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Search Results for " glioblastoma "

20

Compounds

Cat No. Product Name Synonyms Targets
T7008 Vacquinol-1 Vacquinol 1 JNK
Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death.
T14214 AMG 511 PI3K
AMG 511 is a potent and orally available pan inhibitor of class I PI3Ks(Kis of 4 nM, 6 nM, 2 nM and 1 nM for PI3Kα, β, δ and γ, respectively). It exhibits anti-tumor activity in mouse glioblastoma xenograft model[1]. AMG...
T10140 4-Diethylaminobenzaldehyde Dehydrogenase
4-Diethylaminobenzaldehyde is a reversible aldehyde dehydrogenase (ALDH) inhibitor (Ki: 4 nM for ALDH1). It displays a potent anti-androgenic effect (IC50: 1.71μM).
TN2080 Pinoresinol (+)-Pinoresinol Apoptosis , NF-κB , CDK , p53
Pinoresinol ((+)-Pinoresinol) has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury, to increase nitric oxide release and to reduce oxidative st...
T9575 MRTX9768 Histone Methyltransferase
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
T8961 GW280264X Carbamic acid MMP
GW280264X (Carbamic acid) is an inhibitor of ADAM17 .
T8657 KYP-2047 Others
KYP-2047 is a very potent, selective Prolyl oligopeptidase (POP) inhibitor.
T22318 Taletrectinib DS-6051b,AB-106 Trk receptor , ROS , ROS Kinase
Taletrectinib (AB-106) is a new-generation selective inhibitor of ROS1/NTRK including ROS1,NTRK1,NTRK2 and NTRK3 with IC50 of 0.207 nM,0.622 nM,2.28 nM and 0.980 nM, respectively.
T8545 FEN1-IN-4 FEN1 Inhibitor C2 Others
FEN1-IN-4 (FEN1 Inhibitor C2) is an inhibitor of human flap endonuclease-1 (hFEN1)
T6303 CCT128930 Akt , PKA , S6 Kinase , Autophagy
CCT128930 is a potent, ATP-competitive and selective inhibitor of Akt2 with IC50 of 6 nM, 28-fold greater selectivity for Akt2 than the closely related PKA kinase.
T0440 Oxcarbazepine GP 47680 Apoptosis , Sodium Channel
Oxcarbazepine (GP 47680) is an Anti-epileptic Agent. The physiologic effect of oxcarbazepine is by means of Decreased Central Nervous System Disorganized Electrical Activity.
T8421 TED-347 YAP
TED-347 is an irreversible and covalent inhibitor of TEAD4-Yap1 protein-protein interaction(EC50 of 5.9 μM), and inhibits glioblastoma cell viability.
T5622 BAY-218 AHR antagonist 1 AhR , Aryl Hydrocarbon Receptor
BAY-218 (AHR antagonist 1) is an aryl hydrocarbon receptor (AHR) antagonist , has an IC50 of 39.9 nM in human cell line.
T0192 Levetiracetam UCB L059,SIB-S1 DNA Methyltransferase , Others , Calcium Channel
Levetiracetam (SIB-S1) is a relatively unique anticonvulsant that is typically used in combination with other antiepileptic medications for partial onset seizures. Levetiracetam has been linked to rare instances of serum...
T8333 Aurintricarboxylic acid ATA,NSC-4056,NSC4056,NSC 4056 Apoptosis , P2X Receptor , Influenza Virus , Topoisomerase
Aurintricarboxylic acid (NSC-4056) is a strong inhibitor of topoisomerases and other nucleases. It is a potent inhibitor of ribonuclease and topoisomerase II by preventing the binding of the nucleic acid to the enzyme.
T6303L CCT128930 hydrochloride CCT128930 hydrochloride(885499-61-6 Free base) Apoptosis , Akt , PKA , mTOR , Autophagy
CCT128930 hydrochloride (CCT128930 hydrochloride) is a potent and selective inhibitor of AKT with IC50 of 6 nM. CCT128930 hydrochloride induces cell cycle arrest, DNA damage, and autophagy. CCT128930 hydrochloride has 28...
T41151L K34c hydrochloride K34c hydrochloride(939769-93-4 Free base) Integrin
K34c hydrochloride is an alpha5β1 integrin antagonist for glioblastoma study.
T5017 Nimustine Hydrochloride Nidran hydrochloride Apoptosis , Others , DNA Alkylator/Crosslinker , DNA/RNA Synthesis
Nimustine Hydrochloride (Nidran hydrochloride) has been used in trials studying the treatment of Glioblastoma.
T15373 Gboxin ATPase , Mitochondrial Metabolism
Gboxin is an inhibitor of oxidative phosphorylation that targets glioblastoma,inhibits the activity of F0F1 ATP synthase, with antitumour activity.
T40222 FTO-IN-3 Others
FTO-IN-3 is a FTO inhibitor. FTO-IN-3 impairs self-renewal in glioblastoma stem cells.
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