Anti-infection Apoptosis Metabolic Enzyme/Protease Immunology/Inflammation NF-κB Epigenetics Cell Cycle/DNA Damage PI3K/Akt/mTOR
Bacterial Apoptosis Reactive Oxygen Species (ROS) MDM-2/p53 Caspase PARP MMP Bcl-2 Family HIF/HIF Prolyl-Hydroxylase TNF Receptor Interleukin Related NF-κB mTOR Lactate Dehydrogenase CDK Glutathione Peroxidase SOD
Beta-Sitosterol (purity>98%)

製品番号: HY-N0171A

Beta-Sitosterol (purity>98%)

(別名: β-Sitosterol (purity>98%); 22,23-Dihydrostigmasterol (purity>98%))

22 Cited Publications

カスタマーレビュー

Based on 22 publication(s) in Google Scholar

Beta-Sitosterol (purity>98%) is orally active. Beta-Sitosterol exhibits multiple activities, including anti-inflammatory, anticancer, antioxidant, antimicrobial, antidiabetic, antioxidant enzyme, and analgesic. Beta-Sitosterol inhibits inflammation and impaired adipogenesis in bovine mammary epithelial cells by reducing levels of ROS, TNF-α, IL-1β, and NF-κB p65 and restoring the activity of the HIF-1α/mTOR signaling pathway. Beta-Sitosterol induces apoptosis in cancer cells through ROS-mediated mitochondrial dysregulation and p53 activation. Beta-Sitosterol exerts its anticancer effects in cancer cells by activating caspase-3, caspase-8, and caspase-9, mediating PARP inactivation, MMP loss, altered Bcl-2-Bax ratio, and cytochrome c release. Beta-Sitosterol modulates macrophage polarization and reduces rheumatoid inflammation in mice. Beta-Sitosterol inhibits tumor growth in multiple mouse cancer models. Beta-Sitosterol can be used in the research of arthritis, lung cancer, breast cancer and other cancers, diabetes, etc.

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純度: 99.74%
CAS 番号: 83-46-5
分子式: C₂₉H₅₀O
分子量:414.71

保管条件:

-20°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Beta-Sitosterol (purity>98%) 構造式

CAS 番号: 83-46-5

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生物活性
- 製品説明
- IC₅₀ & Target
- Cellular Effect
- 体外実験
- 体内実験
化学情報
Publications (22)
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参考文献
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生物活性

製品説明

IC₅₀ & Target^[1]^[2]^[3]^[4]^[5]^[6]^[7]^[8]^[9]^[10]

Caspase 3

Caspase-8

Caspase-9

IL-1

HIF-1α

IL-1β

Bax

Bcl-2

Caspase アイソフォーム固有の製品をすべて表示 :

PARP アイソフォーム固有の製品をすべて表示 :

MMP アイソフォーム固有の製品をすべて表示 :

Bcl-2 Family アイソフォーム固有の製品をすべて表示 :

HIF/HIF Prolyl-Hydroxylase アイソフォーム固有の製品をすべて表示 :

TNF Receptor アイソフォーム固有の製品をすべて表示 :

Interleukin Related アイソフォーム固有の製品をすべて表示 :

NF-κB アイソフォーム固有の製品をすべて表示 :

mTOR アイソフォーム固有の製品をすべて表示 :

CDK アイソフォーム固有の製品をすべて表示 :

Glutathione Peroxidase アイソフォーム固有の製品をすべて表示 :

GPX1
GPX4

Cellular Effect

Cell Line	Type	Value	Description	References
1A9	ED₅₀	10.6 μg/mL Compound: 17	Cytotoxicity against human 1A9 cells after 6 days by SRB assay Cytotoxicity against human 1A9 cells after 6 days by SRB assay	[PMID: 14640511]
1A9	ED₅₀	16.8 μg/mL Compound: 17	Cytotoxicity against human 1A9 cells after 3 days by SRB assay Cytotoxicity against human 1A9 cells after 3 days by SRB assay	[PMID: 14640511]
1A9/ptx-10	ED₅₀	20 μg/mL Compound: 17	Cytotoxicity against human 1A9/PTX10 cells after 3 days by SRB assay Cytotoxicity against human 1A9/PTX10 cells after 3 days by SRB assay	[PMID: 14640511]
1A9/ptx-10	ED₅₀	9.5 μg/mL Compound: 17	Cytotoxicity against human 1A9/PTX10 cells after 6 days by SRB assay Cytotoxicity against human 1A9/PTX10 cells after 6 days by SRB assay	[PMID: 14640511]
A2780	IC₅₀	>10 μg/mL Compound: page 1629, R26C1	Cytotoxicity against human A2780 cells after 96 hrs by MTT assay Cytotoxicity against human A2780 cells after 96 hrs by MTT assay	[PMID: 17125236]
A549	ED₅₀	>20 μg/mL Compound: 17	Cytotoxicity against human A549 cells after 3 days by SRB assay Cytotoxicity against human A549 cells after 3 days by SRB assay	[PMID: 14640511]
A549	IC₅₀	>10 μg/mL Compound: page 1629, R26C1	Cytotoxicity against human A549 cells after 96 hrs by MTT assay Cytotoxicity against human A549 cells after 96 hrs by MTT assay	[PMID: 17125236]
Bel-7402	IC₅₀	>10 μg/mL Compound: page 1629, R26C1	Cytotoxicity against human Bel-7402 cells after 96 hrs by MTT assay Cytotoxicity against human Bel-7402 cells after 96 hrs by MTT assay	[PMID: 17125236]
BGC-823	IC₅₀	>10 μg/mL Compound: page 1629, R26C1	Cytotoxicity against human BGC-823 cells after 96 hrs by MTT assay Cytotoxicity against human BGC-823 cells after 96 hrs by MTT assay	[PMID: 17125236]
ECV-304	IC₅₀	472 μM Compound: beta-sitosterol	Membranolytic activity in human ECV304 cells assessed as leakage of intracellular lactate dehydrogenase after 2 hrs by spectrophotometry Membranolytic activity in human ECV304 cells assessed as leakage of intracellular lactate dehydrogenase after 2 hrs by spectrophotometry	[PMID: 22503361]
ECV-304	IC₅₀	472 μM Compound: Beta-sitosterol	Membrane toxicity against human ECV304 cells after 2 hrs by LDH release assay Membrane toxicity against human ECV304 cells after 2 hrs by LDH release assay	[PMID: 24084294]
ECV-304	IC₅₀	61 μM Compound: beta-sitosterol	Cytotoxicity against human ECV304 cells after 72 hrs by Hoechst 33258 staining based fluorescence assay Cytotoxicity against human ECV304 cells after 72 hrs by Hoechst 33258 staining based fluorescence assay	[PMID: 22503361]
ECV-304	IC₅₀	61 μM Compound: Beta-sitosterol	Cytotoxicity against human ECV304 cells after 72 hrs by MTT assay Cytotoxicity against human ECV304 cells after 72 hrs by MTT assay	[PMID: 24084294]
HCT-8	ED₅₀	>20 μg/mL Compound: 17	Cytotoxicity against human HCT8 cells after 3 days by SRB assay Cytotoxicity against human HCT8 cells after 3 days by SRB assay	[PMID: 14640511]
HCT-8	IC₅₀	>10 μg/mL Compound: page 1629, R26C1	Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay	[PMID: 17125236]
HeLa	IC₅₀	46.22 μM Compound: 9	Cytotoxicity against human HeLa cells by MTT assay Cytotoxicity against human HeLa cells by MTT assay	[PMID: 19447618]
HEp-2	IC₅₀	11.4 μM Compound: 119	Antiproliferative activity against human Hep2 cells by MTT assay Antiproliferative activity against human Hep2 cells by MTT assay	[PMID: 30830783]
HT-1080	IC₅₀	2.5 μM Compound: Angelicin	Cytotoxicity against human HT1080 cells assessed as reduction in cell viability Cytotoxicity against human HT1080 cells assessed as reduction in cell viability	[PMID: 30660827]
HUVEC	ED₅₀	>5 μg/mL Compound: beta-sitosterol	Cytotoxicity against HUVEC Cytotoxicity against HUVEC	[PMID: 15043409]
J774	IC₅₀	>241.1 μM Compound: 11	Cytotoxicity against mouse J774 cells by alamar blue assay Cytotoxicity against mouse J774 cells by alamar blue assay	[PMID: 17637068]
KB	ED₅₀	>20 μg/mL Compound: 17	Cytotoxicity against human KB cells after 3 days by SRB assay Cytotoxicity against human KB cells after 3 days by SRB assay	[PMID: 14640511]
KB	IC₅₀	>10 μg/mL Compound: 119	Antiproliferative activity against human KB cells assessed as reduction in cell viability Antiproliferative activity against human KB cells assessed as reduction in cell viability	[PMID: 30830783]
KB	IC₅₀	>241.5 μM Compound: 119	Antiproliferative activity against human KB/HeLa cells assessed as reduction in cell viability Antiproliferative activity against human KB/HeLa cells assessed as reduction in cell viability	[PMID: 30830783]
LNCaP	ED₅₀	>5 μg/mL Compound: beta-sitosterol	Cytotoxicity against human LNCAP cells Cytotoxicity against human LNCAP cells	[PMID: 15043409]
Lu1	ED₅₀	>5 μg/mL Compound: beta-sitosterol	Cytotoxicity against human Lu1 cells Cytotoxicity against human Lu1 cells	[PMID: 15043409]
MCF7	ED₅₀	>20 μg/mL Compound: 17	Cytotoxicity against human MCF7 cells after 3 days by SRB assay Cytotoxicity against human MCF7 cells after 3 days by SRB assay	[PMID: 14640511]
MCF7	ED₅₀	>5 μg/mL Compound: beta-sitosterol	Cytotoxicity against human MCF7 cells Cytotoxicity against human MCF7 cells	[PMID: 15043409]
MCF7	IC₅₀	42.1 μM Compound: 9	Cytotoxicity against human MCF7 cells by MTT assay Cytotoxicity against human MCF7 cells by MTT assay	[PMID: 19447618]
PC-3	ED₅₀	>20 μg/mL Compound: 17	Cytotoxicity against human PC3 cells after 3 days by SRB assay Cytotoxicity against human PC3 cells after 3 days by SRB assay	[PMID: 14640511]
SK-MEL-1	IC₅₀	>50 μM Compound: 9	Cytotoxicity against human SK-MEL-1 cells by MTT assay Cytotoxicity against human SK-MEL-1 cells by MTT assay	[PMID: 19447618]
U-87MG ATCC	ED₅₀	>20 μg/mL Compound: 17	Cytotoxicity against human U87MG cells after 3 days by SRB assay Cytotoxicity against human U87MG cells after 3 days by SRB assay	[PMID: 14640511]
Vero	IC₅₀	>128 μg/mL Compound: 4	Cytotoxicity against african green monkey Vero cells Cytotoxicity against african green monkey Vero cells	[PMID: 18818073]

体外実験

Beta-Sitosterol (0-40 µM, 24 h) decreases cell viability with concentrations exceeding 5 µM in MAC-T cells ^[1].
Beta-Sitosterol (1 µM, 24 h) increases the levels of CAT, GSH, T-AOC, T-SOD and decreases the level of ROS, TNF-α, IL-1β, NF-κB p65 in LPS (HY-D1056)-induced MAC‐T cells^[1].
Beta-Sitosterol (1 µM, 24 h) inhibits apoptosis, attenuates the expression levels of caspase-3 and Bax, increases the levels of Bcl-2 and Bcl-2/Bax radio in LPS-induced MAC‐T cells^[1].
Beta-Sitosterol (1 µM, 24 h) restores HIF-1α/mTOR signaling pathway viability and the expression of fat synthesis-related Genes (SCD, PSMA5, FASN, SREBP1) in LPS-induced MAC-T cells^[1].
Beta-Sitosterol (25-200 µM, 24-72 h) affectes the growth of A549 cells, with an IC₅₀ of 24.7 μM at 72 h, increases the release of LDH in A549 cells, affects the viability of NCI-H460 cells, but does not affect the growth and viability of normal human lung, PBMC cells and NCI-H23 cells^[2].
Beta-Sitosterol (25-200 µM, 24-72 h) induces cell cycle arrest at Sub-G1 phase, reduces the expression of Cyclin D1 and CDK2 in A549 cells^[2].
Beta-Sitosterol (25-200 µM, 0-72 h) induces apoptosis occurred via mitochondrial dysfunction and ROS mediated DNA damage in A549 cells^[2].
Beta-Sitosterol (25-200 µM, 0-72 h) elevates the expression levels of caspase-3, caspase-9, cleavage PARP, Bax, p53 and pSer15-p53, suppresses the expression levels of Bcl-2 in A549 cells^[2].
Beta-Sitosterol (25-200 µM, 72 h) induces apoptosis occurred via the activation of p53 in NCI-H460 cells^[2].
Beta-Sitosterol decreases the expression of both TrxR1 and Trx1 in A549 and NCI-H460 cells^[2].
Beta-Sitosterol (5-50 µM, 24 h) blocks M1 but promotes M2 macrophage polarization in IFN-γ/IL-4-stimulated BMBMs^[3].
Beta-Sitosterol (1-150 μM/L, 5 days) increases MCF-7 cells proliferation^[5].
Beta-Sitosterol (8-16 μM, 5 days) causes a significant reduction in cell growth, alters composition of cell membranes in MCF-7 and MDA-MB-231 cells^[6].
Beta-Sitosterol (16 μM, 1-3 days) increases caspase-8 activity and Fas protein levels in MCF-7 and MDA-MB-231 cells^[6].
Beta-Sitosterol (0.1-100 μM, 18 h) reduces VCAM-1 and ICAM-1 expression, attenuates phosphorylation of NFkB p65 in TNF-α- stimulated HAEC, inhibits binding of U937 cells to TNF-α-stimulated HAEC^[7].
Beta-Sitosterol (50 μM, 1-6 h) reverts the enhancement of GSSG levels and the impairment of GSH levels or the GSH/total glutathione ratio induced by PMA (HY-18739) in RAW 264.7 cells^[8].
Beta-Sitosterol (50 μM, 1-6 h) increases GPx and Mn SOD activities, and decreases catalase activity in RAW 264.7 cells^[8].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay^[1]

Cell Line:

MAC-T cells
Concentration:

0, 0.01, 0.1, 1, 5, 10, 20, 30, and 40 µM
Incubation Time:

24 h
Result:

Decreased cell viability with concentrations exceeding 5 µM.

Immunofluorescence^[1]

Cell Line:

LPS (1 µg/mL)-induced MAC-T cells
Concentration:

1 µM
Incubation Time:

24 h
Result:

Decreased the level of DCFH-DA.

RT-PCR^[1]

Cell Line:

LPS (1 µg/mL)-induced MAC-T cells
Concentration:

1 µM
Incubation Time:

24 h
Result:

Slowed the mRNA expression levels of pro-inflammatory factors TNF-α and IL-1β down.
Upregulated the mRNA levels of HIF-1α and mTOR.
Restored the mRNA expression of fatty acid synthase (FASN) and sterol regulatory element-binding protein 1 (SREBP1) to the controls.

Western Blot Analysis^[1]

Cell Line:

LPS (1 µg/mL)-induced MAC-T cells
Concentration:

1 µM
Incubation Time:

24 h
Result:

Attenuated NF-κB p65 production by LPS-induced and restored it to the same level as the control group.
Upregulated the protein expression of HIF-1α and the ratio of p-mTOR/mTOR.
Restored the protein expression of stearoyl coenzyme A dehydrogenase (SCD), proteasome 20 s subunit α5 (PSMA5) to the controls.

Apoptosis Analysis^[1]

Cell Line:

LPS (1 µg/mL)-induced MAC-T cells
Concentration:

1 µM
Incubation Time:

24 h
Result:

Inhibited the apoptosis caused by LPS, attenuated the expression levels of mRNA and protein of caspase-3 and pro-apoptotic protein B-cell lymphoma-2-associated X protein (Bax), increased the protein levels of Bcl-2 and Bcl-2/Bax radio.

Cell Cycle Analysis^[2]

Cell Line:

A549 cells
Concentration:

25, 50, 100, 200 µM
Incubation Time:

24, 48 and 72 h
Result:

Affected the growth of cells in a concentration and time diferent manner.

Immunofluorescence^[2]

Cell Line:

A549 cells
Concentration:

25, 50, 100, 200 µM
Incubation Time:

72 h
Result:

Increased the number of PI positive cells.

Cell Cycle Analysis^[2]

Cell Line:

A549 cells
Concentration:

25, 50, 100, 200 µM
Incubation Time:

24, 48, 72 h
Result:

Induced cell cycle arrest at Sub-G1 phase in a time dependent, reduced the expression of both Cyclin D1 and CDK2.

Apoptosis^[2]

Cell Line:

A549 cells
Concentration:

25, 50, 100, 200 µM
Incubation Time:

0, 1, 6, 24, 48, 72 h
Result:

Increased early apoptotic cells and few late apoptotic cells upon 25μM exposure, elevated the protein expression levels of caspase-3, caspase-9, cleavage PARP.
Induced a concentration dependent disruption of ΔΨm afer 72h treatment, induced the release of cytochrome c into the cell cytoplasm in a dose dependent manner, suppressed the Bcl-2 and strongly increased the expression of Bax in a dose dependent manner.
Induced generation of DCF fuorescence at 6h of BS treatment and peaked at 12-48h time point, decreased at 72 h, caused severe DSBs and elevation of tail and olive movement, caused chromatin condensation and morphological alteration.
Up-regulated the protein expression of p53 and pSer15-p53.

Apoptosis Analysis^[2]

Cell Line:

NCI-H460 cells
Concentration:

25, 50, 100, 200 µM
Incubation Time:

72 h
Result:

Induced cell shrinkage, elongation and reduced cell populations, elevated the protein expression levels of caspase-3, caspase-9, cleavage PARP.
Reduced the expression of Bcl-2 protein and signifcant elevated Bax and cytochrome c, up-regulated p53, pSer15-p53 and p21 expression.

RT-PCR^[3]

Cell Line:

BMDMs
Concentration:

5, 25, 50 µM + 10 ng/mL IFN-γ/IL-4
Incubation Time:

24 h
Result:

Decreased NOS and IL-1β to 50.2% and 47.1% at 25 μM in the presence of IFN-γ, and increased the expression of arginase-1 by approximately 0.5-fold and IL-10 by approximately 1-fold in the presence of IL-4, compared with vehicle-treated BMDMs.

ELISA Assay^[3]

Cell Line:

HAECs
Concentration:

0.1, 1, 10, 50, 100 µM + TNF-α (1 ng/mL), 24 h
Incubation Time:

18 h
Result:

Significantly dose-dependent reduced VCAM-1 and ICAM-1 expression.

体内実験

Beta-Sitosterol (20-50 mg/kg, i.p., every 2 days, 31 days; 2 × 10⁶ BMDMs treating with 25 μM BS, i.v., once) inhibits pathological changes by suppressing humoral and cellular immune responsesin, in part, through IL-10 transfer in Collagen (HY-NP003)-induced arthritis (CIA) mice model^[3].
Beta-Sitosterol (2-5 mg/20 g mouse, i.p., once) plays an analgesic role in Acetic acid (HY-Y0319)-induced Swiss Webster albino mice model^[4].
Beta-Sitosterol (2 mg/20 g mouse, i.p., once) plays an anti-inflammatory role in Carrageenan (HY-125474)-induced mouse paw oedema model^[4].
Beta-Sitosterol (9.8 g/kg diet, o.p., 18 weeks) inhibits the growth of estrogen-responsive breast cancer cells of MCF-7 tumors implanted in ovariectomized athymic mice^[5].
Beta-Sitosterol (10-20 mg/kg, o.p., once a day, 21 days) has antidiabetic as well as antioxidant effects in Streptozotocin (HY-13753)-induced diabetes Wistar rats model^[9].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

CIA mice (six-week-old male C57BL/6) model^[3]
Dosage:

20, 50 mg/kg + 30 μg LPS, i.p., on day 3
Administration:

i.p., every 2 days, 31 days
Result:

Suppressed hind paw swelling and the production of collagen-specific IgG and IgG1, but not IgG2c.
Decreased IL-1β, IL-6, and IL-12 levels and increased IL-10 levels.

Animal Model:

CIA mice (six-week-old male C57BL/6) model^[3]
Dosage:

2 × 10⁶ BMDMs treating with 25 μM BS + 30 μg LPS, i.p., on day 3
Administration:

i.v., once
Result:

Reduced ankle swelling and synovial inflammation, reduced serum collagen-specific IgG, IgG1, and IgG2a antibodies, as well as IL-1β and IL-6, and increased serum IL-10 levels.

Animal Model:

Acetic acid-induced (0.7%, 0.2 mL/20 g mouse, i.p.) Swiss Webster albino mice (20-25 g) model^[4]
Dosage:

2, 5 mg/20 g mouse
Administration:

i.p., once
Result:

Reduced peristalsis by 70%, exhibited a 300% increase in pain tolerance.

Animal Model:

Carrageenan-induced mouse paw oedema model^[4]
Dosage:

2 mg/20 g mouse
Administration:

i.p., once
Result:

Changed paw oedema volume by 16.7%.

Animal Model:

MCF-7 tumors implanted (1 × 10⁵, 40 μL) ovariectomized athymic nude mice (female athymic BALB/c) model^[5]
Dosage:

9.8 g/kg diet
Administration:

o.p., 18 weeks
Result:

Did not affect tumor growth, regressed tumors after removal of the E2 pellet at wk 7, reduced 1:47 E2-induced tumor growth by 38.9%.
Downregulated Bcl-2 expression in the 1:47 E2 group by 38%, lowered the serum E2 level in the 1:47 E2 group by 35.1%.

Animal Model:

Streptozotocin-induced (i.p., 50 mg/kg) diabetes male albino Wistar rats (170-190 g) model^[9]
Dosage:

10, 15, 20 mg/kg
Administration:

o.p., once a day, 21 days
Result:

Reduced blood glucose (37.5%, 45.2%, and 50.4% in diabetic rats) and NO (16.4%, 28.4%, and 47.1% in diabetic rats).
Prevented the induction of diabetes by 77.8% and 100% at 10, 15 mg/kg, increased insulin levels and lowered HbA1c levels, dose-dependent increased pancreatic protein content.
Improved antioxidant activity and significantly reduced LPO levels, caused the pancreatic cells to rejuvenate.

化学情報

CAS 番号 83-46-5
性状 Solid
分子量 414.71
分子式 C₂₉H₅₀O
Color White to off-white
SMILES

CC[C@@H](C(C)C)CC[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C
別名

β-Sitosterol (purity>98%); 22,23-Dihydrostigmasterol (purity>98%)
Structure Classification
- Steroids
Initial Source
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件

-20°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Publications (22)

All Cell Proliferation/Viability AssayELISAIn Vivo Efficacy StudyWB

Sort by:

Journal Impact Factor

Signal Transduct Target Ther

Selective depletion of tumor-associated SAMHD1 enhances chemotherapeutic efficacy and antitumor immune responses. [Abstract]

2025 Dec 15;10(1):406. PMID: 41392286
J Control Release

Single intravitreal injection of lipid nanoparticles delivering circular mRNA of nicotinamide phosphoribosyltransferase protects against dry AMD. [Abstract]

2026 Apr 10:392:114691. PMID: 41672305
Phytomedicine

β-sitosterol alleviates pulmonary arterial hypertension by altering smooth muscle cell phenotype and DNA damage/cGAS/STING signaling. [Abstract]

2024 Sep 7:135:156030. PMID: 39265206
Int J Pharm X

Cutaneous delivery of bioactive components from a rice bran oil nanoemulsion and their biodistribution in porcine and human skin. [Abstract]

2026 Apr 13:11:100543. PMID: 42028061
Phytother Res

β-Sitosterol Suppresses Osteoclastogenesis and Alleviates Bone Loss by Targeting Tmed10 to Inhibit RANKL-Induced Hedgehog/MAPK Signaling and ROS. [Abstract]

2026 May;40(5):2491-2513. PMID: 41703993
Plant J

Unveiling the inequivalent biochemical functions of OsSMO2-1 and OsSMO2-2 in rice phytosterol biosynthesis using a customized sterol standards mixture. [Abstract]

2025 Nov;124(3):e70559. PMID: 41194406
Acta Neuropathol Commun

Unilateral intranigral administration of β-sitosterol β-D-glucoside triggers pathological α-synuclein spreading and bilateral nigrostriatal dopaminergic neurodegeneration in the rat. [Abstract]

2020 Apr 22;8(1):56. PMID: 32321590
J Ethnopharmacol

Ethanol extract of Liriodendron tulipifera leaves displays anti-inflammatory activity by suppressing the Syk/Src/NF-κB pathway. [Abstract]

2025 Sep 9;355(Pt A):120590. PMID: 40935214
Biosci Rep

Experimental evidence and network pharmacology-based analysis reveal the molecular mechanism of Tongxinluo capsule administered in coronary heart diseases. [Abstract]

2020 Oct 30;40(10):BSR20201349. PMID: 32990315

Beta-Sitosterol (purity>98%) purchased from MedChemExpress. Usage Cited in: Biosci Rep. 2020 Oct 30;40(10):BSR20201349. [Abstract]

Beta-sitosterol (5–100 μM; 48 h). Different concentrations of active compounds on improvement rate.

Beta-Sitosterol (purity>98%) purchased from MedChemExpress. Usage Cited in: Biosci Rep. 2020 Oct 30;40(10):BSR20201349. [Abstract]

Beta-Sitosterol (40 μM; 30 min) reduced IL-6 concentration.
Sci Rep

Beta sitosterol inhibits the proliferation and migration of synoviocytes in rheumatoid arthritis via lactylation of GPI. [Abstract]

2025 Jul 11;15(1):25045. PMID: 40646091
Mol Med Rep

Mechanism of β‑sitosterol in treating keloids: Network pharmacology, molecular docking and experimental verification. [Abstract]

2025 Apr;31(4):95. PMID: 39981895
Front Oncol

Salvia chinensis Benth Inhibits Triple-Negative Breast Cancer Progression by Inducing the DNA Damage Pathway. [Abstract]

2022 Aug 10;12:882784. PMID: 36033499

Beta-Sitosterol (purity>98%) purchased from MedChemExpress. Usage Cited in: Front Oncol. 2022 Aug 10;12:882784. [Abstract]

TNBC cells were simultaneously treated with quercetin and/or β-sitosterol for 48 h. Cell viability was measured via CCK-8 assay.

Beta-Sitosterol (purity>98%) purchased from MedChemExpress. Usage Cited in: Front Oncol. 2022 Aug 10;12:882784. [Abstract]

Mice were administered β-sitosterol (75 mg/kg) each day via oral gavage. Nude mice were subcutaneously injected with MDA-MB-231 cells. Representative images showed the dissected tumors in distinct treatment groups as specified at the endpoint.

Beta-Sitosterol (purity>98%) purchased from MedChemExpress. Usage Cited in: Front Oncol. 2022 Aug 10;12:882784. [Abstract]

Mice were administered β-sitosterol (75 mg/kg) each day via oral gavage. Tumor lysates were collected, and the protein profile was established by immunoblotting analysis.
Processes (Basel)

2026 Jan;14(9):1351.
Int J Clin Pract

2025 Aug 25.
Int J Environ Health Res

Green extraction and RSM optimization of Peganum harmala shoots for antioxidant and anti-inflammatory properties: modulation of pro-inflammatory cytokines. [Abstract]

2026 Feb 17:1-12. PMID: 41700732
Lett Drug Des Discov

2026 Feb 11.
Discover Pharmaceutical Sciences

2026 Jan 7;2(1):1.
SSRN

2025 May 6.
Res Sq

2025 May 16.
Patent

US20240209361A1.
Research Square Preprint

2021. Jul.
Evid Based Complement Alternat Med

Ethanol Extract of the Infructescence of Platycarya strobilacea Sieb. et Zucc. Induces Methuosis of Human Nasopharyngeal Carcinoma Cells. [Abstract]

2020 Apr 29;2020:2760979. PMID: 32419796

溶剤 & 溶解度

体外:

Ethanol : 5 mg/mL (12.06 mM; ultrasonic and warming and heat to 60°C)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

2.4113 mL

12.0566 mL

24.1132 mL

5 mM

0.4823 mL

2.4113 mL

4.8226 mL

10 mM

0.2411 mL

1.2057 mL

2.4113 mL

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 (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

モル濃度計算機

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass

濃度

体積

分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始)

体積 _(開始)

濃度 _(終了)

体積 _(終了)

体内:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% EtOH 40% PEG300 5% Tween-80 45% Saline

Solubility: ≥ 1 mg/mL (2.41 mM); Suspended solution

This protocol yields a suspended solution of ≥ 1 mg/mL (saturation unknown). Suspended solution can be used for oral and intraperitoneal injection.

Taking 1 mL working solution as an example, add 100 μL EtOH stock solution (10.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% EtOH 90% (20% SBE-β-CD in Saline)

Solubility: 1 mg/mL (2.41 mM); Suspended solution; Need ultrasonic

This protocol yields a suspended solution of 1 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

Taking 1 mL working solution as an example, add 100 μL EtOH stock solution (10.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

Protocol 3

Add each solvent one by one: 10% EtOH 90% Corn Oil

Solubility: ≥ 1 mg/mL (2.41 mM); Clear solution

This protocol yields a clear solution of ≥ 1 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL EtOH stock solution (10.0 mg/mL) to 900 μL Corn oil, and mix evenly.

Working Solution

For the following dissolution methods, please prepare the working solution directly:

It is recommended to prepare fresh solutions and use them promptly within a short period of time.

The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: Corn Oil

Solubility: 10 mg/mL (24.11 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

Protocol 2

Add each solvent one by one: 15% Cremophor EL 85% Saline

Solubility: 5 mg/mL (12.06 mM); Suspended solution; Need ultrasonic and warming and heat to 60°C

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage
mg/kg
Animal Weight (Per Animal)
g
Dosing Volume (Per Animal)
μL
Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Working solution concentration: 0.22 mg/mL

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

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- Portuguese - PT (648 KB)
COA (2659 KB)
元素分析報告書 (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Fan Y, et al. β-Sitosterol Suppresses Lipopolysaccharide-Induced Inflammation and Lipogenesis Disorder in Bovine Mammary Epithelial Cells. Int J Mol Sci. 2023 Sep 27;24(19):14644. [Content Brief]

[2]. Rajavel T, et al. β-Sitosterol targets Trx/Trx1 reductase to induce apoptosis in A549 cells via ROS mediated mitochondrial dysregulation and p53 activation. Sci Rep. 2018 Feb 1;8(1):2071. [Content Brief]

[3]. Liu R, et al. β-Sitosterol modulates macrophage polarization and attenuates rheumatoid inflammation in mice. Pharm Biol. 2019 Dec;57(1):161-168. [Content Brief]

[4]. Villaseñor IM, et al. Bioactivity studies on beta-sitosterol and its glucoside. Phytother Res. 2002 Aug;16(5):417-21. [Content Brief]

[5]. Ju YH, et al. beta-Sitosterol, beta-Sitosterol Glucoside, and a Mixture of beta-Sitosterol and beta-Sitosterol Glucoside Modulate the Growth of Estrogen-Responsive Breast Cancer Cells In Vitro and in Ovariectomized Athymic Mice. J Nutr. 2004 May;134(5):1145-51. [Content Brief]

[6]. Awad AB, et al. beta-Sitosterol activates Fas signaling in human breast cancer cells. Phytomedicine. 2007 Nov;14(11):747-54. [Content Brief]

[7]. Loizou S, et al. Beta-sitosterol exhibits anti-inflammatory activity in human aortic endothelial cells. Mol Nutr Food Res. 2010 Apr;54(4):551-8. [Content Brief]

[8]. Vivancos M, et al. beta-Sitosterol modulates antioxidant enzyme response in RAW 264.7 macrophages. Free Radic Biol Med. 2005 Jul 1;39(1):91-7. [Content Brief]

[9]. Gupta R, et al. Antidiabetic and antioxidant potential of β-sitosterol in streptozotocin-induced experimental hyperglycemia. J Diabetes. 2011 Mar;3(1):29-37. [Content Brief]

[10]. Anwar R, et al. Antimicrobial Activity of β-Sitosterol Isolated from Kalanchoe tomentosa Leaves Against Staphylococcus aureus and Klebsiella pneumonia. Pak J Biol Sci. 2022 Jun;25(7):602-607. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
Ethanol	1 mM	2.4113 mL	12.0566 mL	24.1132 mL	60.2831 mL
	5 mM	0.4823 mL	2.4113 mL	4.8226 mL	12.0566 mL
	10 mM	0.2411 mL	1.2057 mL	2.4113 mL	6.0283 mL

Beta-Sitosterol (purity>98%)

22 Cited Publications

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Beta-Sitosterol (purity>98%)

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