阿帕佐尼

阿帕佐尼（CAS 13539-59-8）的公开数据库记录，列此仅供独立核对。

物理形态与操作说明

• 169.5 Ų [M+H]+ [CCS Type: TW; Method: Major Mix IMS/Tof Calibration Kit (Waters)]

公开数据库收录的理化数据

这个物质在各数据库里的编号

数据库记载的用途

• Breast Feeding; Lactation; Milk, Human; Anti-Inflammatory Agents, Nonsteroidal; Uricosuric Agents
• 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.
• Gout suppressants that act directly on the renal tubule to increase the excretion of uric acid, thus reducing its concentrations in plasma.
• M01 - Antiinflammatory and antirheumatic products
• M01A - Antiinflammatory and antirheumatic products, non-steroids
• M01AX - Other antiinflammatory and antirheumatic agents, non-steroids

它在各数据库里的别名

Azapropazone; APAZONE; 13539-59-8; Cinnopropazone; Azapropazona; Azapropazonum; Azapropazon; AHR-3018; Mi-85; NSC-102824; DTXSID6045408; K2VOT966ZI; 3-Dimethylamino-7-methyl-1,2-(n-propylmalonyl)-1,2-dihydro-1,2,4-benzotriazine; 5-(Dimethylamino)-9-methyl-2-propyl-1H-pyrazolo(1,2-a)(1,2,4)benzotriazine-1,3(2H)-dione; 5-(Dimethylamino)-9-methyl-2-propyl-1H-pyrazolo[1,2-a][1,2,4]benzotriazine-1,3(2H)-dione; 1,2-Dihydro-3-dimethylamino-7-methyl-1,2-(propylmalonyl)-1,2,4-benzotriazine

计算机算出的分子描述符

数据库摘要

Apazone · CAS 13539-59-8 · C16H20N4O2. UNII K2VOT966ZI. 熔点: 187.

数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。