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Merck
CN

485616

Sigma-Aldrich

十二烷基磷酰胆碱-d38

98 atom % D

别名:

十二烷基磷酸胆碱-d38

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About This Item

线性分子式:
[CD3(CD2)11O](O-)P(=O)OCD2CD2N+(CD3)3
分子量:
389.70
MDL编号:
UNSPSC代码:
12352211
PubChem化学物质编号:
NACRES:
NA.12

同位素纯度

98 atom % D

质量水平

形式

solid

技术

NMR: suitable
bio NMR: suitable

mp

247-249 °C (lit.)

质量偏移

M+38

SMILES字符串

[O-]P(OC([2H])(C([N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])([2H])[2H])[2H])(OC([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])(C([2H])([2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H]

InChI

1S/C17H38NO4P/c1-5-6-7-8-9-10-11-12-13-14-16-21-23(19,20)22-17-15-18(2,3)4/h5-17H2,1-4H3/i1D3,2D3,3D3,4D3,5D2,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2

InChI key

QBHFVMDLPTZDOI-DHIOKLJKSA-N

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Ruslan Garifullin et al.
European biophysics journal : EBJ, 48(1), 25-34 (2018-08-15)
Chemical modification of therapeutic peptides is an important approach to improving their physicochemical and pharmacokinetic properties. The triphenylphosphonium (TPP) cation has proved to be a powerful modifier; however, its effects on peptide structure and activity remain uncharacterized. In this study
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Cyclic lipodepsipeptides or CLiPs from Pseudomonas are secondary metabolites that mediate a wide range of biological functions for their producers, and display antimicrobial and anticancer activities. Direct interaction of CLiPs with the cellular membranes is presumed to be essential in
Ting-Wei Chang et al.
PloS one, 12(10), e0186442-e0186442 (2017-10-19)
Antimicrobial peptides are important components of the host innate defense mechanism against invading pathogens, especially for drug-resistant bacteria. In addition to bactericidal activity, the 25 residue peptide TP4 isolated from Nile tilapia also stimulates cell proliferation and regulates the innate
Nelson A Araujo et al.
Archives of biochemistry and biophysics, 698, 108731-108731 (2020-12-29)
Microbial pathogens, such as Trypanosoma brucei, have an enormous impact on global health and economic systems. Protein kinase A of T. brucei is an attractive drug target as it is an essential enzyme which differs significantly from its human homolog.
Soraya Serrano et al.
Biochemistry, 56(41), 5503-5511 (2017-09-21)
Despite extensive characterization of the human immunodeficiency virus type 1 (HIV-1) hydrophobic fusion peptide (FP), the structure-function relationships underlying its extraordinary degree of conservation remain poorly understood. Specifically, the fact that the tandem repeat of the FLGFLG tripeptide is absolutely

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