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TargetMol | Compound Library

Wnt/Hedgehog/Notch Compound Library

Catalog No. L4300

The Wnt signaling pathway is an ancient and evolutionarily conserved pathway that regulates crucial aspects of cell fate determination, cell migration, cell polarity, neural patterning and organogenesis during embryonic development. Aberrant regulation of the Wnt signaling pathway is a prevalent theme in cancer biology. The Hedgehog (Hh) pathway is a major regulator of many fundamental processes in vertebrate embryonic development including stem cell maintenance, cell differentiation, tissue polarity and cell proliferation. Constitutive activation of the Hh pathway leading to tumorigenesis is seen in basal cell carcinomas and medulloblastoma. A variety of other human cancers, including brain, gastrointestinal, lung, breast and prostate cancers, also demonstrate inappropriate activation of this pathway. Targeting the Hh signaling pathway provides a new and exciting therapeutic option for a broad variety of cancers. The Notch signaling pathway is a highly conserved cell signaling system present in most multicellular organisms. The Notch signaling cascade is critical for cell proliferation, differentiation, development and homeostasis. Deregulated Notch signaling is found in various diseases, such as T-cell leukemia, breast cancer, prostate cancer, colorectal cancer and lung cancer as well as central nervous system (CNS) malignancies, CADASIL, Alagille syndrome, spondylocostal dysostosis, etc. Wnt/Hedgehog/Notch Compound Library from TargetMol, a unique collection of 237 Wnt/Hedgehog/Notch signaling targeted compounds, can be used for research in Wnt/Hedgehog/Notch signaling and related drug screening (high throughput and high content screening).

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.

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Catalog No. L4300

Wnt/Hedgehog/Notch Compound Library
sizeIn stock
  • 1 mg
  • 30 μL x 10 mM (in DMSO)
  • 50 μL x 10 mM (in DMSO)
  • 100 μL x 10 mM (in DMSO)
  • 250 μL x 10 mM (in DMSO)
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Product Description Product Description

  • A unique collection of 237 Wnt/Hedgehog/Notch signaling targeted compounds for high throughput and high content screening;
  • Bioactivity and safety confirmed by pre-clinical research and clinical trials;
  • Detailed compound information with structure, target, activity, IC50 value, and biological activity description;
  • Structurally diverse, medicinally active, and cell permeable;
  • NMR and HPLC validated to ensure high purity and quality;

Packaging And Storage | TargetMol Packaging And Storage

  • Powder or pre-dissolved DMSO solutions in 96/384 well plate with optional 2D barcode
  • Shipped with blue ice

Library Customization | TargetMol Library Customization

Compound Library | TargetMol
Targetmol Compound Libraries
can be highly customized!
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Library Customization | TargetMol Library Composition

Wnt/beta-catenin
GSK-3
Autophagy
Apoptosis
Casein Kinase
Hedgehog/Smoothened
Gamma-secretase
CDK
Smo
ROCK
c-Myc
CaMK
Endogenous Metabolite
PARP
PKC
Src
Antifungal
PKA
NF-κB
Reactive Oxygen Species
Antibacterial
Porcupine
HIV Protease
PI3K
Parasite
Beta Amyloid
Phospholipase
p38 MAPK
Mitophagy
Calcium Channel
Aurora Kinase
Lipoxygenase
MEK
S6 Kinase
Carbonic Anhydrase
Estrogen/progestogen Receptor
JNK
ATPase
Ferroptosis
Estrogen Receptor/ERR
ERK
Immunology/Inflammation related
Drug Metabolite
Epigenetic Reader Domain
JAK
COX
SGK
FLT
Antibiotic
MLK
STAT
HDAC
GABA Receptor
Syk
Sodium Channel
DHFR
Histone Methyltransferase
DNA-PK
Arginase
c-Met/HGFR
DYRK
Histamine Receptor
Phosphatase
ABC
Proton pump
Dehydrogenase
Virus Protease
Serine/threonin kinase
VEGFR
Glucocorticoid Receptor
Topoisomerase
RIP kinase
Bcr-Abl
PDE
Raf
Tyrosine Kinases
PPAR
Pim
GRK
P2X Receptor
Glucosidase
BCL
DNA Alkylation
HSV
CXCR
Chk
MMP
GluR
DNA
TGF-beta/Smad
Akt
SARS-CoV
LRRK2
PDGFR
IGF-1R
MAPK
Antiviral
Trk receptor
Methionine Adenosyltransferase (MAT)
Influenza Virus
KLF
PI4K
P450
FGFR
Potassium Channel
cholecystokinin
NO Synthase
ALK
MELK
Microtubule Associated
HIF/HIF Prolyl-Hydroxylase
FAK
Kinesin

Keywords