Deprecated: mysql_connect(): The mysql extension is deprecated and will be removed in the future: use mysqli or PDO instead in /home/content/93/7713193/html/chandraprabhu/includes/dbconfig.php on line 20
acetazolamide manufacturer Chandraprabhu Pharma

acetazolamide manufacturer


Deprecated: mysql_connect(): The mysql extension is deprecated and will be removed in the future: use mysqli or PDO instead in /home/content/93/7713193/html/chandraprabhu/includes/dbconfig.php on line 20
Product Name :
ACETAZOLAMIDE
Chemical Formula :
N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide
CAS No :
59-66-5
Molecular Formula :
C4H6N4O3S2
Molecular Weight :
222.245
acetazolamide
Description :
Acetazolamide is a carbonic anhydrase inhibitor that is used to treat glaucoma, epileptic seizures, Idiopathic intracranial hypertension (pseudotumor cerebri), altitude sickness, cystinuria, periodic paralysis and dural ectasia. Acetazolamide is available as ageneric drug and is also a diuretic. Acetazolamide is a carbonic anhydrase inhibitor. Medically it may be used to treat conditions of moderate to severe metabolic or respiratory alkalosis. It does this by interfering with bicarbonate (HCO3-) reabsorption in the kidneys, thereby re-acidifying the blood (and thus alkalinizing the urine). Carbonic anhydrase (CA) catalyzes the first part of the following reversible reaction (the second half happens spontaneously, favouring production of H+ + HCO3-), in which carbon dioxide (CO2) and water (H2O) are converted to carbonic acid (H2CO3) and vice-versa: CO2 + H2O <--CA--> H2CO3 <--> H+ + HCO3-. In the kidney tubules, locally secreted hydrogen ions normally combine with filtered bicarbonate (HCO3-) to form carbonic acid (H2CO3). Carbonic acid in turn is normally acted upon by carbonic anhydrase, leading to formation of CO2. As CO2 rapidly leaves the tubules by diffusing across cell membranes, the above reaction normally runs shifted strongly to the left (i.e. reversed), and more bicarbonate can be continuously reabsorbed from the preurine. However, in the presence of acetazolamide, carbonic anhydrase is inhibited and carbonic acid levels build up. The inhibition of carbonic anhydrase in turn leads to a slowing of the reverse reaction and a decrease in the body's ability to reabsorb serum bicarbonate, resulting in urinary bicarbonate wasting. This leads to a decreased ability to exchange Na+ for H+ in the presence of acetazolamide (in proximal convoluted tubules of kidney) resulting in a mild diuresis. By contrast, the H+ that is also present in the lumen is reabsorbed via an alternative pathway along with Cl-; it then passes into the bloodstream, leading to hyperchloremic metabolic acidosis.[2] This effect can also be used for therapeutic correction of alkalosis seen in altitude sickness or other forms of respiratory alkalosis.Acetazolamide is often used in the treatment of various diseases.

Submit Enquiry