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Merck
CN

234491

PD 153035

InSolution, ≥97%, potent and specific inhibitor of the tyrosine kinase activity of EGFR

别名:

InSolution PD 153035

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关于此项目

经验公式(希尔记法):
C16H14BrN3O2
分子量:
360.21
UNSPSC Code:
12352200
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产品名称

PD 153035, InSolution, ≥97%, potent and specific inhibitor of the tyrosine kinase activity of EGFR

assay

≥97% (HPLC)

form

liquid

potency

25 pM IC50

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)
protect from light

shipped in

wet ice

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

Target Ki: 6 pM against the tyrosine kinase activity of the epidermal growth factor receptor (EGFR)
Product competes with ATP.
Reversible: yes
Cell permeable: yes

Disclaimer

Toxicity: Irritant (B)

General description

An extremely potent and specific inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR; IC50 = 25 pM; Ki = 6 pM). Rapidly suppresses autophosphorylation of EGFR at low nanomolar concentrations in fibroblasts or in human epidermoid carcinoma cells. Also selectively blocks EGF-mediated cellular processes including mitogenesis, early gene expression and oncogenic transformation.

Packaging

Packaged under inert gas

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Physical form

A 10 mM (500 µg/139 µl) solution of PD 153035 (Cat. No. 234490 ) in DMSO.

存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

188.6 °F - closed cup - (Dimethylsulfoxide)

flash_point_c

87 °C - closed cup - (Dimethylsulfoxide)


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Thibaut Renard et al.
Scientific reports, 12(1), 21228-21228 (2022-12-10)
The reproductive division of labour is a hallmark of eusocial Hymenoptera. Females are either reproductive queens or non-reproductive workers. In ants, workers often display further task specialisation that is associated with variation in size and/or morphology. Because female polyphenism is
Carolina Franco Nitta et al.
eLife, 10 (2021-11-26)
Crosstalk between different receptor tyrosine kinases (RTKs) is thought to drive oncogenic signaling and allow therapeutic escape. EGFR and RON are two such RTKs from different subfamilies, which engage in crosstalk through unknown mechanisms. We combined high-resolution imaging with biochemical

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