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文件

485616

十二烷基磷酰胆碱-d₃₈

Name: 十二烷基磷酰胆碱-d<SUB>38</SUB>
Brand: ALDRICH

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

CAS号:

130890-78-7

分子量:

389.70

MDL號碼:

MFCD01321393

分類程式碼代碼:

12352211

PubChem物質ID:

24872104

NACRES:

NA.12

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同位素純度

98 atom % D

形狀

solid

技術

NMR: suitable
bio NMR: suitable

mp

247-249 °C (lit.)

質量偏移

M+38

SMILES 字串

[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 密鑰

QBHFVMDLPTZDOI-DHIOKLJKSA-N

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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Effect of triphenylphosphonium moiety on spatial structure and biointeractions of stereochemical variants of YRFK motif.

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

Conformation and Dynamics of the Cyclic Lipopeptide Viscosinamide at the Water-Lipid Interface.

Niels Geudens et al.

Molecules (Basel, Switzerland), 24(12) (2019-06-20)

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

Disorder and partial folding in the regulatory subunit hinge region of Trypanosoma brucei protein kinase A: The C-linker portion inhibits the parasite's protein kinase A.

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.

Hydrophobic residues are critical for the helix-forming, hemolytic and bactericidal activities of amphipathic antimicrobial peptide TP4.

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

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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十二烷基磷酰胆碱-d₃₈