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EAI-045

EAI-045

CAS: 1942114-09-1

Molecular Formula: C19H14FN3O3S

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EAI-045 - Names and Identifiers

Name EAI-045
Synonyms EA1045
EAI045
EAI-045
CS-2350
EAI 045
2-(5-fluoro-2-hydroxyphenyl)-2-(1-oxoisoindolin-2-yl)-N-(thiazol-2-yl)acetamide
N-(3-((5-fluoroethoxy)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide (EAI-045)
α-(5-fluoro-2-hydroxyphenyl)-1,3-dihydro-1-oxo-N-2-thiazolyl-2H-Isoindole-2-acetamide
N-(3-((5-fluoroethoxy)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide (EAI-045)
CAS 1942114-09-1

EAI-045 - Physico-chemical Properties

Molecular FormulaC19H14FN3O3S
Molar Mass383.4
Density1.546±0.06 g/cm3(Predicted)
Solubility DMSO: ≥ 28 mg/mL
pKa7.20±0.50(Predicted)
Storage Condition2-8°C
Physical and Chemical PropertiesBioactive EAI045 is an allosteric inhibitor targeting specific drug-resistant EGFR mutants. No effect on wild-type receptors.
UseApplication EAI045 is an allosteric inhibitor of EGFR mutants targeting specific drug resistance. No effect on wild-type receptors. It can be used as a pharmaceutical raw material.
In vitro studyEAI045 potently inhibited phosphorylation of EGFR(Y1173) in H1975 cells (EC50=2 nM), but not in HaCaT cells with wild EGFR (keratinocyte cell line). Despite the inhibitory effect of EAI045 on EGFR mutants, EAI had no anti-proliferative effect in H1975 and H3255 cells despite reaching concentrations of 10 μm. EAI045 was able to inhibit EGFR(L858R and T790M) mutants with an IC50 of 3 nM. However, it was not able to completely prevent the autophosphorylation of EGFR in H1975 cells with EGFR(L858R/T790M) mutants. The dimerization defective/independent mutant was more sensitive to eai045. Because kinase activation of EGFR requires the formation of dimers, EAI045 may have inhibitory activity against one of the subunits of the EGFR heteromer.
In vivo studyPharmacokinetic studies in mice showed a maximum plasma concentration of 0.57 μm for EAI045 with a half-life of 2.15 hours. At a concentration of 20 mg/kg, the bioavailability was 26%. When EAI045 was used in combination with cetuximab, another compound that prevented EGFR dimerization, EAI045 significantly reduced tumor growth in a mouse model of lung cancer driven by EGFR(L858R/T790M) mutants. Mice dosed with EAI045 alone had no therapeutic effect. EAI045 in combination with cetuximab also induced tumor volume reduction in mice with the L858R/T790M/C797S mutation. EAI045 and cetuximab showed a synergistic effect.

EAI-045 - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.608 ml13.041 ml26.083 ml
5 mM0.522 ml2.608 ml5.217 ml
10 mM0.261 ml1.304 ml2.608 ml
5 mM0.052 ml0.261 ml0.522 ml
Last Update:2024-01-02 23:10:35

EAI-045 - Reference Information

application EAI045 is an allosteric inhibitor targeting EGFR mutants with specific drug resistance. No effect on wild-type receptors. It can be used as a pharmaceutical raw material.
biological activity EAI045 is an allosteric inhibitor targeting EGFR mutants with specific drug resistance. No effect on wild-type receptors.
target TargetValue EGFR mutants ()
TargetValue
In vitro study EAI045 effectively inhibits the phosphorylation of EGFR(Y1173) in H1975 cells (EC50=2 nM), but has no such effect in HaCaT cells (keratinocytes) with wild EGFR. Although EAI045 had an inhibitory effect on the mutant of EGFR, in H1975 and H3255 cells, EAI also had no antiproliferative effect despite reaching a concentration of 10 μM. EAI045 was able to inhibit EGFR(L858R and T790M) mutants with an IC50 of 3 nM. However, it is not able to completely prevent the autophosphorylation of EGFR in H1975 cells with EGFR(L858R/T790M) mutants. The dimerization-deficient/independent mutants were more sensitive to EAI045. Because EGFR kinase activation requires the formation of dimers, EAI045 may have inhibitory activity on a certain subunit of EGFR heteromers.
In vivo studies Pharmacokinetic studies in mice showed that the maximum plasma concentration of EAI045 is 0.57 μM, and its half-life is 2.15 hours. At an administration concentration of 20 mg/kg, its bioavailability is 26%. When EAI045 is cetuximab combined with another compound that prevents EGFR dimerization, EAI045 can significantly reduce tumor growth in a mouse model of lung cancer driven by EGFR(L858R/T790M) mutants. Mice given EAI045 alone had no therapeutic effect. EAI045 combined with cetuximab also induced tumor volume reduction in mice with L858R/T790M/C797S mutation. This shows that EAI045 and cetuximab have synergistic effect.
Last Update:2024-04-09 22:09:11
EAI-045
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Shanghai Macklin Biochemical Co., Ltd
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CAS: 1942114-09-1
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CAS: 1942114-09-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
Shanghai Macklin Biochemical Co., Ltd
Featured ProductsSpot supply
Product Name: EAI045 Visit Supplier Webpage Request for quotation
CAS: 1942114-09-1
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: EAI045 Request for quotation
CAS: 1942114-09-1
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
MedChemExpress (MCE)
Multiple SpecificationsSpot supply
Product Name: EAI045 (Standard) Visit Supplier Webpage Request for quotation
CAS: 1942114-09-1
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: EAI045 Visit Supplier Webpage Request for quotation
CAS: 1942114-09-1
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
WhatsApp: +86-18621343501
BOC Sciences
Spot supply
Product Name: EAI045 Visit Supplier Webpage Request for quotation
CAS: 1942114-09-1
Tel: +16314854226
Email: info@bocsci.com
Mobile: +16314854226
Linkedin: https://www.linkedin.com/company/boc-sciences
Product List: View Catalog
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: EAI045 Visit Supplier Webpage Request for quotation
CAS: 1942114-09-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
EAI-045
38775-38-1
Chromic Acid
CYCLOPENTANEACETIC ACID
2,4-DCAD
65166-97-4
C.I. Vat Blue 6
colloidalmercury
C.I. Disperse Yellow 37
4-METHYLPENTYL BROMIDE
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