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TargetMol | Compound Library

Cancer Cell Differentiation Compound Library

Catalog No. L2140

Cell differentiation is a multifaceted process that depends on complex regulatory networks that involve transcriptional, post-transcriptional and epigenetic regulation of gene expression. In cancer, this describes how much or how little tumor tissue looks like the normal tissue it came from. Well-differentiated cancer cells look more like normal cells and tend to grow and spread more slowly than poorly differentiated or undifferentiated cancer cells. Differentiation is used in tumor grading systems, which are different for each type of cancer. In addition to apoptosis resistance and cell proliferation capacities, the undifferentiated state also characterizes most cancer cells, especially leukemia cells. The induction of cancer cell differentiation is considered an alternative approach to elicit cell death and proliferation arrest. Differentiation therapy has mainly been developed to treat acute myeloid leukemia, notably with all-trans retinoic acid (ATRA). Numerous molecules from diverse natural or synthetic origins are effective alone or in association with ATRA in both in vitro and in vivo experiments. During the last two decades, pharmaceuticals and natural compounds with various chemical structures, including alkaloids, flavonoids and polyphenols, were identified as potential differentiating agents of hematopoietic pathways and osteogenesis. TargetMol collects 406 reported compounds inducing cancer cell differentiation as Cancer Cell Differentiation Compound Library, which can be used for high throughput and high content screening for 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. L2140

Cancer Cell Differentiation 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 406 cancer cell differentiation inducing compounds for high throughput and high content screening;
  • 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

Autophagy
Apoptosis
PI3K
p38 MAPK
STAT
TGF-beta/Smad
mTOR
HDAC
ERK
Akt
GSK-3
DNA-PK
Wnt/beta-catenin
NF-κB
ALK
ATM/ATR
CDK
AMPK
Antibacterial
Endogenous Metabolite
S6 Kinase
Parasite
Gamma-secretase
Mitophagy
Antibiotic
Casein Kinase
HIV Protease
Reactive Oxygen Species
PDK
Src
PKA
Caspase
PKC
MEK
Dehydrogenase
BCL
DNA/RNA Synthesis
JAK
COX
MAPK
Virus Protease
PARP
VEGFR
PDE
Raf
PPAR
Chk
Influenza Virus
Carbonic Anhydrase
JNK
Antifungal
Adenosine Receptor
ROCK
HSV
MMP
Aurora Kinase
Epigenetic Reader Domain
EGFR
Beta Amyloid
FGFR
TNF
FLT
Phosphatase
Calcium Channel
Adrenergic Receptor
Topoisomerase
Bcr-Abl
HBV
Tyrosine Kinases
Drug Metabolite
IL Receptor
Lipoxygenase
P-gp
TLR
PDGFR
IGF-1R
AChE
Porcupine
IκB/IKK
c-Fms
PI4K
P450
CRISPR/Cas9
HER
NOS
DHFR
HCV Protease
Estrogen/progestogen Receptor
Arginase
c-Met/HGFR
BACE
NADPH
Histamine Receptor
Tie-2
c-Myc
ATPase
Integrin
YAP
Ferroptosis
Antioxidant
Estrogen Receptor/ERR
Antifolate
Serine Protease
RIP kinase
UGT
Hck
Nucleoside Antimetabolite/Analog
Smo
Fatty Acid Synthase
CXCR
GluR
DNA
Beta-Secretase
SARS-CoV
transporter
Isocitrate Dehydrogenase (IDH)
Hedgehog/Smoothened
CCR
PTEN
PAD
MNK
Antiviral
5-HT Receptor
SGK
Potassium Channel
MLK
Nrf2
hCE
MELK
Retinoid Receptor
Aromatase
Phospholipase
GABA Receptor
HIF
PLK
AChR
c-Kit
Sodium Channel
Ras
HIF/HIF Prolyl-Hydroxylase
FAK

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