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Merck
CN

870510C

Avanti

16:0 CDP DG

Avanti Research™ - A Croda Brand

别名:

1,2-dipalmitoyl-sn-glycero-3-(cytidine diphosphate) (ammonium salt)

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关于此项目

经验公式（希尔记法）:
C44H87N5O15P2
化学文摘社编号:
384835-55-6
分子量:
988.13
MDL编号:
MFCD22416912
UNSPSC代码:
12352211
NACRES:
NA.25

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产品名称

16:0 CDP DG, Avanti Research™ - A Croda Brand 870510C

方案

>99% (TLC)

表单

liquid

包装

pkg of 1 × 1 mL (870510C-10mg)
pkg of 1 × 1 mL (870510C-5mg)

制造商/商品名称

Avanti Research™ - A Croda Brand 870510C

浓度

10 mg/mL (870510C-10mg)
5 mg/mL (870510C-5mg)

脂质类型

phosphoglycerides
bioactive lipids

运输

dry ice

储存温度

−20°C

SMILES字符串

[H][C@@](COP(OP(OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C(N=C(N)C=C2)=O)O1)([O-])=O)([O-])=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[NH4+].[NH4+]

InChI

1S/C44H81N3O15P2.2H3N/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-39(48)57-33-36(60-40(49)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)34-58-63(53,54)62-64(55,56)59-35-37-41(50)42(51)43(61-37)47-32-31-38(45)46-44(47)52;;/h31-32,36-37,41-43,50-51H,3-30,33-35H2,1-2H3,(H,53,54)(H,55,56)(H2,45,46,52);2*1H3/t36-,37-,41+,42?,43-;;/m1../s1

InChI key

IAUUMXARBJMHDT-LWJUINKDSA-N

应用

Cytidine diphosphate-diacylglycerol (CDP-DG) is suitable for liposome preparation.

生化/生理作用

Cytidine diphosphate-diacylglycerol (CDP-DG) acts as a precursor for synthesis of phosphatidylglycerol (PG) and phosphatidylinositol (PI) in alveolar type II cells.

包装

5 mL Clear Glass Sealed Ampule (870510C-10mg)
5 mL Clear Glass Sealed Ampule (870510C-5mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形图

Skull and crossbonesHealth hazard
GHS06,GHS08

警示用语：

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Oral - STOT SE 3

靶器官

Liver,Kidney, Respiratory system

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

闪点(°F)

does not flash

闪点(°C)

does not flash

法规信息

危险化学品
易制毒化学品（2类）
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Changes in phospholipids in bronchoalveolar lavage fluid of patients with interstitial lung diseases
Honda Y, et al.
Lung, 166(1), 293-301 (1988)
A steric gating mechanism dictates the substrate specificity of a Rab-GEF
Thomas L, et al.
Developmental Cell, 48(1), 100-114 (2019)
Julia Alvarez-Malmagro et al.
Bioelectrochemistry (Amsterdam, Netherlands), 132, 107416-107416 (2020-01-26)
A hybrid bilayer lipid membrane (hBLM), constructed with a 1-hexadecanethiol self-assembled interior leaflet and a 1,2-dipalmitoyl-sn-glycero-3-cytidine nucleolipid exterior leaflet, was deposited at the surface of a gold (111) electrode. This system was used to investigate the molecular recognition reaction between
Ru-Yin Huang et al.
Current microbiology, 77(5), 710-715 (2020-01-04)
Phosphatidylserine synthase (Pss) is involved in the metabolic pathway in phospholipid synthesis in different organisms. In this study, Pss expression in Vibrio parahaemolyticus was verified through liquid chromatography tandem-mass spectrometry. To analyze the characteristics of Pss, the recombinant Pss was

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