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TargetMol | Compound Library

Immuno-Oncology Compound Library

Catalog No. L2170

Traditional cancer therapies include surgery, radiation therapy, and chemotherapy. With the rapid development of science and technology in medicine, new cancer therapies such as immunotherapy, targeted therapy, radiofrequency ablation for cancer are actively developed to help patients fight cancer. Cancer immunotherapy, also known as immuno-oncology, is a form of cancer treatment that uses the power of the body's own immune system to prevent, control, and eliminate cancer. Science magazine—America's leading scientific journal—has deemed cancer immunotherapy the 2013 "Breakthrough of the Year," beating out nine other contenders. There are several types of immunotherapy, including: Non-specific immunotherapies, CAR T-cell therapy, cancer vaccines, checkpoint inhibitors, etc. Most cancer immunotherapy agents being developed or approved are engineered T cells targeting tumors or mostly antibody-based biologics that target the immune checkpoint cascade. The success of these biologics in the clinic is now inspiring the discovery and development of small molecules that act on intracellular targets affecting immuno-modulatory pathways in cancer. Small molecule agents as opposed to biologics that steer or enable the immune system to attack cancer cells, represent an emerging area of R&D focus in the oncology drug development industry. Small molecules are being investigated as stand-alone agents and synergistically with approved biologics because of the ability of small molecules to reach intracellular targets and the greater patient convenience offered by their oral bioavailability. The foundation for the pursuit of small molecule immune therapies for cancer is the wide spectrum of cells and their molecular pathways that are used by the immune system to suppress or enhance cellular immunity. Such novel immunotherapeutic approaches can either negate immune suppression in the tumor milieu or facilitate cytolytic lymphocyte responses to the tumor. TargetMol's Immuno-Oncology Compound Library carefully collects 523 bioactive compounds targeting intracellular pathways modulating the innate and adaptive immune response is a powerful tool for your research and drug discovery.

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

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Catalog No. L2170

Immuno-Oncology 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 523 compounds acting on immune-oncology therapeutic targets can be used for high throughput and high content screening;
  • Targets include PD-1/PD-L1, HER2, STAT3, CTLA4, IDO, STING, CCR, CXCR, TLR, etc.
  • Detailed compound information with structure, target, and biological activity description;
  • NMR and HPLC validated to ensure high purity and quality.

Packaging And Storage Packaging And Storage

  • Powder or pre-dissolved DMSO solutions in 96/384 well plate with optional 2D barcode
  • Shipped with blue ice
  • This compound library is provided at a concentration of 10 mM in DMSO. A small number of compounds may be provided in different solvents or concentrations due to solubility or stability requirements. Please refer to the specific product information for details.

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Library Customization | TargetMol Library Composition

Apoptosis
TNF
TLR
STAT
PI3K
Autophagy
CCR
EGFR
CXCR
NF-κB
HER
IL Receptor
TGF-beta/Smad
STING
PD-1/PD-L1
HIV Protease
IDO
Indoleamine 2,3-Dioxygenase (IDO)
Interleukin
Adenosine Receptor
mTOR
COX
Antibacterial
VEGFR
Endogenous Metabolite
RIP kinase
JAK
ALK
p38 MAPK
Parasite
Akt
Epigenetic Reader Domain
c-Fms
DNA-PK
c-Met/HGFR
Virus Protease
CSF-1R
SARS-CoV
FLT
Antibiotic
NO Synthase
ERK
Reactive Oxygen Species
PDGFR
HCV Protease
Src
Arginase
IFNAR
MMP
Potassium Channel
c-Kit
BTK
Ferroptosis
PDE
Raf
Bcl-2 Family
Casein Kinase
Influenza Virus
MyD88
Antioxidant
Wnt/beta-catenin
Topoisomerase
CDK
Antifection
Aurora Kinase
P-gp
HSP
Nrf2
HDAC
5-HT Receptor
FGFR
MEK
AChR
NOD
Tyrosinase
HIF/HIF Prolyl-Hydroxylase
Carbonic Anhydrase
DHFR
Arrestin
Histone Demethylase
JNK
c-Myc
HBV
Tyrosine Kinases
PPAR
Caspase
TRP/TRPV Channel
Bcr-Abl
Drug Metabolite
Mitochondrial Metabolism
Stearoyl-CoA Desaturase (SCD)
HSV
Cholinesterase (ChE)
PTEN
Cytochromes P450
IGF-1R
OXPHOS
PGE Synthase
MAPK
Antiviral
Prostaglandin Receptor
IκB/IKK
PI4K
AMPK
DNA Methyltransferase
Ras
NOD-like Receptor (NLR)
FOXO3
Apelin receptor
GPCR
Proteasome
Chloride channel
Proton pump
NOS
ROR
Dynamin
Integrin
Amino Acids and Derivatives
Dehydrogenase
Antifungal
LTR
Tie-2
Glutathione Peroxidase
Phosphatase
Mitophagy
VDA
Progesterone Receptor
PKA
Estrogen Receptor/ERR
Serine Protease
Serine/threonin kinase
Liver X Receptor
Leukotriene Receptor
NAMPT
Calcium Channel
PKC
LDLR
Amylase
Adrenergic Receptor
Immunology/Inflammation related
iGluR
E1/E2/E3 Enzyme
UGT
ROS
ACK1
PAD
DNA
Target Protein Ligand-Linker Conjugate
SGLT
BCRP
DNA/RNA Synthesis
MNK
Survivin
Trk receptor
Sirtuin
Ephrin Receptor
AIM2
Histone Acetyltransferase
Decarboxylase
hCE
ATM/ATR
Beta Amyloid
Reverse Transcriptase
PLK
HIF
Syk
NADPH-oxidase
S6 Kinase
ROS Kinase
CFTR
MLK
PKM

Keywords