(2E)-N-hydroxy-3-[4-({[2-(2-methyl-1H-indol-3-yl)ethyl]amino}methyl)phenyl]prop-2-enamide
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Modulations of DNMT1 and HDAC1 are involved in the OTA-induced cytotoxicity and apoptosis in vitro. | Chemico-biological interactions 20171225 |
Fingerprinting of neurotoxic compounds using a mouse embryonic stem cell dual luminescence reporter assay. | Archives of toxicology 20170101 |
Definition of transcriptome-based indices for quantitative characterization of chemically disturbed stem cell development: introduction of the STOP-Tox(ukn) and STOP-Tox(ukk) tests. | Archives of toxicology 20170101 |
The Bromodomain Inhibitor JQ1 and the Histone Deacetylase Inhibitor Panobinostat Synergistically Reduce N-Myc Expression and Induce Anticancer Effects. | Clinical cancer research : an official journal of the American Association for Cancer Research 20160515 |
Keap1-Independent Regulation of Nrf2 Activity by Protein Acetylation and a BET Bromodomain Protein. | PLoS genetics 20160501 |
Panobinostat for the Treatment of Multiple Myeloma. | Clinical cancer research : an official journal of the American Association for Cancer Research 20151101 |
A transcriptome-based classifier to identify developmental toxicants by stem cell testing: design, validation and optimization for histone deacetylase inhibitors. | Archives of toxicology 20150101 |
Highly active combination of BRD4 antagonist and histone deacetylase inhibitor against human acute myelogenous leukemia cells. | Molecular cancer therapeutics 20140501 |
SIRT1 activation enhances HDAC inhibition-mediated upregulation of GADD45G by repressing the binding of NF-κB/STAT3 complex to its promoter in malignant lymphoid cells. | Cell death & disease 20130501 |
Synergistic effect of panobinostat and bortezomib on chemoresistant acute myelogenous leukemia cells via AKT and NF-κB pathways. | Cancer letters 20121230 |
Resveratrol sensitizes acute myelogenous leukemia cells to histone deacetylase inhibitors through reactive oxygen species-mediated activation of the extrinsic apoptotic pathway. | Molecular pharmacology 20121201 |
Selective histone deacetylase 6 inhibitors bearing substituted urea linkers inhibit melanoma cell growth. | Journal of medicinal chemistry 20121126 |
Phase I dose-escalating study of panobinostat (LBH589) administered intravenously to Japanese patients with advanced solid tumors. | Investigational new drugs 20121001 |
Characterizing the disposition, metabolism, and excretion of an orally active pan-deacetylase inhibitor, panobinostat, via trace radiolabeled 14C material in advanced cancer patients. | Cancer chemotherapy and pharmacology 20121001 |
[Inhibitory effect of histone deacetylase inhibitor LBH589 on multiple myeloma MM1R cells in vitro]. | Zhongguo shi yan xue ye xue za zhi 20121001 |
Downregulation of HMGA2 by the pan-deacetylase inhibitor panobinostat is dependent on hsa-let-7b expression in liver cancer cell lines. | Experimental cell research 20120910 |
Phase II trial of the pan-deacetylase inhibitor panobinostat as a single agent in advanced relapsed/refractory multiple myeloma. | Leukemia & lymphoma 20120901 |
Phase II study of melphalan, thalidomide and prednisone combined with oral panobinostat in patients with relapsed/refractory multiple myeloma. | Leukemia & lymphoma 20120901 |
A phase I trial of oral administration of panobinostat in combination with paclitaxel and carboplatin in patients with solid tumors. | Cancer chemotherapy and pharmacology 20120901 |
LBH589 enhances T cell activation in vivo and accelerates graft-versus-host disease in mice. | Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 20120801 |
Phase I study of bevacizumab, everolimus, and panobinostat (LBH-589) in advanced solid tumors. | Cancer chemotherapy and pharmacology 20120801 |
Panobinostat (LBH589)-induced acetylation of tubulin impairs megakaryocyte maturation and platelet formation. | Experimental hematology 20120701 |
Pan-histone deacetylase inhibitor panobinostat sensitizes gastric cancer cells to anthracyclines via induction of CITED2. | Gastroenterology 20120701 |
Histone deacetylase inhibition modulates E-cadherin expression and suppresses migration and invasion of anaplastic thyroid cancer cells. | The Journal of clinical endocrinology and metabolism 20120701 |
Panobinostat in patients with relapsed/refractory Hodgkin's lymphoma after autologous stem-cell transplantation: results of a phase II study. | Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20120620 |
Brentuximab vedotin and panobinostat: new drugs for Hodgkin's lymphoma--can they make one of medical oncology's chemotherapy success stories more successful? | Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20120620 |
A phase I study of oral panobinostat (LBH589) in Japanese patients with advanced solid tumors. | Investigational new drugs 20120601 |
Regulation of STAT3 by histone deacetylase-3 in diffuse large B-cell lymphoma: implications for therapy. | Leukemia 20120601 |
Histone deacetylase inhibitors are unable to synergize with ABT-737 in killing primary chronic lymphocytic leukaemia cells in vitro. | Leukemia 20120601 |
Combination therapy for hepatocellular carcinoma: additive preclinical efficacy of the HDAC inhibitor panobinostat with sorafenib. | Journal of hepatology 20120601 |
Bortezomib and panobinostat combination is effective against PTCL. | Leukemia research 20120601 |
Biocatalytic synthesis and structure elucidation of cyclized metabolites of the deacetylase inhibitor panobinostat (LBH589). | Drug metabolism and disposition: the biological fate of chemicals 20120501 |
Panobinostat for the treatment of multiple myeloma. | Expert opinion on investigational drugs 20120501 |
The pan-deacetylase inhibitor panobinostat induces cell death and synergizes with everolimus in Hodgkin lymphoma cell lines. | Blood 20120426 |
The HDAC inhibitor LBH589 enhances the antimyeloma effects of the IGF-1RTK inhibitor picropodophyllin. | Clinical cancer research : an official journal of the American Association for Cancer Research 20120415 |
LBH-589 (panobinostat) potentiates fludarabine anti-leukemic activity through a JNK- and XIAP-dependent mechanism. | Leukemia research 20120401 |
Fludarabine and a histone deacetylase inhibitor - strange bedfellows. | Leukemia research 20120401 |
Combination of pan-histone deacetylase inhibitor and autophagy inhibitor exerts superior efficacy against triple-negative human breast cancer cells. | Molecular cancer therapeutics 20120401 |
Phase I study of panobinostat in combination with bevacizumab for recurrent high-grade glioma. | Journal of neuro-oncology 20120301 |
Phase II study of panobinostat and bortezomib in patients with pancreatic cancer progressing on gemcitabine-based therapy. | Anticancer research 20120301 |
KLF9 is a novel transcriptional regulator of bortezomib- and LBH589-induced apoptosis in multiple myeloma cells. | Blood 20120209 |
Histone deacetylases mediate the silencing of miR-15a, miR-16, and miR-29b in chronic lymphocytic leukemia. | Blood 20120202 |
Cytotoxic activity of the histone deacetylase inhibitor panobinostat (LBH589) in anaplastic thyroid cancer in vitro and in vivo. | International journal of cancer 20120201 |
The effect of food on the bioavailability of panobinostat, an orally active pan-histone deacetylase inhibitor, in patients with advanced cancer. | Cancer chemotherapy and pharmacology 20120201 |
Histone deacetylase inhibitors induce growth arrest and differentiation in uveal melanoma. | Clinical cancer research : an official journal of the American Association for Cancer Research 20120115 |
Preclinical evaluation of dual PI3K-mTOR inhibitors and histone deacetylase inhibitors in head and neck squamous cell carcinoma. | British journal of cancer 20120103 |
Phase II study of the histone deacetylase inhibitor panobinostat (LBH589) in patients with low or intermediate-1 risk myelodysplastic syndrome. | American journal of hematology 20120101 |
HDAC gene expression in pancreatic tumor cell lines following treatment with the HDAC inhibitors panobinostat (LBH589) and trichostatine (TSA). | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 20120101 |
Targeting triple-negative breast cancer cells with the histone deacetylase inhibitor panobinostat. | Breast cancer research : BCR 20120101 |
ING1 and 5-azacytidine act synergistically to block breast cancer cell growth. | PloS one 20120101 |
Inhibition of DNA methyltransferase activity and expression by treatment with the pan-deacetylase inhibitor panobinostat in hepatocellular carcinoma cell lines. | BMC cancer 20120101 |
The histone deacetylase inhibitor panobinostat demonstrates marked synergy with conventional chemotherapeutic agents in human ovarian cancer cell lines. | Investigational new drugs 20111201 |
HDAC inhibitors and decitabine are highly synergistic and associated with unique gene-expression and epigenetic profiles in models of DLBCL. | Blood 20111117 |
Development and validation of ultra high performance liquid chromatography-mass spectrometry method for LBH589 in mouse plasma and tissues. | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20111115 |
Addition of a histone deacetylase inhibitor redirects tamoxifen-treated breast cancer cells into apoptosis, which is opposed by the induction of autophagy. | Breast cancer research and treatment 20111101 |
Anti-angiogenic therapies in the treatment of Waldenstrom's Macroglobulinemia. | Current cancer drug targets 20111101 |
Discovery, synthesis, and biological evaluation of novel SMN protein modulators. | Journal of medicinal chemistry 20110922 |
Effect of ketoconazole-mediated CYP3A4 inhibition on clinical pharmacokinetics of panobinostat (LBH589), an orally active histone deacetylase inhibitor. | Cancer chemotherapy and pharmacology 20110901 |
[Effect of RAD001 or plus LBH589 on the proliferation, apoptosis and drug resistance in chemoresistant acute myeloid leukemic cells]. | Zhonghua yi xue za zhi 20110830 |
A phase II trial of panobinostat, a histone deacetylase inhibitor, in the treatment of patients with refractory metastatic renal cell carcinoma. | Cancer investigation 20110801 |
[Reversal effect of LBH589 alone or in combination with bortezomib on drug-resistance in myeloid leukemia and its mechanism]. | Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 20110801 |
Discovery of (2E)-3-{2-butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl}-N-hydroxyacrylamide (SB939), an orally active histone deacetylase inhibitor with a superior preclinical profile. | Journal of medicinal chemistry 20110714 |
Antitumor activities and on-target toxicities mediated by a TRAIL receptor agonist following cotreatment with panobinostat. | International journal of cancer 20110601 |
Clinical development of panobinostat in classical Hodgkin's lymphoma. | Expert review of hematology 20110601 |
Low-dose LBH589 increases the sensitivity of cisplatin to cisplatin-resistant ovarian cancer cells. | Taiwanese journal of obstetrics & gynecology 20110601 |
The dual EGFR/HER2 inhibitor lapatinib synergistically enhances the antitumor activity of the histone deacetylase inhibitor panobinostat in colorectal cancer models. | Cancer research 20110515 |
Overexpression of Enhancer of zeste homolog 2 with trimethylation of lysine 27 on histone H3 in adult T-cell leukemia/lymphoma as a target for epigenetic therapy. | Haematologica 20110501 |
Discovery, synthesis, and pharmacological evaluation of spiropiperidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors. | Journal of medicinal chemistry 20110428 |
LBH589, a deacetylase inhibitor, induces apoptosis in adult T-cell leukemia/lymphoma cells via activation of a novel RAIDD-caspase-2 pathway. | Leukemia 20110401 |
The synergistic effect of panobinostat (LBH589) with melphalan or doxorubicin on multiple myeloma cells; rationale for the use of combination regimens in myeloma patients. | Leukemia research 20110301 |
A phase I study of panobinostat in combination with gemcitabine in the treatment of solid tumors. | Clinical advances in hematology & oncology : H&O 20110301 |
Induction of cell cycle arrest and DNA damage by the HDAC inhibitor panobinostat (LBH589) and the lipid peroxidation end product 4-hydroxynonenal in prostate cancer cells. | Free radical biology & medicine 20110115 |
Knockdown of MTDH sensitizes endometrial cancer cells to cell death induction by death receptor ligand TRAIL and HDAC inhibitor LBH589 co-treatment. | PloS one 20110101 |
Concurrent HDAC and mTORC1 inhibition attenuate androgen receptor and hypoxia signaling associated with alterations in microRNA expression. | PloS one 20110101 |
Comparative analysis of novel and conventional Hsp90 inhibitors on HIF activity and angiogenic potential in clear cell renal cell carcinoma: implications for clinical evaluation. | BMC cancer 20110101 |
Pan-histone deacetylase inhibitor panobinostat depletes CXCR4 levels and signaling and exerts synergistic antimyeloid activity in combination with CXCR4 antagonists. | Blood 20101209 |
To selectivity and beyond. | Nature biotechnology 20101201 |
Activity of deacetylase inhibitor panobinostat (LBH589) in cutaneous T-cell lymphoma models: Defining molecular mechanisms of resistance. | International journal of cancer 20101101 |
Role of CAAT/enhancer binding protein homologous protein in panobinostat-mediated potentiation of bortezomib-induced lethal endoplasmic reticulum stress in mantle cell lymphoma cells. | Clinical cancer research : an official journal of the American Association for Cancer Research 20101001 |
Combinations of DNA methyltransferase and histone deacetylase inhibitors induce DNA damage in small cell lung cancer cells: correlation of resistance with IFN-stimulated gene expression. | Molecular cancer therapeutics 20100801 |
In vitro and in vivo rationale for the triple combination of panobinostat (LBH589) and dexamethasone with either bortezomib or lenalidomide in multiple myeloma. | Haematologica 20100501 |
A phase I study of oral panobinostat alone and in combination with docetaxel in patients with castration-resistant prostate cancer. | Cancer chemotherapy and pharmacology 20100501 |
Treatment with panobinostat induces glucose-regulated protein 78 acetylation and endoplasmic reticulum stress in breast cancer cells. | Molecular cancer therapeutics 20100401 |
IGF-1 suppresses Bim expression in multiple myeloma via epigenetic and posttranslational mechanisms. | Blood 20100325 |
The enhancement of antiproliferative and proapoptotic activity of HDAC inhibitors by curcumin is mediated by Hsp90 inhibition. | Cellular and molecular life sciences : CMLS 20100301 |
Chemical phylogenetics of histone deacetylases. | Nature chemical biology 20100301 |
Induction of bicalutamide sensitivity in prostate cancer cells by an epigenetic Puralpha-mediated decrease in androgen receptor levels. | The Prostate 20100201 |
Synthesis and biological evaluation of N-hydroxyphenylacrylamides and N-hydroxypyridin-2-ylacrylamides as novel histone deacetylase inhibitors. | Journal of medicinal chemistry 20100128 |
Induction of TAp63 by histone deacetylase inhibitors. | Biochemical and biophysical research communications 20100122 |
The pan-deacetylase inhibitor panobinostat inhibits growth of hepatocellular carcinoma models by alternative pathways of apoptosis. | Cellular oncology : the official journal of the International Society for Cellular Oncology 20100101 |
The oral histone deacetylase inhibitor LBH589 is a potential and promising therapeutic agent in multiple myeloma after at least two lines of chemotherapy including bortezomib or lenalidomide. | Onkologie 20100101 |
c-FLIP degradation mediates sensitization of pancreatic cancer cells to TRAIL-induced apoptosis by the histone deacetylase inhibitor LBH589. | PloS one 20100101 |
Polycomb target genes are silenced in multiple myeloma. | PloS one 20100101 |
Histone deacetylase inhibitors downregulate checkpoint kinase 1 expression to induce cell death in non-small cell lung cancer cells. | PloS one 20100101 |
Cotreatment with panobinostat and JAK2 inhibitor TG101209 attenuates JAK2V617F levels and signaling and exerts synergistic cytotoxic effects against human myeloproliferative neoplastic cells. | Blood 20091203 |
The synergy of panobinostat plus doxorubicin in acute myeloid leukemia suggests a role for HDAC inhibitors in the control of DNA repair. | Leukemia 20091201 |
LBH589 induces up to 10-fold SMN protein levels by several independent mechanisms and is effective even in cells from SMA patients non-responsive to valproate. | Human molecular genetics 20091001 |
Inhibition of histone deacetylase overcomes rapamycin-mediated resistance in diffuse large B-cell lymphoma by inhibiting Akt signaling through mTORC2. | Blood 20091001 |
Preliminary evidence of disease response to the pan deacetylase inhibitor panobinostat (LBH589) in refractory Hodgkin Lymphoma. | British journal of haematology 20091001 |
Combined epigenetic therapy with the histone methyltransferase EZH2 inhibitor 3-deazaneplanocin A and the histone deacetylase inhibitor panobinostat against human AML cells. | Blood 20090924 |
Development of the pan-DAC inhibitor panobinostat (LBH589): successes and challenges. | Cancer letters 20090808 |
The HDAC inhibitor panobinostat (LBH589) inhibits mesothelioma and lung cancer cells in vitro and in vivo with particular efficacy for small cell lung cancer. | Molecular cancer therapeutics 20090801 |
Clinical studies of histone deacetylase inhibitors. | Clinical cancer research : an official journal of the American Association for Cancer Research 20090615 |
High efficacy of panobinostat towards human gastrointestinal stromal tumors in a xenograft mouse model. | Clinical cancer research : an official journal of the American Association for Cancer Research 20090615 |
Acquired vorinostat resistance shows partial cross-resistance to 'second-generation' HDAC inhibitors and correlates with loss of histone acetylation and apoptosis but not with altered HDAC and HAT activities. | Anti-cancer drugs 20090601 |
Panobinostat (LBH589): a potent pan-deacetylase inhibitor with promising activity against hematologic and solid tumors. | Future oncology (London, England) 20090601 |
Panobinostat treatment depletes EZH2 and DNMT1 levels and enhances decitabine mediated de-repression of JunB and loss of survival of human acute leukemia cells. | Cancer biology & therapy 20090501 |
Cotreatment with BCL-2 antagonist sensitizes cutaneous T-cell lymphoma to lethal action of HDAC7-Nur77-based mechanism. | Blood 20090423 |
Identification and characterization of small molecule inhibitors of a class I histone deacetylase from Plasmodium falciparum. | Journal of medicinal chemistry 20090423 |
A systematic assessment of radiation dose enhancement by 5-Aza-2'-deoxycytidine and histone deacetylase inhibitors in head-and-neck squamous cell carcinoma. | International journal of radiation oncology, biology, physics 20090301 |
Caspase cleavage of Itch in chronic lymphocytic leukemia cells. | Biochemical and biophysical research communications 20090213 |
A histone deacetylase inhibitor LBH589 downregulates XIAP in mesothelioma cell lines which is likely responsible for increased apoptosis with TRAIL. | Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 20090201 |
Dual degradation of aurora A and B kinases by the histone deacetylase inhibitor LBH589 induces G2-M arrest and apoptosis of renal cancer cells. | Clinical cancer research : an official journal of the American Association for Cancer Research 20090201 |
DNA microarray profiling of genes differentially regulated by the histone deacetylase inhibitors vorinostat and LBH589 in colon cancer cell lines. | BMC medical genomics 20090101 |
The potential role of histone deacetylase inhibitors in the treatment of non-small-cell lung cancer. | Critical reviews in oncology/hematology 20081001 |
Molecular and biologic characterization and drug sensitivity of pan-histone deacetylase inhibitor-resistant acute myeloid leukemia cells. | Blood 20081001 |
Histone deacetylase inhibitor panobinostat induces clinical responses with associated alterations in gene expression profiles in cutaneous T-cell lymphoma. | Clinical cancer research : an official journal of the American Association for Cancer Research 20080715 |
Experimental treatment of pancreatic cancer with two novel histone deacetylase inhibitors. | World journal of gastroenterology 20080621 |
Role of acetylation and extracellular location of heat shock protein 90alpha in tumor cell invasion. | Cancer research 20080615 |
Mitochondrial Bax translocation partially mediates synergistic cytotoxicity between histone deacetylase inhibitors and proteasome inhibitors in glioma cells. | Neuro-oncology 20080601 |
Combination strategy targeting the hypoxia inducible factor-1 alpha with mammalian target of rapamycin and histone deacetylase inhibitors. | Clinical cancer research : an official journal of the American Association for Cancer Research 20080601 |
Epigenetic silencing of the tetraspanin CD9 during disease progression in multiple myeloma cells and correlation with survival. | Clinical cancer research : an official journal of the American Association for Cancer Research 20080515 |
Inhibition of histone deacetylases promotes ubiquitin-dependent proteasomal degradation of DNA methyltransferase 1 in human breast cancer cells. | Molecular cancer research : MCR 20080501 |
Histone deacetylase inhibitors in lymphoma and solid malignancies. | Expert review of anticancer therapy 20080301 |
Histone deacetylase inhibitors induce growth arrest and apoptosis of HTLV-1-infected T-cells via blockade of signaling by nuclear factor kappaB. | Leukemia research 20080201 |
Determination of the class and isoform selectivity of small-molecule histone deacetylase inhibitors. | The Biochemical journal 20080115 |
Inhibition of histone deacetylase for the treatment of biliary tract cancer: a new effective pharmacological approach. | World journal of gastroenterology 20070921 |
Effect of the histone deacetylase inhibitor LBH589 against epidermal growth factor receptor-dependent human lung cancer cells. | Molecular cancer therapeutics 20070901 |
Targeted therapy and the T315I mutation in Philadelphia-positive leukemias. | Haematologica 20070401 |
Abrogation of MAPK and Akt signaling by AEE788 synergistically potentiates histone deacetylase inhibitor-induced apoptosis through reactive oxygen species generation. | Clinical cancer research : an official journal of the American Association for Cancer Research 20070215 |
Histone deacetylase inhibitor LBH589 reactivates silenced estrogen receptor alpha (ER) gene expression without loss of DNA hypermethylation. | Cancer biology & therapy 20070101 |
Aggresome induction by proteasome inhibitor bortezomib and alpha-tubulin hyperacetylation by tubulin deacetylase (TDAC) inhibitor LBH589 are synergistic in myeloma cells. | Blood 20061115 |
Combined effects of novel tyrosine kinase inhibitor AMN107 and histone deacetylase inhibitor LBH589 against Bcr-Abl-expressing human leukemia cells. | Blood 20060715 |
The histone deacetylase inhibitor LBH589 is a potent antimyeloma agent that overcomes drug resistance. | Cancer research 20060601 |
Meeting highlights from: 47th Annual Meeting of the American Society of Hematology December 2005, Atlanta, GA. | Clinical lymphoma & myeloma 20060501 |
Targeting tumor angiogenesis with histone deacetylase inhibitors: the hydroxamic acid derivative LBH589. | Clinical cancer research : an official journal of the American Association for Cancer Research 20060115 |
[Novel inhibitors of Bcr-Abl]. | Postepy higieny i medycyny doswiadczalnej (Online) 20060101 |
Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3. | Blood 20050215 |
The American Society of Hematology--46th Annual Meeting and Exposition. HDAC, Flt and farnesyl transferase inhibitors. | IDrugs : the investigational drugs journal 20050101 |