Icotinib

$120$670

Products Details

Product Description

– Icotinib (BPI-2009) is a potent and specific EGFR inhibitor with an IC50 of 5 nM; also inhibits mutant EGFRL858R, EGFRL858R/T790M, EGFRT790M and EGFRL861Q. Icotinib is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Web ID

– HY-15164A

Storage Temperature

– -20°C, 3 years (Powder)

Shipping

– Blue Ice

Applications

– Cancer-Kinase/protease

Molecular Formula

– C22H21N3O4

Citations

– Cell Rep Med. 2023 Jan 10;100911.|Clin Chim Acta. 2022 Jan 6;S0009-8981(21)00457-5.|Eur J Pharmacol. 2019 May 5;850:141-149.|J Pharmaceut Biomed. 2023 Jan 26.|Sci Transl Med. 2018 Jul 18;10(450):eaaq1093.|Biochem Pharmacol. 2016 Dec 1;121:67-77. |Science. 2017 Dec 1;358(6367):eaan4368.

References

– [1]Tan F, et al. Icotinib (BPI-2009H), a novel EGFR tyrosine kinase inhibitor, displays potent efficacy in preclinical studies. Lung Cancer. 2012 May;76(2):177-82.

CAS Number

– 610798-31-7

Molecular Weight

– 391.42

Compound Purity

– 99.99

SMILES

– C#CC1=CC(NC2=C(C=C(OCCOCCOCCO3)C3=C4)C4=NC=N2)=CC=C1

Clinical Information

– Launched

Research Area

– Cancer

Solubility

– DMSO : ≥ 155 mg/mL

Target

– EGFR

Isoform

– EGFR/ErbB1/HER1

Pathway

– JAK/STAT Signaling;Protein Tyrosine Kinase/RTK

Product type

– Reference compound

Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.

My Cart
Close Wishlist
Close Recently Viewed
Categories

Please fill out this form to request the file. We will send it to your Email address shortly. Thanks.

Please enable JavaScript in your browser to complete this form.

=

Please fill out this form to request the pricing.
We will send it to your email address shortly.
Thanks.

Please enable JavaScript in your browser to complete this form.

=