Evaluation of Rhenium and Technetium-99m Complexes Bearing Quinazoline Derivatives as Potential EGFR Agents

被引：4

作者：

Makrypidi, Konstantina ^{[1
]}

Kiritsis, Christos ^{[1
]}

Roupa, Ioanna ^{[1
]}

Triantopoulou, Sotiria ^{[1
]}

Shegani, Antonio ^{[1
]}

Paravatou-Petsotas, Maria ^{[1
]}

Chiotellis, Aristeidis ^{[1
]}

Pelecanou, Maria ^{[2
]}

Papadopoulos, Minas ^{[1
]}

Pirmettis, Ioannis ^{[1
]}

机构：

[1] NCSR Demokritos, Inst Nucl & Radiol Sci & Technol, Energy & Safety, Athens 15310, Greece

[2] NCSR Demokritos, Inst Biosci & Applicat, Athens 15310, Greece

来源：

MOLECULES | 2023年 / 28卷 / 04期

关键词：

EGFR; TKI; PAMA; cysteine; rhenium; technetium-99m; tricarbonyl; STRUCTURAL-CHARACTERIZATION; KINASE INHIBITORS; TECHNETIUM; BIOMARKER; CYSTEINE; CANCER; PET;

D O I：

10.3390/molecules28041786

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

tau he Epidermal Growth Factor Receptor tyrosine kinase inhibitor (EGFR-TKI) 6-amino-4-[(3-bromophenyl) amino]quinazoline was derivatized with 6-bromohexanoyl-chloride and coupled with the tridentate chelating agents N-(2-pyridylmethyl) aminoethyl acetic acid (PAMA) and L(+)-cysteine bearing the donor atom set NNO and SNO, respectively. The rhenium precursors ReBr(CO)(5) and fac-[NEt4](2)[ReBr3(CO)(3)] were used for the preparation of the Re complexes fac-[Re(NNO)(CO)(3)] (5a) and fac-[Re(SNO)(CO)(3)] (7a) which were characterized by NMR and IR spectroscopies. Subsequently, the new potential EGFR inhibitors were labeled with the fac-[Tc-99m(CO)(3)](+) core in high yield and radiochemical purity (>90%) by ligand exchange reaction using the fac-[Tc-99m][Tc(OH2)(3)(CO)(3)](+) precursor. The radiolabeled complexes were characterized by comparative HPLC analysis with the analogous rhenium (Re) complexes as references. In vitro studies in the A431 cell lines showed that both ligands and Re complexes inhibit A431 cell growth. Complex 5a demonstrated the highest potency (IC50 = 8.85 +/- 2.62 mu M) and was further assessed for its capacity to inhibit EGFR autophosphorylation, presenting an IC50 value of 26.11 nM. Biodistribution studies of the Tc-99m complexes in healthy mice showed high in vivo stability for both complexes and fast blood and soft tissue clearance with excretion occurring via the hepatobiliary system.

引用

页数：15

共 25 条

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