ChemicalBook >> CAS DataBase List >>AG 1478

AG 1478

CAS No.
175178-82-2
Chemical Name:
AG 1478
Synonyms
AG 1517;AG 1478;SU 5271;WHI-P 79;NSC 669364;PD-153,035;COMPOUND 32;Tyrphostin AG;AG 1478 USP/EP/BP;TYRPHOSTIN AG 1517
CBNumber:
CB8751920
Molecular Formula:
C16H14ClN3O2
Molecular Weight:
315.75
MDL Number:
MFCD00270914
MOL File:
175178-82-2.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:34

AG 1478 Properties

Melting point 180 - 183°C
storage temp. 2-8°C
solubility 0.1 M HCl: soluble <0.4 mg/mL
form Pale yellow solid
color Off-white
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
FDA UNII TC62B68RSL

SAFETY

Risk and Safety Statements

WGK Germany  3
NFPA 704
1
2 0

AG 1478 price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 658552 AG 1478 175178-82-2 5mg $187 2024-03-01 Buy
Sigma-Aldrich 658548 InSolution? AG 1478 175178-82-2 1mg $113 2024-03-01 Buy
Sigma-Aldrich T4182 Tyrphostin AG 1478 ≥98% 175178-82-2 1mg $76.2 2024-03-01 Buy
Sigma-Aldrich T4182 Tyrphostin AG 1478 ≥98% 175178-82-2 5mg $228 2024-03-01 Buy
American Custom Chemicals Corporation KIN0001450 AG 1478 95.00% 175178-82-2 1G $798 2021-12-16 Buy
Product number Packaging Price Buy
658552 5mg $187 Buy
658548 1mg $113 Buy
T4182 1mg $76.2 Buy
T4182 5mg $228 Buy
KIN0001450 1G $798 Buy

AG 1478 Chemical Properties,Uses,Production

Description

AG-1478 (175478-82-2; base) is a potent and selective inhibitor of the EGFR kinase (IC50 = 3 nM). Inhibits proliferation of a variety human cancer cell lines.1,2 AG-1478 reduces pulmonary fibrosis in a rat model.3?Cell permeable.

Uses

A highly potent and specific EGFR tyrosine kinase inhibitor with an IC50 of 3 nM.

Uses

Tyrphostin AG 1478 is a potent and selective inhibitor of EGFR.

Uses

Tyrphostin AG 1478 has been used as epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor to study its effect on desmoid cell mobility in boyden chamber motility assays. It has also been used to inhibit phosphorylation of c-Met by exogenous transforming growth factor α in epidermoid carcinoma cell line A431.

Definition

ChEBI: Tyrphostin AG 1478 is a member of the class of quinazolines that is quinazoline substituted by methoxy groups at positions 6 and 7 and a (3-chlorophenyl)nitrilo group at position 4. It acts as an epidermal growth factor receptor antagonist. It has a role as an epidermal growth factor receptor antagonist, an antineoplastic agent, a geroprotector and an antiviral agent. It is a member of quinazolines, an aromatic ether and a member of monochlorobenzenes.

General Description

Highly potent and specific inhibitor of the epidermal growth factor (EGF) receptor tyrosine kinase (IC50 = 3 nM). Much higher concentrations are required for inhibition of the kinase activity of the closely related HER2 (neu/erb-B2) receptor (IC50 >100 μM), the platelet-derived growth factor (PDGF) receptor (IC50 >100 μM), and p210Bcr-Abl (IC50 >50 μM). Its mechanism of inhibition likely mimics that of the related compound, 4-(3-chloroanilino)quinazoline (CAQ), a competitive inhibitor with respect to ATP.

Biochem/physiol Actions

Primary TargetEpidermal growth factor receptor kinase

References

1) Han et al. (1996), Tyrphostin AG 1478 preferentially inhibits human glioma cells expressing truncated rather than wild-type epidermal growth factor receptors; Cancer Res., 56 3859 2) Partik et al. (1999), Inhibition of epidermal-growth-factor-receptor-dependent signaling by tyrphostins A25 and AG1478 blocks growth and induces apoptosis in colorectal tumor cells in vitro; J. Cancer Res. Clin. Oncol., 125 379 3) Rice et al. (1999), Specific inhibitors of platelet-derived growth factor or epidermal growth factor receptor tyrosine kinase reduce pulmonary fibrosis in rats; Am. J. Pathol., 155 213

AG 1478 Preparation Products And Raw materials

Raw materials

Preparation Products

AG 1478 Suppliers

Global( 115)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49391 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 27644 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131980 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
Shanghai Paulshine Chemical Co., Ltd. +86-021-37788663 China 186 64
Jinan Trio PharmaTech Co., Ltd. +86 (531) 88811783 sales@trio-pharmatech.com (International market) China 1856 62
Spectrum Chemical Manufacturing Corp. 021-021-021-67601398-809-809-809 15221380277 marketing_china@spectrumchemical.com China 9664 60
UHN Shanghai Research & Development Co., Ltd. 021-58958002 18930822973 SALES@UHNSHANGHAI.COM China 977 58
NSC 669364 N-[3-CHLOROPHENYL]-6,7-DIMETHOXY-4-QUINAZOLINAMINE N-(3-CHLOROPHENYL)-N-(6,7-DIMETHOXY-4-QUINAZOLINYL)AMINE SU 5271 WHI-P 79 TYRPHOSTIN AG 1478 TYRPHOSTIN AG 1517 AG 1478 AG 1517 4-(N-3-CHLOROPHENYL)-AMINO-6,7-DIMETHOXYQUINAZOLINE 4-QUINAZOLINAMINE, N-(3-BROMOPHENYL)-6,7-DIMETHOXY- 4-(3-BROMOPHENYLAMINO)-6,7-BIS(METHOXY)QUINAZOLINE 4-[(3-BROMOPHENYL)AMINO]-6,7-DIMETHOXYQUINAZOLINE 4-(3-BROMOPHENYLAMINO)-6,7-DIMETHYLQUINAZOLINE 4-(3-CHLOROANILINO)-6,7-DIMETHOXYQUINAZOLINE 4-(3-CHLOROANILLINO)-6,7-DIMETHOXYQUINAZOLINE 4-(3-BROMOANILINO)-6,7-DIMETHOXYQUINAZOLINE COMPOUND 32 TYRPHOSTIN AG 1478, 99+% 4-(3-Chloro-benzyl)-6,7-dimethoxy-quinazoline 4-Quinazolinamine,N-(3-chlorophenyl)-6,7-dimethoxy- N-(3-chlorophenyl)-6,7-dimethoxyquinazolin-4-amine Tyrphostin AG 1478, Methanesulfonate Salt InSolution? AG 1478 PD-153,035 Tyrphostin AG InSolution AG 1478 - CAS 175178-82-2 - Calbiochem AG 1478 - CAS 175178-82-2 - Calbiochem 4-[(3-chlorophenyl)methyl]-6,7-dimethoxyquinazoline AG 1478 USP/EP/BP 175178-82-2 174178-82-2 BioChemical Cell Signaling and Neuroscience Cell Biology Kinase/Phosphatase Biology Epidermal Growth Factor Receptor (EGFR) Receptor Tyrosine Kinase Inhibitors