Next Article in Journal
Phytoalexin Accumulation in Colombian Bean Varieties and Aminosugars as Elicitors
Previous Article in Journal
Easy Preparation of [Bis(trifluoroacetoxy)iodo]arenes from Iodoarenes, with Sodium Percarbonate as the Oxidant
Molecules 2002, 7(11), 813-816; doi:10.3390/71100813
Article

Nα-Urocanylhistamine: A Natural Histamine Derivative

1,2,* , 1 and 1
1 Department of Chemistry, 111 Willard Hall, Kansas State University, Manhattan, Kansas, 66506, USA 2 Current Address: Signature BioScience, Inc., 1240 S. 47th Street, Richmond, CA 94804, USA
* Author to whom correspondence should be addressed.
Received: 22 October 2002 / Revised: 2 December 2002 / Accepted: 2 December 2002 / Published: 2 December 2002
View Full-Text   |   Download PDF [34 KB, uploaded 18 June 2014]   |   Browse Figures
SciFeed

Abstract

Nα-Urocanylhistamine and two related compounds were synthesized by using PyBOP coupling protocols. These compounds represent naturally occurring histamine derivatives.
Keywords: Amide coupling; histamine; urocanic acid; imidazole Amide coupling; histamine; urocanic acid; imidazole
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

Share & Cite This Article

Further Mendeley | CiteULike
Export to BibTeX |
EndNote |
RIS
MDPI and ACS Style

Baures, P.W.; Kaliyan, K.; Desper, J. Nα-Urocanylhistamine: A Natural Histamine Derivative. Molecules 2002, 7, 813-816.

View more citation formats

Related Articles

Article Metrics

For more information on the journal, click here

Comments

[Return to top]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert