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首页> 外文期刊>Biological & pharmaceutical bulletin >A phenoxazine compound, 2-amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one reverses the phenylephrine or high-K+ induced contraction of smooth muscles in rat aorta and guinea pig tenia cecum.
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A phenoxazine compound, 2-amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one reverses the phenylephrine or high-K+ induced contraction of smooth muscles in rat aorta and guinea pig tenia cecum.

机译:苯恶嗪化合物2-氨基-4,4α-二氢-4α-7-二甲基-3H-苯恶嗪-3-酮可逆转去氧肾上腺素或高K +诱导的大鼠主动脉和豚鼠盲肠平滑肌收缩。

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摘要

2-Amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one (Phx-1) reversed concentration dependently the contraction of both rat aorta and guinea pig tenia cecum induced by phenylephrine or high-K(+). Since Phx-1 suppresses the responses of human mononuclear cells to phytohemagglutinin, (Akazawa et al. Tohoku J. Exp. Med., 196, 185-192, 2002), Phx-1 may be useful for developing new vasorelaxing agents with immunosuppressive action.
机译:2-氨基-4,4alpha-二氢-4alpha-7-二甲基-3H-吩恶嗪-3-one(Phx-1)逆转浓度依赖于去氧肾上腺素或高K诱导的大鼠主动脉和豚鼠盲肠的收缩+)。由于Phx-1抑制人单核细胞对植物血凝素的反应(Akazawa等人Tohoku J.Exp.Med。,196,185-192,2002),因此Phx-1可用于开发具有免疫抑制作用的新血管舒张剂。

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