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Vemurafenib
Known as:
1-propanesulfonamide, N-(3-((5-(4-chlorophenyl)-1H-pyrrolo(2,3-b)pyridin-3- yl)carbonyl)-2,4-difluorophenyl)-
, 1-propanesulfonamide, n-(3-((5-(4-chlorophenyl)-1h-pyrrolo(2,3-b)pyridin-3-yl)carbonyl)-2,4-difluorophenyl)-
, N-(3-((5-(4-chlorophenyl)-1H-pyrrolo(2,3-b)pyridin-3-yl)carbonyl)-2,4- difluorophenyl)propane-1-sulfonamide
An orally bioavailable, ATP-competitive, small-molecule inhibitor of BRAF(V600E) kinase with potential antineoplastic activity. Vemurafenib…
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National Institutes of Health
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Related topics
Related topics
13 relations
Broader (4)
Antineoplastic Agents
Enzyme Inhibitors
Indoles
Sulfonamides
BRAF protein, human
Inhibition of Cell Proliferation
NCIt Antineoplastic Agent Terminology
Positive Regulation of Apoptosis
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Narrower (3)
PLX4032
RG7204
Zelboraf
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
BRAFV600E-mutant cancers display a variety of networks by SWIM analysis: prediction of vemurafenib clinical response
R. Falcone
,
F. Conte
,
+7 authors
A. Verrienti
Endocrine
2019
Corpus ID: 73512988
PurposeSeveral studies have shown that different tumour types sharing a driver gene mutation do not respond uniformly to the same…
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2015
2015
Melanoma patient derived xenografts acquire distinct Vemurafenib resistance mechanisms.
D. Monsma
,
David Cherba
,
+11 authors
N. Monks
American Journal of Cancer Research
2015
Corpus ID: 1711186
Variable clinical responses, tumor heterogeneity, and drug resistance reduce long-term survival outcomes for metastatic melanoma…
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Highly Cited
2014
Highly Cited
2014
Phase 1 study of the BRAF inhibitor dabrafenib (D) with or without the MEK inhibitor trametinib (T) in combination with ipilimumab (Ipi) for V600E/K mutation–positive unresectable or metastatic…
I. Puzanov
,
M. Callahan
,
+11 authors
A. Hoos
2014
Corpus ID: 77065869
2511 Background: D, T, and Ipi are each indicated for treatment of patients (pts) with MM (D+T in BRAF V600 mutation–positive MM…
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2014
2014
COX‐2 inhibition prevents the appearance of cutaneous squamous cell carcinomas accelerated by BRAF inhibitors
Helena Escuin-Ordinas
,
M. Atefi
,
+12 authors
A. Ribas
Molecular Oncology
2014
Corpus ID: 8595929
Highly Cited
2014
Highly Cited
2014
BRAF inhibitors in cancer therapy.
C. Johansson
,
S. E. Brage
2014
Corpus ID: 196597474
2014
2014
Molecular Pathways Molecular Pathways : Response and Resistance to BRAF and MEK Inhibitors in BRAFV 600 E Tumors
M. Thakur
,
D. Stuart
2014
Corpus ID: 7157516
The RAS–RAF–MEK (MAP–ERK kinase)–ERK (extracellular signal–regulated kinase) pathway plays a central role in driving…
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2014
2014
Case of vemurafenib‐induced Sweet's syndrome
J. Yorio
,
S. Mays
,
+6 authors
Kevin B. Kim
Journal of dermatology (Print)
2014
Corpus ID: 13573072
Vemurafenib is a targeted therapy that has become standard treatment for patients with advanced melanoma with a V600E BRAF…
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Review
2013
Review
2013
Advances in therapy for melanoma brain metastases.
Jaclyn C Flanigan
,
Lucia B. Jilaveanu
,
V. Chiang
,
H. Kluger
Clinical Dermatology
2013
Corpus ID: 1253322
Review
2013
Review
2013
High-Dose Interleukin-2 (HD IL-2) Therapy Should Be Considered for Treatment of Patients with Melanoma Brain Metastases
M. Chu
,
M. Fesler
,
E. Armbrecht
,
S. Fosko
,
E. Hsueh
,
J. Richart
Chemotherapy Research and Practice
2013
Corpus ID: 15455813
A retrospective review was performed on patients with stable melanoma brain metastases treated with HD IL-2 therapy (720,000 IU…
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2012
2012
Vemurafenib-induced neutrophilic panniculitis.
J. Monfort
,
C. Pagès
,
+6 authors
C. Lebbé
Melanoma research
2012
Corpus ID: 23635407
Vemurafenib is a targeted therapy, used in patients with metastatic cutaneous melanoma who carry the BRAF V600E mutation, with a…
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