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TargetMol | Compound Library

Tyrosine Kinase Inhibitor Library

Catalog No. L2200

A protein kinase is a kinase enzyme that modifies other molecules, mostly proteins, by chemically adding phosphate groups to them (phosphorylation) to regulate the majority of cellular pathways, especially those involved in signal transduction. Phosphorylation usually results in a functional change of the target protein (substrate) by changing enzyme activity, cellular location, or association with other proteins. Of the 518 known kinases, the most successful class for drug targeting is the tyrosine kinase family consisting of 90 distinct and diverse members. Abnormal expression of PTK usually leads to cell proliferation disorders, and is closely related to tumor invasion, metastasis and tumor angiogenesis. More recently, PTKs play a pivotal role in inflammatory diseases such as idiopathic pulmonary fibrosis.

The Tyrosine Kinase Inhibitors Library by TargetMol, containing 1350 tyrosine kinase inhibitors, can be used for research in tyrosine kinase signaling, and drug screening for related diseases.

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

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Catalog No. L2200

Tyrosine Kinase Inhibitor 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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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.

Product Description Product Description

  • A unique collection of 1350 tyrosine kinase inhibitors for high throughput screening and high content screening for drug discovery in tyrosine kinase related diseases;
  • Bioactivity and safety confirmed by pre-clinical research and clinical trials, and some of them are approved by FDA;
  • Targets include c-Kit, c-Met, EGFR, FGFR, SRC, JAK, SYK, Btk, Bcr-Abl, etc;
  • 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;

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Library Customization | TargetMol Library Composition

Apoptosis
EGFR
VEGFR
JAK
Src
FLT
Autophagy
PDGFR
FGFR
c-Met/HGFR
c-Kit
Bcr-Abl
ALK
PKA
IGF-1R
Akt
Tyrosine Kinases
CDK
STAT
FAK
Trk receptor
NF-κB
c-RET
ERK
c-Fms
TGF-beta/Smad
TAM Receptor
p38 MAPK
Syk
PKC
Endogenous Metabolite
ROS
Potassium Channel
HER
ROS Kinase
Aurora Kinase
Raf
DYRK
BTK
PI3K
Antibacterial
Caspase
mTOR
GSK-3
Ephrin Receptor
Interleukin
5-HT Receptor
TNF
CSF-1R
Parasite
S6 Kinase
AMPK
Reactive Oxygen Species
JNK
Discoidin Domain Receptor (DDR)
MAPK
Tie-2
Tyrosinase
Cytochromes P450
Bcl-2 Family
IL Receptor
HIV Protease
Calcium Channel
ROCK
Adrenergic Receptor
COX
DNA/RNA Synthesis
MEK
Serine/threonin kinase
PYK2
MMP
Influenza Virus
Microtubule Associated
Ferroptosis
PPAR
SARS-CoV
Phosphatase
NO Synthase
Drug Metabolite
PARP
Antibiotic
PROTACs
Chk
TLR
Virus Protease
Casein Kinase
IκB/IKK
PDE
Sodium Channel
HDAC
Integrin
Histamine Receptor
Mitophagy
AChR
Pim
SGK
MLK
Histone Methyltransferase
RIP kinase
MDM-2/p53
Antioxidant
Ligands for Target Protein for PROTAC
Antifungal
Mitochondrial Metabolism
PLK
HIF/HIF Prolyl-Hydroxylase
HSP
Dehydrogenase
GRK
ACK1
CaMK
MAO
PERK
HSV
Epigenetic Reader Domain
Phospholipase
IFNAR
Hck
TRP/TRPV Channel
Antiviral
Beta Amyloid
Anti-infection
Nrf2
PAK
GABA Receptor
HIF
IRAK
GDNF
iGluR
Cholinesterase (ChE)
GluR
Sigma receptor
Serine Protease
LIM Kinase
Immunology/Inflammation related
MNK
Ras
Estrogen Receptor/ERR
Serotonin Transporter
PDK
Monoamine Oxidase
NOS
HCV Protease
Topoisomerase
LDL
CXCR
P-gp
Prostaglandin Receptor
Dopamine Receptor
Antifection
GPCR
Adenosine Receptor
Rho
Lipoxygenase
Reverse Transcriptase
PD-1/PD-L1
HBV
Wnt/beta-catenin
Glucokinase
Haspin Kinase
Angiotensin-converting Enzyme (ACE)
DUB
DHFR
Myosin
Transferase
NADPH
transporter
NOD-like Receptor (NLR)
MyD88
FXR
IRE1
PTEN
Norepinephrine
p53
Wee1
BCRP
Survivin
HMG-CoA Reductase
Kinesin
IKZF
FOXO3
Na+/Ca2+ Exchanger
GTPase
c-Myc
Liver X Receptor
NAMPT
Vasopressin Receptor
cAMP
GHR
Histone Acetyltransferase
PAI-1
MELK
Gap Junction Protein
Platelet aggregation
NOD
ATPase
Carbonic Anhydrase
Nucleoside Antimetabolite/Analog
IAP
LAG-3
E1/E2/E3 Enzyme
ABC Transporter
Monoamine Transporter
PROTAC Linker
FAAH
CCR
E3 Ligase Ligand-Linker Conjugates
Sirtuin
cGAS
Hippo pathway
Kras
CRISPR/Cas9
Hydroxylase
ROR
Cell Cycle Arrest
Gamma-secretase
NMDAR
GPCR19
RSV
Protease
Melanin-concentrating Hormone Receptor (MCHR)
DNA-PK
RAAS
Cholecystokinin Receptor
AAK1
SIK
Glucosidase
Hedgehog/Smoothened
DNA Alkylation
Acyltransferase
ATM/ATR
FOXO
YAP
Glucocorticoid Receptor
MT Receptor
Phosphorylase
Stearoyl-CoA Desaturase (SCD)
Telomerase
Proton pump
Arrestin
Leukotriene Receptor
Aryl Hydrocarbon Receptor
STING
LRRK2
Pyroptosis
Acetyl-CoA Carboxylase
CGRP Receptor
NADPH-oxidase
Estrogen/progestogen Receptor
Antifolate
Glutaminase
UGT
Fatty Acid Synthase
PAD
Thrombopoietin Receptor
Androgen Receptor
PGE Synthase
DAPK
Protease-activated Receptor
p97
Ferroportin
IGF-2R
Vitamin
PGC-1α