KYNURAMINE DIHYDROBROMIDE structure, CAS 304-47-2

KYNURAMINE DIHYDROBROMIDE

CAS Number304-47-2

Synonyms3-(2-Aminophenyl)-3-oxopropanamine; 3-amino-1-(2-aminophenyl)propan-1-one,hydrobromide

Molecular FormulaC9H14Br2N2O

Molecular Weight326.02800

Purity98.00%

Density

Boiling Point367.3ºC at 760mmHg

Melting Point

Flash Point

AppearanceWhite, yellow, brown crystal

EINECS

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Cat. No.: 2A-1184269 Purity: 98.00%
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Quality Control of [ 304-47-2 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number304-47-2
Catalog No.2A-1184269
Chinese Name犬尿胺 二氢溴酸
Synonyms3-(2-Aminophenyl)-3-oxopropanamine; 3-amino-1-(2-aminophenyl)propan-1-one,hydrobromide
Molecular FormulaC9H14Br2N2O
Molecular Weight326.02800
Purity98.00
Boiling Point367.3ºC at 760mmHg
AppearanceWhite, yellow, brown crystal
Storage Condition20°C
ApplicationKynuramine (dihydrobromide) is an endogenous amine and a fluorescent substrate and probe for plasma amine oxidase [1][2].
PubChem ID24896227
SMILESBr.Br.NCCC(=O)c1ccccc1N
InChIInChI=1S/C9H12N2O.BrH/c10-6-5-9(12)7-3-1-2-4-8(7)11;/h1-4H,5-6,10-11H2;1H
InChI KeyKNLPLQJBAIXOQE-UHFFFAOYSA-N
Hazard Symbolstransportation
BioactivityKynuramine (dihydrobromide), an endogenously occurring amine, is a fluorescent substrate and probe of plasma amine oxidase[1][2]. Related Catalog Signaling Pathways >> Neuronal Signaling >> Monoamine Oxidase Research Areas >> Metabolic Disease In Vitro Kynuramine (dihydrobromide) inhibits presynaptic and postsynaptic α-adrenergic receptors in vitro[2]. Kynuramine has been shown to be a partial agonist of serotonin receptors in the cerebral arteries of dogs [2]. Kynuramine (20 μg/mL) often causes mild contraction of the ileum but fails to alter the twitching response to cholinergic stimulation [2]. In Vivo Kynuramine (dihydrobromide) (0.064, 0.32, 1.6, or 8 μg; intracerebroventricular; single dose) promotes estrogen-stimulated lordotic behavior in ovariectomized rats [3]. Kynuramine (1.25, 2.5, and 5.0 mg/kg; intravenously; single dose) increases heart rate and blood pressure in rats [4]. Animal Model: Female rats[3]. Dosage: 0.064-8 μg. Administration: Intraventricular injection; single does. Result: Produced facilitation of lordosis behavior. Animal Model: Male rats (about 200g)[4]. Dosage: 1.25-5.0 mg/kg. B Massey, et al. Kynuramine, a fluorescent substrate and probe of plasma amine oxidase. J Biol Chem. 1977 Nov 25;252(22):8081-4. [2]. T D Johnson, An alpha-adrenoceptor inhibitory action of kynuramine. Eur J Pharmacol. 1981 Jul 10;72(4):351-6. [3]. S D Mendelson, et al. Intraventricular administration of l-kynurenine and kynuramine facilitates lordosis in the female rat. Eur J Pharmacol. 1987 Oct 27;142(3):447-51. [4]. T D Johnson, et al. Blood pressure and heart rate effects of kynuramine in pithed rats. Eur J Pharmacol. 1983 Feb 18;87(2-3):323-6. Chemical & Physical Properties Boiling Point 367.3ºC at 760mmHg Molecular Formula C9H14Br2N2O Molecular Weight 326.02800 Flash Point 175.9ºC Exact Mass 323.94700 PSA 69.11000 LogP 3.99800 InChIKey KNLPLQJBAIXOQE-UHFFFAOYSA-N SMILES Br.Br.NCCC(=O)c1ccccc1N Storage condition 20°C
Use ofProperties Name Kynuramine dihydrobromide Synonym More Synonyms Kynuramine Dihydrobromide Biological Activity Description Kynuramine (dihydrobromide), an endogenously occurring amine, is a fluorescent substrate and probe of plasma amine oxidase[1][2]. Related Catalog Signaling Pathways >> Neuronal Signaling >> Monoamine Oxidase Research Areas >> Metabolic Disease In Vitro Kynuramine (dihydrobromide) inhibits presynaptic and postsynaptic alpha-adrenergic receptors in vitro[2]. Kynuramine has been shown to be a partial agonist of serotonin receptors in the cerebral arteries of dogs [2]. Kynuramine (20 μg/mL) often causes mild contraction of the ileum but fails to alter the twitching response to cholinergic stimulation [2]. References [1]. J B Massey, et al. Kynuramine, a fluorescent substrate and probe of plasma amine oxidase. J Biol Chem. 1977 Nov 25;252(22):8081-4. [2]. T D Johnson, An alpha-adrenoceptor inhibitory action of kynuramine. Eur J Pharmacol. 1981 Jul 10;72(4):351-6. [3]. S D Mendelson, et al. Intraventricular administration of l-kynurenine and kynuramine facilitates lordosis in the female rat. Eur J Pharmacol. 1987 Oct 27;142(3):447-51. [4]. T D Johnson, et al. Blood pressure and heart rate effects of kynuramine in pitted rats. Eur J Pharmacol. 1983 Feb 18;87(2-3):323-6. Chemical & Physical Properties Molecular Formula C9H14Br2N2O Exact Mass 323.94700 PSA 69.11000 LogP 3.99800 InChIKey KNLPLQJBAIXOQE-UHFFFAOYSA-N
Transport InfoProduct name: Purity: 97.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
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