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858897

Nω-Acetylhistamine

Name: <I>Nω</I>-Acetylhistamine
Brand: ALDRICH

98%

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About This Item

Empirical Formula (Hill Notation):

C₇H₁₁N₃O

CAS Number:

673-49-4

Molecular Weight:

153.18

PubChem Substance ID:

24888477

eCl@ss:

32160406

UNSPSC Code:

12352005

NACRES:

NA.22

EC Number:

211-610-3

MDL number:

MFCD00005209

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

147-149 °C (lit.)

functional group

amide

SMILES string

CC(=O)NCCc1c[nH]cn1

InChI

1S/C7H11N3O/c1-6(11)9-3-2-7-4-8-5-10-7/h4-5H,2-3H2,1H3,(H,8,10)(H,9,11)

InChI key

XJWPISBUKWZALE-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Detection of Novel Cytotoxic Imidazole Alkaloids in Tomato Products by LC-MS/MS.

Yannick Hövelmann et al.

Journal of agricultural and food chemistry, 67(13), 3670-3678 (2019-03-13)

Imidazole alkaloids represent a rather small group of alkaloids and are assumed not to be of significance to the human food chain so far. In this study, novel imidazole alkaloids occurring in tomato products were synthesized and structurally characterized by

Properties of N-acetylhistamine deacetylase in mammalian brain.

L R Hegstrand et al.

Journal of neurochemistry, 45(1), 300-307 (1985-07-01)

Properties of N-acetylhistamine deacetylase in rat brain were studied, utilizing a sensitive coupled radioenzymatic assay. The Km for N-acetylhistamine for this deacetylase was 660 microM and its Vmax was 330 pmol/h/mg protein. N-Acetylhistamine deacetylase activity increased 80% in the presence

[Molecular mechanism of the interaction of histamine with hyaluronic acid].

K L Erzinkian et al.

Izvestiia Akademii nauk SSSR. Seriia biologicheskaia, (2)(2), 206-210 (1985-03-01)

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Global Trade Item Number

SKU	GTIN
858897-1G	04061826664957