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  2. Sulfacetamide - Wikipedia

    en.wikipedia.org/wiki/Sulfacetamide

    Sulfacetamide is a sulfonamide antibiotic commonly used in the treatment of bacterial infections, particularly those affecting the eyes and skin. It functions by inhibiting the synthesis of folic acid in bacteria, which is essential for their growth and reproduction, thereby exerting a bacteriostatic effect.

  3. Sulfur in pharmacy - Wikipedia

    en.wikipedia.org/wiki/Sulfur_in_pharmacy

    Pulverised sulfur. Flowers of sulfur or sublimed sulfur (Latin: sulfur sublimatum) is the naturally occurring, unpurified form. [1] It comes in yellow flakes and has been used in traditional and alternative medicine for humans and animals, as well as in alchemy and sulfuring fruit before drying.

  4. Sulfacetamide/sulfur - Wikipedia

    en.wikipedia.org/wiki/Sulfacetamide/sulfur

    The drug combination sulfacetamide/sulfur is a topical acne medication [1] manufactured by Medicis under the trade name Plexion and also available under other trade names such as Clenia, Prascion, and Avar. It combines sodium sulfacetamide, a sulfonamide antibiotic, and sulfur, a keratolytic agent. [2]

  5. 5 Things to Avoid When You Have Alopecia Areata - AOL

    www.aol.com/5-things-avoid-alopecia-areata...

    2. Excessive Stress. Stress is a natural, normal part of the human experience, and your body knows how to handle it. When you’re under stress, your body releases stress hormones that activate ...

  6. List of sulfonamides - Wikipedia

    en.wikipedia.org/wiki/List_of_sulfonamides

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  7. Acylsulfonamide - Wikipedia

    en.wikipedia.org/wiki/Acylsulfonamide

    Chemical structure of a generic acylsulfonamide. Acylsulfonamide is a functional group in organic chemistry that is sometimes used in medicinal chemistry. [1] It consists of a sulfonamide group (SO 2 NH) linked to an acyl group (RCO), forming the structure R 1-CO-NH-SO 2-R 2.

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