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Merck
CN

P4509

Sigma-Aldrich

棕榈酰-DL-肉碱氯化物

powder

别名:

DL-Hexadecanoylcarnitine, Hexadecanoyl-DL-carnitine, NSC 628323, ​DL-Palmitoylcarnitine

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About This Item

线性分子式:
C23H46NO4 · Cl
CAS号:
分子量:
436.07
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

生物来源

synthetic (organic)

质量水平

方案

≥98% (TLC)

表单

powder

颜色

white

溶解性

H2O: 25 mg/mL (with heat or sonication)

储存温度

−20°C

SMILES字符串

Cl.CCCCCCCCCCCCCCCC(=O)OC(CC(O)=O)C[N](C)(C)C

InChI

1S/C23H46NO4.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-23(27)28-21(19-22(25)26)20-24(2,3)4;/h21H,5-20H2,1-4H3,(H,25,26);1H

InChI key

LGVBWSFTXDIBPB-UHFFFAOYSA-N

应用

使用前列腺癌的体外模型,已使用棕榈酰-DL-肉碱氯化物研究其对炎性细胞因子和钙(Ca2+)内流的影响。

生化/生理作用

已知棕榈酰-DL-肉碱氯化物可抑制铜绿假单胞菌大肠埃希菌介导的生物膜形成。它是一种磷酸激酶C抑制剂。
长链酰基肉碱和线粒体脂肪酸氧化的众所周知的中间体。改变心脏中高能磷酸盐和游离脂肪酸的心肌水平。增加培养物中红细胞集落的形成。减少红细胞和心肌细胞的表面负电荷。据报道,通过抑制内皮细胞内钙信号转导,影响电流并抑制乙酰胆碱和物质P诱导的内皮依赖性舒张,呈剂量依赖性。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Signal transduction of the prophenoloxidase-activating system of prawn haemocytes triggered by CpG oligodeoxynucleotides
Chuo CP, et al.
Fish & Shellfish Immunology, 18(2), 149-162 (2005)
Journal of Chemical and Pharmaceutical Sciences , 76(14), 29-29 (2012)
Accumulation of Palmitoylcarnitine and Its Effect on Pro-Inflammatory Pathways and Calcium Influx in Prostate Cancer
Al-Bakheit A, et al.
Prostate, 76(14), 1326-1337 (2016)
Yige Fu et al.
Experimental cell research, 396(1), 112275-112275 (2020-09-09)
Limited treatment options and development of resistance to targeted therapy within few months pose significant challenges in the treatment of BRAF-mutated malignant melanoma. Moreover, extensive angiogenesis and vasculogenic mimicry promote the rapid progression of disease. The purpose of this study
T Nakadate et al.
Cancer research, 47(24 Pt 1), 6537-6542 (1987-12-15)
Palmitoylcarnitine, a reported protein kinase C inhibitor, enhanced the phorbol ester dependency of the enzyme, augmenting protein kinase C activity in the presence of phorbol esters such as phorbol 12,13-dibutyrate while inhibiting the basal activity measured in the presence of

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