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Momordin Ic/地肤子皂苷Ic {[allProObj[0].p_purity_real_show]}

货号:A829165

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。

Momordin Ic/地肤子皂苷Ic 化学结构 CAS号:96990-18-0
Momordin Ic/地肤子皂苷Ic 化学结构
CAS号:96990-18-0
Momordin Ic/地肤子皂苷Ic 3D分子结构
CAS号:96990-18-0
Momordin Ic/地肤子皂苷Ic 化学结构 CAS号:96990-18-0
Momordin Ic/地肤子皂苷Ic 3D分子结构 CAS号:96990-18-0
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Momordin Ic/地肤子皂苷Ic 纯度/质量文件 产品仅供科研

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Momordin Ic/地肤子皂苷Ic 生物活性

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].

Momordin Ic/地肤子皂苷Ic 细胞实验

Cell Line
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

Momordin Ic/地肤子皂苷Ic 动物实验

Species
Animal Model
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

Momordin Ic/地肤子皂苷Ic 参考文献

[1]Wang J, Yuan L, et al. Momordin Ic induces HepG2 cell apoptosis through MAPK and PI3K/Akt-mediated mitochondrial pathways. Apoptosis. 2013 Jun;18(6):751-65.

[2]Kim NY, Lee MK, et al. Momordin Ic and oleanolic acid from Kochiae Fructus reduce carbon tetrachloride-induced hepatotoxicity in rats. J Med Food. 2005 Summer;8(2):177-83.

[3]Mi Y, Xiao C, Du Q, Wu W, Qi G, Liu X. Momordin Ic couples apoptosis with autophagy in human hepatoblastoma cancer cells by reactive oxygen species (ROS)-mediated PI3K/Akt and MAPK signaling pathways. Free Radic Biol Med. 2016 Jan;90:230-42

[4]Wang J, Liu Q, Xiao H, Luo X, Liu X. Suppressive effects of Momordin Ic on HepG2 cell migration and invasion by regulating MMP-9 and adhesion molecules: Involvement of p38 and JNK pathways. Toxicol In Vitro. 2019 Apr;56:75-83

[5]Xianjun F, Xirui X, Jie T, Huiwen M, Shaojun Z, Qiaoyun L, Yunxin L, Xuqun S. Momordin Ic induces G0/1 phase arrest and apoptosis in colon cancer cells by suppressing SENP1/c-MYC signaling pathway. J Pharmacol Sci. 2021 Aug;146(4):249-258

[6]Zheng C, Li D, Zhan W, He K, Yang H. Downregulation of SENP1 suppresses LPS-induced macrophage inflammation by elevating Sp3 SUMOylation and disturbing Sp3-NF-κB interaction. Am J Transl Res. 2020 Nov 15;12(11):7439-7448

[7]Yoo SR, Jeong SJ, Lee NR, Shin HK, Seo CS. Quantification Analysis and In Vitro Anti-Inflammatory Effects of 20-Hydroxyecdysone, Momordin Ic, and Oleanolic Acid from the Fructus of Kochia scoparia. Pharmacogn Mag. 2017 Jul-Sep;13(51):339-344

Momordin Ic/地肤子皂苷Ic 实验方案

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

Momordin Ic/地肤子皂苷Ic 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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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