GLPBio

AG-18 (Tyrphostin 23)

Catalog No.: GC17647Purity:>98.50%Synonyms: RG50810, RG50858, TX 825, Tyrphostin 23, Tyrphostin AG18
AG-18 (Tyrphostin A23) is an EGFR inhibitor with an IC50 and Kiof 35 and 11 μM, respectively.

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AG-18 (Tyrphostin 23)
Cas No.: 118409-57-7
10mM (in 1mL DMSO)In Stock
$25.00
1
5mgIn Stock
$23.00
1
10mgIn Stock
$39.00
1
50mgIn Stock
$139.00
1
100mgIn Stock
$209.00
1

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Description

AG-18 (Tyrphostin 23) is a cell-permeable tyrosine kinase and epidermal growth factor receptor (EGFR) inhibitor, with an IC50 of 35μM for EGFR[1]. AG-18 blocks receptor autophosphorylation and activation of downstream signaling pathways by acting on the ATP-binding site or substrate-binding site of EGFR[2]. AG-18 is commonly applied to study EGFR-mediated signal transduction, regulation of cell proliferation, and receptor tyrosine kinase-related mechanisms[3,4].

In vitro, treatment of primary rat astrocytes with AG-18 (100μM) for 2h significantly increased lactate release and glucose consumption to 220% and 260% of the control, respectively[5]. Pretreatment of human alveolar epithelial A549 cells with AG-18 (30, 100, 300μM) for 30min, followed by continued treatment with TNF-α (10ng/mL) for 4.5h, dose-dependently inhibited TNF-α-induced surface expression of intercellular adhesion molecule-1 (ICAM-1)[6]. Co-incubation of AG-18 (25-200μM) with mouse striatal homogenate at 30℃ for 2min, using 10nM [3H]dopamine as the substrate, concentration-dependently inhibited dopamine uptake[7].

In vivo, LKB1null LUAD organoids were subcutaneously injected into NOD-SCID mice, and after palpable tumors formed, oral administration of AG-18 (100mg/kg; once daily) for 14 days significantly reduced tumor volume (by approximately 60-70%)[8].

References:
[1] Boschelli D H. Small molecule inhibitors of receptor tyrosine kinases[J]. Drugs of the Future, 1999, 24(5): 515-538.
[2] Levitzki A, Gazit A. Tyrosine kinase inhibition: an approach to drug development[J]. Science, 1995, 267(5205): 1782-1788.
[3] Breen M E, Soellner M B. Small molecule substrate phosphorylation site inhibitors of protein kinases: approaches and challenges[J]. ACS chemical biology, 2015, 10(1): 175-189.
[4] Hohnholt M C, Blumrich E M, Waagepetersen H S, et al. The tricarboxylic acid cycle activity in cultured primary astrocytes is strongly accelerated by the protein tyrosine kinase inhibitor tyrphostin 23[J]. Neurochemistry international, 2017, 102: 13-21.
[5] Blumrich E M, Kadam R, Dringen R. The protein tyrosine kinase inhibitor tyrphostin 23 strongly accelerates glycolytic lactate production in cultured primary astrocytes[J]. Neurochemical research, 2016, 41(10): 2607-2618.
[6] Chen C C, Chou C Y, Sun Y T, et al. Tumor necrosis factor α-induced activation of downstream NF-κB site of the promoter mediates epithelial ICAM-1 expression and monocyte adhesion: involvement of PKCα, tyrosine kinase, and IKK2, but not MAPKs, pathway[J]. Cellular Signalling, 2001, 13(8): 543-553.
[7] Simon J R, Bare D J, Ghetti B, et al. A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatum[J]. Neuroscience letters, 1997, 224(3): 201-205.
[8] Angelopoulou A, Theocharous G, Valakos D, et al. Loss of the tumour suppressor LKB1/STK11 uncovers a leptin-mediated sensitivity mechanism to mitochondrial uncouplers for targeted cancer therapy[J]. Molecular Cancer, 2024, 23(1): 147.

Protocol

Cell experiment [1]:

Cell lines

Primary rat astrocytes

Preparation Method

Primary rat astrocytes were incubated with 100μM AG-18 for 2h, then the extracellular lactate content and glucose consumption were determined using coupled enzymatic assays with lactate dehydrogenase/glutamate pyruvate transaminase and hexokinase/glucose-6-phosphate dehydrogenase, respectively.

Reaction Conditions

100μM; 2h

Applications

Incubation of cultured primary rat astrocytes with 100μM AG-18 for 2h significantly increased lactate release and glucose consumption to 220% and 260% of control values, respectively.
Animal experiment [2]:

Animal models

NOD-SCID mice bearing LKB1null LUAD organoid xenografts

Preparation Method

LKB1null LUAD organoids were subcutaneously injected into NOD-SCID mice. After palpable tumours had formed, mice were administered AG-18 (100mg/kg; once daily; per os) for 14 days, and tumour volume was monitored and calculated.

Dosage form

100mg/kg; once daily; 14 days; p.o.

Applications

Treatment with AG-18 resulted in a statistically significant decrease in tumour volume in the absence of LKB1 (60-70% reduction).

References:
[1] Blumrich E M, Kadam R, Dringen R. The protein tyrosine kinase inhibitor tyrphostin 23 strongly accelerates glycolytic lactate production in cultured primary astrocytes[J]. Neurochemical research, 2016, 41(10): 2607-2618.
[2] Angelopoulou A, Theocharous G, Valakos D, et al. Loss of the tumour suppressor LKB1/STK11 uncovers a leptin-mediated sensitivity mechanism to mitochondrial uncouplers for targeted cancer therapy[J]. Molecular Cancer, 2024, 23(1): 147.

Product Documents

Purity:>98.50%Appearance:A solid

Chemical Properties

CAS No.
118409-57-7
Synonyms
RG50810, RG50858, TX 825, Tyrphostin 23, Tyrphostin AG18
Chemical Name
2-[(3,4-dihydroxyphenyl)methylidene]propanedinitrile
SMILES
C1=CC(=C(C=C1C=C(C#N)C#N)O)O
Molecular Formula
C10H6N2O2
Molecular Weight
186.17
Solubility
≥ 9.3mg/mL in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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