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C6 Ceramide {[allProObj[0].p_purity_real_show]}

货号:A464869 同义名: C6-Cer; N-Hexanoylsphingosine

C6 Ceramide是一种神经酰胺途径的激活剂,对多种癌细胞系具有活性,并可作为化疗药物的佐剂以增强抗肿瘤作用。

C6 Ceramide 化学结构 CAS号:124753-97-5
C6 Ceramide 化学结构
CAS号:124753-97-5
C6 Ceramide 3D分子结构
CAS号:124753-97-5
C6 Ceramide 化学结构 CAS号:124753-97-5
C6 Ceramide 3D分子结构 CAS号:124753-97-5
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C6 Ceramide 纯度/质量文件 产品仅供科研

货号:A464869 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 PLK1 PLK2 PLK3 PLK4 其他靶点 纯度
HMN-214 99%+
SBE13 HCl ++++

PLK1, IC50: 200 pM

98%
Onvansertib +++

PLK1, IC50: 2 nM

99%+
Volasertib ++++

PLK1, IC50: 0.87 nM

97%
GSK461364 +++

PLK1, Ki: 2.2 nM

99%+
MLN0905 +++

PLK1, IC50: 2 nM

99%+
Ro3280 ++

PLK1, IC50: 3 nM

99%
(E/Z)-Rigosertib sodium +

PLK1, IC50: 9 nM

+

PLK2, IC50: 260 nM

Bcr-Abl 99%+
BI 2536 ++++

PLK1, IC50: 0.83 nM

++

PLK2, IC50: 3.5 nM

+

PLK3, IC50: 9.0 nM

99%+
CFI-400945 ++

PLK4, IC50: 2.8 nM

Tie-2 98%
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。

C6 Ceramide 细胞实验

Cell Line
Concentration Treated Time Description References
MCF-7 cells 50 μM 24 h Induced MCF-7 cell death via autophagy Int J Biol Sci. 2011;7(5):629-44
HT-29 cells 5 μM 72 h Facilitated ABC294640-induced cytotoxicity against HT-29 cells J Exp Clin Cancer Res. 2015 Sep 4;34(1):94.
NCI/ADR-RES cells 25 μM 48 hr C6-ceramide substantially increased the levels of phosphorylated p53 and enhanced the expression of p53-responsive genes such as p21Waf1/Cip1, Bax, and Puma. Cancer Res. 2011 Mar 15;71(6):2276-85
p56lck-reconstituted JCaM1.6 cells 10 μM 15-25 min Reconstitution of p56lck partially restored the inhibitory effect of C6-ceramide on n-K1 channels. Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7661-6
p56lck-deficient JCaM1.6 cells 10 μM 20 min In p56lck-deficient cells, the inhibitory effect of C6-ceramide on n-K1 channels was significantly reduced. Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7661-6
Jurkat T lymphocytes 10 μM 15-25 min C6-ceramide significantly inhibited n-K1 channel currents, with a 41±5% decrease at 15 min and 67±6% decrease at 25 min. Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7661-6
Human adipose derived stem cells (hADSC) 20 µM 48 h C6-ceramide increased cellular and exosomal MALAT1 levels and promoted migration and mitochondrial function in human dermal fibroblasts. Cell Commun Signal. 2023 Aug 24;21(1):221
Bone marrow-derived macrophages (BMMs) 25 µM 24 h LipC6 significantly inhibited ROS production in both GMCSF-induced M1 BMMs and MCSF-induced M2 BMMs, promoted M1 cytokine production, and suppressed M2 cytokine production. Gastroenterology. 2018 Mar;154(4):1024-1036. e9
HEK293 cells 40 μM 24 h To evaluate the effect of CNL on non-transformed cells. CNL treatment did not affect the viability of HEK293 cells or STAT3 phosphorylation. Signal Transduct Target Ther. 2017 Oct 27;2:17051
Mec-2 cells 40 μM 24 h To evaluate the effect of CNL on STAT3 phosphorylation. A reduction in STAT3 phosphorylation at Y705 and S727 residues was observed. Signal Transduct Target Ther. 2017 Oct 27;2:17051
JVM-3 cells 40 μM 24 h To evaluate the effect of CNL on STAT3 phosphorylation. A reduction in STAT3 phosphorylation at both Y705 and S727 residues was observed in six out of seven patient samples, while total STAT3 levels remained unchanged. Signal Transduct Target Ther. 2017 Oct 27;2:17051

C6 Ceramide 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Chick embryos CAM assay Topical application 50 μM 24 hours Reduced new vessel formation Int J Biol Sci. 2011;7(5):629-44
C57BL/6 mice Hepatocellular carcinoma model in a fibrotic/cirrhotic liver setting Tail vein injection 35 mg/kg Every other day for 2 weeks LipC6 injection slowed tumor growth, reduced the number and immunosuppressive function of tumor-associated macrophages (TAMs), and promoted TAM differentiation into an M1 phenotype, thereby enhancing the antitumor activity of CD8+ T cells. Gastroenterology. 2018 Mar;154(4):1024-1036. e9

C6 Ceramide 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.51mL

0.50mL

0.25mL

12.57mL

2.51mL

1.26mL

25.15mL

5.03mL

2.51mL

C6 Ceramide 技术信息

CAS号124753-97-5
分子式C24H47NO3
分子量 397.63
SMILES Code CCCCCCCCCCCCC/C=C/[C@H]([C@H](CO)NC(CCCCC)=O)O
MDL No. MFCD00870174
别名 C6-Cer; N-Hexanoylsphingosine; N-C6:0-D-erythro-Ceramide; N-Hexanoyl-D-erythro-sphingosine
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 105 mg/mL(264.06 mM),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

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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