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。
规格 | 价格 | 会员价 | 库存 | 数量 | |||
---|---|---|---|---|---|---|---|
{[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
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。 |
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 |
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 |
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 |
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 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
|