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The flavokawains: uprising medicinal chalcones.黄烷酮:新兴的药用查尔酮。
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In vitro Toxicity and in vivo Immunomodulatory Effects of Flavokawain A and Flavokawain B in Balb/C Mice.黄樟素A和黄樟素B对Balb/C小鼠的体外毒性及体内免疫调节作用
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Flavokawains B and C, melanogenesis inhibitors, isolated from the root of Piper methysticum and synthesis of analogs.从卡瓦胡椒根中分离出的黑素生成抑制剂黄烷卡瓦因B和C及其类似物的合成。
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Multienzymatic biotransformation of flavokawain B by entomopathogenic filamentous fungi: structural modifications and pharmacological predictions.多酶法生物转化法对 flavokawain B 的作用:结构修饰和药理学预测。
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Beneficial biological effects of Flavokawain A, a chalcone constituent from kava, on surgically induced endometriosis rat model.金纳黄酮 A,一种来自卡瓦胡椒的查尔酮成分,对手术诱导的子宫内膜异位症大鼠模型具有有益的生物学效应。
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Induction of Apoptosis and Cell Cycle Arrest by Flavokawain C on HT-29 Human Colon Adenocarcinoma via Enhancement of Reactive Oxygen Species Generation, Upregulation of p21, p27, and GADD153, and Inactivation of Inhibitor of Apoptosis Proteins.黄樟素C通过增强活性氧生成、上调p21、p27和GADD153以及使凋亡抑制蛋白失活诱导HT-29人结肠腺癌细胞凋亡和细胞周期停滞
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Effects of the kava chalcone flavokawain A differ in bladder cancer cells with wild-type versus mutant p53.卡瓦查尔酮黄酮卡瓦因A对携带野生型与突变型p53的膀胱癌细胞的作用有所不同。
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Flavokawain A suppresses the malignant progression of neuroblastoma in vitro depending on inactivation of ERK/VEGF/MMPs signaling pathway.黄樟素A通过使ERK/VEGF/MMPs信号通路失活,在体外抑制神经母细胞瘤的恶性进展。
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Natural 2',4-Dihydroxy-4',6'-dimethoxy Chalcone Isolated from Inhibits Breast Cancer Cell Growth through Autophagy and Mitochondrial Apoptosis.从[具体来源未给出]中分离出的天然2',4-二羟基-4',6'-二甲氧基查耳酮通过自噬和线粒体凋亡抑制乳腺癌细胞生长。
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Flavokawain C inhibits proliferation and migration of liver cancer cells through FAK/PI3K/AKT signaling pathway.Flavokawain C 通过 FAK/PI3K/AKT 信号通路抑制肝癌细胞的增殖和迁移。
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Flavokawain B Inhibits Growth of Cholangiocarcinoma Cells by Suppressing the Akt Pathway. flavokawain B 通过抑制 Akt 通路抑制胆管癌细胞生长。
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Flavokawain A is a natural inhibitor of PRMT5 in bladder cancer.Flavokawain A 是膀胱癌中 PRMT5 的天然抑制剂。
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and inhibitory potential of Kava extract on monoamine oxidase B activity in mice.以及卡瓦提取物对小鼠单胺氧化酶B活性的抑制潜力。
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本文引用的文献

1
Flavokawain B, a kava chalcone, inhibits growth of human osteosarcoma cells through G2/M cell cycle arrest and apoptosis.黄烷酮 B,一种卡瓦胡椒查尔酮,通过 G2/M 细胞周期阻滞和细胞凋亡抑制人骨肉瘤细胞的生长。
Mol Cancer. 2013 Jun 10;12:55. doi: 10.1186/1476-4598-12-55.
2
Suppression of iNOS and COX-2 expression by flavokawain A via blockade of NF-κB and AP-1 activation in RAW 264.7 macrophages. flavokawain A 通过阻断 NF-κB 和 AP-1 激活抑制 RAW 264.7 巨噬细胞中 iNOS 和 COX-2 的表达。
Food Chem Toxicol. 2013 Aug;58:479-86. doi: 10.1016/j.fct.2013.05.031. Epub 2013 May 28.
3
Flavokawain B induces apoptosis of non-small cell lung cancer H460 cells via Bax-initiated mitochondrial and JNK pathway. flavokawain B 通过 Bax 起始的线粒体和 JNK 途径诱导非小细胞肺癌 H460 细胞凋亡。
Biotechnol Lett. 2012 Oct;34(10):1781-8. doi: 10.1007/s10529-012-0976-6. Epub 2012 Jun 23.
4
Multispectroscopic and molecular modeling approach to investigate the interaction of flavokawain B with human serum albumin.采用多光谱和分子建模方法研究 flavokawain B 与人血清白蛋白的相互作用。
J Agric Food Chem. 2012 Jun 13;60(23):5899-908. doi: 10.1021/jf301139h. Epub 2012 Jun 4.
5
Flavokawain B, a novel, naturally occurring chalcone, exhibits robust apoptotic effects and induces G2/M arrest of a uterine leiomyosarcoma cell line.黄樟素B是一种新型的天然查尔酮,具有强大的凋亡作用,并能诱导子宫平滑肌肉瘤细胞系发生G2/M期阻滞。
J Obstet Gynaecol Res. 2012 Aug;38(8):1086-94. doi: 10.1111/j.1447-0756.2011.01841.x. Epub 2012 Apr 30.
6
Kava components down-regulate expression of AR and AR splice variants and reduce growth in patient-derived prostate cancer xenografts in mice.卡瓦成分下调 AR 和 AR 剪接变异体的表达,并减少小鼠来源的前列腺癌异种移植瘤的生长。
PLoS One. 2012;7(2):e31213. doi: 10.1371/journal.pone.0031213. Epub 2012 Feb 9.
7
The chalcone flavokawain B induces G2/M cell-cycle arrest and apoptosis in human oral carcinoma HSC-3 cells through the intracellular ROS generation and downregulation of the Akt/p38 MAPK signaling pathway.查尔酮 flavokawain B 通过细胞内 ROS 的产生和下调 Akt/p38 MAPK 信号通路诱导人口腔鳞癌细胞 HSC-3 的 G2/M 期细胞周期阻滞和凋亡。
J Agric Food Chem. 2012 Mar 7;60(9):2385-97. doi: 10.1021/jf205053r. Epub 2012 Feb 27.
8
Flavokawain B, a kava chalcone, induces apoptosis in synovial sarcoma cell lines.黄烷酮 B,一种卡瓦内酯,可诱导滑膜肉瘤细胞系凋亡。
J Orthop Res. 2012 Jul;30(7):1045-50. doi: 10.1002/jor.22050. Epub 2011 Dec 29.
9
Flavokawain B induces apoptosis of human oral adenoid cystic cancer ACC-2 cells via up-regulation of Bim and down-regulation of Bcl-2 expression.黄樟素B通过上调Bim和下调Bcl-2表达诱导人涎腺腺样囊性癌ACC-2细胞凋亡。
Can J Physiol Pharmacol. 2011 Dec;89(12):875-83. doi: 10.1139/y11-088. Epub 2011 Nov 24.
10
Flavokawain B inhibits growth of human squamous carcinoma cells: Involvement of apoptosis and cell cycle dysregulation in vitro and in vivo.Flavokawain B 抑制人鳞状细胞癌细胞的生长:体外和体内的细胞凋亡和细胞周期失调的参与。
J Nutr Biochem. 2012 Apr;23(4):368-78. doi: 10.1016/j.jnutbio.2011.01.002. Epub 2011 May 2.

黄烷酮:新兴的药用查尔酮。

The flavokawains: uprising medicinal chalcones.

机构信息

Bright Sparks Unit, University Malaya, 53500, Kuala Lumpur, Malaysia.

出版信息

Cancer Cell Int. 2013 Oct 22;13(1):102. doi: 10.1186/1475-2867-13-102.

DOI:10.1186/1475-2867-13-102
PMID:24148263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4015927/
Abstract

Plant-based compounds have been in the spotlight in search of new and promising drugs. Flavokawain A, B and C are naturally occurring chalcones that have been isolated from several medicinal plants; namely the piper methysticum or commercially known as the kava-kava. Multiple researches have been done to evaluate the bioactivities of these compounds. It has been shown that all three flavokawains may hold promising anti-cancer effects. It has also been revealed that both flavokawain A and B are involved in the induction of cell cycle arrest in several cancer cell lines. Nevertheless, flavokawain B was shown to be more effective in treating in vitro cancer cell lines as compared to flavokawain A and C. Flavokawain B also exerts antinociceptive effects as well as anti-inflammation properties. This mini-review attempts to discuss the biological properties of all the flavokawains that have been reported.

摘要

植物化合物一直是寻找新的、有前途的药物的焦点。黄烷酮 A、B 和 C 是天然存在的查耳酮,已从几种药用植物中分离出来;即胡椒 methysticum 或商业上称为卡瓦卡瓦。已经进行了多项研究来评估这些化合物的生物活性。研究表明,这三种黄烷酮可能具有有前途的抗癌作用。研究还表明,黄烷酮 A 和 B 都参与了几种癌细胞系的细胞周期阻滞诱导。然而,与黄烷酮 A 和 C 相比,黄烷酮 B 被证明在治疗体外癌细胞系方面更有效。黄烷酮 B 还具有镇痛作用和抗炎特性。本综述试图讨论已报道的所有黄烷酮的生物学特性。