Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,400,778 papers from all fields of science
Search
Sign In
Create Free Account
panobinostat
Known as:
(2E)-N-hydroxy-3-[4-({[2-(2-methyl-1H-indol-3-yl)ethyl]amino}methyl)phenyl]acrylamide
, 2-Propenamide, N-hydroxy-3-(4-(((2-(2-methyl-1H-indol-3-yl)ethyl)amino) methyl)phenyl)-, (2E)-
A cinnamic hydroxamic acid analogue with potential antineoplastic activity. Panobinostat selectively inhibits histone deacetylase (HDAC), inducing…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
11 relations
Angiogenesis Inhibition
Histone Deacetylase
NCIt Antineoplastic Agent Terminology
Positive Regulation of Apoptosis
Expand
Broader (4)
Antineoplastic Agents
Histone deacetylase inhibitor
Hydroxamic Acids
Indoles
Narrower (1)
LBH589
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Panobinostat: The Small Molecule Metalloenzyme Inhibitor with Marvelous Anticancer Activity.
S. A. Ganai
Current Topics in Medicinal Chemistry
2015
Corpus ID: 32011376
Histone acetyl transferases (HATs) and histone deacetylases (HDACs) are antagonistic enzymes regulating the turnover of histone…
Expand
2015
2015
The thioacetate-ω(γ-lactam carboxamide) HDAC inhibitor ST7612AA1 as HIV-1 latency reactivation agent.
R. Badia
,
Judith Grau
,
E. Riveira-Muñoz
,
E. Ballana
,
G. Giannini
,
J. Esté
Antiviral Research
2015
Corpus ID: 22076785
Review
2014
Review
2014
Rationale for combination therapy in myelofibrosis.
J. Mascarenhas
Baillière's Best Practice & Research: Clinical…
2014
Corpus ID: 37808568
2013
2013
A phase 1/2 study of oral panobinostat combined with melphalan for patients with relapsed or refractory multiple myeloma
J. Berenson
,
J. Hilger
,
+11 authors
R. Vescio
Annals of Hematology
2013
Corpus ID: 21894093
Panobinostat is a histone deacetylase inhibitor that has shown synergistic preclinical anti-myeloma activity when combined with…
Expand
2013
2013
Significant improvement of pig cloning efficiency by treatment with LBH589 after somatic cell nuclear transfer.
Jun-Xue Jin
,
Suo Li
,
+6 authors
Xi-jun Yin
Theriogenology
2013
Corpus ID: 11668192
2012
2012
A phase I study of oral panobinostat (LBH589) in Japanese patients with advanced solid tumors
A. Fukutomi
,
K. Hatake
,
+5 authors
N. Yamamoto
Investigational new drugs
2012
Corpus ID: 26217521
SummaryObjective The objective was to determine the maximum tolerated dose and the dose-limiting toxicity of panobinostat (LBH589…
Expand
Highly Cited
2012
Highly Cited
2012
Downregulation of HMGA2 by the pan-deacetylase inhibitor panobinostat is dependent on hsa-let-7b expression in liver cancer cell lines.
P. Di Fazio
,
R. Montalbano
,
+5 authors
M. Ocker
Experimental Cell Research
2012
Corpus ID: 22589597
Review
2012
Review
2012
Advances in the treatment of relapsed or refractory Hodgkin's lymphoma.
R. Ramchandren
The Oncologist
2012
Corpus ID: 9099371
Hodgkin's lymphoma (HL) is diagnosed in 20,000 men and women annually in North America and Europe. Despite treatment advancements…
Expand
2011
2011
The histone deacetylase inhibitor panobinostat demonstrates marked synergy with conventional chemotherapeutic agents in human ovarian cancer cell lines
D. Budman
,
J. Tai
,
A. Calabro
,
V. John
Investigational new drugs
2011
Corpus ID: 8986851
SummaryAlthough platinum based therapy has improved short term survival of patients with metastatic ovarian cancer, the majority…
Expand
Highly Cited
2010
Highly Cited
2010
The HDAC inhibitor LBH589 (panobinostat) is an inhibitory modulator of aromatase gene expression
Shiuan Chen
,
Jingjing Ye
,
I. Kijima
,
D. Evans
Proceedings of the National Academy of Sciences…
2010
Corpus ID: 40521233
Aromatase converts androgens to estrogens. Although third-generation aromatase inhibitors (AIs) are important drugs in hormonal…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE