4-bromo-2,7-dimethoxyphenothiazin-3-one
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4-bromo-2,7-dimethoxyphenothiazin-3-one
structure -
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CAS No:
93211-49-5
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Formula:
C14H10BrNO3S
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Chemical Name:
4-bromo-2,7-dimethoxyphenothiazin-3-one
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Synonyms:
4-bromo-2,7-dimethoxy-3H-phenothiazin-3-one;L 651.392;L 651392;L-651,392;L-651392;4-Bromo-2,7-dimethoxy-3H-phenothiazin-3-one;L-651392;93211-49-5;4-bromo-2,7-dimethoxyphenothiazin-3-one;UNII-6163B74DJY;6163B74DJY;L 651392;L 651.392;L-651,392;3H-Phenothiazin-3-one, 4-bromo-2,7-dimethoxy-;SCHEMBL2987610;DTXSID60239339;ZINC6018919
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CAS No:
4-bromo-2,7-dimethoxyphenothiazin-3-one Basic Attributes
352.20 g/mol
350.95648 g/mol
6163B74DJY
DTXSID60239339
Drug Information
Compounds that bind to and inhibit that enzymatic activity of LIPOXYGENASES. Included under this category are inhibitors that are specific for lipoxygenase subtypes and act to reduce the production of LEUKOTRIENES. (See all compounds classified as Lipoxygenase Inhibitors.)|Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)
4-bromo-2,7-dimethoxy-3H-phenothiazin-3-one
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