Key Documents

View All Documentation

K3250

Kynuramine dihydrobromide

Name: Kynuramine dihydrobromide
Brand: SIGMA

monoamine oxidase substrate, fluorogenic, ≥97% (TLC), crystalline

Synonym(s):

3-(2-Aminophenyl)-3-oxopropanamine

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₉H₁₂N₂O · 2HBr

CAS Number:

304-47-2

Molecular Weight:

326.03

UNSPSC Code:

12352204

PubChem Substance ID:

24896227

NACRES:

NA.32

MDL number:

MFCD00050683

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Product Name

Kynuramine dihydrobromide, crystalline

assay

≥97% (TLC)

Quality Level

100

form

crystalline

solubility

water: 50 mg/mL, clear to slightly hazy

storage temp.

−20°C

SMILES string

Br.NCCC(=O)c1ccccc1N

InChI

1S/C9H12N2O.BrH/c10-6-5-9(12)7-3-1-2-4-8(7)11;/h1-4H,5-6,10-11H2;1H

InChI key

YUPVVZSYBUIDQR-UHFFFAOYSA-N

Description

General description

Substrate for monoamine oxidase

Application

Kynuramine dihydrobromide has been used as a substrate for monoamine oxidase.

Biochem/physiol Actions

Kynuramine dihydrobromide is a substrate for the enzyme monoamine oxidase. The end product is the formation of fluorescence detectable 4-hydroxyquinoline (4-HOQ) measured in a fluorescence spectrophotometer at 380 nm.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Evidence for the involvement of the noradrenergic system, dopaminergic and imidazoline receptors in the antidepressant-like effect of tramadol in mice

Jesse CR, et al.

Pharmacology, Biochemistry, and Behavior, 95(3), 344-350 (2010)

An investigation of the monoamine oxidase inhibition properties of pyrrolo[3,4-f]indole-5,7-dione and indole-5,6-dicarbonitrile derivatives.

Zhanna V Chirkova et al.

Drug development research, 79(2), 81-93 (2018-03-24)

Hit, Lead & Candidate Discovery In recent studies, we have shown that pyrrolo[3,4-f]indole-5,7-dione and indole-5,6-dicarbonitrile derivatives act as good potency in vitro inhibitors of the monoamine oxidase (MAO) enzymes. To expand on these series and to further derive structure-activity relationships

Chronic dietary mercury exposure causes oxidative stress, brain lesions, and altered behaviour in Atlantic salmon (Salmo salar) parr

Berntssen MHG, et al.

Aquatic Toxicology (Amsterdam, Netherlands), 65(1), 55-72 (2003)

View All Related Papers

Global Trade Item Number

SKU	GTIN
K3250-100MG	04061833868669
K3250-250MG	04061832917818
K3250-25MG	04061833868683