STX-721
Based on 1 publication(s) in Google Scholar
STX-721 is an orally active, irreversible, covalent EGFR exon 20 insertion (ex20ins) inhibitor that selectively targets ex20ins-mutant dynamic protein states. STX-721 potently inhibits the kinase activity of EGFR ex20ins mutants (NPG, ASV, SVD). STX-721 inhibits phosphorylation of EGFR (pEGFR Y1068) and downstream ERK (pERK Thr202/Tyr204), and suppresses proliferation of ex20ins-mutant Ba/F3 cells and human NSCLC cell lines (NCI-H2073 ASV KI, CUTO-14 ASV). STX-721 induces tumor regression in EGFR ex20ins-mutant PDX/CDX models. STX-721 can be used for the study of non-small cell lung cancer (NSCLC) harboring EGFR or HER2 ex20ins mutations.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 98.25%
- CAS 番号: 2765525-82-2
- 分子式: C32H35ClN6O3
- 分子量:587.11
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
MedChemExpress(MCE)の使用を引用している文献 STX-721
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生物活性
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| BaF3 | IC50 |
136.7 nM
Compound: STX-721
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Antiproliferative activity against mouse BaF3 cells harboring wild type EGFR
Antiproliferative activity against mouse BaF3 cells harboring wild type EGFR
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[PMID: 37669428] |
| BaF3 | IC50 |
5.17 nM
Compound: STX-721
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Antiproliferative activity against mouse BaF3 cells harboring EGFR-D770-N771insNPG mutant
Antiproliferative activity against mouse BaF3 cells harboring EGFR-D770-N771insNPG mutant
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[PMID: 37669428] |
STX-721 (10-1000 nM, 2 h) inhibits phosphorylation of EGFR (pEGFR Y1068) and ERK (pERK Thr202/Tyr204) in patient-derived EGFR exon 20 insertion-mutant cell lines (MGH10080-1 SVD, MGH10022-1.19 GF) with higher potency than in EGFR WT NCI-H2073 cells[1].
STX-721 (72 h) shows antiproliferative activity in CRISPR/Cas9-edited NCI-H2073 human cancer cell lines, with IC50 values of 10.1 nM for NCI-H2073 EGFR V769_D770 insASV knock-in (KI) cells and 6.1 nM for NCI-H2073 EGFR D770_N771 insSVD KI cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Tumor tissues with NSCLC harboring EGFR NPH mutation, EGFR ASV mutation, EGFR SVD mutation, HER2 YVMA mutation and NCI-H2073 EGFR_exon20_SVD_ins cells (1×107 cells/mouse in appropriate medium) were subcutaneously implanted into the flanks of 6-8-week-old female BALB/c nude mice[1]
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Dosage:12.5, 25, 50, 100 mg/kg
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Administration:p.o. once daily for 20, 26, 38 or 42 days
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Result:Achieved tumor growth inhibition.
Reduced phosphorylation of EGFR (pEGFR) and ERK (pERK).
化学情報
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CAS 番号 2765525-82-2
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性状 Solid
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分子量 587.11
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分子式 C32H35ClN6O3
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Color Off-white to light yellow
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SMILES
O=C(N1CCC[C@]1(C)C#CC2=C(C=CN=C2)C3=C(C4=C(N3)CCNC4=O)NC5=CC=CC(Cl)=C5OC)/C=C/CN(C)C
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (1)
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Journal Impact Factor
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Most Recent
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Cancer Discov
2025 Oct 15. PMID: 41090369
溶剤 & 溶解度
DMSO : 100 mg/mL (170.33 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
純度とドキュメンテーション
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データシート (284 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Pagliarini RA, et al. STX-721, a Covalent EGFR/HER2 Exon 20 Inhibitor, Utilizes Exon 20-Mutant Dynamic Protein States and Achieves Unique Mutant Selectivity Across Human Cancer Models. Clin Cancer Res. 2025 Jul 15;31(14):3002-3018. [Content Brief]
[2]. Milgram BC, et al. Discovery of STX-721, a Covalent, Potent, and Highly Mutant-Selective EGFR/HER2 Exon20 Insertion Inhibitor for the Treatment of Non-Small Cell Lung Cancer. J Med Chem. 2025 Feb 13;68(3):2403-2421. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 1.7033 mL | 8.5163 mL | 17.0326 mL | 42.5815 mL |
| 5 mM | 0.3407 mL | 1.7033 mL | 3.4065 mL | 8.5163 mL | |
| 10 mM | 0.1703 mL | 0.8516 mL | 1.7033 mL | 4.2581 mL | |
| 15 mM | 0.1136 mL | 0.5678 mL | 1.1355 mL | 2.8388 mL | |
| 20 mM | 0.0852 mL | 0.4258 mL | 0.8516 mL | 2.1291 mL | |
| 25 mM | 0.0681 mL | 0.3407 mL | 0.6813 mL | 1.7033 mL | |
| 30 mM | 0.0568 mL | 0.2839 mL | 0.5678 mL | 1.4194 mL | |
| 40 mM | 0.0426 mL | 0.2129 mL | 0.4258 mL | 1.0645 mL | |
| 50 mM | 0.0341 mL | 0.1703 mL | 0.3407 mL | 0.8516 mL | |
| 60 mM | 0.0284 mL | 0.1419 mL | 0.2839 mL | 0.7097 mL | |
| 80 mM | 0.0213 mL | 0.1065 mL | 0.2129 mL | 0.5323 mL | |
| 100 mM | 0.0170 mL | 0.0852 mL | 0.1703 mL | 0.4258 mL |