3-phenylpropanamine

3-phenylpropanamine Structure
3-phenylpropanamine structure
Common Name 3-phenylpropanamine
CAS Number 2038-57-5 Molecular Weight 135.206
Density 0.9±0.1 g/cm3 Boiling Point 217.3±19.0 °C at 760 mmHg
Molecular Formula C9H13N Melting Point N/A
MSDS Chinese USA Flash Point 90.6±0.0 °C
Symbol GHS05
GHS05
Signal Word Danger

Disulfiram-induced cytotoxicity and endo-lysosomal sequestration of zinc in breast cancer cells.

Biochem. Pharmacol. 93(3) , 332-42, (2015)

Disulfiram, a clinically used alcohol-deterrent has gained prominence as a potential anti-cancer agent due to its impact on copper-dependent processes. Few studies have investigated zinc effects on disulfiram action, despite it having high affinity for this m...

New efficient substrates for semicarbazide-sensitive amine oxidase/VAP-1 enzyme: analysis by SARs and computational docking.

J. Med. Chem. 49 , 6197-208, (2006)

Structure activity relationships for semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1) were studied using a library of arylalkylamine substrates, with the aim of contributing to the discovery of more efficient SSAO substrates. Exp...

Drug-, dose- and sex-dependent effects of chronic fluoxetine, reboxetine and venlafaxine on open-field behavior and spatial memory in rats.

Behav. Brain Res. 281 , 43-54, (2015)

In an effort to address the need to include both sexes in studies of effects of the SSRI fluoxetine, the NRI reboxetine and the SNRI venlafaxine on anxiety-related behavior and memory along with the use of chronic drug administration, male and female PVG/c ra...

Determination of amphetamine and related compounds in urine using on-line derivatization in octadecyl silica columns with 9-fluorenylmethyl chloroformate and liquid chromatography.

J. Chromatogr. B, Biomed. Appl. 679(1-2) , 69-78, (1996)

A method for the determination of amphetamine and related compounds in urine based on on-line derivatization with 9-fluorenylmethyl chloroformate (FMOC) and high-performance liquid chromatography is described. Derivatization is performed in a 20 x 2.1 mm I.D....

Use of alternate substrates to probe the order of substrate addition to dopamine beta-hydroxylase.

Arch. Biochem. Biophys. 249(1) , 70-5, (1986)

In order to determine the order of substrate binding to dopamine beta-hydroxylase during catalysis, the effect of alternate substrates upon kinetic parameters was examined. The V/K value for ascorbate was unchanged when tyramine, phenylpropylamine, p-Cl-phene...