[CAS NO. 118409-57-7]  AG-18

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PRODUCTS SPECIFICATIONS [118409-57-7]

Store
Catalog
SLK-S8009
Brand
Selleck
CAS
118409-57-7

DESCRIPTION [118409-57-7]

Overview

MDLMFCD00133899
Molecular Weight186.17
Molecular FormulaC10H6N2O2
SMILESC(=C(C#N)C#N)C1=CC(O)=C(O)C=C1

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM5.3714 mL26.8572 mL53.7143 mL
5 mM1.0743 mL5.3714 mL10.7429 mL
10 mM0.5371 mL2.6857 mL5.3714 mL
50 mM0.1074 mL0.5371 mL1.0743 mL

Description

AG-18 (RG-50810, Tyrphostin A23, TX 825) inhibits with of 35 μM.

Targets

EGFR [1]
35 μM

In vitro

AG 18 inhibits EGFR and IR with K of 11 μM and 12 mM. AG 18 inhibits EGF-induced EGFR autophoshporylation with IC50 of 15 μM in A431 cells. AG 18 (10 μM) inhibits EGF-induced proliferation of GH3 cells. AG 18 (10 μM) causes significant inhibition of the cell proliferation induced by 10 nM and 1 μM ghrelin. AG 18 (10 μM) blocks the ghrelin-stimulated increase in ERK 1/2 phosphorylation in GH3 cells. AG 18 inhibits the volume-sensitive release of [3H]taurine in primary astrocyte cultures in a dose-dependent manner. AG 18 activates swelling-induced volume-dependent D-[3H]aspartate release from primary astrocytic cultures. AG 18 (300 μM) inhibits TPA-induced stimulation of ICAM-1 expression in a dose dependent manner in A549 epithelial cells. AG 18 (300 μM) also inhibits TPA stimulated NF-kappaB DNA-protein binding and ICAM-1 promoter activity in A549 epithelial cells. AG 18 (300 μM) inhibits TNF-alpha-induced NF-kappaB DNA-protein binding and ICAM-1 promoter activity in a dose dependent manner in A549 epithelial cells. IKK activity is stimulated by both TNF-alpha and TPA, and these effects are inhibited by AG 18 (100 μM) in A549 epithelial cells. AG 18 (10 μM) decreases the potency of 5-HT 4-fold and reduces the maximal contraction to 5-HT in the carotid artery. AG 18 (10 μM) shifts KCl-induced contraction 2-fold and causes the maximum significantly inhibition.


Synonyms

Propanedinitrile, 2-[(3,4-dihydroxyphenyl)methylene]-
Propanedinitrile, [(3,4-dihydroxyphenyl)methylene]-
2-[(3,4-Dihydroxyphenyl)methylene]propanedinitrile
RG 50810
RG 50858
AG 18
AG 18 (pharmaceutical)
TX 825
Tyrphostin 23
Tyrphostin AG 18
Tyrphostin A 23
2-(3,4-Dihydroxybenzylidene)malononitrile
(3,4-Dihydroxybenzylidene)malononitrile
2-[(3,4-Dihydroxyphenyl)methylidene]propanedinitrile