Sandbox1996: Difference between revisions
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== Structure == | == Structure == | ||
<scene name='75/756546/Chlorothiazide/1'>Chlorothiazide</scene> is a semisynthetic chemical compound known chemically as 6-chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide (Figure 1) | <scene name='75/756546/Chlorothiazide/1'>Chlorothiazide</scene> is a semisynthetic chemical compound known chemically as 6-chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide (Figure 1) <ref name "one. It has a chemical formula of C<sub>7</sub>H<sub>8</sub>ClN<sub>3</sub>O<sub>4</sub>S<sub>2</sub> and a molecular weight of 298 Da. This chemical compound consists of an aromatic ring, benzothiadiazine, a sulfonamide group, and a chloride. It has a melting point of 272 degrees Celsius, a flash po int of 302.7 degrees Celsius, a solubility of 60 mg/ml in DMSO and less than 1 mg/ml in water, and appears as a white crystalline powder(reference). The structure was determined by X-Ray diffraction and was measured at a resolution of 2.1 Angstroms (reference). <scene name='75/756546/Drug/1'>Chlorothiazide was determined when bound to glutamate receptor 2</scene>. The enzyme cave of glutamate receptor 2 contained <scene name='75/756546/Inprogess/1'>specific amino acids</scene> that enabled binding of chlorothiazide. Binding involved hydrogen bonding between the <scene name='75/756546/Inprogess1/3'>nitrogen 12 and serine 242B, nitrogen 1 and serines 108B and 108E, and oxygen 17 and glycine 219 E</scene> (Figure 2 & 3). Synthesis of chlorothiazide occurs through the reaction between 3-chloroaniline, chlorosulfonic acid, and ammonia; and it is catalyzed by formic acid (Figure 4)(reference). | ||
<center>[[Image:Duiril.png|thumb|left|200px|Figure 1. Molecular structure of chlorothiazide.]]</center> | <center>[[Image:Duiril.png|thumb|left|200px|Figure 1. Molecular structure of chlorothiazide.]]</center> | ||