貨號:A1155000
同義名:
索托拉西布(AMG510) / AMG-510
Sotorasib 是一種 KRAS G12C 抑制劑,對 KRAS G12C 的 IC50 值為 5.3 nM。Sotorasib 具有抗腫瘤作用,可用于 KRAS 突變相關癌癥的研究。


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| 描述 | Sotorasib (AMG-510) 是一種高效、高選擇性的 KRAS G12C 共價抑制劑。 該分子通過與 KRAS G12C 突變體 Switch II 口袋 (SIIP) 鄰近的半胱氨酸殘基特異性結合,形成不可逆的共價鍵,從而將 KRAS 鎖定在不活躍的 GDP 結合狀態,阻斷其下游信號通路。作為首個針對該突變的候選藥物,Sotorasib 在多種 KRAS G12C 突變細胞系中表現出強效的抗增殖活性,并能誘導細胞凋亡 (apoptosis)。在臨床前研究中,Sotorasib 處理可上調 HLA 的表達,增強腫瘤抗原遞呈[1]。由于其對突變型與野生型 KRAS 具有極高的選擇性,Sotorasib 已成為研究 KRAS 信號傳導及開發針對難治性實體瘤靶向策略的里程碑式工具化合物。 |
| 作用機制 | AMG-510 selectively forms an irreversible covalent bond to the sulfur atom in the cysteine residue that is present in the mutated form of KRAS, but not in the normal form. KRASG12C can be targeted with covalent small molecule inhibitor AMG-510 which react with the mutant cysteine adjacent to the switch II pocket (SIIP), locking KRAS in its inactive GDP-bound state[1]. |
| Concentration | Treated Time | Description | References | |
| MIAPACA2 cells | 40 nM | 72 h | Investigate the effect of Sotorasib on MIAPACA2 cells, results showed that ALDH1A1 knockout enhanced the effect of Sotorasib | Redox Biol. 2024 Nov;77:103361. |
| H2122 cells | 100 nM | 72 h | Investigate the effect of Sotorasib on H2122 cells, results showed that ALDH1A1 knockout enhanced the effect of Sotorasib | Redox Biol. 2024 Nov;77:103361. |
| MIA-PaCa-2 cells | 30 nM | 2 days | Suppressed the activation of MEK/ERK, leading to cell growth inhibition and increased protein aggregation | Science. 2023 Sep 8;381(6662):eabn4180. |
| H358 cells | 30 nM | 2 days | Suppressed the activation of MEK/ERK, leading to cell growth inhibition and increased protein aggregation | Science. 2023 Sep 8;381(6662):eabn4180. |
| MiaPaCa2 | 6 nM | 72 h | To evaluate the synergistic effects of Sotorasib with various drugs and identify potential combination therapies | Mol Oncol. 2025 Feb;19(2):295-310. |
| H358 | 1 μM | 72 h | Evaluate the anti-proliferative effect of Sotorasib on KRASG12C mutant lung cancer cells | Nat Commun. 2024 Aug 30;15(1):7554. |
| H23 | 1 μM | 72 h | Evaluate the anti-proliferative effect of Sotorasib on KRASG12C mutant lung cancer cells | Nat Commun. 2024 Aug 30;15(1):7554. |
| H1792 | 1 μM | 72 h | Evaluate the anti-proliferative effect of Sotorasib on KRASG12C mutant lung cancer cells | Nat Commun. 2024 Aug 30;15(1):7554. |
| H2030 | 1 μM | 72 h | Evaluate the anti-proliferative effect of Sotorasib on KRASG12C mutant lung cancer cells | Nat Commun. 2024 Aug 30;15(1):7554. |
| H2122 | 1 μM | 72 h | Evaluate the anti-proliferative effect of Sotorasib on KRASG12C mutant lung cancer cells | Nat Commun. 2024 Aug 30;15(1):7554. |
| MIA PaCa-2 | 5 μM | > 2 weeks | Establish sotorasib-resistant cells | J Biomed Sci. 2023 Jun 29;30(1):50. |
| NCI-H23 | 5 μM | > 2 weeks | Establish sotorasib-resistant cells | J Biomed Sci. 2023 Jun 29;30(1):50. |
| LU65 | 5 μM | > 2 weeks | Establish sotorasib-resistant cells | J Biomed Sci. 2023 Jun 29;30(1):50. |
| Administration | Dosage | Frequency | Description | References | ||
| Mice | UMUC3 and H358 subcutaneous xenograft models | Oral gavage | 100 mg/kg | Once daily until the end of the experiment | To evaluate the antitumor efficacy of Sotorasib and its combination with radiolabeled P1B7 IgG. Results showed that the combination of Sotorasib with radiolabeled P1B7 IgG significantly inhibited tumor growth. | Cancer Res. 2025 Jan 15;85(2):329-341 |
| Nude mice | MIAPACA2 xenograft model | Oral | 30 mg/kg | Once daily for 2 weeks | Investigate the anti-tumor effect of Sotorasib in MIAPACA2 xenograft model, results showed that Sotorasib significantly inhibited tumor growth | Redox Biol. 2024 Nov;77:103361. |
| ICR-SCID mice | PDAC (MIA PaCa-2) cell-derived xenograft model | Oral | 25 mg/kg | Daily for 3 weeks | The combination of KPT9274 and Sotorasib significantly reduced tumor volumes, tumor weights, and tumor sizes. | Mol Cancer Ther. 2023 Dec 1;22(12):1422-1433. |
| ICR-SCID mice | MIA PaCa-2 cell-derived tumor xenograft model | Oral | 25 mg/kg | Daily administration for 3 weeks | Significant reduction in tumor volumes, tumor weights, and tumor sizes | Mol Cancer Ther. 2023 Dec 1;22(12):1422-1433. |
| Mice | MIA-PaCa-2 xenograft tumor model | Oral | 30 mg/kg | Daily for 6 weeks | Initially sensitive to sotorasib but relapsed after 6 weeks, with increased protein aggregation and restored proteostasis in relapsed tumors | Science. 2023 Sep 8;381(6662):eabn4180. |
| Mice | Subcutaneous tumor model | Oral | 30 mg/kg | Once daily for 3 weeks | Evaluate the in vivo anti-tumor effect of Sotorasib on KRASG12C mutant tumors | Nat Commun. 2024 Aug 30;15(1):7554. |
| NOD/SCID mice | Subcutaneous xenograft model | Oral | 10 mg/kg | Once daily for 14 days | Evaluate the effect of combined treatment with sotorasib and BRAF inhibitor | J Biomed Sci. 2023 Jun 29;30(1):50. |
| Mice | NCI-H358-R xenograft model | Subcutaneous injection | 250 mg/kg | 4 days on, 2 days off | Evaluate the efficacy of GNE-7883 in combination with sotorasib in overcoming KRAS G12C inhibitor resistance | Nat Cancer. 2023 Jun;4(6):812-828 |
| 計算器 | ||||
| 存儲液制備 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.78mL 0.36mL 0.18mL |
8.92mL 1.78mL 0.89mL |
17.84mL 3.57mL 1.78mL |
|
| CAS號 | 2296729-00-3 |
| 分子式 | C30H30F2N6O3 |
| 分子量 | 560.59 |
| SMILES Code | O=C1N(C2=C(C)C=CN=C2C(C)C)C3=NC(C4=C(O)C=CC=C4F)=C(F)C=C3C(N5[C@@H](C)CN(C(C=C)=O)CC5)=N1 |
| MDL No. | MFCD32062763 |
| 別名 | 索托拉西布(AMG510) ;AMG-510 |
| 英文名稱 | (1R)-4-((S)-4-Acryloyl-2-methylpiperazin-1-yl)-6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(2-isopropyl-4-methylpyridin-3-yl)pyrido[2,3-d]pyrimidin-2(1H)-one |
| 運輸 | 藍冰 |
| InChI Key | NXQKSXLFSAEQCZ-SFHVURJKSA-N |
| Pubchem ID | 137278711 |
| 存儲條件 |
In solvent -20°C: 3-6個月 -80°C: 12個月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO 中的溶解度 : 50 mg/mL (89.19 mM; 超聲助溶; 吸濕的 DMSO 對產品的溶解度有顯著影響,請使用新開封的 DMSO) H2O 中的溶解度 : 33.33 mg/mL (59.46 mM; ultrasonic and adjust pH to 11 with NaOH) 以下溶解方案都請先按照體外實驗的方式配制澄清的儲備液,再依次添加助溶劑: ——為保證實驗結果的可靠性,澄清的儲備液可以根據儲存條件,適當保存;體內實驗的工作液,建議現用現配,當天使用; 以下溶劑前顯示的百分比是指該溶劑在終溶液中的體積占比;如在配制過程中出現沉淀、析出現象,可以通過加熱和/或超聲的方式助溶
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