Momordin Ic 是一种 SUMO 特异性蛋白酶 1 (SENP1) 抑制剂,SENP1/c-MYC 信号通路抑制剂。Momordin Ic通过MAPK 和 PI3K 介导的 iNOS 和 HO-1 通路的氧化应激调节线粒体功能障碍来诱导细胞凋亡。


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| 描述 | Momordin Ic (MI), a natural product isolated and purified from the fruits of Kochia scoparia (L.) Schrad., might represent a potential source of anticancer candidate, by inducing apoptosis through oxidative stress-regulated mitochondrial dysfunction involving the MAPK and PI3K-mediated iNOS and HO-1 pathways. Momordin Ic promoted the formation of autophagic vacuole and expression of Beclin 1 and LC-3 in a dose- and time-dependent manner[3]. Momordin Ic prevent cell invasion by inhibiting VCAM-1, ICAM-1, MMP-9 but inducing E-cadherin expression via p38 and JNK pathways[4]. MI inhibited cell proliferation with G0/1 phase cell cycle arrest in colon cancer cells. MI exerted an anti-tumor activity in colon cancer cells via SENP1/c-Myc signaling pathway[5]. MI, a new type of SENP1 inhibitor, reduces LPS-induced cellular inflammation by depressing SENP1 expression. Furthermore, MI-depressed Sp3 expression disturbed Sp3-nuclear factor (NF)-κB interaction and then alleviated LPS-induced cellular inflammation[6]. Momordin Ic, but not 20-hydroxyecdysone and oleanolic acid, had inhibitory effects on the production of inflammatory cytokines TNF-α and IL-6 in LPS-treated RAW264.7 macrophages[7]. |
| Concentration | Treated Time | Description | References | |
| MDA-MB-231 breast cancer cells | 25 µM | 9 days | Combined treatment with Momordin Ic and Gallic Acid significantly inhibits tumor spheroid growth | Cells. 2023 Mar 7;12(6):825 |
| MIAPaCa-2 pancreatic cancer cells | 25 µM | 9 days | Combined treatment with Momordin Ic and Gallic Acid significantly inhibits tumor spheroid growth | Cells. 2023 Mar 7;12(6):825 |
| HCT116 colon cancer cells | 25 µM | 9 days | Combined treatment with Momordin Ic and Gallic Acid significantly inhibits tumor spheroid growth | Cells. 2023 Mar 7;12(6):825 |
| C-33A cervical cancer cells | 25 µM | 6, 12, 24, 48 hours | Momordin Ic inhibits tumor cell proliferation by promoting abnormal SUMOylation of pH3(Ser10) | Cells. 2023 Mar 7;12(6):825 |
| CaSki cervical cancer cells | 25 µM | 6, 12, 24, 48 hours | Momordin Ic inhibits tumor cell proliferation by promoting abnormal SUMOylation of pH3(Ser10) | Cells. 2023 Mar 7;12(6):825 |
| WM793 | 2.0 µg/mL (24 h), 1.0 µg/mL (48 h) | 24 h and 48 h | Exhibits potent cytotoxicity against WM793 cells | Molecules. 2024 Aug 10;29(16):3794 |
| A375 | 1.9 µg/mL (24 h), 0.9 µg/mL (48 h) | 24 h and 48 h | Exhibits potent cytotoxicity against A375 cells | Molecules. 2024 Aug 10;29(16):3794 |
| HCT-116 | 9.4 µg/mL (24 h), 8.3 µg/mL (48 h) | 24 h and 48 h | Inhibits HCT-116 cell proliferation via suppression of SENP1/c-Myc signaling pathway | Molecules. 2024 Aug 10;29(16):3794 |
| HT-29 | 4.2 µg/mL (24 h), 2.9 µg/mL (48 h) | 24 h and 48 h | Inhibits HT-29 cell proliferation via suppression of SENP1/c-Myc signaling pathway | Molecules. 2024 Aug 10;29(16):3794 |
| HepG2 | 12.5 µg/mL (24 h), 9.5 µg/mL (48 h) | 24 h and 48 h | Induces apoptosis in HepG2 cells via MAPK- and PI3K/Akt-mediated pathways | Molecules. 2024 Aug 10;29(16):3794 |
| Du-145 | 5.4 µg/mL (24 h), 2.8 µg/mL (48 h) | 24 h and 48 h | Inhibits Du-145 cell proliferation via suppression of SENP1/c-Myc signaling pathway | Molecules. 2024 Aug 10;29(16):3794 |
| PC3 | 5.5 µg/mL (24 h), 3.4 µg/mL (48 h) | 24 h and 48 h | Inhibits PC3 cell proliferation via suppression of SENP1/c-Myc signaling pathway | Molecules. 2024 Aug 10;29(16):3794 |
| TOV2414 | 24.3 µM ±13.09 | 5 days | Evaluate the cytotoxic effect of Momordin Ic on TOV2414 cells, IC50 was 24.3 µM ±13.09 | Int J Mol Sci. 2025 Jan 8;26(2):472 |
| MCAS | 33.01 µM ±10.53 | 5 days | Evaluate the cytotoxic effect of Momordin Ic on MCAS cells, IC50 was 33.01 µM ±10.53 | Int J Mol Sci. 2025 Jan 8;26(2):472 |
| OCM.72 | 10.68 µM ±1.08 | 5 days | Evaluate the cytotoxic effect of Momordin Ic on OCM.72 cells, IC50 was 10.68 µM ±1.08 | Int J Mol Sci. 2025 Jan 8;26(2):472 |
| EFO27 | 13.19 ±1.43 µM | 5 days | Evaluate the cytotoxic effect of Momordin Ic on EFO27 cells, IC50 was 13.19 ±1.43 µM | Int J Mol Sci. 2025 Jan 8;26(2):472 |
| THP1 macrophages | 2 µM | 24 hours | Evaluate the inhibitory effect of Momordin Ic on THP1 macrophage infection, results showed Momordin Ic significantly inhibited HCMV infection | Pathogens. 2024 Jun 28;13(7):546 |
| Adult retinal pigment epithelial cells (ARPE-19) | 2 µM | 24 hours | Evaluate the inhibitory effect of Momordin Ic on ARPE-19 cell infection, results showed Momordin Ic significantly inhibited HCMV infection | Pathogens. 2024 Jun 28;13(7):546 |
| Human foetal foreskin fibroblasts (HFFs) | 1.25 µM | 24 hours | Evaluate the inhibitory effect of Momordin Ic on HCMV infection, results showed Momordin Ic significantly inhibited HCMV infection | Pathogens. 2024 Jun 28;13(7):546 |
| Administration | Dosage | Frequency | Description | References | ||
| Mice | Pressure overload-induced cardiac hypertrophy model | Intraperitoneal injection | 10 mg/kg | Once daily for 20 consecutive days | Momordin Ic accelerated pressure overload-induced cardiac remodeling | J Am Heart Assoc. 2022 Nov 15;11(22):e027004 |
| NOD/SCID mice | AML xenograft model | Intraperitoneal injection | 10 mg/kg | Ara-C for 5 consecutive days, Momordin Ic every two days for a week | To evaluate the effect of Momordin Ic combined with Ara-C on AML xenograft model, results showed that combination therapy significantly reduced AML cell survival and improved mouse survival. | Int J Mol Sci. 2022 Jul 27;23(15):8282 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.31mL 0.26mL 0.13mL |
6.54mL 1.31mL 0.65mL |
13.07mL 2.61mL 1.31mL |
|
| CAS号 | 96990-18-0 |
| 分子式 | C41H64O13 |
| 分子量 | 764.94 |
| SMILES Code | O[C@H]([C@H]([C@@H]([C@@H](C(O)=O)O1)O)O[C@H]2[C@@H]([C@H]([C@@H](CO2)O)O)O)[C@@H]1O[C@H]3CC[C@]4(C)[C@@]5([H])CC=C6[C@]7([H])CC(C)(C)CC[C@]7(C(O)=O)CC[C@](C)6[C@@](C)5CC[C@@]4([H])C3(C)C |
| MDL No. | MFCD11042256 |
| 别名 | |
| 运输 | 蓝冰 |
| InChI Key | HWYBGIDROCYPOE-WEAQAMGWSA-N |
| Pubchem ID | 176596 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(137.27 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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