Synthesis and antihistamine evaluations of novel loratadine analogues

Bioorganic & Medicinal Chemistry Letters
Yue WangDeng-Ke Liu

Abstract

A series of loratadine analogues containing hydroxyl group and chiral center were synthesized. The effect of the synthesized compounds on the histamine-induced contractions of guinea-pig ileum muscles was studied. In addition, the in vivo asthma-relieving effect of the analogues in the histamine induced asthmatic reaction in guinea-pigs was determined. Most of the compounds exhibited definite H(1) antihistamine activity. The S-enantiomers, compounds 2, 4 and 8, are more potent than the R-enantiomers, compounds 1, 3 and 7. Compound 6 was the most active one among the eight synthesized compounds.

References

Aug 1, 1991·Journal of Computer-aided Molecular Design·M J van DroogeH Timmerman
Apr 9, 2001·Allergy·F M Baroody, R M Naclerio

Related Concepts

Asthma
Cavia porcellus
Ceplene
Histamine Antagonists
Ileum
Molecular Stereochemistry
Clarium
Anti-Allergic Agents
Analogs & derivatives
Antihistamines

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