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LFM-A13

Catalog No. T6217   CAS 244240-24-2

LFM-A13(IC50=2.5 μM), a specific Bruton's tyrosine kinase (BTK), is more than 100-fold specificity than other protein kinases, such as JAK1, JAK2, HCK, EGFR, and IRK.

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LFM-A13 Chemical Structure
LFM-A13, CAS 244240-24-2
Pack Size Availability Price/USD Quantity
2 mg In stock $ 31.00
5 mg In stock $ 47.00
10 mg In stock $ 74.00
25 mg In stock $ 167.00
50 mg In stock $ 283.00
100 mg In stock $ 479.00
1 mL * 10 mM (in DMSO) In stock $ 47.00
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Purity: 99.9%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description LFM-A13(IC50=2.5 μM), a specific Bruton's tyrosine kinase (BTK), is more than 100-fold specificity than other protein kinases, such as JAK1, JAK2, HCK, EGFR, and IRK.
Targets&IC50 BTK:2.5 μM
In vitro In BTK+ B-lineage leukemic cells, LFM-A13 enhances their sensitivity to ceramide- or vincristine-induced apoptosis. [1] In BCL-1 cells, NALM-6 cells, or normal BALB/c splenocytes, LFM-13 inhibits the enzymatic activity of BTK in BCL-1 cells without affecting the BTK protein expression levels [2] In human neutrophils, LFM-A13 decreases the tyrosine phosphorylation induced by fMet-Leu-Phe and inhibits the production of superoxide anions and the stimulation of adhesion, chemotaxis, and phospholipase D activity. [3]
In vivo In BALB/c mice bearing BCL-1 leukemia, combination of LFM-A13 (50 mg/kg/day i.p.) and the standard triple-drug VPL prolongs the median survival time. [2] In primary myeloma-bearing SCID-rab mice, LFM-A13 inhibits osteoclast activity, prevents myeloma-induced bone resorption and suppresss myeloma growth. [4]
Molecular Weight 360
Formula C11H8Br2N2O2
CAS No. 244240-24-2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 67 mg/mL (186.1 mM)

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: < 1 mg/mL (insoluble or slightly soluble)

TargetMolReferences and Literature

1. Mahajan S, et al. J Biol Chem. 1999, 274(14), 9587-9599. 2. Uckun FM, et al. Clin Cancer Res. 2002, 8(5), 1224-1233. 3. Gilbert C, et al. J Immunol. 2003, 170(10), 5235-5243. 4. Bam R, et al. Am J Hematol. 2013, 88(6), 463-471.

TargetMolCitations

1. Wan J, Yu X, Niu J Q, et al. Inhibition of Bruton's Tyrosine Kinase Protects Against Burn Sepsis-Induced Intestinal Injury. Frontiers in Medicine. 2022, 9.

Related compound libraries

This product is contained In the following compound libraries:
Tyrosine Kinase Inhibitor Library Highly Selective Inhibitor Library Inhibitor Library Anti-Cancer Active Compound Library Anti-Prostate Cancer Compound Library Anti-Cancer Compound Library Reprogramming Compound Library Stem Cell Differentiation Compound Library Anti-Lung Cancer Compound Library Anti-Aging Compound Library

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Keywords

LFM-A13 244240-24-2 Angiogenesis Cell Cycle/Checkpoint Chromatin/Epigenetic JAK/STAT signaling Stem Cells Tyrosine Kinase/Adaptors PLK JAK BTK Janus kinase LFM-A-13 Inhibitor LFMA13 Polo-like Kinase (PLK) Bruton tyrosine kinase Btk LFM A13 inhibit inhibitor

 

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