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pan FGFR Inhibitor PRN1371
Known as:
FGFR 1-4 Inhibitor PRN1371
, PRN 1371
, PRN1371
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A highly specific covalent inhibitor of human fibroblast growth factor receptor types 1, 2, 3 and 4 (FGFR1-4) with potential antiangiogenic and…
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National Institutes of Health
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Related topics
Related topics
1 relation
Receptor Tyrosine Kinase Inhibition
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Abstract B22: Exposure of AZD4547 FGFR-TKI to a lung squamous carcinoma cell line induces resistance by small cell lung cancer-like transformation associated with ASCL1
Y. Amano
,
T. Ando
,
+4 authors
H. Kage
Tumor Microenvironment
2018
Corpus ID: 91324285
Molecular targeted medicine has progressed in non-small cell lung cancer in recent years, and acquired resistance to molecular…
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2017
2017
Abstract 2091: PRN1371, an irreversible, covalent inhibitor of FGFR1-4 exhibits sustained pathway inhibition in cancer cell lines
E. Venetsanakos
,
Y. Xing
,
+11 authors
S. Gourlay
2017
Corpus ID: 80514827
Introduction: Multiple human cancers harbor alterations in FGFRs that drive tumor growth, including mutations, translocations and…
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2016
2016
A phase 1, multicenter, dose-escalation study of PRN1371, an irreversible covalent FGFR1-4 kinase inhibitor, in patients with advanced solid tumors, followed by expansion cohorts in patients with…
S. Piha-Paul
,
C. Hierro
,
+5 authors
J. Tabernero
2016
Corpus ID: 56910292
TPS2602Background: FGFR inhibition is a promising therapeutic approach in a number of solid tumors where genetic alterations of…
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2016
2016
Abstract 4996: Targeting FGFR4 with monoclonal antibodies as therapeutic agents for the treatment of rhabdomyosarcoma
S. Baskar
2016
Corpus ID: 78157858
Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA Rhabdomyosarcoma (RMS) is the most common soft…
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2016
2016
Abstract SY30-01: Discovery of the highly selective covalent FGFR1-4 inhibitor PRN1371, currently in development for the treatment of solid tumors
K. Brameld
2016
Corpus ID: 78504024
Discovering drug candidates that exhibit durable on-target pharmacology upon oral dosing has been extremely challenging for the…
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2016
2016
Abstract 1249: PRN1371, an irreversible, covalent inhibitor of FGFR1, 2, 3 and 4 is highly efficacious in preclinical tumor models
E. Venetsanakos
,
M. Bradshaw
,
+10 authors
K. Brameld
2016
Corpus ID: 79375595
Introduction: Multiple human cancers harbor alterations in FGFRs that drive tumor growth, including mutations, translocations and…
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2016
2016
Polythérapie fgfr/pd-1 destinée au traitement du cancer
Matthew V. Lorenzi
,
Suso Platero
,
Raluca Verona
,
Jayaprakash Karkera
2016
Corpus ID: 131955350
La presente invention concerne des polytherapies destinees au traitement du cancer. En particulier, les procedes de l'invention…
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2012
2012
FGFR-Fc 융합단백질 및 용도
팡 지앤민
2012
Corpus ID: 187977091
본 발명은 생물기술영역에 속하며 질병의 치료에 관련되고 더욱이 FGF의 과도발현과 상관되는 질병의 치료에 연관된다. 구체적으로 본 발명은 FGFR-Fc 융합단백질 및 FGFR-Fc…
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2012
2012
A Computational Model of Fibroblast Growth Factor-2 Binding to Endothelial Cells Under Fluid Flow
Nisha S. Patel
,
K. Reisig
,
A. Clyne
Annals of Biomedical Engineering
2012
Corpus ID: 254186949
Fibroblast growth factor-2 (FGF2) is an angiogenic growth factor that binds to cell surface receptors (FGFR) and heparan sulfate…
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2001
2001
Mechanisms Growth by Both Angiogenesis-dependent and-independent Factor Receptor Activity in Glioma Cells Impedes Tumor Inhibition of Fibroblast Growth Factor / Fibroblast Growth
P. Auguste
,
Demirkan B. Gürsel
,
+5 authors
A. Bikfalvi
2001
Corpus ID: 17952875
We undertook a series of systematic studies to address the role of fibroblast growth factor/fibroblast growth factor receptor…
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