-
-
53749087120
-
Histone deacetylase inhibitors: Mechanism of action and therapeutic use in cancer
-
Martinez-Iglesias, O.; Ruiz-Llorente, L.; Sanchez-Martinez, R.; Garcia, L.; Zambrano, A.; Aranda, A. Histone deacetylase inhibitors: Mechanism of action and therapeutic use in cancer. Clin. Transl. Oncol., 2008, 10, 395-398.
-
(2008)
Clin. Transl. Oncol.
, vol.10
, pp. 395-398
-
-
Martinez-Iglesias, O.1
Ruiz-Llorente, L.2
Sanchez-Martinez, R.3
Garcia, L.4
Zambrano, A.5
Aranda, A.6
-
7
-
-
67650090545
-
Histone deacetylase inhibitors: Potential in cancer therapy
-
Marks, P.A.; Xu, W.S. Histone deacetylase inhibitors: Potential in cancer therapy. J. Cell. Biochem., 2009, 107, 600-608.
-
(2009)
J. Cell. Biochem.
, vol.107
, pp. 600-608
-
-
Marks, P.A.1
Xu, W.S.2
-
8
-
-
77955646151
-
Macrocyclic histone deacetylase inhibitors
-
Mwakwari, S.C.; Patil, V.; Guerrant, W.; Oyelere, A.K. Macrocyclic histone deacetylase inhibitors. Curr. Top. Med. Chem., 2010, 10, 1423-1440.
-
(2010)
Curr. Top. Med. Chem.
, vol.10
, pp. 1423-1440
-
-
Mwakwari, S.C.1
Patil, V.2
Guerrant, W.3
Oyelere, A.K.4
-
9
-
-
77955643796
-
The clinical development of histone deacetylase inhibitors as targeted anticancer drugs
-
Marks, P.A. The clinical development of histone deacetylase inhibitors as targeted anticancer drugs. Expert. Opin. Investig. Drugs, 2010, 19, 1049-1066.
-
(2010)
Expert. Opin. Investig. Drugs
, vol.19
, pp. 1049-1066
-
-
Marks, P.A.1
-
10
-
-
27644556419
-
Inhibitors of histone deacetylases target the Rb-E2F1 pathway for apoptosis induction through activation of proapoptotic protein Bim
-
DOI 10.1073/pnas.0505585102
-
Zhao, Y.; Tan, J.; Zhuang, L.; Jiang, X.; Liu, E.T.; Yu, Q. Inhibitors of histone deacetylases target the Rb-E2F1 pathway for apoptosis induction through activation of proapoptotic protein Bim. Proc. Natl. Acad. Sci. USA, 2005, 102, 16090-16095. (Pubitemid 41552872)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.44
, pp. 16090-16095
-
-
Zhao, Y.1
Tan, J.2
Zhuang, L.3
Jiang, X.4
Liu, E.T.5
Yu, Q.6
-
11
-
-
58149310725
-
Histone deacetylase inhibitors and genomic instability
-
Eot-Houllier, G.; Fulcrand, G.; Magnaghi-Jaulin, L.; Jaulin, C. Histone deacetylase inhibitors and genomic instability. Cancer. Lett, 2009, 274, 169-176.
-
(2009)
Cancer. Lett
, vol.274
, pp. 169-176
-
-
Eot-Houllier, G.1
Fulcrand, G.2
Magnaghi-Jaulin, L.3
Jaulin, C.4
-
12
-
-
37649015347
-
HDAC inhibitor PCI-24781 decreases RAD51 expression and inhibits homologous recombination
-
Adimoolam, S.; Sirisawad, M.; Chen, J.; Thiemann, P.; Ford, J.M.; Buggy, J.J. HDAC inhibitor PCI-24781 decreases RAD51 expression and inhibits homologous recombination. Proc. Natl. Acad. Sci. USA, 2007, 104, 19482-19487.
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 19482-19487
-
-
Adimoolam, S.1
Sirisawad, M.2
Chen, J.3
Thiemann, P.4
Ford, J.M.5
Buggy, J.J.6
-
13
-
-
34548564426
-
Attenuated DNA damage repair by trichostatin a through BRCA1 suppression
-
DOI 10.1667/RR0811.1
-
Zhang, Y.; Carr, T.; Dimtchev, A.; Zaer, N.; Dritschilo, A.; Jung, M. Attenuated DNA damage repair by trichostatin A through BRCA1 suppression. Radiat. Res, 2007, 168, 115-124. (Pubitemid 351292932)
-
(2007)
Radiation Research
, vol.168
, Issue.1
, pp. 115-124
-
-
Zhang, Y.1
Carr, T.2
Dimtchev, A.3
Zaer, N.4
Dritschilo, A.5
Jung, M.6
-
14
-
-
0037472924
-
DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation
-
DOI 10.1038/nature01368
-
Bakkenist, C.J.; Kastan, M.B. DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation. Nature, 2003, 421, 499-506. (Pubitemid 36168436)
-
(2003)
Nature
, vol.421
, Issue.6922
, pp. 499-506
-
-
Bakkenist, C.J.1
Kastan, M.B.2
-
15
-
-
79958695612
-
Vorinostat induces reactive oxygen species and DNA damage in acute myeloid leukemia cells
-
Petruccelli, L.A.; Dupere-Richer, D.; Pettersson, F.; Retrouvey, H.; Skoulikas, S.; Miller Jr, W.H. Vorinostat induces reactive oxygen species and DNA damage in acute myeloid leukemia cells. PLoS. One 2011, 6, e20987.
-
(2011)
PLoS. One
, vol.6
-
-
Petruccelli, L.A.1
Dupere-Richer, D.2
Pettersson, F.3
Retrouvey, H.4
Skoulikas, S.5
Miller Jr., W.H.6
-
16
-
-
77951241720
-
Histone deacetylase inhibitors activate NF-kappaB in human leukemia cells through an ATM/NEMO-related pathway
-
Rosato, R.R.; Kolla, S.S.; Hock, S.K.; Almenara, J.A.; Patel, A.; Amin, S.; Atadja, P.; Fisher, P.B.; Dent, P.; Grant, S. Histone deacetylase inhibitors activate NF-kappaB in human leukemia cells through an ATM/NEMO-related pathway. J. Biol. Chem, 2010, 285, 10064-10077.
-
(2010)
J. Biol. Chem
, vol.285
, pp. 10064-10077
-
-
Rosato, R.R.1
Kolla, S.S.2
Hock, S.K.3
Almenara, J.A.4
Patel, A.5
Amin, S.6
Atadja, P.7
Fisher, P.B.8
Dent, P.9
Grant, S.10
-
17
-
-
66249124267
-
PCI-24781 induces caspase and reactive oxygen species-dependent apoptosis through NF-kappaB mechanisms and is synergistic with bortezomib in lymphoma cells
-
Bhalla, S.; Balasubramanian, S.; David, K.; Sirisawad, M.; Buggy, J.; Mauro, L.; Prachand, S.; Miller, R.; Gordon, L.I.; Evens, A.M. PCI-24781 induces caspase and reactive oxygen species-dependent apoptosis through NF-kappaB mechanisms and is synergistic with bortezomib in lymphoma cells. Clin. Cancer. Res, 2009, 15, 3354-3365.
-
(2009)
Clin. Cancer. Res
, vol.15
, pp. 3354-3365
-
-
Bhalla, S.1
Balasubramanian, S.2
David, K.3
Sirisawad, M.4
Buggy, J.5
Mauro, L.6
Prachand, S.7
Miller, R.8
Gordon, L.I.9
Evens, A.M.10
-
18
-
-
39849093997
-
Histone deacetylase inhibitors induce mitotic slippage
-
DOI 10.1038/sj.onc.1210779, PII 1210779
-
Stevens, F.E.; Beamish, H.; Warrener, R.; Gabrielli, B. Histone deacetylase inhibitors induce mitotic slippage. Oncogene, 2008, 27, 1345-1354. (Pubitemid 351317466)
-
(2008)
Oncogene
, vol.27
, Issue.10
, pp. 1345-1354
-
-
Stevens, F.E.1
Beamish, H.2
Warrener, R.3
Gabrielli, B.4
-
19
-
-
33748706179
-
A novel histone deacetylase pathway regulates mitosis by modulating Aurora B kinase activity
-
DOI 10.1101/gad.1455006
-
Li, Y.; Kao, G.D.; Garcia, B.A.; Shabanowitz, J.; Hunt, D.F.; Qin, J.; Phelan, C.; Lazar M.A. A novel histone deacetylase pathway regulates mitosis by modulating Aurora B kinase activity. Genes. Dev, 2006, 20, 2566-2579. (Pubitemid 44396841)
-
(2006)
Genes and Development
, vol.20
, Issue.18
, pp. 2566-2579
-
-
Li, Y.1
Kao, G.D.2
Garcia, B.A.3
Shabanowitz, J.4
Hunt, D.F.5
Qin, J.6
Phelan, C.7
Lazar, M.A.8
-
20
-
-
43249095919
-
Tumor angiogenesis
-
DOI 10.1056/NEJMra0706596
-
Kerbel, R.S. Tumor angiogenesis. N. Engl. J. Med, 2008, 358, 2039-2049. (Pubitemid 351656458)
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.19
, pp. 2039-2049
-
-
Kerbel, R.S.1
-
21
-
-
34247850849
-
Regulation of the HIF-1alpha stability by histone deacetylases
-
Kim, S.H.; Jeong, J.W.; Park, J.A.; Lee, J.W.; Seo, J.H.; Jung, B.K.; Bae, M.K.; Kim, K.W. Regulation of the HIF-1alpha stability by histone deacetylases. Oncol. Rep, 2007, 17, 647-651.
-
(2007)
Oncol. Rep
, vol.17
, pp. 647-651
-
-
Kim, S.H.1
Jeong, J.W.2
Park, J.A.3
Lee, J.W.4
Seo, J.H.5
Jung, B.K.6
Bae, M.K.7
Kim, K.W.8
-
22
-
-
78651352243
-
Histone deacetylase inhibitors: Potential targets responsible for their anti-cancer effect
-
Dickinson, M.; Johnstone, R.W.; Prince, H.M. Histone deacetylase inhibitors: Potential targets responsible for their anti-cancer effect. Invest. New. Drugs, 2010, 28, Suppl 1: S3-20.
-
(2010)
Invest. New. Drugs
, vol.28
, Issue.SUPPL. 1
-
-
Dickinson, M.1
Johnstone, R.W.2
Prince, H.M.3
-
23
-
-
79959804516
-
Histone deacetylases as regulators of inflammation and immunity
-
Shakespear, M.R.; Halili, M.A.; Irvine, K.M.; Fairlie, D.P.; Sweet, M.J. Histone deacetylases as regulators of inflammation and immunity. Trends. Immunol, 2011, 32,. 335-343.
-
(2011)
Trends. Immunol
, vol.32
, pp. 335-343
-
-
Shakespear, M.R.1
Halili, M.A.2
Irvine, K.M.3
Fairlie, D.P.4
Sweet, M.J.5
-
24
-
-
79959344464
-
Autophagic and apoptotic effects of HDAC inhibitors on cancer cells
-
Rikiishi, H. Autophagic and apoptotic effects of HDAC inhibitors on cancer cells. J. Biomed. Biotechnol, 2011, 2011, 830260.
-
(2011)
J. Biomed. Biotechnol
, vol.2011
, pp. 830260
-
-
Rikiishi, H.1
-
25
-
-
33750284176
-
Autophagy in cancer: Good, bad, or both?
-
Hippert, M.M.; O'Toole, P.S.; Thorburn, A. Autophagy in cancer: Good, bad, or both? Cancer. Res, 2006, 66, 9349-9351.
-
(2006)
Cancer. Res
, vol.66
, pp. 9349-9351
-
-
Hippert, M.M.1
O'Toole, P.S.2
Thorburn, A.3
-
26
-
-
0345166111
-
Beclin 1, an autophagy gene essential for early embryonic development, is a haploinsufficient tumor suppressor
-
DOI 10.1073/pnas.2436255100
-
Yue, Z.; Jin, S.; Yang, C.; Levine, A.J.; Heintz, N. Beclin 1, an autophagy gene essential for early embryonic development, is a haploinsufficient tumor suppressor. Proc. Natl. Acad. Sci. USA, 2003, 100, 15077-15082. (Pubitemid 37518019)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.25
, pp. 15077-15082
-
-
Yue, Z.1
Jin, S.2
Yang, C.3
Levine, A.J.4
Heintz, N.5
-
27
-
-
0035967169
-
Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death
-
DOI 10.1038/35069004
-
Joza, N.; Susin, S.A.; Daugas, E.; Stanford, W.L.; Cho, S.K.; Li, C.Y.J.; Sasaki, T.; Elia, A.J.; Mary Cheng, H.Y.; Ravagnan, L.; Ferri, K.F.; Zamzami, N.; Wakeham, A.; Hakem, R.; Yoshida, H.; Kong, Y.Y.; Mak, T.W.; Zuniga-Pflucker, J.C.; Kroemer, G.; Penninger, J.M. Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death. Nature, 2001, 410, 549-554. (Pubitemid 32267191)
-
(2001)
Nature
, vol.410
, Issue.6828
, pp. 549-554
-
-
Joza, N.1
Susin, S.A.2
Daugas, E.3
Stanford, W.L.4
Cho, S.K.5
Li, C.Y.J.6
Sasaki, T.7
Elia, A.J.8
Cheng, H.-Y.M.9
Ravagnan, L.10
Ferri, K.F.11
Zamzami, N.12
Wakeham, A.13
Hakem, R.14
Yoshida, H.15
Kong, Y.-Y.16
Mak, T.W.17
Zuniga-Pflucker, J.C.18
Kroemer, G.19
Penninger, J.M.20
more..
-
28
-
-
33644812102
-
Caspase family proteases and apoptosis
-
DOI 10.1111/j.1745-7270.2005.00108.x
-
Fan, T.J.; Han, L.H.; Cong, R.S.; Liang, J. Caspase family proteases and apoptosis. Acta. Biochim. Biophys. Sin, 2005, 37, 719-727. (Pubitemid 44890981)
-
(2005)
Acta Biochimica et Biophysica Sinica
, vol.37
, Issue.11
, pp. 719-727
-
-
Fan, T.-J.1
Han, L.-H.2
Cong, R.-S.3
Liang, J.4
-
29
-
-
26444560960
-
Caspase: Pharmacological manipulation of cell death
-
DOI 10.1172/JCI26252
-
Lavrik, I.N.; Golks, A.; Krammer, P.H. Caspases: Pharmacological manipulation of cell death. J. Clin. Invest., 2005, 115, 2665-2672. (Pubitemid 41434390)
-
(2005)
Journal of Clinical Investigation
, vol.115
, Issue.10
, pp. 2665-2672
-
-
Lavrik, I.N.1
Golks, A.2
Krammer, P.H.3
-
30
-
-
0036716281
-
The BCL2 family: Regulators of the cellular life-or-death switch
-
DOI 10.1038/nrc883
-
Cory, S.; Adams, J.M. The Bcl2 family: Regulators of the cellular life-or-death switch. Nature. Rev. Cancer,. 2002, 2, 647-656. (Pubitemid 37328916)
-
(2002)
Nature Reviews Cancer
, vol.2
, Issue.9
, pp. 647-656
-
-
Cory, S.1
Adams, J.M.2
-
31
-
-
0032575714
-
Death receptors: Signaling and modulation
-
Ashkenazi, A.; Dixit, V.M. Death receptors: Signaling and modulation. Science, 1998, 281, 1305-1308. (Pubitemid 28406815)
-
(1998)
Science
, vol.281
, Issue.5381
, pp. 1305-1308
-
-
Ashkenazi, A.1
Dixit, V.M.2
-
32
-
-
0037276437
-
The CD95(APO-1/Fas) DISC and beyond
-
DOI 10.1038/sj.cdd.4401186
-
Peter, M.E.; Krammer, P.H. The CD95(APO-1/Fas) DISC and beyond. Cell. Death. Differ, 2003, 10, 26-35. (Pubitemid 36511830)
-
(2003)
Cell Death and Differentiation
, vol.10
, Issue.1
, pp. 26-35
-
-
Peter, M.E.1
Krammer, P.H.2
-
33
-
-
0041853690
-
Induction of TNF receptor I-mediated apoptosis via two sequential signaling complexes
-
DOI 10.1016/S0092-8674(03)00521-X
-
Micheau, O.; Tschopp, J. Induction of TNF receptor I-mediated apoptosis via two sequential signaling complexes. Cell, 2003, 114, 181-190. (Pubitemid 36936912)
-
(2003)
Cell
, vol.114
, Issue.2
, pp. 181-190
-
-
Micheau, O.1
Tschopp, J.2
-
34
-
-
1342285692
-
Tumor Necrosis Factor: An Apoptosis JuNKie?
-
DOI 10.1016/S0092-8674(04)00166-7
-
Varfolomeev, E.E.; Ashkenazi, A. Tumor necrosis factor: An apoptosis JuNKie?. Cell,. 2004, 116, 491-497. (Pubitemid 38264427)
-
(2004)
Cell
, vol.116
, Issue.4
, pp. 491-497
-
-
Varfolomeev, E.E.1
Ashkenazi, A.2
-
35
-
-
21444446872
-
Selective knockdown of the long variant of cellular FLICE inhibitory protein augments death receptor-mediated caspase-8 activation and apoptosis
-
DOI 10.1074/jbc.M413962200
-
Sharp, D.A.; Lawrence, D.A.; Ashkenazi, A. Selective knockdown of the long variant of cellular FLICE inhibitory protein augments death receptor-mediated caspase-8 activation and apoptosis. J. Biol. Chem., 2005, 280, 19401-19409. (Pubitemid 41379648)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.19
, pp. 19401-19409
-
-
Sharp, D.A.1
Lawrence, D.A.2
Ashkenazi, A.3
-
36
-
-
0035496099
-
Regulation of lymphocyte proliferation and death by flip
-
Thome, M.; Tschopp, J. Regulation of lymphocyte proliferation and death by FLIP. Nature. Rev. Immunol., 2001, 1, 50-58. (Pubitemid 33741975)
-
(2001)
Nature Reviews Immunology
, vol.1
, Issue.1
, pp. 50-58
-
-
Thome, M.1
Tschopp, J.2
-
37
-
-
0035156737
-
Insights into cancer therapeutic design based on p53 and TRAIL receptor signaling
-
DOI 10.1038/sj.cdd.4400943
-
El-Deiry, W.S. Insights into cancer therapeutic design based on p53 and TRAIL receptor signaling. Cell. Death. Differ., 2001, 8, 1066-1075. (Pubitemid 33061824)
-
(2001)
Cell Death and Differentiation
, vol.8
, Issue.11
, pp. 1066-1075
-
-
El-Deiry, W.S.1
-
38
-
-
0033981577
-
Bid induces the oligomerization and insertion of Bax into the outer mitochondrial membrane
-
DOI 10.1128/MCB.20.3.929-935.2000
-
Eskes, R.; Desagher, S.; Antonsson, B.; Martinou, J.C. Bid induces the oligomerization and insertion of Bax into the outer mitochondrial membrane. Mol. Cell. Biol., 2000, 20, 929-935. (Pubitemid 30044230)
-
(2000)
Molecular and Cellular Biology
, vol.20
, Issue.3
, pp. 929-935
-
-
Eskes, R.1
Desagher, S.2
Antonsson, B.3
Martinou, J.-C.4
-
39
-
-
0034663829
-
TBID, a membrane-targeted death ligand, oligomerizes BAK to release cytochrome c
-
Wei, M.C.; Lindsten, T.; Mootha, V.K.; Weiler, S.; Gross, A.; Ashiya, M.; Thompson, C.B.; Korsmeyer, S.J. tBID, a membranetargeted death ligand, oligomerizes BAK to release cytochrome-c. Genes. Dev., 2000, 14, 2060-2071. (Pubitemid 30637355)
-
(2000)
Genes and Development
, vol.14
, Issue.16
, pp. 2060-2071
-
-
Wei, M.C.1
Lindsten, T.2
Mootha, V.K.3
Weiler, S.4
Gross, A.5
Ashiya, M.6
Thompson, C.B.7
Korsmeyer, S.J.8
-
40
-
-
0034616946
-
Apoptotic pathways: Paper wraps stone blunts scissors
-
Green, D.R. Apoptotic pathways: Paper wraps stone blunts scissors. Cell, 2000, 102, 1-4.
-
(2000)
Cell
, vol.102
, pp. 1-4
-
-
Green, D.R.1
-
41
-
-
82255165408
-
Targeting of Bcl-2 family proteins for treatment of acute leukaemia
-
Spec No: S3-S12
-
Jurecekova, J.; Hatok, J.; Stefanikova, A.; Dobrota, D.; Racay, P. Targeting of Bcl-2 family proteins for treatment of acute leukaemia. Gen. Physiol. Biophys., 2011, 30, Spec No: S3-S12.
-
(2011)
Gen. Physiol. Biophys.
, vol.30
-
-
Jurecekova, J.1
Hatok, J.2
Stefanikova, A.3
Dobrota, D.4
Racay, P.5
-
42
-
-
78650048538
-
Bcl-2 inhibits apoptosis by increasing the time-to-death and intrinsic cell-to-cell variations in the mitochondrial pathway of cell death
-
Skommer, J.; Brittain, T.; Raychaudhuri, S. Bcl-2 inhibits apoptosis by increasing the time-to-death and intrinsic cell-to-cell variations in the mitochondrial pathway of cell death. Apoptosis, 2010, 15, 1223-1233.
-
(2010)
Apoptosis
, vol.15
, pp. 1223-1233
-
-
Skommer, J.1
Brittain, T.2
Raychaudhuri, S.3
-
43
-
-
33750619845
-
How do Bax and Bak lead to permeabilization of the outer mitochondrial membrane?
-
DOI 10.1016/j.ceb.2006.10.004, PII S0955067406001578
-
Antignani, A.; Youle, R.J. How do Bax and Bak lead to permeabilization of the outer mitochondrial membrane?. Curr. Opin. Cell. Biol., 2006, 18, 685-689. (Pubitemid 44692478)
-
(2006)
Current Opinion in Cell Biology
, vol.18
, Issue.6
, pp. 685-689
-
-
Antignani, A.1
Youle, R.J.2
-
44
-
-
80051995190
-
Fas-mediated neutrophil apoptosis is accelerated by Bid, Bak, and Bax and inhibited by Bcl-2 and Mcl-1
-
Croker, B.A.; O'Donnell, J.A.; Nowell, C.J.; Metcalf, D.; Dewson, G.; Campbell, K.J.; Rogers, K.L.; Hu, Y.; Smyth, G.K.; Zhang, J.G.; White, M.; Lackovic, K.; Cengia, L.H.; O'Reilly, L.A.; Bouillet, P.; Cory, S.; Strasser, A.; Roberts, A.W. Fas-mediated neutrophil apoptosis is accelerated by Bid, Bak, and Bax and inhibited by Bcl-2 and Mcl-1. Proc. Natl. Acad. Sci. U. S. A., 2011, 108, 13135-13140.
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 13135-13140
-
-
Croker, B.A.1
O'Donnell, J.A.2
Nowell, C.J.3
Metcalf, D.4
Dewson, G.5
Campbell, K.J.6
Rogers, K.L.7
Hu, Y.8
Smyth, G.K.9
Zhang, J.G.10
White, M.11
Lackovic, K.12
Cengia, L.H.13
O'Reilly, L.A.14
Bouillet, P.15
Cory, S.16
Strasser, A.17
Roberts, A.W.18
-
45
-
-
0033107657
-
The apoptosome: Heart and soul of the cell death machine
-
Chinnaiyan, A.M. The apoptosome: Heart and soul of the cell death machine. Neoplasia, 1999, 1, 5-15.
-
(1999)
Neoplasia
, vol.1
, pp. 5-15
-
-
Chinnaiyan, A.M.1
-
46
-
-
0036792475
-
The role of mitochondrial factors in apoptosis: A Russian roulette with more than one bullet
-
Van Loo, G.; Saelens, X.; Van Gurp, M.; MacFarlane, M.; Martin, S.J.; Vandenabeele, P. The role of mitochondrial factors in apoptosis: A Russian roulette with more than one bullet. Cell. Death. Differ., 2002, 9, 1031-1042.
-
(2002)
Cell. Death. Differ.
, vol.9
, pp. 1031-1042
-
-
Van Loo, G.1
Saelens, X.2
Van Gurp, M.3
MacFarlane, M.4
Martin, S.J.5
Vandenabeele, P.6
-
47
-
-
0036674617
-
Live or let die: The cell's response to p53
-
DOI 10.1038/nrc864
-
Vousden, K.H.; Lu, X. Live or let die: The cell's response to p53. Nature. Rev. Cancer, 2002, 2, 594-604. (Pubitemid 37328926)
-
(2002)
Nature Reviews Cancer
, vol.2
, Issue.8
, pp. 594-604
-
-
Vousden, K.H.1
Lu, X.2
-
48
-
-
0037291871
-
A unified model for apical caspase activation
-
DOI 10.1016/S1097-2765(03)00051-0
-
Boatright, K.M.; Renatus, M.; Scott, F.L.; Sperandio, S.; Shin, H.; Pedersen, I.M.; Ricci, J.E.; Edris, W.A.; Sutherlin, D.P.; Green, D.R.; Salvesen, G.S. A unified model for apical caspase activation. Mol. Cell, 2003, 11, 529-541. (Pubitemid 36293843)
-
(2003)
Molecular Cell
, vol.11
, Issue.2
, pp. 529-541
-
-
Boatright, K.M.1
Renatus, M.2
Scott, F.L.3
Sperandio, S.4
Shin, H.5
Pedersen, I.M.6
Ricci, J.-E.7
Edris, W.A.8
Sutherlin, D.P.9
Green, D.R.10
Salvesen, G.S.11
-
49
-
-
0034630317
-
Apoptotic DNA fragmentation
-
Nagata, S. Apoptotic DNA fragmentation. Exp. Cell. Res., 2006, 256, 12-18.
-
(2006)
Exp. Cell. Res.
, vol.256
, pp. 12-18
-
-
Nagata, S.1
-
50
-
-
33645116726
-
Chemoenzymatic and templatedirected synthesis of bioactive macrocyclic peptides
-
Gruenewald, J.; Marahiel, M.A. Chemoenzymatic and templatedirected synthesis of bioactive macrocyclic peptides. Microbiol. Mol. Biol. Rev., 2006, 70(1), 121-146.
-
(2006)
Microbiol. Mol. Biol. Rev.
, vol.70
, Issue.1
, pp. 121-146
-
-
Gruenewald, J.1
Marahiel, M.A.2
-
51
-
-
0036735385
-
FK228 (depsipeptide) as a natural prodrug that inhibits class I histone deacetylases
-
Furumai, R.; Matsuyama, A.; Kobashi, N.; Lee, K.H.; Nishiyama, M.; Nakajima, H.; Tanaka, A.; Komatsu, Y.; Nishino, N.; Yoshida, M.; Horinouchi, S. FK228 (Depsipeptide) as a natural prodrug that inhibits class I histone deacetylases. Cancer. Res., 2002, 62, 4916-4921. (Pubitemid 34984414)
-
(2002)
Cancer Research
, vol.62
, Issue.17
, pp. 4916-4921
-
-
Furumai, R.1
Matsuyama, A.2
Kobashi, N.3
Lee, K.-H.4
Nishiyama, M.5
Nakajima, H.6
Tanaka, A.7
Komatsu, Y.8
Nishino, N.9
Yoshida, M.10
Horinouchi, S.11
-
52
-
-
36148975704
-
The first biologically active synthetic analogues of FK228, the depsipeptide histone deacetylase inhibitor
-
DOI 10.1021/jm0703800
-
Yurek-George, A.; Cecil, A.R.; Mo, A.H.; Wen, S.; Rogers, H.; Habens, F.; Maeda, S.; Yoshida, M.; Packham, G.; Ganesan, A. The first biologically active synthetic analogues of FK228, the depsipeptide histone deacetylase inhibitor. J. Med. Chem., 2007, 50, 5720-5726. (Pubitemid 350106026)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.23
, pp. 5720-5726
-
-
Yurek-George, A.1
Cecil, A.R.L.2
Mo, A.H.K.3
Wen, S.4
Rogers, H.5
Habens, F.6
Maeda, S.7
Yoshida, M.8
Packham, G.9
Ganesan, A.10
-
53
-
-
0033566643
-
Depsipeptide (FR901228): A novel therapeutic agent with selective, in vitro activity against human B-cell chronic lymphocytic leukemia cells
-
Byrd, J.C.; Shinn, C.; Ravi, R.; Willis, C.R.; Waselenko, J.K.; Flinn, I.W.; Dawson, N.A.; Grever, M.R. Depsipep tide (FR901228): A novel therapeutic agent with selective, in. vitro activity against human B-cell chronic lymphocytic leukemia cells. Blood, 1999, 94, 1401-1408. (Pubitemid 29380421)
-
(1999)
Blood
, vol.94
, Issue.4
, pp. 1401-1408
-
-
Byrd, J.C.1
Shinn, C.2
Ravi, R.3
Willis, C.R.4
Waselenko, J.K.5
Flinn, I.W.6
Dawson, N.A.7
Grever, M.R.8
-
54
-
-
2942535832
-
T-cell lymphoma as a model for the use of histone deacetylase inhibitors in cancer therapy: Impact of depsipeptide on molecular markers, therapeutic targets, and mechanisms of resistance
-
DOI 10.1182/blood-2003-09-3068
-
Piekarz, R.L.; Robey, R.W.; Zhan, Z.; Kayastha, G.; Sayah, A.; Abdeldaim, A.H.; Torrico, S.; Bates, S.E. T-cell lymphoma as a model for the use of histone deacetylase inhibitors in cancer therapy: Impact of depsipeptide on molecular markers, therapeutic targets, and mechanisms of resistance. Blood,. 2004, 103, 4636-4643. (Pubitemid 38745996)
-
(2004)
Blood
, vol.103
, Issue.12
, pp. 4636-4643
-
-
Piekarz, R.L.1
Robey, R.W.2
Zhan, Z.3
Kayastha, G.4
Sayah, A.5
Abdeldaim, A.H.6
Torrico, S.7
Bates, S.E.8
-
55
-
-
19944432566
-
A phase 1 and pharmacodynamic study of depsipeptide (FK228) in chronic lymphocytic leukemia and acute myeloid leukemia
-
DOI 10.1182/blood-2004-05-1693
-
Byrd, J.C.; Marcucci, G.; Parthun, M.R.; Xiao, J.J.; Klisovic, R.B.; Moran, M.; Lin, T.S.; Liu, S.; Sklenar, A.R.; Davis, M.E.; Lucas, D.M.; Fischer, B.; Shank, R.; Tejaswi, S.L.; Binkley, P.; Wright, J.; Chan, K.K; Grever, M.R. A phase 1 and pharmacodynamic study of depsipeptide (FK228) in chronic lymphocytic leukemia and acute myeloid leukemia. Blood, 2005, 105, 959-967. (Pubitemid 40170861)
-
(2005)
Blood
, vol.105
, Issue.3
, pp. 959-967
-
-
Byrd, J.C.1
Marcucci, G.2
Parthun, M.R.3
Xiao, J.J.4
Klisovic, R.B.5
Moran, M.6
Lin, T.S.7
Liu, S.8
Sklenar, A.R.9
Davis, M.E.10
Lucas, D.M.11
Fischer, B.12
Shank, R.13
Tejaswi, S.L.14
Binkley, P.15
Wright, J.16
Chan, K.K.17
Grever, M.R.18
-
56
-
-
73949149251
-
Phase II multi-institutional trial of the histone deacetylase inhibitor romidepsin as monotherapy for patients with cutaneous T-cell lymphoma
-
Piekarz, R.L.; Frye, R.; Turner, M.; Wright, J.J.; Allen, S.L.; Kirschbaum, M.H.; Zain, J.; Prince, H.M.; Leonard, J.P.; Geskin, L.J.; Reeder, C.; Joske, D.; Figg, W.D.; Gardner, E.R.; Steinberg, S.M.; Jaffe, E.S.; Stetler-Stevenson, M.; Lade, S.; Fojo, A.T.; Bates, S.E. Phase II multi-institutional trial of the histone deacetylase inhibitor romidepsin as monotherapy for patients with cutaneous T-cell lymphoma. J. Clin. Oncol., 2009, 27, 5410-5417.
-
(2009)
J. Clin. Oncol.
, vol.27
, pp. 5410-5417
-
-
Piekarz, R.L.1
Frye, R.2
Turner, M.3
Wright, J.J.4
Allen, S.L.5
Kirschbaum, M.H.6
Zain, J.7
Prince, H.M.8
Leonard, J.P.9
Geskin, L.J.10
Reeder, C.11
Joske, D.12
Figg, W.D.13
Gardner, E.R.14
Steinberg, S.M.15
Jaffe, E.S.16
Stetler-Stevenson, M.17
Lade, S.18
Fojo, A.T.19
Bates, S.E.20
more..
-
57
-
-
77958185126
-
Phase II study of the histone deacetylase inhibitor Romidepsin in relapsed small cell lung cancer (Cancer and Leukemia Group B 30304
-
Otterson, G.A.; Hodgson, L.; Pang, H.; Vokes, E.E. Phase II study of the histone deacetylase inhibitor Romidepsin in relapsed small cell lung cancer (Cancer and Leukemia Group B 30304). J. Thorac. Oncol., 2010, 5, 1644-1648.
-
(2010)
J. Thorac. Oncol.
, vol.5
, pp. 1644-1648
-
-
Otterson, G.A.1
Hodgson, L.2
Pang, H.3
Vokes, E.E.4
-
58
-
-
0242660847
-
Total Synthesis of the Depsipeptide FR-901375
-
DOI 10.1021/jo034765b
-
Chen, Y.; Gambs, C.; Abe, Y.; Wentworth, P.Jr.; Janda, K.D. Total synthesis of the depsipeptide FR-901375. J. Org. Chem., 2003, 68, 8902-8905. (Pubitemid 37409537)
-
(2003)
Journal of Organic Chemistry
, vol.68
, Issue.23
, pp. 8902-8905
-
-
Chen, Y.1
Gambs, C.2
Abe, Y.3
Wentworth Jr., P.4
Janda, K.D.5
-
59
-
-
39749098365
-
Improved total synthesis of the potent HDAC inhibitor FK228 (FR-901228
-
Greshock, T.J.; Johns, D.M.; Noguchi, Y.; Williams, R.M. Improved total synthesis of the potent HDAC inhibitor FK228 (FR-901228). Org. Lett., 2008, 10(4), 613-616.
-
(2008)
Org. Lett.
, vol.10
, Issue.4
, pp. 613-616
-
-
Greshock, T.J.1
Johns, D.M.2
Noguchi, Y.3
Williams, R.M.4
-
60
-
-
79851478834
-
Histone deacetylase inhibitors as a tool to up-regulate new fungal biosynthetic products -isolation of EGM-556, a cyclodepsipeptide, from Microascus. sp
-
Vervoort, H.C.; Draskovic, M.; Crews, P. Histone deacetylase inhibitors as a tool to up-regulate new fungal biosynthetic products -isolation of EGM-556, a cyclodepsipeptide, from Microascus. sp. Org. Lett., 2011, 13, 410-413.
-
(2011)
Org. Lett.
, vol.13
, pp. 410-413
-
-
Vervoort, H.C.1
Draskovic, M.2
Crews, P.3
-
61
-
-
67749124307
-
Synthesis and conformation-activity relationships of the peptide isosteres of FK228 and Largazole
-
Bowers, A.A.; Greshock, T.J.; West, N.; Estiu, G.; Schreiber, S.L.; Wiest, O.; Williams, R.M.; Bradner, J.E. Synthesis and conformation-activity relationships of the peptide isosteres of FK228 and Largazole. J. Am. Chem. Soc., 2009, 131, 2900-2905.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2900-2905
-
-
Bowers, A.A.1
Greshock, T.J.2
West, N.3
Estiu, G.4
Schreiber, S.L.5
Wiest, O.6
Williams, R.M.7
Bradner, J.E.8
-
62
-
-
46049100010
-
Total synthesis and molecular target of largazole, a histone deacetylase inhibitor
-
DOI 10.1021/ja8013727
-
Ying, Y.; Taori, K.; Kim, H.; Hong, J.; Luesch, H. Total synthesis and molecular target of largazole, a histone deacetylase inhibitor. J. Am. Chem. Soc., 2008, 130, 8455-8459. (Pubitemid 351898566)
-
(2008)
Journal of the American Chemical Society
, vol.130
, Issue.26
, pp. 8455-8459
-
-
Ying, Y.1
Taori, K.2
Kim, H.3
Hong, J.4
Luesch, H.5
-
63
-
-
79959603291
-
Synthetic routes and biological evaluation of largazole and its analogues as potent histone deacetylase inhibitors
-
Li, S.; Yao, H.; Xu, J.; Jiang, S. Synthetic routes and biological evaluation of largazole and its analogues as potent histone deacetylase inhibitors. Molecules, 2011, 16(6), 4681-4694.
-
(2011)
Molecules
, vol.16
, Issue.6
, pp. 4681-4694
-
-
Li, S.1
Yao, H.2
Xu, J.3
Jiang, S.4
-
64
-
-
64049106355
-
Synthesis and histone deacetylase inhibitory activity of largazole analogs: Alteration of the zinc-binding domain and macrocyclic scaffold
-
Bowers, A.A.; West, N.; Newkirk, T.L.; Troutman-Youngman, A.E.; Schreiber, S.L.; Wiest, O.; Bradner, J.E.; Williams, R.M. Synthesis and histone deacetylase inhibitory activity of largazole analogs: Alteration of the zinc-binding domain and macrocyclic scaffold. Org. Lett., 2009, 11(6), 1301-1304.
-
(2009)
Org. Lett.
, vol.11
, Issue.6
, pp. 1301-1304
-
-
Bowers, A.A.1
West, N.2
Newkirk, T.L.3
Troutman-Youngman, A.E.4
Schreiber, S.L.5
Wiest, O.6
Bradner, J.E.7
Williams, R.M.8
-
65
-
-
80455162618
-
Largazole and analogues with modified metal-binding motifs targeting histone deacetylases: Synthesis and biological evaluation
-
Bhansali, P.; Hanigan, C.L.; Casero Jr., R.A.; Tillekeratne, L.M.V. Largazole and analogues with modified metal-binding motifs targeting histone deacetylases: Synthesis and biological evaluation. J. Med. Chem., 2011, 54(21), 7453-7463.
-
(2011)
J. Med. Chem.
, vol.54
, Issue.21
, pp. 7453-7463
-
-
Bhansali, P.1
Hanigan, C.L.2
Casero Jr., R.A.3
Tillekeratne, L.M.V.4
-
66
-
-
50249144006
-
Total synthesis and biological mode of action of largazole: A potent class I histone deacetylase inhibitor
-
Bowers, A.; West, N.; Taunton, J.; Schreiber, S.L.; Bradner, J.E.; Williams, R.M. Total synthesis and biological mode of action of largazole: A potent class I histone deacetylase inhibitor. J. Am. Chem. Soc., 2008, 130, 11219-11222.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 11219-11222
-
-
Bowers, A.1
West, N.2
Taunton, J.3
Schreiber, S.L.4
Bradner, J.E.5
Williams, R.M.6
-
67
-
-
55949094932
-
Synthesis and activity of largazole analogues with linker and macrocycle modification
-
Ying, Y.; Liu, Y.; Byeon, S.R.; Kim, H.; Luesch, H.; Hong, J. Synthesis and activity of largazole analogues with linker and macrocycle modification. Org. Lett., 2008, 10(18), 4021-4024.
-
(2008)
Org. Lett.
, vol.10
, Issue.18
, pp. 4021-4024
-
-
Ying, Y.1
Liu, Y.2
Byeon, S.R.3
Kim, H.4
Luesch, H.5
Hong, J.6
-
68
-
-
79951632653
-
Total syntheses of the histone deacetylase inhibitors largazole and 2-epi-largazole: Application of N-heterocyclic carbene mediated acylations in complex molecule synthesis
-
Wang, B.; Huang, P.H.; Chen, C.S.; Forsyth, C.J. Total syntheses of the histone deacetylase inhibitors largazole and 2-epi-largazole: Application of N-heterocyclic carbene mediated acylations in complex molecule synthesis. J. Org. Chem., 2011, 76, 1140-1150.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 1140-1150
-
-
Wang, B.1
Huang, P.H.2
Chen, C.S.3
Forsyth, C.J.4
-
69
-
-
80051599485
-
Structural basis of the antiproliferative activity of largazole, a depsipeptide inhibitor of the histone deacetylases
-
Cole, K.E.; Dowling, D.P.; Boone, M.A.; Phillips, A.J.; Christianson, D.W. Structural basis of the antiproliferative activity of largazole, a depsipeptide inhibitor of the histone deacetylases. J. Am. Chem. Soc., 2011, 133, 12474-12477.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 12474-12477
-
-
Cole, K.E.1
Dowling, D.P.2
Boone, M.A.3
Phillips, A.J.4
Christianson, D.W.5
-
70
-
-
84861157767
-
Largazole: From discovery to broadspectrum therapy
-
Hong, J.; Luesch, H. Largazole: From discovery to broadspectrum therapy. Nat. Prod. Rep., 2012, 29(4), 449-456.
-
(2012)
Nat. Prod. Rep.
, vol.29
, Issue.4
, pp. 449-456
-
-
Hong, J.1
Luesch, H.2
-
71
-
-
78149267515
-
Anticolon cancer activity of largazole, a marine-derived tunable histone deacetylase inhibitor
-
Liu, Y.; Salvador, L.A.; Byeon, S.; Ying, Y.; Kwan, J.C.; Law, B.K.; Hong, J.; Luesch, H. Anticolon cancer activity of largazole, a marine-derived tunable histone deacetylase inhibitor. The. J. Pharmacol. Exp. Ther., 2010, 335(2), 351-361.
-
(2010)
The. J. Pharmacol. Exp. Ther.
, vol.335
, Issue.2
, pp. 351-361
-
-
Liu, Y.1
Salvador, L.A.2
Byeon, S.3
Ying, Y.4
Kwan, J.C.5
Law, B.K.6
Hong, J.7
Luesch, H.8
-
72
-
-
34147096292
-
Functions of cyclin D1 as an oncogene and regulation of cyclin D1 expression
-
DOI 10.1111/j.1349-7006.2007.00449.x
-
Tashiro, E.; Tsuchiya, A.; Imoto, M. Functions of cyclin D1 as an oncogene and regulation of cyclin D1 expression. Cancer. Sci,. 2007, 98, 629-635. (Pubitemid 46563437)
-
(2007)
Cancer Science
, vol.98
, Issue.5
, pp. 629-635
-
-
Tashiro, E.1
Tsuchiya, A.2
Imoto, M.3
-
73
-
-
70349554391
-
Combinatorial strategies by marine cyanobacteria: Symplostatin 4, an antimitotic natural dolastatin 10/15 hybrid that synergizes with the coproduced HDAC inhibitor largazole
-
Taori, K.; Liu, Y.; Paul, V.J.; Luesch, H. Combinatorial strategies by marine cyanobacteria: Symplostatin 4, an antimitotic natural dolastatin 10/15 hybrid that synergizes with the coproduced HDAC inhibitor largazole. Chembiochem., 2009, 10(10), 1634-1639.
-
(2009)
Chembiochem.
, vol.10
, Issue.10
, pp. 1634-1639
-
-
Taori, K.1
Liu, Y.2
Paul, V.J.3
Luesch, H.4
-
74
-
-
79958264627
-
Total synthesis of largazole and analogues: HDAC inhibition, antiproliferative activity and metabolic stability
-
Benelkebir, H.; Marie, S.; Hayden, A.L.; Lyle, J.; Loadman, P.M.; Crabb, S.J.; Packham, G.; Ganesan, A. Total synthesis of largazole and analogues: HDAC inhibition, antiproliferative activity and metabolic stability. Bioorg. Med. Chem., 2011, 19, 3650-3658.
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 3650-3658
-
-
Benelkebir, H.1
Marie, S.2
Hayden, A.L.3
Lyle, J.4
Loadman, P.M.5
Crabb, S.J.6
Packham, G.7
Ganesan, A.8
-
75
-
-
0035180541
-
Spiruchostatins A and B, novel gene expression-enhancing substances produced by Pseudomonas sp
-
DOI 10.1016/S0040-4039(00)01874-8, PII S0040403900018748
-
Masuoka, Y.; Nagai, A.; Shin-ya, K.; Furihata, K.; Nagai, K.; Suzuki, K.; Hayakawa, Y.; Seto, H. Spiruchostatins A and B, novel gene expression-enhancing substances produced by Pseudomonas. sp. Tetrahedron. Lett., 2001, 42(1), 41-44. (Pubitemid 32011701)
-
(2001)
Tetrahedron Letters
, vol.42
, Issue.1
, pp. 41-44
-
-
Masuoka, Y.1
Nagai, A.2
Shin-ya, K.3
Furihata, K.4
Nagai, K.5
Suzuki, K.-I.6
Hayakawa, Y.7
Seto, H.8
-
76
-
-
0942265466
-
Total Synthesis of Spiruchostatin A, a Potent Histone Deacetylase Inhibitor
-
DOI 10.1021/ja039258q
-
Yurek-George, A.; Habens, F.; Brimmell, M.; Packham, G.; Ganesan, A. Total synthesis of spiruchostatin A, a potent histone deacetylase inhibitor. J. Am. Chem. Soc., 2004, 126, 1030-1031. (Pubitemid 38140727)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.4
, pp. 1030-1031
-
-
Yurek-George, A.1
Habens, F.2
Brimmell, M.3
Packham, G.4
Ganesan, A.5
-
77
-
-
84860529331
-
Spiruchostatin A inhibits proliferation and differentiation of fibroblasts from patients with pulmonary fibrosis
-
Davies, E.R.; Haitchi, H.M.; Thatcher, T.H.; Sime, P.J.; Kottmann, R.M.; Ganesan, A.; Packham, G.; O'Reilly, K.M.; Davies, D.E. Spiruchostatin A inhibits proliferation and differentiation of fibroblasts from patients with pulmonary fibrosis. Am. J. Respir. Cell. Mol. Biol., 2012, 46(5), 687-694.
-
(2012)
Am. J. Respir. Cell. Mol. Biol.
, vol.46
, Issue.5
, pp. 687-694
-
-
Davies, E.R.1
Haitchi, H.M.2
Thatcher, T.H.3
Sime, P.J.4
Kottmann, R.M.5
Ganesan, A.6
Packham, G.7
O'Reilly, K.M.8
Davies, D.E.9
-
78
-
-
48149089435
-
Characterisation of the in. vitro activity of the depsipeptide histone deacetylase inhibitor spiruchostatin A
-
Crabb, S.J.; Howell, M.; Rogers, H.; Ishfaq, M.; Yurek-George, A.; Carey, K.; Pickering, B.M.; East, P.; Mitter, R.; Maeda, S.; Johnson, P.W.M.; Townsend, P.; Shin-ya, K.; Yoshida, M.; Ganesan, A.; Packham, G. Characterisation of the in. vitro activity of the depsipeptide histone deacetylase inhibitor spiruchostatin A. Biochem. Pharmacol., 2008, 76, 463-475.
-
(2008)
Biochem. Pharmacol.
, vol.76
, pp. 463-475
-
-
Crabb, S.J.1
Howell, M.2
Rogers, H.3
Ishfaq, M.4
Yurek-George, A.5
Carey, K.6
Pickering, B.M.7
East, P.8
Mitter, R.9
Maeda, S.10
Johnson, P.W.M.11
Townsend, P.12
Shin-ya, K.13
Yoshida, M.14
Ganesan, A.15
Packham, G.16
-
79
-
-
0035577768
-
The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells
-
Munster, P.N.; Troso-Sandoval, T.; Rosen, N.; Rifkind, R.; Marks, P.A.; Richon, V.M. The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells. Cancer. Res., 2001, 61, 8492-8497. (Pubitemid 33131130)
-
(2001)
Cancer Research
, vol.61
, Issue.23
, pp. 8492-8497
-
-
Munster, P.N.1
Troso-Sandoval, T.2
Rosen, N.3
Rifkind, R.4
Marks, P.A.5
Richon, V.M.6
-
80
-
-
84860314336
-
Involvement of p21waf1/cip1 expression in the cytotoxicity of the potent histone deacetylase inhibitor spiruchostatin B towards susceptible NALM-6 human B cell leukemia cells
-
Kanno, S.-I.; Maeda, N.; Tomizawa, A.; Yomogida, S.; Katoh, T.; Ishikawa, M. Involvement of p21waf1/cip1 expression in the cytotoxicity of the potent histone deacetylase inhibitor spiruchostatin B towards susceptible NALM-6 human B cell leukemia cells. Int. J. Oncol., 2012, 40, 1391-1396.
-
(2012)
Int. J. Oncol.
, vol.40
, pp. 1391-1396
-
-
Kanno, S.-I.1
Maeda, N.2
Tomizawa, A.3
Yomogida, S.4
Katoh, T.5
Ishikawa, M.6
-
81
-
-
65249112206
-
A solid-phase total synthesis of the cyclic depsipeptide HDAC inhibitor spiruchostatin A
-
Lijima, Y.; Munakata, A.; Shinya, K.; Ganesan, A.; Doi, T.; Takahashi, T. A solid-phase total synthesis of the cyclic depsipeptide HDAC inhibitor spiruchostatin A. Tetrahedron. Lett., 2009, 50, 2970-2972.
-
(2009)
Tetrahedron. Lett.
, vol.50
, pp. 2970-2972
-
-
Lijima, Y.1
Munakata, A.2
Shinya, K.3
Ganesan, A.4
Doi, T.5
Takahashi, T.6
-
82
-
-
65549147694
-
Total synthesis of spiruchostatin A via chemoselective macrocyclization using an accessible enantiomerically pure latent thioester
-
Calandra, N.A.; Cheng, Y.L.; Kocak, K.A.; Miller, J.S. Total synthesis of spiruchostatin A via chemoselective macrocyclization using an accessible enantiomerically pure latent thioester. Org. Lett., 2009, 11(9), 1971-1974.
-
(2009)
Org. Lett.
, vol.11
, Issue.9
, pp. 1971-1974
-
-
Calandra, N.A.1
Cheng, Y.L.2
Kocak, K.A.3
Miller, J.S.4
-
83
-
-
79955447251
-
Total synthesis of spiruchostatin B aided by an automated synthesizer
-
Fuse, S.; Okada, K.; Iijima, Y.; Munakata, A.; Machida, K.; Takahashi, T.; Takagi, M.; Shin-yad, K.; Doi, T. Total synthesis of spiruchostatin B aided by an automated synthesizer. Org. Biomol. Chem., 2011, 9, 3825-3833.
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 3825-3833
-
-
Fuse, S.1
Okada, K.2
Iijima, Y.3
Munakata, A.4
Machida, K.5
Takahashi, T.6
Takagi, M.7
Shin-yad, K.8
Doi, T.9
-
84
-
-
70350507928
-
Total synthesis of the bicyclic depsipeptide HDAC inhibitors spiruchostatins A and B, 5''-epi-spiruchostatin B, FK228 (FR901228) and preliminary evaluation of their biological activity
-
Narita, K.; Kikuchi, T.; Watanabe, K.; Takizawa, T.; Oguchi, T.; Kudo, K.; Matsuhara, K.; Abe, H.; Yamori, T.; Yoshida, M.; Katoh, T. Total synthesis of the bicyclic depsipeptide HDAC inhibitors spiruchostatins A and B, 5''-epi-spiruchostatin B, FK228 (FR901228) and preliminary evaluation of their biological activity. Chemistry, 2009, 15(42), 11174-11186.
-
(2009)
Chemistry
, vol.15
, Issue.42
, pp. 11174-11186
-
-
Narita, K.1
Kikuchi, T.2
Watanabe, K.3
Takizawa, T.4
Oguchi, T.5
Kudo, K.6
Matsuhara, K.7
Abe, H.8
Yamori, T.9
Yoshida, M.10
Katoh, T.11
-
85
-
-
80055086046
-
Histone deacetylase inhibitors from Burkholderia. thailandensis
-
Klausmeyer, P.; Shipley, S.M.; Zuck, K.M.; McCloud, T.G. Histone deacetylase inhibitors from Burkholderia. thailandensis. J. Nat. Prod., 2011, 74, 2039-2044.
-
(2011)
J. Nat. Prod.
, vol.74
, pp. 2039-2044
-
-
Klausmeyer, P.1
Shipley, S.M.2
Zuck, K.M.3
McCloud, T.G.4
-
86
-
-
80055098514
-
Thailandepsins: Bacterial products with potent histone deacetylase inhibitory activities and broadspectrum antiproliferative activities
-
Wang, C.; Henkes, L.M.; Doughty, L.B.; He, M.; Wang, D.; Meyer-Almes, F.-J.; Cheng, Y.-Q. Thailandepsins: Bacterial products with potent histone deacetylase inhibitory activities and broadspectrum antiproliferative activities. J. Nat. Prod., 2011, 74, 2031-2038.
-
(2011)
J. Nat. Prod.
, vol.74
, pp. 2031-2038
-
-
Wang, C.1
Henkes, L.M.2
Doughty, L.B.3
He, M.4
Wang, D.5
Meyer-Almes, F.-J.6
Cheng, Y.-Q.7
-
87
-
-
79952593656
-
Acyldepsipeptide HDAC inhibitor production induced in Burkholderia. thailandensis
-
Biggins, J.B.; Gleber, C.D.; Brady, S.F. Acyldepsipeptide HDAC inhibitor production induced in Burkholderia. thailandensis. Org. Lett.,. 2011, 13(6), 1536-1539.
-
(2011)
Org. Lett.,.
, vol.13
, Issue.6
, pp. 1536-1539
-
-
Biggins, J.B.1
Gleber, C.D.2
Brady, S.F.3
-
88
-
-
84055178563
-
Total synthesis and stereochemical assignment of burkholdac B, a depsipeptide HDAC inhibitor
-
Benelkebir, H.; Donlevy, A.M.; Packham, G.; Ganesan, A. Total synthesis and stereochemical assignment of burkholdac B, a depsipeptide HDAC inhibitor. Org. Lett.,. 2011, 13(24), 6334-6337.
-
(2011)
Org. Lett.,.
, vol.13
, Issue.24
, pp. 6334-6337
-
-
Benelkebir, H.1
Donlevy, A.M.2
Packham, G.3
Ganesan, A.4
-
89
-
-
0035024737
-
Histone deacetylase: A target for antiproliferative and antiprotozoal agents
-
Meinke, P.T.; Liberator, P. Histone deacetylase: A target for antiproliferative and antiprotozoal agents. Curr. Med. Chem., 2001, 8(2), 211-235. (Pubitemid 32416448)
-
(2001)
Current Medicinal Chemistry
, vol.8
, Issue.2
, pp. 211-235
-
-
Meinke, P.T.1
Liberator, P.2
-
90
-
-
0023946967
-
Conformationally constrained biologically active peptides: Tentative identification of the antimitogenic bioactive conformer of the naturally occurring cyclic tetrapeptides
-
DOI 10.1016/S0040-4020(01)86109-3
-
Shute, R.E.; Kawai, M.; Rich, D.H. Conformationally constrained biologically active peptides: Tentative identification of the antimi togenic bioactive confomer of the naturally occurring cyclic tetrapeptides. Tetrahedron, 1988, 44(3), 685-695. (Pubitemid 18051776)
-
(1988)
Tetrahedron
, vol.44
, Issue.3
, pp. 685-695
-
-
Shute, R.E.1
Kawai, M.2
Rich, D.H.3
-
91
-
-
70349956393
-
Probing the bioactive conformation of an archetypal natural product HDAC inhibitor with conformationally homogeneous triazole-modified cyclic tetrapeptides
-
Horne, W.S.; Olsen, C.A.; Beierle, J.M.; Montero, A.; Ghadiri, M.R. Probing the bioactive conformation of an archetypal natural product HDAC inhibitor with conformationally homogeneous triazole-modified cyclic tetrapeptides. Angew. Chem. Int. Ed. Engl., 2009, 48, 4718-4724.
-
(2009)
Angew. Chem. Int. Ed. Engl.
, vol.48
, pp. 4718-4724
-
-
Horne, W.S.1
Olsen, C.A.2
Beierle, J.M.3
Montero, A.4
Ghadiri, M.R.5
-
92
-
-
84862800182
-
Synthesis, evaluation and molecular modeling of cyclic tetrapeptide histone deacetylase inhibitors as anticancer agents
-
Huang, D.; Li, X.; Sun, L.; Xiu, Z.; Nishino, N. Synthesis, evaluation and molecular modeling of cyclic tetrapeptide histone deacetylase inhibitors as anticancer agents. J. Pept. Sci., 2012, 18(4), 242-251.
-
(2012)
J. Pept. Sci.
, vol.18
, Issue.4
, pp. 242-251
-
-
Huang, D.1
Li, X.2
Sun, L.3
Xiu, Z.4
Nishino, N.5
-
93
-
-
57349171593
-
N-Methylation of peptides: A new perspective in medicinal chemistry
-
Chatterjee, J.; Gilon, C.; Hoffman, A.; Kessler, H. N-Methylation of peptides: A new perspective in medicinal chemistry. Acc. Chem. Res.,. 2008, 41(10), 1331-1342.
-
(2008)
Acc. Chem. Res.,.
, vol.41
, Issue.10
, pp. 1331-1342
-
-
Chatterjee, J.1
Gilon, C.2
Hoffman, A.3
Kessler, H.4
-
94
-
-
20944452022
-
Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide scaffolds
-
DOI 10.1021/jm050009h
-
Tamamura, H.; Araki, T.; Ueda, S.; Wang, Z.; Oishi, S.; Esaka, A.; Trent, J.O.; Nakashima, H.; Yamamoto, N.; Peiper, S.C.; Otaka, A.; Fujii, N. Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide scaffolds. J. Med. Chem., 2005, 48, 3280-3289. (Pubitemid 40628048)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.9
, pp. 3280-3289
-
-
Tamamura, H.1
Araki, T.2
Ueda, S.3
Wang, Z.4
Oishi, S.5
Esaka, A.6
Trent, J.O.7
Nakashima, H.8
Yamamoto, N.9
Peiper, S.C.10
Otaka, A.11
Fujii, N.12
-
95
-
-
0037460144
-
Conformationally homogeneous cyclic tetrapeptides: Useful new three-dimensional scaffolds
-
DOI 10.1021/ja029205t
-
Glenn, M.P.; Kelso, M.J.; Tyndall, J.D.A.; Fairlie, D.P. Conformationally homogeneous cyclic tetrapeptides: Useful new threedimensional scaffolds. J. Am. Chem. Soc., 2003, 125(3), 640-641. (Pubitemid 36109919)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.3
, pp. 640-641
-
-
Glenn, M.P.1
Kelso, M.J.2
Tyndall, J.D.A.3
Fairlie, D.P.4
-
96
-
-
33750430831
-
2-amino acids in the design of conformationally homogeneous cyclo-peptide scaffolds
-
DOI 10.1021/jo060854n
-
Norgren, A.S.; Buettner, F.; Prabpai, S.; Kongsaeree, P.; Arvidsson, P.I. Beta2-amino acids in the design of conformationally homogeneous cyclo-peptide scaffolds. J. Org. Chem., 2006, 71(18), 6814-6821. (Pubitemid 44645656)
-
(2006)
Journal of Organic Chemistry
, vol.71
, Issue.18
, pp. 6814-6821
-
-
Norgren, A.S.1
Buttner, F.2
Prabpai, S.3
Kongsaeree, P.4
Arvidsson, P.I.5
-
97
-
-
0030569401
-
Apicidins: Novel cyclic tetrapeptides as coccidiostats and antimalarial agents from Fusarium pallidoroseum
-
DOI 10.1016/0040-4039(96)01844-8, PII S0040403996018448
-
Singh, S.B.; Zink, D.L.; Polishook, J.D.; Dombrowski, A.W.; Darkin-Rattray, S.J.; Schmatz, D.M.; Goetz, M.A. Apicidins: Novel cyclic tetrapeptides as coccidiostats and antimalarial agents from Fusarium. pallidoroseum. Tetrahedron. Lett., 1996, 37, 8077-8080. (Pubitemid 26366232)
-
(1996)
Tetrahedron Letters
, vol.37
, Issue.45
, pp. 8077-8080
-
-
Singh, S.B.1
Zink, D.L.2
Polishook, J.D.3
Dombrowski, A.W.4
Darkin-Rattray, S.J.5
Schmatz, D.M.6
Goetz, M.A.7
-
98
-
-
10544250252
-
Apicidin: A novel antiprotozoal agent that inhibits parasite histone deacetylase
-
DOI 10.1073/pnas.93.23.13143
-
Darkin-Rattray, S.J.; Gurnett, A.M.; Myers, R.W.; Dulski, P.M.; Crumley, T.M.; Allocco, J.J.; Cannova, C.; Meinke, P.T.; Colletti, S.L.; Bednarik, M.A.; Singh, S.B.; Goetz, M.A.; Dombrowski, A.W.; Polishook, J.D.; Schmatz, D.M. Apicidin: A novel antiprotozoal agent that inhibits parasite histone deacetylase. Proc. Natl. Acad. Sci. U.S.A., 1996, 93, 13143-13147. (Pubitemid 26382783)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.23
, pp. 13143-13147
-
-
Darkin-Rattray, S.J.1
Gurnett, A.M.2
Myers, R.W.3
Dulski, P.M.4
Crumley, T.M.5
Allocco, J.J.6
Cannova, C.7
Meinke, P.T.8
Colletti, S.L.9
Bednarek, M.A.10
Singh, S.B.11
Goetz, M.A.12
Dombrowski, A.W.13
Polishook, J.D.14
Schmatz, D.M.15
-
99
-
-
33847796188
-
Apicidin a novel histone deacetylase inhibitor, has profound anti-growth activity in human endometrial and ovarian cancer cells
-
Ueda, T.; Takai, N.; Nishida, M.; Nasu, K.; Narahara, H. Apicidin, a novel histone deacetylase inhibitor, has profound anti-growth activity in human endometrial and ovarian cancer cells. Int. J. Mol. Med., 2007, 19, 301-308.
-
(2007)
Int. J. Mol. Med.
, vol.19
, pp. 301-308
-
-
Ueda, T.1
Takai, N.2
Nishida, M.3
Nasu, K.4
Narahara, H.5
-
100
-
-
0034326799
-
Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin
-
Han, J.W.; Ahn, S.H.; Park, S.H.; Wang, S.Y.; Bae, G.-U.; Seo, D.-W.; Kwon, H.-K.; Hong, S.; Lee, H.Y.; Lee, Y.W.; Lee, H.-W. Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin. Cancer. Res., 2000, 60, 6068-6074.
-
(2000)
Cancer. Res.
, vol.60
, pp. 6068-6074
-
-
Han, J.W.1
Ahn, S.H.2
Park, S.H.3
Wang, S.Y.4
Bae, G.-U.5
Seo, D.-W.6
Kwon, H.-K.7
Hong, S.8
Lee, H.Y.9
Lee, Y.W.10
Lee, H.-W.11
-
101
-
-
0142157097
-
Induction of Apoptosis by Apicidin, a Histone Deacetylase Inhibitor, via the Activation of Mitochondria-Dependent Caspase Cascades in Human Bcr-Abl-Positive Leukemia Cells
-
Cheong, J.-W.; Chong, S.Y.; Kim, J.Y.; Eom, J.I.; Jeung, H.K.; Maeng, H.Y.; Lee, S.T.; Min, Y.H. Induction of apoptosis by apicidin, a histone deacetylase inhibitor, via the activation of mitochondria-dependent caspase cascades in human Bcr-Abl-positive leukemia cells. Clin. Cancer. Res., 2003, 9, 5018-5027. (Pubitemid 37323309)
-
(2003)
Clinical Cancer Research
, vol.9
, Issue.13
, pp. 5018-5027
-
-
Cheong, J.-W.1
Chong, S.Y.2
Kim, J.Y.3
Eom, J.I.4
Jeung, H.K.5
Maeng, H.Y.6
Lee, S.T.7
Min, Y.H.8
-
102
-
-
1642580501
-
Apicidin potentiates the imatinibinduced apoptosis of Bcr-Abl-positive human leukaemia cells by enhancing the activation of mitochondria-dependent caspase cascades
-
Kim, J.S.; Jeung, H.K.; Cheong, J.-W.; Maeng, H.; Lee, S.T.; Hahn, J.S.; Ko, Y.W.; Min, Y.H. Apicidin potentiates the imatinibinduced apoptosis of Bcr-Abl-positive human leukaemia cells by enhancing the activation of mitochondria-dependent caspase cascades. British. J. Haematol., 2003, 124, 166-178.
-
(2003)
British. J. Haematol.
, vol.124
, pp. 166-178
-
-
Kim, J.S.1
Jeung, H.K.2
Cheong, J.-W.3
Maeng, H.4
Lee, S.T.5
Hahn, J.S.6
Ko, Y.W.7
Min, Y.H.8
-
103
-
-
0037039919
-
Structure and chemistry of apicidins, a class of novel cyclic tetrapeptides without a terminal α-keto epoxide as inhibitors of histone deacetylase with potent antiprotozoal activities
-
DOI 10.1021/jo016088w
-
Singh, S.B.; Zink, D.L.; Liesch, J.M.; Mosley, R.T.; Dombrowski, A.W.; Bills, G.F. Structure and chemistry of apicidins, a class of novel cyclic tetrapeptides without a terminal ?-keto epoxide as inhibitors of histone deacetylase with potent antiprotozoal activities. J. Org. Chem., 2002, 67, 815-825. (Pubitemid 34135683)
-
(2002)
Journal of Organic Chemistry
, vol.67
, Issue.3
, pp. 815-825
-
-
Singh, S.B.1
Zink, D.L.2
Liesch, J.M.3
Mosley, R.T.4
Dombrowski, A.W.5
Bills, G.F.6
Darkin-Rattray, S.J.7
Schmatz, D.M.8
Goetz, M.A.9
-
104
-
-
0035931503
-
Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 1
-
DOI 10.1016/S0960-894X(00)00604-1, PII S0960894X00006041
-
Colletti, S.L.; Myers, R.W.; Darkin-Rattray, S.J.; Gurnett, A.M.; Dulski, P.M.; Galuska, S.; Allocco, J.J.; Ayer, M.B.; Li, C.; Lim, J.; Crumley, T.M.; Cannova, C.; Schmatz, D.M.; Wyvratt, M.J.; Fisher, M.H.; Meinke, P.T. Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 1. Bioorg. Med. Chem. Lett., 2001, 11, 107-111. (Pubitemid 32099620)
-
(2001)
Bioorganic and Medicinal Chemistry Letters
, vol.11
, Issue.2
, pp. 107-111
-
-
Colletti, S.L.1
Myers, R.W.2
Darkin-Rattray, S.J.3
Gurnett, A.M.4
Dulski, P.M.5
Galuska, S.6
Allocco, J.J.7
Ayer, M.B.8
Li, C.9
Lim, J.10
Crumley, T.M.11
Cannova, C.12
Schmatz, D.M.13
Wyvratt, M.J.14
Fisher, M.H.15
Meinke, P.T.16
-
105
-
-
0034649616
-
Synthesis of apicidin-derived quinolone derivatives: Parasite-selective histone deacetylase inhibitors and antiproliferative agents
-
DOI 10.1021/jm0001976
-
Meinke, P.T.; Colletti, S.L.; Doss, G.; Myers, R.W.; Gurnett, A.M.; Dulski, P.M.; Darkin-Rattray, S.J.; Allocco, J.J.; Galuska, S.; Schmatz, D.M.; Wyvratt, M.J.; Fisher, M.H. Synthesis of apicidinderived quinolone derivatives: Parasite-selective histone deacetylase inhibitors and antiproliferative agents. J. Med. Chem., 2000, 43, 4919-4922. (Pubitemid 32002704)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.25
, pp. 4919-4922
-
-
Meinke, P.T.1
Colletti, S.L.2
Doss, G.3
Myers, R.W.4
Gurnett, A.M.5
Dulski, P.M.6
Darkin-Rattray, S.J.7
Allocco, J.J.8
Galuska, S.9
Schmatz, D.M.10
Wyvratt, M.J.11
Fisher, M.H.12
-
106
-
-
33845199114
-
Azumamides A-E: Histone deacetylase inhibitory cyclic tetrapeptides from the marine sponge Mycale izuensis
-
DOI 10.1002/anie.200602047
-
Nakao, Y.; Yoshida, S.; Matsunaga, S.; Shindoh, N.; Terada, Y.; Nagai, K.; Yamashita, J.K.; Ganesan, A.; Van Soest, R.W.M.; Fusetani, N. Azumamides A-E: Histone deacetylase inhibitory cyclic tetrapeptides from the marine sponge Mycale. izuensis. Angew. Chem. Int. Ed., 2006, 45, 7553-7557. (Pubitemid 44851680)
-
(2006)
Angewandte Chemie - International Edition
, vol.45
, Issue.45
, pp. 7553-7557
-
-
Nakao, Y.1
Yoshida, S.2
Matsunaga, S.3
Shindoh, N.4
Terada, Y.5
Nagai, K.6
Yamashita, J.K.7
Ganesan, A.8
Van Soest, R.W.M.9
Fusetani, N.10
-
107
-
-
33947239221
-
Molecular insights into azumamide E histone deacetylases inhibitory activity
-
DOI 10.1021/ja0686256
-
Maulucci, N.; Chini, M.G.; Di Micco, S.; Izzo, I.; Cafaro, E.; Russo, A.; Gallinari, P.; Paolini, C.; Nardi, M.C.; Casapullo, A.; Riccio, R.; Bifulco, G.; De Riccardis, F. Molecular insights into azumamide E histone deacetylases inhibitory activity. J. Am. Chem. Soc., 2007, 129, 3007-3012. (Pubitemid 46417978)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.10
, pp. 3007-3012
-
-
Maulucci, N.1
Chini, M.G.2
Di Micco, S.3
Izzo, I.4
Cafaro, E.5
Russo, A.6
Gallinari, P.7
Paolini, C.8
Nardi, M.C.9
Casapullo, A.10
Riccio, R.11
Bifulco, G.12
De Riccardis, F.13
-
108
-
-
33947586979
-
Total synthesis of azumamide A and azumamide E, evaluation as histone deacetylase inhibitors, and design of a more potent analogue
-
Wen, S.; Carey, K.L.; Nakao, Y.; Fusetani, N.; Packham, G.; Ganesan, A. Total synthesis of azumamide A and azumamide E, evaluation as histone deacetylase inhibitors, and design of a more potent analogue. Org. Lett., 2007, 9, 1105-1108.
-
(2007)
Org. Lett.
, vol.9
, pp. 1105-1108
-
-
Wen, S.1
Carey, K.L.2
Nakao, Y.3
Fusetani, N.4
Packham, G.5
Ganesan, A.6
-
109
-
-
58149305980
-
Total synthesis of Azumamide E and sugar amino acid-containing analogue
-
Chandrasekhar, S.; Rao, C.L.; Seenaiah, M.; Naresh, P.; Jagadeesh, B.; Manjeera, D.; Sarkar, A.; Bhadra M.P. Total synthesis of Azumamide E and sugar amino acid-containing analogue. J. Org. Chem., 2009, 74, 401-404.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 401-404
-
-
Chandrasekhar, S.1
Rao, C.L.2
Seenaiah, M.3
Naresh, P.4
Jagadeesh, B.5
Manjeera, D.6
Sarkar, A.7
Bhadra, M.P.8
-
110
-
-
42949139951
-
Evaluation of antiangiogenic activity of azumamides by the in vitro vascular organization model using mouse induced pluripotent stem (iPS) cells
-
DOI 10.1016/j.bmcl.2008.03.053, PII S0960894X08003272
-
Nakao, Y.; Narazaki, G.; Hoshino, T.; Maeda, S.; Yoshida, M.; Maejima, H.; Yamashita, J.K. Evaluation of antiangiogenic activity of azumamides by the in. vitro vascular organization model using mouse induced pluripotent stem (iPS) cells. Bioorg. Med. Chem. Lett., 2008, 18, 2982-2984. (Pubitemid 351608862)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.9
, pp. 2982-2984
-
-
Nakao, Y.1
Narazaki, G.2
Hoshino, T.3
Maeda, S.4
Yoshida, M.5
Maejima, H.6
Yamashita, J.K.7
-
111
-
-
84862757536
-
Evaluation of functional groups on amino acids in cyclic tetrapeptides in histone deacetylase inhibition
-
Islam, M.S.; Bhuiyan, M.P.; Islam, M.N.; Nsiama, T.K.; Oishi, N.; Kato, T.; Nishino, N.; Ito, A.; Yoshida, M. Evaluation of functional groups on amino acids in cyclic tetrapeptides in histone deacetylase inhibition. Amino. Acids, 2012, 42(6), 2103-2110.
-
(2012)
Amino. Acids
, vol.42
, Issue.6
, pp. 2103-2110
-
-
Islam, M.S.1
Bhuiyan, M.P.2
Islam, M.N.3
Nsiama, T.K.4
Oishi, N.5
Kato, T.6
Nishino, N.7
Ito, A.8
Yoshida, M.9
-
112
-
-
6344247464
-
Chlamydocin-hydroxamic acid analogues as histone deacetylase inhibitors
-
DOI 10.1016/j.bmc.2004.08.041, PII S0968089604006650
-
Nishino, N.; Jose, B.; Shinta, R.; Kato, T.; Komatsub, Y.; Yoshida M. Chlamydocin-hydroxamic acid analogues as histone deacetylase inhibitors. Bioorg. Med. Chem.,. 2004, 12, 5777-5784. (Pubitemid 39388176)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.22
, pp. 5777-5784
-
-
Nishino, N.1
Jose, B.2
Shinta, R.3
Kato, T.4
Komatsu, Y.5
Yoshida, M.6
-
113
-
-
33645892015
-
Chlamydocin analogs bearing carbonyl group as possible ligand toward zinc atom in histone deacetylases
-
Bhuiyan, M.P.I.; Kato, T.; Okauchi, T.; Nishino, N.; Maeda, S.; Nishino, T.G.; Yoshida, M. Chlamydocin analogs bearing carbonyl group as possible ligand toward zinc atom in histone deacetylases. Bioorg. Med. Chem., 2006, 14, 3438-3446.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 3438-3446
-
-
Bhuiyan, M.P.I.1
Kato, T.2
Okauchi, T.3
Nishino, N.4
Maeda, S.5
Nishino, T.G.6
Yoshida, M.7
-
114
-
-
0016366116
-
Isolation and structural clarification of chlamydocin
-
Closse, A.; Huguenin, R. Isolation and structural clarification of chlamydocin. Helv. Chim. Acta., 1974, 57, 533-545.
-
(1974)
Helv. Chim. Acta.
, vol.57
, pp. 533-545
-
-
Closse, A.1
Huguenin, R.2
-
115
-
-
35348816926
-
Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework
-
DOI 10.1016/j.bmc.2007.08.041, PII S0968089607007444
-
Shivashimpi, G.M.; Amagai, S.; Kato, T.; Nishino, N.; Maeda, S.; Nishino, T.G.; Yoshida, M. Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework. Bioorg. Med. Chem.,. 2007, 15, 7830-7839. (Pubitemid 47575905)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.24
, pp. 7830-7839
-
-
Shivashimpi, G.M.1
Amagai, S.2
Kato, T.3
Nishino, N.4
Maeda, S.5
Nishino, T.G.6
Yoshida, M.7
-
116
-
-
38049001966
-
Interaction of aliphatic cap group in inhibition of histone deacetylases by cyclic tetrapeptides
-
Nishino, N.; Shivashimpi, G.M.; Soni, P.B.; Bhuiyan, M.P.I.; Kato, T.; Maeda, S.; Nishino, T.G.; Yoshida, M. Interaction of aliphatic cap group in inhibition of histone deacetylases by cyclic tetrapeptides. Bioorg. Med. Chem., 2008, 16, 437-445.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 437-445
-
-
Nishino, N.1
Shivashimpi, G.M.2
Soni, P.B.3
Bhuiyan, M.P.I.4
Kato, T.5
Maeda, S.6
Nishino, T.G.7
Yoshida, M.8
-
117
-
-
0037310955
-
Inhibition of histone deacetylases by chlamydocin induces apoptosis and proteasome-mediated degradation of survivin
-
DOI 10.1124/jpet.102.042903
-
De Schepper, S.; Bruwiere, H.; Verhulst, T.; Steller, U.; Andries, L.; Wouters, W.; Janicot, M.; Arts, J.; Van Heusden, J. Inhibition of histone deacetylases by chlamydocin induces apoptosis and proteasome-mediated degradation of survivin. J. Pharmacol. Exp. Ther.,. 2003, 304(2), 881-888. (Pubitemid 36152369)
-
(2003)
Journal of Pharmacology and Experimental Therapeutics
, vol.304
, Issue.2
, pp. 881-888
-
-
De Schepper, S.1
Bruwiere, H.2
Verhulst, T.3
Steller, U.4
Andries, L.5
Wouters, W.6
Janicot, M.7
Arts, J.8
Van Heusden, J.9
-
118
-
-
0035361402
-
Cyclic hydroxamic-acid-containing peptide 31, a potent synthetic histone deacetylase inhibitor with antitumor activity
-
Komatsu, Y.; Tomizaki, K.; Tsukamoto, M.; Kato, T.; Nishino, N.; Sato, S.; Yamori, T.; Tsuruo, T.; Furumai, R.; Yoshida, M.; Horinouchi, S.; Hayashi, H. Cyclic hydroxamic acid-containing peptide 31, a potent synthetic histone deacetylase inhibitor with antitumor activity. Cancer. Res., 2001, 61, 4459-4466. (Pubitemid 32685775)
-
(2001)
Cancer Research
, vol.61
, Issue.11
, pp. 4459-4466
-
-
Komatsu, Y.1
Tomizaki, K.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
Hayashi, H.12
-
119
-
-
4744370522
-
Subtype selective substrates for histone deacetylases
-
DOI 10.1021/jm0497592
-
Heltweg, B.; Dequiedt, F.; Marshall, B.L.; Brauch, C.; Yoshida, M.; Nishino, N.; Verdin, E.; Jung, M. Subtype selective substrates for histone deacetylases. J. Med. Chem., 2004, 47, 5235-5243. (Pubitemid 39314921)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.21
, pp. 5235-5243
-
-
Heltweg, B.1
Dequiedt, F.2
Marshall, B.L.3
Brauch, C.4
Yoshida, M.5
Nishino, N.6
Verdin, E.7
Jung, M.8
-
120
-
-
0035793107
-
Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin
-
DOI 10.1073/pnas.011405598
-
Furumai, R.; Komatsu, Y.; Nishino, N.; Khochbin, S.; Yoshida, M.; Horinouchi, S. Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin. Proc. Natl. Acad. Sci. USA., 2001, 98, 87-92. (Pubitemid 32095868)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, 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
-
121
-
-
77649320563
-
CHAP31 induces apoptosis only via the intrinsic pathway in human esophageal cancer cells
-
Murakami, K.; Matsubara, H.; Hoshino, I.; Akutsu, Y.; Miyazawa, Y.; Matsushita, K.; Sakata, H.; Nishimori, T.; Usui, A.; Kano, M.; Nishino, N.; Yoshida, M. CHAP31 induces apoptosis only via the intrinsic pathway in human esophageal cancer cells. Oncol., 2010, 78(1), 62-74.
-
(2010)
Oncol.
, vol.78
, Issue.1
, pp. 62-74
-
-
Murakami, K.1
Matsubara, H.2
Hoshino, I.3
Akutsu, Y.4
Miyazawa, Y.5
Matsushita, K.6
Sakata, H.7
Nishimori, T.8
Usui, A.9
Kano, M.10
Nishino, N.11
Yoshida, M.12
-
122
-
-
13644251766
-
Impact of novel histone deacetylase inhibitors, CHAP31 and FR901228 (FK228), on adenovirus-mediated transgene expression
-
DOI 10.1002/jgm.546
-
Taura, K.; Yamamoto, Y.; Nakajima, A.; Hata, K.; Uchinami, H.; Yonezawa, K.; Hatano, E.; Nishino, N.; Yamaoka, Y. Impact of novel histone deacetylase inhibitors, CHAP31 and FR901228 (FK228), on adenovirus-mediated transgene expression. J. Gene. Med., 2004, 6(5), 526-536. (Pubitemid 40228068)
-
(2004)
Journal of Gene Medicine
, vol.6
, Issue.5
, pp. 526-536
-
-
Taura, K.1
Yamamoto, Y.2
Nakajima, A.3
Hata, K.4
Uchinami, H.5
Yonezawa, K.6
Hatano, E.7
Nishino, N.8
Yamaoka, Y.9
-
123
-
-
75149186089
-
Effects of carbon-ion radiotherapy combined with a novel histone deacetylase inhibitor, cyclic hydroxamic-acid-containing peptide 31 in human esophageal squamous cell carcinoma
-
Kano, M.; Yamada, S.; Hoshino, I.; Murakami, K.; Akutsu, Y.; Sakata, H.; Nishimori, T.; Usui, A.; Miyazawa, Y.; Kamada, T.; Tsujii, H.; Matsubara, H. Effects of carbon-ion radiotherapy combined with a novel histone deacetylase inhibitor, cyclic hydroxamic-acid-containing peptide 31 in human esophageal squamous cell carcinoma. Anticancer. Res., 2009, 29, 4433-4438.
-
(2009)
Anticancer. Res.
, vol.29
, pp. 4433-4438
-
-
Kano, M.1
Yamada, S.2
Hoshino, I.3
Murakami, K.4
Akutsu, Y.5
Sakata, H.6
Nishimori, T.7
Usui, A.8
Miyazawa, Y.9
Kamada, T.10
Tsujii, H.11
Matsubara, H.12
-
124
-
-
1542331640
-
Toward an HDAC6 inhibitor: Synthesis and conformational analysis of cyclic hexapeptide hydroxamic acid designed from α-tubulin sequence
-
DOI 10.1016/j.bmc.2004.01.014, PII S0968089604000471
-
Jose, B.; Okamura, S.; Kato, T.; Nishino, N.; Sumida, Y.; Yoshida, M. Toward an HDAC6 inhibitor: Synthesis and conformational analysis of cyclic hexapeptide hydroxamic acid designed from ?-tubulin sequence. Bioorg. Med. Chem., 2004, 12, 1351-1356. (Pubitemid 38296525)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.6
, pp. 1351-1356
-
-
Jose, B.1
Okamura, S.2
Kato, T.3
Nishino, N.4
Sumida, Y.5
Yoshida, M.6
-
125
-
-
74049094482
-
Bicyclic peptides as potent inhibitors of histone deacetylases: Optimization of alkyl loop length
-
Islam, N.M.; Kato, T.; Nishino, N.; Kim, H.-J.; Ito, A.; Yoshida, M. Bicyclic peptides as potent inhibitors of histone deacetylases: Optimization of alkyl loop length. Bioorg. Med. Chem. Lett., 2010, 20, 997-999.
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 997-999
-
-
Islam, N.M.1
Kato, T.2
Nishino, N.3
Kim, H.-J.4
Ito, A.5
Yoshida, M.6
-
126
-
-
84867582251
-
Cyclic tetrapeptides with thioacetate tails or intramolecular disulfide bridge as potent inhibitors of histone deacetylases
-
10.1016/j.bmcl.2012.03.004
-
Hoque, M.A.; Arai, T.; Nishino, N.; Kim, H.-J.; Ito, A.; Yoshida, M. Cyclic tetrapeptides with thioacetate tails or intramolecular disulfide bridge as potent inhibitors of histone deacetylases. Bioorg. Med. Chem. Lett., 2012,. 10.1016/j.bmcl.2012.03.004.
-
(2012)
Bioorg. Med. Chem. Lett.
-
-
Hoque, M.A.1
Arai, T.2
Nishino, N.3
Kim, H.-J.4
Ito, A.5
Yoshida, M.6
-
127
-
-
77951207678
-
Synthesis and biological activity of cyclotetrapeptide analogues of the natural HDAC inhibitor FR235222
-
Terracciano, S,; Micco, S.D.; Bifulco, G.; Gallinari, P.; Riccio, R.; Bruno, I. Synthesis and biological activity of cyclotetrapeptide analogues of the natural HDAC inhibitor FR235222. Bioorg. Med. Chem., 2010, 18, 3252-3260.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 3252-3260
-
-
Terracciano, S.1
Micco, S.D.2
Bifulco, G.3
Gallinari, P.4
Riccio, R.5
Bruno, I.6
-
128
-
-
41849134699
-
Synthesis and biological evaluation of histone deacetylase inhibitors that are based on FR235222: A cyclic tetrapeptide scaffold
-
DOI 10.1016/j.bmcl.2008.03.047, PII S0960894X0800320X
-
Singh, E.K.; Ravula, S.; Pan, C.-M.; Pan, P.-S.; Vasko, R.C.; Lapera, S.A.; Weerasinghe, S.V.W.; Pflum, M.K.H.; McAlpine, S.R. Synthesis and biological evaluation of histone deacetylase inhibitors that are based on FR235222: A cyclic tetrapeptide scaffold. Bioorg. Med. Chem. Lett., 2008, 18, 2549-2554. (Pubitemid 351503893)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.8
, pp. 2549-2554
-
-
Singh, E.K.1
Ravula, S.2
Pan, C.-M.3
Pan, P.-S.4
Vasko, R.C.5
Lapera, S.A.6
Weerasinghe, S.V.W.7
Pflum, M.K.H.8
McAlpine, S.R.9
-
129
-
-
67649646671
-
Design and synthesis of novel hybrid benzamide-peptide histone deacetylase inhibitors
-
Hu, F.; Chou, C.J.; Gottesfeld, J.M. Design and synthesis of novel hybrid benzamide-peptide histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2009, 19, 3928-3931.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3928-3931
-
-
Hu, F.1
Chou, C.J.2
Gottesfeld, J.M.3
-
130
-
-
67749142082
-
Design synthesis, biological evaluation, and structural characterization of potent histone deacetylase inhibitors based on cyclic ?/?-tetrapeptide architectures
-
Montero, A.; Beierle, J.M.; Olsen, C.A.; Ghadiri, M.R. Design, synthesis, biological evaluation, and structural characterization of potent histone deacetylase inhibitors based on cyclic ?/?-tetrapeptide architectures. J. Am. Chem. Soc.,. 2009, 131, 3033-3041.
-
(2009)
J. Am. Chem. Soc.,.
, vol.131
, pp. 3033-3041
-
-
Montero, A.1
Beierle, J.M.2
Olsen, C.A.3
Ghadiri, M.R.4
-
131
-
-
78649876797
-
Non-natural macrocyclic inhibitors of histone deacetylases: Design, synthesis, and activity
-
Auzzas, L.; Larsson, A.; Matera, R.; Baraldi, A.; Deschenes-Simard, B.; Giannini, G.; Cabri, W.; Battistuzzi, G.; Gallo, G.; Ciacci, A.; Vesci, L.; Pisano, C.; Hanessian, S. Non-natural macrocyclic inhibitors of histone deacetylases: Design, synthesis, and activity. J. Med. Chem., 2010, 53(23), 8387-8399.
-
(2010)
J. Med. Chem.
, vol.53
, Issue.23
, pp. 8387-8399
-
-
Auzzas, L.1
Larsson, A.2
Matera, R.3
Baraldi, A.4
Deschenes-Simard, B.5
Giannini, G.6
Cabri, W.7
Battistuzzi, G.8
Gallo, G.9
Ciacci, A.10
Vesci, L.11
Pisano, C.12
Hanessian, S.13
-
132
-
-
72249094958
-
Discovery of potent and selective histone deacetylase inhibitors via focused combinatorial libraries of cyclic ?3?-tetrapeptides
-
Olsen, C.A.; Ghadiri, M.R. Discovery of potent and selective histone deacetylase inhibitors via focused combinatorial libraries of cyclic ?3?-tetrapeptides. J. Med. Chem., 2009, 52(23), 7836-7846.
-
(2009)
J. Med. Chem.
, vol.52
, Issue.23
, pp. 7836-7846
-
-
Olsen, C.A.1
Ghadiri, M.R.2
-
133
-
-
79953777824
-
Macrocycles are great cycles: Applications, opportunities, and challenges of synthetic macrocycles in drug discovery
-
Marsault, E.; Peterson, M.L. Macrocycles are great cycles: Applications, opportunities, and challenges of synthetic macrocycles in drug discovery. J. Med. Chem., 2011, 54, 1961-2004.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 1961-2004
-
-
Marsault, E.1
Peterson, M.L.2
-
134
-
-
77955430918
-
Histone deacetylase inhibitors: Synthesis of cyclic tetrapeptides and their triazole analogues
-
Singh, E.K.; Nazarova, L.A.; Lapera, S.A.; Alexander, L.D.; McAlpine, S.R. Histone deacetylase inhibitors: Synthesis of cyclic tetrapeptides and their triazole analogues. Tetrahedron. Lett., 2010, 51(33), 4357-4360.
-
(2010)
Tetrahedron. Lett.
, vol.51
, Issue.33
, pp. 4357-4360
-
-
Singh, E.K.1
Nazarova, L.A.2
Lapera, S.A.3
Alexander, L.D.4
McAlpine, S.R.5
-
135
-
-
0346025398
-
Cyclic Tetrapeptides Bearing a Sulfhydryl Group Potently Inhibit Histone Deacetylases
-
DOI 10.1021/ol036098e
-
Nishino, N.; Jose, B.; Okamura, S.; Ebisusaki, S.; Kato, T.; Sumida, Y.; Yoshida, M. Cyclic tetrapeptides bearing a sulfhydryl group potently inhibit histone deacetylases. Org. Lett., 2003, 5(26), 5079-5082. (Pubitemid 38073003)
-
(2003)
Organic Letters
, vol.5
, Issue.26
, pp. 5079-5082
-
-
Nishino, N.1
Jose, B.2
Okamura, S.3
Ebisusaki, S.4
Kato, T.5
Sumida, Y.6
Yoshida, M.7
-
136
-
-
84863232466
-
Multi-targeted histone. Deacetylase inhibitors in cancer therapy
-
Ai, T.; Cui, H.; Chen, L. Multi-targeted histone. deacetylase inhibitors in cancer therapy. Curr. Med. Chem., 2012, 19, 475-487.
-
(2012)
Curr. Med. Chem.
, vol.19
, pp. 475-487
-
-
Ai, T.1
Cui, H.2
Chen, L.3
|