InChI key
DEZFNHCVIZBHBI-ZHACJKMWSA-N
InChI
1S/C30H28O8/c1-15-24(33)19(27(36)22(16(2)31)25(15)34)14-20-26(35)18-12-13-30(3,4)38-29(18)23(28(20)37)21(32)11-10-17-8-6-5-7-9-17/h5-13,33-37H,14H2,1-4H3/b11-10+
SMILES string
CC(=O)c1c(O)c(C)c(O)c(Cc2c(O)c3C=CC(C)(C)Oc3c(c2O)C(=O)\C=C\c4ccccc4)c1O
biological source
plant (Mallotus philippinensis)
assay
≥95% (HPLC)
form
powder
mp
200.0 °C
solubility
ethanol: 1 mg/mL
storage temp.
2-8°C
Gene Information
human ... CDK2(1017)
General description
粗糠柴毒素从粗糠柴( Mallotus philippinensis)中提取。是蛋白激酶 Cδ (PKCδ)抑制剂。粗糠柴毒素作为解偶联剂,将线粒体进行的呼吸作用与氧化磷酸化解偶联。具有抗肿瘤、自噬、抗增殖、抗转移和抗侵袭特性。
Application
粗糠柴毒素用于:
- 作为蛋白激酶 C δ (PKCδ) 抑制剂,分析大鼠体内蛋白含量和磷酸化情况
- 检查早期成骨细胞标记物的基因表达
- 通过琥珀酸,减弱丙酮酸脱氢酶(PDH)的磷酸化作用
- 使线粒体去极化
- 研究其在胰腺癌细胞(Pc)中的抗肿瘤活性
Biochem/physiol Actions
大电导电压的有效激活剂和 Ca2+ 激活 K + 通道;hERG 通道激活剂。
最近,粗糠紫毒素已被证明是大电导电压和 Ca2 激活 K+通道的有效激活剂,并可使通道的电导-电压关系向左偏移。在 hERG 通道上测试的粗糠紫毒素通过左移 hERG 激活的电压依赖性和减缓通道失活,增加了阶跃和尾部 hERG 电流。这些作用将粗糠紫毒素区分为一种新型天然存在的 hERG 通道激活剂。
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
The unfolded protein response plays a predominant homeostatic role in response to mitochondrial stress in pancreatic stellate cells
Su HY, et al.
Testing, 11(2), e0148999-e0148999 (2016)
Succinate accumulation impairs cardiac pyruvate dehydrogenase activity through GRP91-dependent and independent signaling pathways: Therapeutic effects of ginsenoside Rb1
Li J, et al.
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1863(11), 2835-2847 (2017)
Intermittent Administration of Parathyroid Hormone 1-34 Enhances Osteogenesis of Human Mesenchymal Stem Cells by Regulating Protein Kinase Cdelta
Kuo SW, et al.
International Journal of Molecular Sciences, 18(10), 2221-2221 (2017)
Haoyu Zeng et al.
The Journal of pharmacology and experimental therapeutics, 319(2), 957-962 (2006-08-25)
Human ether-a-go-go-related gene (hERG) encodes a rapidly activating delayed rectifier potassium channel that plays important roles in cardiac action potential repolarization. Although many drugs and compounds block hERG channels, activators of the channel have only recently been described. Three structurally
Jui-Ling Hsu et al.
Biochemical pharmacology, 84(1), 59-67 (2012-04-12)
Combination therapy, which can optimize killing activity to cancers and minimize drug resistance, is a mainstream therapy against hormone-refractory prostate cancers (HRPCs). Rottlerin, a natural polyphenolic component, synergistically increased PC-3 (a HRPC cell line) apoptosis induced by camptothecin (a topoisomerase
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持