H6759

L-Histidine β-naphthylamide

Name: <SC>L</SC>-Histidine β-naphthylamide
Brand: SIGMA
Price: 1620 MYR

≥98% (TLC)

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250 MG

RM 1,620.00

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About This Item

Empirical Formula (Hill Notation):

C₁₆H₁₆N₄O

CAS Number:

7424-15-9

Molecular Weight:

280.32

NACRES:

NA.26

PubChem Substance ID:

24895761

UNSPSC Code:

12352209

EC Number:

231-052-4

MDL number:

MFCD00051166

Key Documents

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Product Name

L-Histidine β-naphthylamide, powder

InChI key

DKDILZBBFKZMRO-HNNXBMFYSA-N

InChI

1S/C16H16N4O/c17-15(8-14-9-18-10-19-14)16(21)20-13-6-5-11-3-1-2-4-12(11)7-13/h1-7,9-10,15H,8,17H2,(H,18,19)(H,20,21)/t15-/m0/s1

SMILES string

N[C@@H](Cc1cnc[nH]1)C(=O)Nc2ccc3ccccc3c2

assay

≥98% (TLC)

form

powder

color

white to faint yellow

storage temp.

−20°C

Quality Level

200

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1 of 4

This Item	T3384	I4879	S5628
Sigma-Aldrich H6759 L-Histidine β-naphthylamide	Sigma-Aldrich T3384 L-Tyrosine β-naphthylamide	Sigma-Aldrich I4879 L-Isoleucine β-naphthylamide	Sigma-Aldrich S5628 Ser-Tyr β-naphthylamide
form powder	form powder	form powder	form powder
assay ≥98% (TLC)	assay ≥98% (TLC)	assay ≥98% (TLC)	assay ≥98% (TLC)
storage temp. −20°C	storage temp. −20°C	storage temp. 2-8°C	storage temp. −20°C
color white to faint yellow	color white to off-white	color white to off-white	color off-white
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200

Biochem/physiol Actions

L-Histidine β-naphthylamide is an analogue of L-histidine used to study structural roles of L-histidine in functions such as the activation of HutP protein transcription. L-Histidine β-naphthylamide may also be used to study the specificity and kinetics of various proteases and peptidases.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Allosteric activation of HutP protein, that regulates transcription of hut operon in Bacillus subtilis, mediated by various analogs of histidine.

Kumarevel T, Mizuno H, Kumar PK.

Nucleic Acids Research, 3, 199-200 (2003)

Histidines, histamines and imidazoles as glycosidase inhibitors.

R A Field et al.

The Biochemical journal, 274 ( Pt 3), 885-889 (1991-03-15)

This present study reports the ability of a range of derivatives of L-histidine, histamine and imidazole to act as inhibitors of sweet-almond beta-glucosidase, yeast alpha-glucosidase and Escherichia coli beta-galactosidase. The addition of a hydrophobic group to the basic imidazole nucleus

Purification and characterization of a halotolerant intracellular protease from Bacillus subtilis strain FP-133.

Endang Setyorini et al.

Journal of basic microbiology, 46(4), 294-304 (2006-07-19)

A halotolerant strain FP-133, able to grow at concentrations of 0-12.5% (w/v) NaCl, was isolated from a fish paste and identified as Bacillus subtilis . B. subtilis strain FP-133 produced an intracellular protease which showed catalytic activity under saline conditions.

Histidine 450 plays a critical role in catalysis and, with Ca2+, contributes to the substrate specificity of aminopeptidase A.

X Iturrioz et al.

Biochemistry, 39(11), 3061-3068 (2000-03-15)

Aminopeptidase A (EC 3.4.11.7, APA) is a 130 kDa membrane-bound protease that contains the HEXXH consensus sequence found in the zinc metalloprotease family, the zincins. In addition to the catalytic zinc atom, APA contains a Ca2+ ion that increases its

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L-Histidine β-naphthylamide