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Pharmacological properity of S103. a new benzopyrans potassium channel opener
作者姓名:王霆  刘国卿  李刚峰  孙宏斌  华维一  彭司勋
作者单位:Department of Pharmacology,Department of MedicalChemistry,China Pharmaceutical University,Nanjing210009,China,Department of Pharmacology,Department of MedicalChemistry,China Pharmaceutical University,Nanjing210009,China,Department of Pharmacology,Department of MedicalChemistry,China Pharmaceutical University,Nanjing210009,China,Department of Pharmacology,Department of MedicalChemistry,China Pharmaceutical University,Nanjing210009,China,Department of Pharmacology,Department of MedicalChemistry,China Pharmaceutical University,Nanjing210009,China,Department of Pharmacology,Department of MedicalChemistry,China Pharmaceutical University,Nanjing210009,China
摘    要:AIM: To study the pharmacological properity of S103, a new potassium channel opener(KCO). METHODS:(1) Relaxation of smooth muscle (thoracic aorta of rat andspontaneous response of portal vein of rat); (2) ~(86)Rb~ efflux from rat aorta. RESULTS:(1) S103 inhibited the

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