5'-G A N T C-3' 3'-C T N A G-5'
ATO, but not GANT in combination with Gos reduces GSC marker and Hh and... | Download Scientific Diagram
Effects of an apoptotic inhibitor on GANT-61 treated NB cells. (A)... | Download Scientific Diagram
IJMS | Free Full-Text | Glioma-Associated Oncogene Homolog Inhibitors Have the Potential of Suppressing Cancer Stem Cells of Breast Cancer
Schematic overview of different GANT61 target sites. Inhibition of the... | Download Scientific Diagram
Inhibition of autophagy potentiates the efficacy of Gli inhibitor GANT-61 in MYCN-amplified neuroblastoma cells | BMC Cancer | Full Text
GANT 58 (NSC 75503) | GLI Antagonist | MedChemExpress
Inhibition of the sonic hedgehog pathway activates TGF-β-activated kinase (TAK1) to induce autophagy and suppress apoptosis in thyroid tumor cells | Cell Death & Disease
Gant 61 counteracts the pro-fibrotic effects and autophagy inhibition... | Download Scientific Diagram
NMDAR inhibition-independent antidepressant actions of ketamine metabolites | Nature
Nanoquinacrine induced apoptosis in cervical cancer stem cells through the inhibition of hedgehog-GLI1 cascade: Role of GLI-1 | Scientific Reports
Antileishmanial Chemotherapy through Clemastine Fumarate Mediated Inhibition of the Leishmania Inositol Phosphorylceramide Synthase | ACS Infectious Diseases
Inhibition of autophagy potentiates the efficacy of Gli inhibitor GANT-61 in MYCN-amplified neuroblastoma cells | BMC Cancer | Full Text
APExBIO - GANT 58|GLI antagonist,novel and potent|CAS# 64048-12-0
Nitroreductase‐Mediated Release of Inhibitors of Lysine‐Specific Demethylase 1 (LSD1) from Prodrugs in Transfected Acute Myeloid Leukaemia Cells - Herrlinger - 2020 - ChemBioChem - Wiley Online Library
GANT 61 (CAS 500579-04-4): R&D Systems
Dissecting Histone Deacetylase 3 in Multiple Disease Conditions: Selective Inhibition as a Promising Therapeutic Strategy | Journal of Medicinal Chemistry
IJMS | Free Full-Text | Responsiveness to Hedgehog Pathway Inhibitors in T-Cell Acute Lymphoblastic Leukemia Cells Is Highly Dependent on 5′AMP-Activated Kinase Inactivation
