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