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N5637

3-(1-Naphthyl)-DL-alanine

Name: 3-(1-Naphthyl)-<SC>DL</SC>-alanine
Brand: SIGMA

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关于此项目

经验公式（希尔记法）:

C₁₃H₁₃NO₂

化学文摘社编号:

28095-56-9

分子量:

215.25

UNSPSC Code:

12352202

PubChem Substance ID:

24897744

MDL number:

MFCD00067507

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属性

form

solid

storage temp.

2-8°C

SMILES string

NC(Cc1cccc2ccccc12)C(O)=O

InChI

1S/C13H13NO2/c14-12(13(15)16)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7,12H,8,14H2,(H,15,16)

InChI key

OFYAYGJCPXRNBL-UHFFFAOYSA-N

说明

Biochem/physiol Actions

3-(1-Naphthyl)-DL-alanine is an amino acid derivative that has been used to synthesize cholecystokinin analogues.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

057H0561

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Separation of the enantiomeric intermediates of some platelet-activating factor analogues on a naphthylalanine-type Pirkle column.

P L Camacho et al.

Journal of chromatography, 506, 611-616 (1990-05-11)

A chiral high-performance liquid-chromatographic separation method was developed for the analysis of some glycerol-based, ether-linked platelet-activating factor precursors. Using a D-naphthylalanine-type Pirkle-column and tetrahydrofuran-hexane eluents, the retention-structure relationships were determined for a large number of glycerol ether derivatives. The derivatives

Loop formation in unfolded polypeptide chains on the picoseconds to microseconds time scale.

Beat Fierz et al.

Proceedings of the National Academy of Sciences of the United States of America, 104(7), 2163-2168 (2007-02-08)

Intrachain loop formation allows unfolded polypeptide chains to search for favorable interactions during protein folding. We applied triplet-triplet energy transfer between a xanthone moiety and naphthylalanine to directly measure loop formation in various unfolded polypeptide chains with loop regions consisting

Highly potent antidiuretic antagonists: conformational studies of vasopressin analogues modified with 1-naphthylalanine enantiomers at position 2.

Emilia A Lubecka et al.

Chemical biology & drug design, 79(6), 1033-1042 (2012-02-11)

In this paper, we investigated the structure-activity relationship of two vasopressin analogues, [Cpa(1),(L-1-Nal)(2) ]AVP (I) and [Cpa(1),(D-Nal)(2) ]AVP (II) by NMR spectroscopy and molecular modeling. Both peptides exhibit antioxytocic and antipressor potency. Inversion of configuration of the residue at position

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全球贸易项目编号

货号	GTIN
N5637-1G	04061826061183