AK-778-XXMU
AK-778-XXMU is a potent DNA binding inhibitor 2 (ID2) antagonist with a KD of 129 nM. AK-778-XXMU can inhibit cell migration and invasion of glioma cell lines, induce apoptosis, and exhibits significant cancer-suppressing potency. AK-778-XXMU inhibits the ID2-KDR signaling axis, thereby down-regulating the downstream angiogenic factors (VEGFA) and invasion-related proteins (MMP2/9), and up-regulating the tumor suppressor factor (PTEN) . AK-778-XXMU can be used for the study of glioma[1].
Product Specifications
CAS Number
[1227045-76-2]
UNSPSC
12352005
Target
Apoptosis; MMP; PTEN; VEGFR
Type
Reference compound
Related Pathways
Apoptosis; Metabolic Enzyme/Protease; PI3K/Akt/mTOR; Protein Tyrosine Kinase/RTK
Applications
Cancer-programmed cell death
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/ak-778-xxmu.html
Purity
99.96
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
O=C(C1=CC=CC=N1)CC2(C(N(C3=C2C=CC=C3)CC4=CC=CC(Cl)=C4)=O)O
Molecular Formula
C22H17ClN2O3
Molecular Weight
392.83
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
MMP-2; MMP-9
Available Sizes
Explore Other Products
Browse additional items from our catalog
Rbms2 sgRNA CRISPR Lentivector (Rat) (Target 1)
Recombinant Bacillus thuringiensis subsp. konkukian UPF0295 protein BT9727_0449 (BT9727_0449), partial
Rat Vascuoar endothelial cell growth factor receptor 1,VEGFR-1 ELISA Kit