antihistaminic agent
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BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Ankit Siwach ◽  
Prabhakar Kumar Verma

Abstract Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. The imidazole name was reported by Arthur Rudolf Hantzsch (1857–1935) in 1887. 1, 3-diazole is an amphoteric in nature i.e. it shows both acidic and basic properties. It is a white or colorless solid that is highly soluble in water and other polar solvents. Due to the presence of a positive charge on either of two nitrogen atom, it shows two equivalent tautomeric forms. Imidazole was first named glyoxaline because the first synthesis has been made by glyoxal and ammonia. It is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. The derivatives of 1, 3-diazole show different biological activities such as antibacterial, antimycobacterial, anti-inflammatory, antitumor, antidiabetic, anti-allergic, antipyretic, antiviral, antioxidant, anti-amoebic, antihelmintic, antifungal and ulcerogenic activities, etc. as reported in the literature. There are different examples of commercially available drugs in the market which contains 1, 3-diazole ring such as clemizole (antihistaminic agent), etonitazene (analgesic), enviroxime (antiviral), astemizole (antihistaminic agent), omeprazole, pantoprazole (antiulcer), thiabendazole (antihelmintic), nocodazole (antinematodal), metronidazole, nitroso-imidazole (bactericidal), megazol (trypanocidal), azathioprine (anti rheumatoid arthritis), dacarbazine (Hodgkin's disease), tinidazole, ornidazole (antiprotozoal and antibacterial), etc. This present review summarized some pharmacological activities and various kinds of synthetic routes for imidazole and their derived products.


2017 ◽  
Vol 35 (2) ◽  
pp. e12244 ◽  
Author(s):  
Gerrit Frommeyer ◽  
Magdalena Sterneberg ◽  
Dirk G. Dechering ◽  
Sven Kaese ◽  
Nils Bögeholz ◽  
...  

2012 ◽  
Vol 22 (3) ◽  
pp. 1065-1072 ◽  
Author(s):  
Sunil V. Gupta ◽  
Kamalkishor G. Baheti ◽  
Saurabh B. Ganorkar ◽  
Deepak Dekhane ◽  
Shivaji Pawar ◽  
...  

2005 ◽  
Vol 38 (12) ◽  
pp. 1913-1931 ◽  
Author(s):  
Ayşegul Golcu ◽  
Burcu Dogan ◽  
Sibel A. Ozkan

2005 ◽  
Vol 22 (3) ◽  
pp. 499-514 ◽  
Author(s):  
Dorra Dridi ◽  
Naceur A. Boughattas ◽  
Karim Aouam ◽  
Alain Reinberg ◽  
Mossadok Ben Attia

2004 ◽  
Vol 61 (4) ◽  
pp. 445-447 ◽  
Author(s):  
Aca Vacic

Subcutaneous emphysema is a rare complication in dentistry, which may lead to diagnostic errors and inadequate therapy. A 17 years old female patient, in whom the separation of tooth roots was performed by the use of air-powered drill during the extraction of the first right lower molar, is presented in this paper. During the intervention, swelling of the right half of the face and the lower eyelid suddenly occurred, accompanied with simultaneous feeling of choking, and pressure in the neck and chest. Because of the suspicion of the allergic reaction, the patient was administered antihistaminic agent, together with parenteral corticosteroid, and was sent to an institution where she was treated as an in-patient. During hospitalization, subcutaneous emphysema of the face and neck was diagnosed by physical and x-ray examination. The emphysema completely disappeared after the use of oxygen and antibiotics.


1996 ◽  
Vol 12 (4) ◽  
pp. 389-400 ◽  
Author(s):  
J.M. YANNI ◽  
D.J. STEPHENS ◽  
S.T. MILLER ◽  
L.K. WEIMER ◽  
G. GRAFF ◽  
...  

1990 ◽  
Vol 31 (3-4) ◽  
pp. 210-218
Author(s):  
J. C. Nolan ◽  
M. H. Foxwell ◽  
L. L. Whitman ◽  
D. N. Johnson ◽  
J. M. Yanni ◽  
...  

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