Bumetanide
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(New page: <StructureSection load='' size='340' side='right' caption='Caption for this structure' scene=''> Bumetanide, sold under the brand name Bumex among others, is a medication used to treat swe...) |
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| - | <StructureSection load='' size='340' side='right' caption='Caption for this structure' scene=''> | + | <StructureSection load='' size='340' side='right' caption='Caption for this structure' scene='10/1022891/Cv/1'> |
| - | Bumetanide, sold under the brand name Bumex among others, is a medication used to treat swelling and high blood pressure. This includes swelling as a result of heart failure, liver failure, or kidney problems. It may work for swelling when other medications have not.[ | + | Bumetanide, sold under the brand name Bumex among others, is a medication used to treat swelling and high blood pressure. This includes swelling as a result of heart failure, liver failure, or kidney problems. It may work for swelling when other medications have not.<ref name="a2">[https://www.drugs.com/monograph/bumetanide.html "Bumetanide Monograph for Professionals".] Drugs.com. American Society of Health-System Pharmacists. Retrieved 8 April 2019.</ref> See also [https://en.wikipedia.org/wiki/Bumetanide Bumetanide]. |
| + | Bumetanide is a loop diuretic and works by decreasing the reabsorption of sodium by the kidneys. The main difference between bumetanide and furosemide is in their bioavailability and potency. About 60% of furosemide is absorbed in the intestine, and there are substantial inter- and intraindividual differences in bioavailability (range 10-90%). About 80% of bumetanide is absorbed, and its absorption does not change when it is taken with food. It is said to be a more predictable diuretic, meaning that the predictable absorption is reflected in a more predictable effect. Bumetanide is 40 times more potent than furosemide for people with normal renal function.<ref name="a15">Brunton L, Lazo JS, Parker KL, eds. (2006). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11th ed.). New York: McGraw-Hill. pp. 749–753. ISBN 0-07-142280-3.</ref> Bumetanide blocks the NKCC1 cation-chloride co-transporter. | ||
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| + | <scene name='10/1022891/Cv/2'>Human Cation-chloride cotransporter NKCC1 K289NA492EL671C bound with bumetanide</scene> ([[7s1x]]). | ||
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| + | <scene name='10/1022891/Cv/4'>Bumetanide binding site</scene>. | ||
</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
<references/> | <references/> | ||
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References
- ↑ "Bumetanide Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 8 April 2019.
- ↑ Brunton L, Lazo JS, Parker KL, eds. (2006). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11th ed.). New York: McGraw-Hill. pp. 749–753. ISBN 0-07-142280-3.
