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  2. Tamsulosin - Wikipedia

    en.wikipedia.org/wiki/Tamsulosin

    Tamsulosin is a selective α 1 receptor antagonist that has preferential selectivity for the α 1A receptor in the prostate versus the α 1B receptor in the blood vessels. [ 25 ] When alpha 1 receptors in the bladder neck, prostate, ureter, and urethra are blocked, a relaxation in smooth muscle tissue results. [ 16 ]

  3. List of sulfonamides - Wikipedia

    en.wikipedia.org/wiki/List_of_sulfonamides

    List of sulfonamides; Author of The Demon Under the Microscope, a history of the discovery of the sulfa drugs; A History of the Fight Against Tuberculosis in Canada (Chemotherapy) Presentation speech, Nobel Prize in Physiology and Medicine, 1939; The History of WW II Medicine "Five Medical Miracles of the Sulfa Drugs".

  4. Sulfonamide (medicine) - Wikipedia

    en.wikipedia.org/wiki/Sulfonamide_(medicine)

    Sulfonamide functional group Hydrochlorothiazide is a sulfonamide and a thiazide. Furosemide is a sulfonamide, but not a thiazide. Sulfamethoxazole is an antibacterial sulfonamide. Sulfonamide is a functional group (a part of a molecule) that is the basis of several groups of drugs, which are called sulphonamides, sulfa drugs or sulpha drugs.

  5. Sulfonamide - Wikipedia

    en.wikipedia.org/wiki/Sulfonamide

    The structure of the sulfonamide group. In organic chemistry, the sulfonamide functional group (also spelled sulphonamide) is an organosulfur group with the structure R−S(=O) 2 −NR 2. It consists of a sulfonyl group (O=S=O) connected to an amine group (−NH 2). Relatively speaking this group is unreactive.

  6. Category:Sulfonamides - Wikipedia

    en.wikipedia.org/wiki/Category:Sulfonamides

    Pages in category "Sulfonamides" The following 200 pages are in this category, out of approximately 224 total. ... Tamsulosin; Terutroban; Tezosentan

  7. Sulfinamide - Wikipedia

    en.wikipedia.org/wiki/Sulfinamide

    General structure of sulfinamides, showing both correct zwitterionic and "expanded octet" simplified convention. In organosulfur chemistry, sulfinamide is a functional group with the structure R−S(O)−NR 2 (where R = alkyl or aryl). [1]

  8. Sulfonyl group - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_group

    Sulfonyl groups can be written as having the general formula R−S(=O) 2 −R′, where there are two double bonds between the sulfur and oxygen. [1]: 53 [2]Sulfonyl groups can be reduced to the sulfide with diisobutylaluminium hydride (DIBALH).

  9. Dutasteride/tamsulosin - Wikipedia

    en.wikipedia.org/wiki/Dutasteride/tamsulosin

    It is a combination of two previously existing medications: dutasteride, brand name Avodart, and tamsulosin, brand name Flomax. It contains 0.5 mg of dutasteride and 0.4 mg of tamsulosin hydrochloride. [2] Jalyn was the result of the CombAT (Combination of Avodart and Tamsulosin) trial of 2008.