货号:A284575
同义名:
Stigmasterin; 5,22-Cholestadien-24-beta-ethyl-3-beta-ol
Stigmasterol是一种植物甾醇,具有抗癌、解热、抗炎和免疫调节作用,也被评估为降低 LDL 胆固醇的潜力成分。


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| 产品名称 | MMP ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Marimastat |
+++
MMP-7, IC50: 16 nM MMP-14, IC50: 3 nM |
98% | |||||||||||||||||
| Ilomastat |
++++
MMP-26, Ki: 0.36 nM MMP-2, Ki: 0.1 nM |
99%+ | |||||||||||||||||
| SB-3CT |
+
MMP-9, Ki: 600 nM MMP-2, Ki: 13.9 nM |
99%+ | |||||||||||||||||
| Doxycycline | ✔ | 95% | |||||||||||||||||
| NSC 405020 | ✔ | 98% | |||||||||||||||||
| Batimastat |
+++
MMP-7, IC50: 4 nM MMP-1, IC50: 3 nM |
99%+ | |||||||||||||||||
| Nobiletin | ✔ | 99% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Stigmasterol, a natural compound isolated from Azadirachta indica, has many biological activities. In vitro studies, stigmasterol could induce apoptosis in hepatocarcimona (HepG2) cells by regulating the expression of some special genes. Besides this, it was found that stigmasterol could inhibit the activity of a partially purified bloodstream T. congolense sialidase with an inhibition binding constant of 356.59 μM. In vivo studies, stigmasterol could contribute to the improvement of skin tumors induced by 7,12-dimethylbenz[a]anthracene in swiss albino mice, possibly because of its oxidative stress response. In addition, stigmasterol has the ability of relieving some special skin inflammatory features in rodents. |
| Concentration | Treated Time | Description | References | |
| B16F10 cells | 0.5-50 µg/mL | 1 hour | To evaluate the inhibitory effect of STIG on H2O2-induced ROS levels. Results showed STIG significantly reduced H2O2-induced ROS levels. | Antioxidants (Basel). 2024 Mar 21;13(3):380 |
| LS174T human colon cancer cells | 200 mM | 16 hours | Evaluate the activity of stigmasterol as an LXR agonist in human intestinal cells, results showed stigmasterol could induce the expression of LXR target gene ABCA1. | J Nutr Biochem. 2020 Feb;76:108263 |
| L6 cells | 40 μg/mL | 20 minutes | Evaluate the effect of stigmasterol on GLUT4 translocation, results showed that stigmasterol treatment increased fluorescence intensity on L6 cell membranes, indicating enhanced GLUT4 translocation activity. | Food Nutr Res. 2017 Aug 23;61(1):1364117 |
| U87 GBM cells | 10, 20, 40, 80, 120, 160, 200, 240 µM | 24 and 48 hours | Stigmasterol suppressed the proliferation of GBM cells in a dose- and time-dependent manner. | Mol Med Rep. 2024 Dec;30(6):227 |
| B16F10 cells | 20 µg/mL | 24 hours | To evaluate the effect of STIG on PD-L1 expression. Results showed STIG significantly reduced IFN-γ-induced PD-L1 mRNA and protein levels. | Antioxidants (Basel). 2024 Mar 21;13(3):380 |
| L6 cells | 10, 20, 40 μg/mL | 24 hours | Detect the effect of stigmasterol on glucose uptake, results showed that stigmasterol increased glucose uptake in a concentration-dependent manner. | Food Nutr Res. 2017 Aug 23;61(1):1364117 |
| RAW264.7 cells | 15 µM | 24 hours | To investigate the effect of stigmasterol-treated LPS-induced Schwann cell-conditioned medium on the proliferation and migration of RAW264.7 cells. Results showed that L-S-CM significantly inhibited the proliferation and migration of RAW264.7 cells. | CNS Neurosci Ther. 2024 Apr;30(4):e14657 |
| RSC96 cells | 15 µM | 24 hours | To investigate the effect of stigmasterol on IL-34 secretion in LPS-induced RSC96 cells. Results showed that stigmasterol significantly reduced the secretion of IL-34 in LPS-induced RSC96 cells. | CNS Neurosci Ther. 2024 Apr;30(4):e14657 |
| OV90 cells | 0, 5, 10, 20 μg/mL | 24 hours | Induced apoptosis, activated caspase-3 and caspase-9 | Pharmaceutics. 2020 May 28;12(6):488 |
| ES2 cells | 0, 5, 10, 20 μg/mL | 24 hours | Induced apoptosis, activated caspase-3 and caspase-9 | Pharmaceutics. 2020 May 28;12(6):488 |
| Ishikawa cells | 10 μg/ml | 24 hours | Stigmasterol enhances the sensitivity of endometrial cancer cells to cisplatin by suppressing Nrf2 expression | Antioxidants (Basel). 2022 Jan 20;11(2):199 |
| Ishikawa cells | 10 μg/ml | 24 hours | Stigmasterol enhances the sensitivity of endometrial cancer cells to cisplatin by suppressing Nrf2 expression | Cancer Cell Int. 2020 Oct 6;20:480 |
| U87 GBM cells | 240 µM | 24 hours | Stigmasterol significantly reduced free fatty acid and total cholesterol levels in U87 GBM cells. | Mol Med Rep. 2024 Dec;30(6):227 |
| U87 GBM cells | 240 µM | 24 hours | Stigmasterol significantly inhibited vasculogenic mimicry formation in U87 GBM cells. | Mol Med Rep. 2024 Dec;30(6):227 |
| U87 GBM cells | 240 µM | 24 hours | Stigmasterol significantly inhibited the migration ability of U87 GBM cells. | Mol Med Rep. 2024 Dec;30(6):227 |
| U87 GBM cells | 240 µM | 24 hours | Stigmasterol significantly reduced the number of invasive U87 GBM cells. | Mol Med Rep. 2024 Dec;30(6):227 |
| U87 GBM cells | 240 µM | 24 hours | Stigmasterol significantly increased the proportion of apoptotic U87 GBM cells. | Mol Med Rep. 2024 Dec;30(6):227 |
| 4T1 isolated breast cancer stem-like cells | 0, 1, 5, 10 µM | 24 hours | Inhibits spheroid formation ability, cell viability, and migration ability, promotes cell apoptosis | J Cancer. 2025 Feb 3;16(5):1618-1630 |
| SUM159 isolated breast cancer stem-like cells | 0, 1, 5, 10 µM | 24 hours | Inhibits spheroid formation ability, cell viability, and migration ability, promotes cell apoptosis | J Cancer. 2025 Feb 3;16(5):1618-1630 |
| Mouse chondrogenic cells (ATDC5 cells) | 5, 10, 20, 40 μg/mL | 24 hours | To detect the effect of stigmasterol on the viability of ATDC5 cells, the results showed that 0-20 μg/ml STM had no significant effect on cell viability, while 40 μg/ml STM showed inhibitory effects. | Bioengineered. 2021 Dec;12(2):9332-9340 |
| Liver epithelial cells THLE-2 | 10, 50, 100 µg/mL | 48 hours | Assessed cytotoxicity and metabolic activity, showing DP3SSt inhibited cell proliferation and viability at 50 and 100 µg/mL, while other derivatives had no significant effect | Sci Rep. 2023 Dec 4;13(1):21375 |
| Colon mucosa cells CCD 841CoN | 10, 50, 100 µg/mL | 48 hours | Assessed cytotoxicity and metabolic activity, showing no toxicity from unheated and heated Stigmasterol derivatives, with DO3SSt promoting cell proliferation at specific concentrations | Sci Rep. 2023 Dec 4;13(1):21375 |
| Small intestine epithelial cells FHS 74Int | 10, 50, 100 µg/mL | 48 hours | Assessed cytotoxicity and metabolic activity, showing no toxicity from unheated and heated Stigmasterol derivatives, with DO3SSt promoting cell proliferation at specific concentrations | Sci Rep. 2023 Dec 4;13(1):21375 |
| MGC-803 | 10, 20 µM | 48 hours | To evaluate the effect of Stigmasterol on cell proliferation, results showed that Stigmasterol significantly inhibited cell viability in a time- and dose-dependent manner in MGC-803 cells. | Front Oncol. 2021 Feb 23;11:629008 |
| SGC-7901 | 10, 20 µM | 48 hours | To evaluate the effect of Stigmasterol on cell proliferation, results showed that Stigmasterol significantly inhibited cell viability in a time- and dose-dependent manner in SGC-7901 cells. | Front Oncol. 2021 Feb 23;11:629008 |
| OV90 cells | 0, 5, 10, 20 μg/mL | 48 hours | Increased mitochondrial depolarization, ROS production, and calcium overload | Pharmaceutics. 2020 May 28;12(6):488 |
| ES2 cells | 0, 5, 10, 20 μg/mL | 48 hours | Increased mitochondrial depolarization, ROS production, and calcium overload | Pharmaceutics. 2020 May 28;12(6):488 |
| Human normal colon mucosa CCD 841 CoN cells | 2.5, 5, 10, 20, 40 μg/mL | 48 hours | To assess the effect of stigmasterol on DNA synthesis. Results showed that non-heated stigmasterol at 5 μg/mL significantly inhibited DNA synthesis, and at 40 μg/mL decreased DNA synthesis by 61%. Heated stigmasterol at 20 and 40 μg/mL reduced DNA synthesis by 31% and 39%, respectively. | Sci Rep. 2023 May 1;13(1):7093 |
| Human normal colon mucosa CCD 841 CoN cells | 1.25, 2.5, 5, 10, 20, 40 μg/mL | 48 hours | To evaluate the cytotoxicity of stigmasterol and its esters on colon mucosa cells. Results showed that non-heated stigmasterol at 40 μg/mL reduced viable cell number by approximately 80%, while heated stigmasterol showed lower cytotoxicity at the same concentration. | Sci Rep. 2023 May 1;13(1):7093 |
| RAW 264.7 cells | 0, 1, 2.5, 5, 10 µM | 48 hours | To evaluate the effect of STG on the viability of RAW 264.7 cells. Results showed no significant change in cytotoxicity within concentrations ranging from 0 to 10 μM, but cellular viability decreased at 20 μM. | Front Pharmacol. 2024 Dec 16;15:1527494 |
| BEAS-2B cells | 10 μg/mL and 20 μg/mL | 48 hours | To verify the anti-inflammatory and antioxidant stress effects of stigmasterol and to reduce NK1-R expression in IL-13-induced BEAS-2B cells. | Pharm Biol. 2023 Dec;61(1):449-458 |
| RAW 264.7 cells | 5, 10 µM | 6-7 days | To evaluate the effect of STG on osteoclast-specific gene expression. Results showed that STG significantly downregulated the expression of Acp5, NFATc1, c-Fos, and CTSK genes. | Front Pharmacol. 2024 Dec 16;15:1527494 |
| RAW 264.7 cells | 0, 1, 2.5, 5, 10 µM | 6-7 days | To assess the effect of STG on RANKL-induced osteoclast differentiation. Results showed that STG significantly inhibited osteoclast formation in a dose-dependent manner. | Front Pharmacol. 2024 Dec 16;15:1527494 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | High cholesterol diet model | Oral | 0.3% (w/w) | 4 consecutive days | Assess the effect of stigmasterol on cholesterol balance and secretion, results showed stigmasterol promoted intestinal cholesterol secretion but did not depend on LXR activation pathway. | J Nutr Biochem. 2020 Feb;76:108263 |
| C57BL/6J male mice | DSS-induced colitis model | Oral via diet | 0.4% diet supplementation | Fed for 1 week followed by 1.5% DSS in drinking water for 5 days | To evaluate the protective effects of Stigmasterol against DSS-induced colitis. Results showed that Stigmasterol significantly inhibited colon shortening, reduced fecal hemoglobin content, decreased colonic inflammation score, and downregulated the expression of NF-κB, COX-2, and CSF-1. | Food Funct. 2017 Nov 15;8(11):4179-4186 |
| Mice | High-fat western-style diet-induced NAFLD model | Diet | 0.4% in diet | 17 weeks | To investigate the effects of stigmasterol and β-sitosterol on high-fat western-style diet-induced NAFLD. Results showed that stigmasterol significantly ameliorated HFWD-induced fatty liver and metabolic abnormalities, including elevated levels of hepatic total lipids, triacylglycerols, cholesterol and liver histopathology. | Biochim Biophys Acta Mol Cell Biol Lipids. 2018 Oct;1863(10):1274-1284 |
| BALB/C nude mice | Breast cancer stem cell transplantation model | Mammary fat pad injection | 10 mg/kg | Once a week for 1.5 months | Significantly inhibits tumor formation ability and reverses its inhibitory effect by suppressing JAK3 expression | J Cancer. 2025 Feb 3;16(5):1618-1630 |
| C57BL/6J mice | OVA-induced asthma mouse model | Intraperitoneal injection | 100 mg/kg | 7 consecutive days | To evaluate the anti-inflammatory and antioxidant stress effects of stigmasterol in OVA-induced asthma mice and to verify the role of NK1-R as a potential target. | Pharm Biol. 2023 Dec;61(1):449-458 |
| Wistar rats | Cerebral ischemia/reperfusion injury model | Oral | 20, 40, 80 mg/kg | 1 week | Stigmasterol alleviates cerebral ischemia/reperfusion injury by attenuating inflammation and improving antioxidant defenses in rats. | Biosci Rep. 2020 Apr 30;40(4):BSR20192133 |
| C57/BL6 male mice | OVA-induced asthma mouse model | Oral | 5 mg/kg, 10 mg/kg, 20 mg/kg | Every 2 days from day 21 to day 43 | Stigmasterol alleviated OVA-induced airway inflammation, reduced the number of inflammatory cells in BALF, decreased levels of IL-1β, IL-5, IL-6, and IL-13, and inhibited the TGF-β1/Smad2 and IL-17A signaling pathways | Aging (Albany NY). 2024 Apr 4;16(7):6478-6487 |
| C57BL/6J female mice | Ovariectomy (OVX) osteoporosis model | Oral | 5, 10 mg/kg | Administered every other day for 8 weeks | To evaluate the protective effect of STG against OVX-induced osteoporosis. Results showed that STG significantly reduced the number and surface area of osteoclasts and effectively prevented bone loss. | Front Pharmacol. 2024 Dec 16;15:1527494 |
| KK-Ay mice | High-fat diet-induced type 2 diabetes model | Oral | 50 mg/kg/day, 100 mg/kg/day | Once daily for 4 weeks | Evaluate the hypoglycemic effect of stigmasterol in type 2 diabetic mice, results showed that stigmasterol significantly reduced fasting blood glucose levels and improved insulin resistance and oral glucose tolerance. | Food Nutr Res. 2017 Aug 23;61(1):1364117 |
| Sprague-Dawley rats | Chronic constriction injury (CCI) model | Oral gavage | 80 mg/kg | Once daily for 21 days | To investigate the effect of stigmasterol on neuropathic pain in CCI rats. Results showed that stigmasterol significantly reduced thermal and cold hyperalgesia in CCI rats and decreased the levels of IL-1β, IL-6, TNF-α, CCL2, SP, and PGE2 in serum. | CNS Neurosci Ther. 2024 Apr;30(4):e14657 |
| Sprague-Dawley (SD) rats | High-fat diet (HFD)-induced hyperlipidemia and hepatic steatosis model | Intragastric administration | Low-dose group: 100 mg/kg; High-dose group: 200 mg/kg | Daily administration for 4 weeks | ST treatment significantly alleviated HFD-induced hyperlipidemia and hepatic fat deposition, mainly dependent on the bile acid metabolic pathway. ST also improved intestinal barrier function and gut microbiota in HFD-fed rats, resulting in changes in bile acid metabolism. | NPJ Sci Food. 2022 Aug 27;6(1):38 |
| Dose | Rat: 20 mg/kg - 80 mg/kg[5] (i.p.); 10 mg/kg - 300 mg/kg[6] (p.o.) Mice: 10 mg/kg - 100 mg/kg[7] (i.p.); 50 mg/kg - 200 mg/kg[7] (p.o.) |
| Administration | i.p., p.o. |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT00698256 | Hypercholesterolemia | Not Applicable | Completed | - | Finland ... 展开 >> University of kuopio Kuopio, Finland, 70211 收起 << |
| NCT02702947 | BPH | Phase 4 | Completed | - | India ... 展开 >> Department of Urology, King George's Medical University, Lucknow, UP, India Lucknow, Uttar Pradesh, India, 226003 收起 << |
| NCT00718796 | Cardiovascular Disease | Phase 3 | Completed | - | Canada, Ontario ... 展开 >> Canadian College of Naturopathic Medicine Toronto, Ontario, Canada, M2K 1E2 收起 << |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.42mL 0.48mL 0.24mL |
12.12mL 2.42mL 1.21mL |
24.23mL 4.85mL 2.42mL |
|
| CAS号 | 83-48-7 |
| 分子式 | C29H48O |
| 分子量 | 412.69 |
| SMILES Code | CC[C@](C(C)C)([H])/C([H])=C([H])/[C@@]([C@@]1([H])CC[C@@]2([H])[C@]([C@]3([H])CC[C@]12C)([H])CC=C4C[C@](O)([H])CC[C@@]43C)([H])C |
| MDL No. | MFCD00003630 |
| 别名 | Stigmasterin; 5,22-Cholestadien-24-beta-ethyl-3-beta-ol |
| 运输 | 蓝冰 |
| InChI Key | HCXVJBMSMIARIN-PHZDYDNGSA-N |
| Pubchem ID | 5280794 |
| 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 |
DMF: 1 mg/mL(2.42 mM),配合低频超声,并水浴加热至45℃助溶
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