6-Geranylnaringenin

Modify Date: 2024-01-16 20:37:56

6-Geranylnaringenin Structure
6-Geranylnaringenin structure
Common Name 6-Geranylnaringenin
CAS Number 97126-57-3 Molecular Weight 408.48682
Density 1.219±0.06 g/cm3 Boiling Point 647.8±55.0 °C at 760 mmHg
Molecular Formula C25H28O5 Melting Point 116-118 °C
MSDS N/A Flash Point N/A

 Use of 6-Geranylnaringenin


Bonannione A (6-Geranylnaringenin; Mimulone), a prenylflavonoid, is an orally active and potent protein tyrosine phosphatase 1B (PTP1B) inhibitor with an IC50 of 14 µM. Bonannione A triggers caspase-dependent Apoptosis. Bonannione A induces Autophagy through p53-mediated AMPK/mTOR pathway. Bonannione A shows anti-inflammatory, antiradical and anti-cancer activity[1][2][3].

 Names

Name 6-Geranylnaringenin

 6-Geranylnaringenin Biological Activity

Description Bonannione A (6-Geranylnaringenin; Mimulone), a prenylflavonoid, is an orally active and potent protein tyrosine phosphatase 1B (PTP1B) inhibitor with an IC50 of 14 µM. Bonannione A triggers caspase-dependent Apoptosis. Bonannione A induces Autophagy through p53-mediated AMPK/mTOR pathway. Bonannione A shows anti-inflammatory, antiradical and anti-cancer activity[1][2][3].
Related Catalog
In Vitro 6-香叶草基柚皮素 (0-80 µM; 12, 24 小时) 在癌细胞系中以剂量和时间依赖性方式显着抑制细胞增殖[2]。 6-香叶草基柚皮素 (0-60 µM; 24 小时) 在 A549 细胞中触发半胱天冬酶依赖性细胞凋亡。6-香叶草基柚皮素增加凋亡亚 G1 期细胞的积累和 G2/M 期细胞的数量[2]。 6-香叶草基柚皮素 (60 µM; 24 小时) 在 A549 细胞中触发自噬而不损害自噬通量[2]。 6-香叶草基柚皮素 (60 µM; 24 小时) 显着降低 p53 和磷酸化 mTOR 的水平[2]。 Cell Proliferation Assay[2] Cell Line: Human lung cancer A549, breast cancer MCF-7, colon cancer HCT116 and osteosarcoma U2OS cells Concentration: 20, 40, 60, 80 µM Incubation Time: 12, 24 h Result: Significantly inhibited cell proliferation in a dose- and time-dependent way in these cancer cell lines. Apoptosis Analysis[2] Cell Line: A549 cells Concentration: 0-60 µM Incubation Time: 24 h Result: Annexin V/PI-positive cells were markedly increased in a dose- and time-dependent way. Induced apoptosis through caspase-3 activation and PARP cleavage. Cell Cycle Analysis[2] Cell Line: A549 cells Concentration: 0-60 µM Incubation Time: 24 h Result: Increased accumulation of cells at the apoptotic sub-G1 phase in a dose-dependent manner. The number of cells at G2/M phase also increased in a dose-dependent manner. Cell Autophagy Assay[2] Cell Line: A549 cells Concentration: 60 µM Incubation Time: 24 h Result: Remarkably increased ATG7 and LC3-II protein levels in a dose-dependent way, but Beclin-1 level was slightly augmented. Western Blot Analysis[2] Cell Line: A549 cells Concentration: 60 µM Incubation Time: 0-24 h Result: Remarkably decreased the levels of p53 and phospho-mTOR. Significantly increased whereas the levels of phospho-AMPK and phospho-Acetyl-CoA Carboxylase (ACC), an AMPK substrate.
In Vivo 6-香叶草基柚皮素 (25 mg/kg; 灌胃; DSS 前 48 和 24 小时,随后每 24 小时一次; 持续 5 天) 改善结肠炎的症状并延迟其发作[3]。 Animal Model: Male Wistar rats (180-220 g)[3] Dosage: 25 mg/kg Administration: Gavage; 48 and 24 h prior to DSS (10% (w/v)) and every 24 h on the following days; for 5days Result: Ameliorated the symptoms of colitis and delayed their onset. Showed the low DAI on the last day of the experiment.
References

[1]. Lai-Bin Zhang, et al. Isoprenylated Flavonoids with PTP1B Inhibition from Macaranga denticulate. Nat Prod Bioprospect. 2016 Feb;6(1):25-30.  

[2]. Hyun-Kyu An, et al. Mimulone-induced autophagy through p53-mediated AMPK/mTOR pathway increases caspase-mediated apoptotic cell death in A549 human lung cancer cells. PLoS One. 2014 Dec 9;9(12):e114607.  

[3]. Zora Vochyánová, et al. Diplacone and mimulone ameliorate dextran sulfate sodium-induced colitis in rats. Fitoterapia. 2015 Mar;101:201-7.  

 Chemical & Physical Properties

Density 1.219±0.06 g/cm3
Boiling Point 647.8±55.0 °C at 760 mmHg
Melting Point 116-118 °C
Molecular Formula C25H28O5
Molecular Weight 408.48682
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