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β-Elemene/β-榄香烯 {[allProObj[0].p_purity_real_show]}

货号:A464324 同义名: B-榄香烯 / Levo-β-elemene; (-)-β-Elemene

β-Elemene是一种天然倍半萜,存在于多种植物中,赋予某些植物花香气味。研究表明该化合物能够抑制多种肿瘤的增殖。

β-Elemene/β-榄香烯 化学结构 CAS号:515-13-9
β-Elemene/β-榄香烯 化学结构
CAS号:515-13-9
β-Elemene/β-榄香烯 3D分子结构
CAS号:515-13-9
β-Elemene/β-榄香烯 化学结构 CAS号:515-13-9
β-Elemene/β-榄香烯 3D分子结构 CAS号:515-13-9
规格 价格 会员价 库存 数量
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β-Elemene/β-榄香烯 纯度/质量文件 产品仅供科研

货号:A464324 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 ERK ERK1 ERK2 ERK5 其他靶点 纯度
DEL-22379 +

ERK, IC50: 0.5 μM

+

ERK, IC50: 0.5 μM

98%
Pluripotin ++

ERK1, Kd: 98 nM

RasGAP 98+%
FR 180204 +

ERK1, Ki: 0.31 μM

++

ERK2, Ki: 0.14 μM

98%
Ravoxertinib +++

ERK1, IC50: 1.1 nM

++++

ERK2, IC50: 0.3 nM

99%+
SCH772984 +++

ERK1, IC50: 4 nM

++++

ERK2, IC50: 1 nM

99%+
Temuterkib +++

ERK1, IC50: 5 nM

+++

ERK2, IC50: 5 nM

99%+
VX-11e +++

ERK2, Ki: <2 nM

99%+
Ulixertinib ++++

ERK2, IC50: <0.3 nM

99%+
XMD17-109 ++

ERK5, IC50: 162 nM

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。

β-Elemene/β-榄香烯 生物活性

描述 β-Elemene is a natural sesquiterpene found in various plants and imparts floral aromas to some plants. This compound has been reported to inhibit the proliferation of a wide range of tumors.

β-Elemene/β-榄香烯 细胞实验

Cell Line
Concentration Treated Time Description References
NCI-H226 cells 10 µg/ml 24 hours Β-Elemene significantly up-regulated C3orf21 expression Front Oncol. 2021 May 7;11:571476
MSTO-211H cells 10 µg/ml 24 hours Β-Elemene significantly up-regulated C3orf21 expression Front Oncol. 2021 May 7;11:571476
U87MG cells 10 μg/mL 1 day Cell viability was significantly decreased in a dose-dependent manner. Am J Cancer Res. 2021 Feb 1;11(2):370-388
SGC7901 human gastric cancer cells 30 μg/mL 18 hours To evaluate the effect of β-elemene on the radiosensitivity of gastric cancer cells, results showed that β-elemene pretreatment decreased clonogenic survival World J Gastroenterol. 2015 Sep 14;21(34):9945-56
MKN45 human gastric cancer cells 15 μg/mL 18 hours To evaluate the effect of β-elemene on the radiosensitivity of gastric cancer cells, results showed that β-elemene pretreatment decreased clonogenic survival World J Gastroenterol. 2015 Sep 14;21(34):9945-56
DBTRG-05MG cells 10 μg/mL 2 days Induced senescence in glioma cells, with the percentage of SA-β-gal positive cells significantly increased to approximately 50%. Am J Cancer Res. 2021 Feb 1;11(2):370-388
C6 cells 10 μg/mL 2 days Induced senescence in glioma cells, including reduction of cell proliferation, hypertrophic morphology, increase of SA-β-Gal activity, upregulation of senescence-associated genes such as p16, p53 and NF-κB, and down-regulation of Lamin B1. Am J Cancer Res. 2021 Feb 1;11(2):370-388
SPC-A-1 cells 120 μg/mL 24 hours To evaluate the effect of β-Elemene on the expression of lysosomal biogenesis-related genes, results showed β-Elemene significantly upregulated mRNA expression of GLA, MCOLN1, and SLC26A11. J Adv Res. 2024 Aug;62:257-272
NCI-H460 cells 120 μg/mL 24 hours To investigate the effect of β-Elemene on TFEB activation and lysosomal function, results showed β-Elemene significantly increased lysosomal acidification and TFEB nuclear translocation. J Adv Res. 2024 Aug;62:257-272
A549 cells 120 μg/mL 24 hours To observe the effect of β-Elemene on TFEB activation and GPX4 lysosomal degradation, results showed β-Elemene significantly reduced TFEB phosphorylation, promoted its nuclear translocation, and increased GPX4 lysosomal degradation. J Adv Res. 2024 Aug;62:257-272
HCT116p53−/− cells 40 μg/ml 24 hours Β-Elemene significantly inhibited the proliferation of HCT116p53−/− cells and reversed their resistance to 5-Fu. Front Bioeng Biotechnol. 2020 May 8;8:378
Human hepatoma HepG2 cells 0.02, 0.04, 0.08 mg/mL 24 hours To detect the effect of β-elemene on microtubule polymerization, results showed that β-elemene reduced microtubule polymerization in a dose-dependent manner. Chin J Cancer Res. 2013 Dec;25(6):770-6
Human hepatoma HepG2 cells 0.02, 0.04, 0.08 mg/mL 24 hours To detect the effect of β-elemene on α-tubulin mRNA expression, results showed that β-elemene down-regulated α-tubulin mRNA expression in a dose-dependent manner. Chin J Cancer Res. 2013 Dec;25(6):770-6
Human hepatoma HepG2 cells 0.02, 0.04, 0.08 mg/mL 24 hours To detect the effect of β-elemene on HepG2 cell cycle, results showed that β-elemene induced cell cycle arrest at S phase in a dose-dependent manner. Chin J Cancer Res. 2013 Dec;25(6):770-6
BV-2 cells 40 µM and 80 µM 24 hours Β-Elemene promoted the transformation of BV-2 cells from M1-like to M2-like phenotype, inhibited inflammatory factor release, thereby reducing neuronal apoptosis. Chin Med. 2024 Jun 15;19(1):86
NCI-H1650 cells 50 μg/ml 24 hours To investigate the effect of β-elemene on the Warburg effect in NCI-H1650 cells and its mechanism. Results showed that β-elemene suppressed the Warburg effect by regulating the miR-301a-3p/AMPKα axis, as evidenced by decreased glucose and lactic acid levels and downregulation of metabolism-related enzymes (GLUT1, HK1, and LDHA). Biosci Rep. 2020 Jun 26;40(6):BSR20194389
CaSki cells 0.18 mg/mL 24 hours Evaluate the inhibitory effect of β-Elemene on CaSki cells, showing nearly 50% inhibition at 0.18 mg/mL Int J Pharm X. 2024 Aug 13;8:100276
Hela cells 0.09 mg/mL 24 hours Evaluate the inhibitory effect of β-Elemene on Hela cells, showing nearly 50% inhibition at 0.09 mg/mL Int J Pharm X. 2024 Aug 13;8:100276
RAW 264 cells 10 μg/ml 24 hours To study the inhibitory effect of β-Elemene on LPS-induced inflammatory response, results showed that β-Elemene significantly reduced the production of inflammatory cytokines. Commun Biol. 2022 May 31;5(1):519
PP-CD11c+ DCs 1, 2, 5, 10 μg/mL 24 hours To evaluate the effects of β-elemene on the expression of TGF-β1, RALDH2, integrin αvβ8, and IL-10 in PP DCs. Results showed that β-elemene significantly increased the expression of these molecules, indicating its role in promoting Tregs generation by modulating DCs function. iScience. 2020 Nov 30;24(1):101883
MLN-CD11c+ DCs 1, 2, 5, 10 μg/mL 24 hours To evaluate the effects of β-elemene on the expression of TGF-β1, RALDH2, integrin αvβ8, and IL-10 in MLN DCs. Results showed that β-elemene significantly increased the expression of these molecules, indicating its role in promoting Tregs generation by modulating DCs function. iScience. 2020 Nov 30;24(1):101883
MAT SVCs 1, 2, 5, 10 μg/mL 24 hours To evaluate the direct anti-inflammatory effects of β-elemene on SVCs from EAT and MAT of obese mice. Results showed that β-elemene had limited effects on LPS-induced inflammation in vitro, with significant effects only at high concentration (10 μg/mL) on CCL2 expression in MAT SVCs. iScience. 2020 Nov 30;24(1):101883
EAT SVCs 1, 2, 5, 10 μg/mL 24 hours To evaluate the direct anti-inflammatory effects of β-elemene on SVCs from EAT and MAT of obese mice. Results showed that β-elemene had limited effects on LPS-induced inflammation in vitro, with significant effects only at high concentration (10 μg/mL) on IL-1β, TGF-β1, and IL-10 expression in EAT SVCs. iScience. 2020 Nov 30;24(1):101883
NRK49F cells 5-20 µM 24 hours Β-elemene inhibited TGF-β-induced fibroblast activation and expression of fiber markers in a dose-dependent manner Int J Mol Sci. 2022 May 16;23(10):5553
NCI-H1650 cells 3 μg/mL 24 hours To evaluate the effect of β-elemene on the survival and apoptosis of NCI-H1650 cells. Results showed that β-elemene significantly reduced cell viability and promoted apoptosis. Am J Cancer Res. 2022 Apr 15;12(4):1535-1555
A549 cells 3 μg/mL 24 hours To evaluate the effect of β-elemene on the survival and apoptosis of A549 cells. Results showed that β-elemene significantly reduced cell viability and promoted apoptosis. Am J Cancer Res. 2022 Apr 15;12(4):1535-1555
NCI-H1975 cells 10 µg/ml 24 hours Β-Elemene significantly up-regulated C3orf21 expression Front Oncol. 2021 May 7;11:571476
PC-9 cells 10 µg/ml 24 hours Β-Elemene significantly up-regulated C3orf21 expression and inhibited cell proliferation, wound healing, and invasion Front Oncol. 2021 May 7;11:571476
A549 cells 10 µg/ml 24 hours Β-Elemene significantly up-regulated C3orf21 expression and inhibited cell proliferation, wound healing, and invasion Front Oncol. 2021 May 7;11:571476
Human hepatoma HepG2 cells 0.1, 0.08, 0.06, 0.04, 0.02, 0.01 mg/mL 24, 48, 72 hours To evaluate the inhibitory effect of β-elemene on HepG2 cell proliferation, results showed that β-elemene inhibited HepG2 cell proliferation in a time- and dose-dependent manner. Chin J Cancer Res. 2013 Dec;25(6):770-6
MCAS cells 20-200 µg/ml 24, 48, 72, and 96 hours To evaluate the antiproliferative effect of β-elemene on MCAS cells, showing IC50 values between 60 and 78 µg/ml. Int J Oncol. 2013 Sep;43(3):721-8
A2780/CP70 cells 20-200 µg/ml 24, 48, 72, and 96 hours To evaluate the antiproliferative effect of β-elemene on A2780/CP70 cells, showing IC50 values at 24, 48, 72, and 96 h were 80, 70, 68, and 65 µg/ml, respectively. Int J Oncol. 2013 Sep;43(3):721-8
A2780 cells 20-200 µg/ml 24, 48, 72, and 96 hours To evaluate the antiproliferative effect of β-elemene on A2780 cells, showing IC50 values at 24, 48, 72, and 96 h were 65, 65, 65, and 60 µg/ml, respectively. Int J Oncol. 2013 Sep;43(3):721-8
H1299 cells 2 mg/mL 24, 48, and 72 hours To evaluate the effects of β-Elemene on proliferation, apoptosis, and autophagy in NSCLC cells. Results showed that β-Elemene significantly inhibited NSCLC cell proliferation and induced autophagy and apoptosis. J Pharm Anal. 2024 Sep;14(9):100961
A549 cells 2 mg/mL 24, 48, and 72 hours To evaluate the effects of β-Elemene on proliferation, apoptosis, and autophagy in NSCLC cells. Results showed that β-Elemene significantly inhibited NSCLC cell proliferation and induced autophagy and apoptosis. J Pharm Anal. 2024 Sep;14(9):100961
PC9 cells 5-60 μg/ml 24-72 hours Β-Elemene inhibited PC9 cell growth in a dose- and time-dependent manner, with a maximal dose of 40 μg/ml observed at 48 hrs. J Cell Mol Med. 2015 Mar;19(3):630-41
A549 cells 5-60 μg/ml 24-72 hours Β-Elemene inhibited A549 cell growth in a dose- and time-dependent manner, with a maximal dose of 40 μg/ml observed at 48 hrs. Additionally, β-Elemene significantly increased the proportion of cells at G0/G1 phase while reducing the proportion at S phase, indicating cell cycle arrest at G0/G1 phase. J Cell Mol Med. 2015 Mar;19(3):630-41
Primary human airway granulation fibroblasts (PHAGF) 160 µg/mL 48 hours Inhibits PHAGF proliferation and induces G0/G1 cell cycle arrest and apoptosis by down-regulating the ILK/Akt pathway Cell Mol Biol Lett. 2021 Jun 12;26(1):28
THLE2 cells 100 µg/mL 48 hours Β-Elemene showed no significant inhibition on the proliferation of normal hepatocytes THLE2. Endocr Relat Cancer. 2019 Feb;26(2):187-199
MHH-ES-1 cells 47.86 µg/mL (IC50) 48 hours Β-Elemene significantly inhibited the proliferation of MHH-ES-1 cells in a dose-dependent manner. Endocr Relat Cancer. 2019 Feb;26(2):187-199
A673 cells 38.02 µg/mL (IC50) 48 hours Β-Elemene significantly inhibited the proliferation of A673 cells in a dose-dependent manner. Endocr Relat Cancer. 2019 Feb;26(2):187-199
SU-DHL-10 cells 60 μg/ml 48 hours To evaluate the effect of β-elemene on apoptosis of DLBCL cells, the results showed that β-elemene significantly up-regulated Bax expression and down-regulated Bcl-2 expression. Biosci Rep. 2020 Feb 28;40(2):BSR20190804
SU-DHL-8 cells 60 μg/ml 48 hours To evaluate the effect of β-elemene on apoptosis of DLBCL cells, the results showed that β-elemene significantly up-regulated Bax expression and down-regulated Bcl-2 expression. Biosci Rep. 2020 Feb 28;40(2):BSR20190804
MHCCLM3 60 μg/mL 48 hours Β-Elemene combined with oxaliplatin significantly enhanced the anti-proliferative effect of oxaliplatin by upregulating CTR1 expression, increasing intracellular platinum accumulation. Sci Rep. 2016 Feb 12;6:21010
Huh7 60 μg/mL 48 hours Β-Elemene combined with oxaliplatin significantly enhanced the anti-proliferative effect of oxaliplatin by upregulating CTR1 expression, increasing intracellular platinum accumulation. Sci Rep. 2016 Feb 12;6:21010
Hep3B 60 μg/mL 48 hours Β-Elemene combined with oxaliplatin significantly enhanced the anti-proliferative effect of oxaliplatin by upregulating CTR1 expression, increasing intracellular platinum accumulation. Sci Rep. 2016 Feb 12;6:21010
MHCC97H 60 μg/mL 48 hours Β-Elemene enhanced the anti-proliferative effect of oxaliplatin by upregulating the expression of copper transporter 1 (CTR1), increasing intracellular platinum accumulation and platinum-DNA adduct formation, thereby enhancing oxaliplatin-induced apoptosis. Sci Rep. 2016 Feb 12;6:21010
Tca-8113-CDDP cells 40 μg/ml 48 hours To explore the sensitizing effect of β-Ele on cisplatin-resistant OSCC cells. The results showed that β-Ele significantly enhanced the chemosensitivity to cisplatin in Tca-8113-CDDP cells. Cancer Cell Int. 2022 Jul 31;22(1):244
Tca-8113 cells 0, 20, 40, 60, 80, 100 μg/ml 48 hours To evaluate the anti-proliferative effect of β-Ele on OSCC cells. The results showed that β-Ele suppressed the growth and proliferation of Tca-8113 and Tca-8113-CDDP cells in dose-dependent manners. Cancer Cell Int. 2022 Jul 31;22(1):244
Primary human airway granulation fibroblasts 40, 80, 120, 160 μg/ml 48 hours Β-Elemene had a dose–responsive inhibitive effect on the proliferation of human airway granulation fibroblasts and didn’t affect normal human airway fibroblasts. Biosci Rep. 2018 Apr 13;38(2):BSR20171386
AGS/IR cells 100 mg/L 48 hours To evaluate the effect of β-Elemene on radiosensitivity, results showed that β-Elemene significantly inhibited cell growth and enhanced ferroptosis. Front Pharmacol. 2024 Oct 17;15:1469180
MKN-45/IR cells 100 mg/L 48 hours To evaluate the effect of β-Elemene on radiosensitivity, results showed that β-Elemene significantly inhibited cell growth and enhanced ferroptosis. Front Pharmacol. 2024 Oct 17;15:1469180
MCF-7 cells 5, 10, 20 and 40 µM 48 hours Β-Elemene at concentrations below 40 μmol/L did not inhibit the viability of MCF-7 cells but significantly inhibited cell migration and invasion. J Cell Mol Med. 2019 Oct;23(10):6846-6858
MDA-MB-231 cells 5, 10, 20 and 40 µM 48 hours Β-Elemene at concentrations below 40 μmol/L did not inhibit the viability of MDA-MB-231 cells but significantly inhibited cell migration and invasion. J Cell Mol Med. 2019 Oct;23(10):6846-6858
Pancreatic cancer peritoneum effusion cells 0, 0.5, 1, 2, 4, 8 and 16 µM 72 hours Β-Elemene suppressed the proliferation of pancreatic cancer peritoneum effusion cells in a dose-dependent manner, with IC50 values of 15.80±0.63 and 14.86±0.69 µM. Oncol Rep. 2019 Dec;42(6):2561-2571
BxPC3 cells 0, 0.5, 1, 2, 4, 8 and 16 µM 72 hours Β-Elemene suppressed the proliferation of BxPC3 cells in a dose-dependent manner, with an IC50 value of 17.36±1.25 µM. Oncol Rep. 2019 Dec;42(6):2561-2571
PANC-1 cells 0, 0.5, 1, 2, 4, 8 and 16 µM 72 hours Β-Elemene suppressed the proliferation of PANC-1 cells in a dose-dependent manner, with an IC50 value of 6.94±0.86 µM. Oncol Rep. 2019 Dec;42(6):2561-2571

β-Elemene/β-榄香烯 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Nude mice Subcutaneous tumor model Gavage 0.2 mL per administration 36 days To evaluate the inhibitory effect of β-Elemene combined with radiotherapy on tumor growth, results showed that the combination therapy significantly inhibited tumor growth. Front Pharmacol. 2024 Oct 17;15:1469180
C57BL/6J neonatal mice Oxygen-induced retinopathy (OIR) model Intravitreal injection 0.25 mg/ml (1 µl) Single injection, lasting 5 days (P12-P17) Β-Elemene reduced retinal neovascularization by upregulating miR-27a expression, leading to decreased VEGF expression. Mol Med Rep. 2019 Mar;19(3):2307-2316
BALB/c nude mice HCT116p53−/− xenograft model Intraperitoneal injection 100 mg/kg/d Once daily for 24 days Β-Elemene significantly inhibited the growth of HCT116p53?/? xenograft tumors and enhanced the anti-tumor effect of 5-Fu. Front Bioeng Biotechnol. 2020 May 8;8:378
BALB/C nude mice Glioma xenograft model Intraperitoneal injection 100 mg/kg/d Once daily for 23 days Β-Elemene treatment induced senescence in glioma cells through inactivation of YAP-CDK6 signaling pathway, which inhibited glioma growth. Am J Cancer Res. 2021 Feb 1;11(2):370-388
NOD/SCID mice Orthotopic non-small cell lung cancer model Tail vein injection 120 mg/kg Once daily for 21 days To evaluate the antitumor effect of β-Elemene in TFEB knockout mice, results showed TFEB knockout attenuated the inhibitory effect of β-Elemene on tumor growth. J Adv Res. 2024 Aug;62:257-272
New Zealand white rabbits Rabbit model of tracheal stenosis Local endotracheal injection 160 µg/mL Once a week for one week Inhibits airway granulation tissue hyperplasia and alleviates tracheal stenosis Cell Mol Biol Lett. 2021 Jun 12;26(1):28
C57BL/6J mice MCAO model and photothrombotic stroke model Intraperitoneal injection 25 mg/kg, 50 mg/kg, 100 mg/kg 1 hour before ischemia and 5 hours after reperfusion Β-Elemene attenuated neurological deficit, reduced the infarction volume and neuroinflammation, thus improving ischemic stroke injury. Chin Med. 2024 Jun 15;19(1):86
C57BL/6 mice Unilateral ureteral obstruction (UUO) model Intraperitoneal injection 40 mg/kg/d Once daily for 7 days Β-Elemene attenuated renal fibrosis in UUO mice by inhibition of STAT3 and Smad3 signaling Int J Mol Sci. 2022 May 16;23(10):5553
BALB/C mice DLBCL xenograft model Intraperitoneal injection 45 mg/kg Once daily for 28 days To evaluate the inhibitory effect of β-Elemene on the growth of DLBCL xenograft, the results showed that β-Elemene significantly suppressed tumor growth, down-regulated HULC expression, up-regulated Bax expression, and down-regulated Bcl-2 expression. Biosci Rep. 2020 Feb 28;40(2):BSR20190804
BALB/c nude mice OSCC xenograft model Intraperitoneal injection 45 mg/kg β-Ele and/or 4 mg/kg cisplatin Every three days for 27 days To evaluate the inhibitory effect of β-Ele and cisplatin combination therapy on the growth of OSCC xenograft tumors. The results showed that β-Ele and cisplatin synergistically suppressed tumor growth and induced apoptosis, possibly by inhibiting the JAK/STAT3 signaling pathway. Cancer Cell Int. 2022 Jul 31;22(1):244
Nude mice Orthotopic transplantation HCC model Intraperitoneal injection 45 mg/kg β-elemene and 5 mg/kg oxaliplatin Twice a week for 7 weeks Β-Elemene combined with oxaliplatin significantly inhibited HCC tumor growth in nude mice by upregulating CTR1 expression, increasing intracellular oxaliplatin accumulation, thereby enhancing the anti-tumor effect of oxaliplatin. Sci Rep. 2016 Feb 12;6:21010
BALB/c-nu mice A549 cell subcutaneous xenograft model Intraperitoneal injection 5 mg/kg Once daily for 7 days To evaluate the inhibitory effect of β-Elemene on the growth of A549 cell subcutaneous xenografts. Results showed that β-Elemene significantly suppressed tumor growth. Am J Cancer Res. 2022 Apr 15;12(4):1535-1555
BALB/c nude mice NSCLC xenograft model Oral gavage 50 mg/kg Every other day for 2 weeks Β-Elemene suppresses tumor growth by downregulating ALDH3A1 expression, reducing glucose uptake, and inhibiting glycolysis. Cell Death Dis. 2023 Sep 20;14(9):617
BALB/c nude mice Orthotopic breast cancer xenograft model Intraperitoneal injection 50 mg/kg Once daily for 21 days Β-Elemene significantly reduced metastatic foci of breast cancer in the lung and liver. J Cell Mol Med. 2019 Oct;23(10):6846-6858
Nude mice HCC827/GR xenograft model Intravenous injection 50 mg/kg Daily for an unspecified duration To evaluate the antitumor efficacy of β-Elemene in combination with gefitinib, results showed that the combination treatment significantly suppressed tumor growth. Pharmaceuticals (Basel). 2024 May 14;17(5):626
BALB/c nude mice A673 xenograft model Peritumoral injection 50 mg/kg and 100 mg/kg Once daily for 17 days Β-Elemene significantly inhibited the growth of A673 xenografts, with a 72% inhibition rate in the high-dose group. Endocr Relat Cancer. 2019 Feb;26(2):187-199
C57BL/6 male mice High-fat diet-induced obese mouse model Gavage 7.5 mg/kg/d Once daily for 3 weeks Β-Elemene suppressed experimental obesity-induced chronic inflammation by adjusting the intestinal immune system of obese mice and partially reversed HFD-induced changes in the composition and contents of mouse gut bacteria. Biomedicines. 2021 Jun 22;9(7):704
Mice High-fat diet-induced obesity model Gavage 7.5 mg/kg/d Once daily for 3 weeks To study the regulatory effect of β-Elemene on inflammatory response in obese mice, results showed that β-Elemene significantly reduced blood glucose levels and the expression of inflammatory cytokines. Commun Biol. 2022 May 31;5(1):519
C57BL/6 male mice High-fat diet-induced obese mouse model Oral gavage 7.5 mg/kg/d Once daily for 3 weeks To evaluate the effects of β-Elemene on adipose tissue inflammation and Tregs in obese mice. Results showed that oral administration of β-Elemene significantly downregulated the expression of inflammatory cytokines (TNF-α, IL-1β, IL-6) in adipose tissue and increased the proportion of Foxp3+CD4+ T cells, indicating its role in alleviating obesity-induced chronic inflammation by modulating DCs function in the intestinal immune system. iScience. 2020 Nov 30;24(1):101883

β-Elemene/β-榄香烯 参考文献

[1]Chen J, Wang R, et al. Antioxidant Properties of Novel Dimers Derived from Natural β-Elemene through Inhibiting H(2)O(2)-Induced Apoptosis. ACS Med Chem Lett. 2017 Mar 13;8(4):443-448.

[2]Li X, Lin Z, Zhang B, et al. β-elemene sensitizes hepatocellular carcinoma cells to oxaliplatin by preventing oxaliplatin-induced degradation of copper transporter 1. Sci Rep. 2016 Feb 12;6:21010.

β-Elemene/β-榄香烯 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.89mL

0.98mL

0.49mL

24.47mL

4.89mL

2.45mL

48.94mL

9.79mL

4.89mL

β-Elemene/β-榄香烯 技术信息

CAS号515-13-9
分子式C15H24
分子量 204.35
SMILES Code C=C[C@@]1(C)[C@H](C(C)=C)C[C@H](C(C)=C)CC1
MDL No. MFCD00468041
别名 B-榄香烯 ;Levo-β-elemene; (-)-β-Elemene
运输蓝冰
InChI Key OPFTUNCRGUEPRZ-QLFBSQMISA-N
Pubchem ID 6918391
存储条件

In solvent -20°C:3-6个月-80°C:12个月

溶解方案

DMSO: 50 mg/mL(244.68 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

无水乙醇: 50 mg/mL(244.68 mM),配合低频超声助溶,注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇

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
方案 一
方案 二
方案 三
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