“betaine hydrochloride”的搜索结果
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adrenergic receptor/5-HT receptor 抑制剂
Asenapine hydrochloride抑制肾上腺素能受体(α1,α2A,α2B,α2C)的Ki为0.25-1.2 nM,还抑制5-HT受体(1A,1B,2A,2B,2C,5A,6、7),Ki为0.03- 4.0 nM。
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5-HT2 receptors inhibitor
Nefazodone HCl is an inhibitor of 5-HT2 receptors, SERT, NET, and hERG K+ channels used to treat mood disorders. It decreases immobility time in the forced swim test.
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Thromboxane A2 synthesis 抑制剂
Ozagrel hydrochloride是一种抗血小板剂,用作血栓烷a2合成抑制剂。
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norepinephrine (NE) transporter 抑制剂
Atomoxetine HCl是SLC6A2的一种竞争性特异性抑制剂,同时在大鼠下丘脑突触体中显示出微弱的ST和DAT抑制作用。
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Histamine H1 receptor 抑制剂
Antazoline HCl是第一代抗组胺药,可与组胺H1受体结合并阻断内源性组胺的作用。
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dopamine re-uptake 抑制剂
Vanoxerine 2HCl (GBR-12909)是哌嗪衍生物,是一种有效的、选择性的多巴胺摄取(dopamine uptake)抑制剂。
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DAT and SLC6A2 抑制剂
GBR-12935 dihydrochloride是一种有效的选择性多巴胺再摄取抑制剂。
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COX 抑制剂/histamine H1 receptor 激动剂
Fexofenadine Hydrochloride是一种抗组胺药,可抑制Cox-1,Cox-2,并且是组胺H1受体激动剂,IC50为246 nM。
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dopamine uptake 抑制剂
GBR 12783 dihydrochloride是一种非常有效的选择性多巴胺摄取抑制剂(抑制大鼠纹状体突触体中[3H]-多巴胺摄取的IC50为1.8 nM)。
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S1P inhibitor
PF429242 dihydrochloride is a reversible and competitive S1P inhibitor with an IC50 of 175 nM.
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α-adrenergic (AR) 拮抗剂/CaM 抑制剂
Phenoxybenzamine hydrochloride是一种细胞可渗透的,非特异性的,不可逆的α-肾上腺素(AR)拮抗剂,也可作为CaM抑制剂。
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SNR 抑制剂
Sibutramine hydrochloride是5-HT和去甲肾上腺素再摄取抑制剂(SNRI)。
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noradrenalin re-uptake 抑制剂
Maprotiline hydrochloride是选择性去甲肾上腺素再摄取抑制剂。
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SphK2 抑制剂
K145 hydrochloride是选择性鞘氨醇激酶2(SphK2)抑制剂和抗癌剂。
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Adenosine deaminase inhibitor
EHNA hydrochloride is a specific inhibitor of adenosine deaminase, prevents dAdo degradation and increases mitochondrial dATP levels in fibroblasts.
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dopamine transporter/norepinephrine transportertransporters inhibitor
Radafaxine hydrochloride (GW-353162A) is a DAT (dopamine transporter) and NET(norepinephrine transporter) transporters inhibitor, and nAChR family modulator.
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D2DR inhibitor
Promazine Hydrochloride is a phenothiazine compound and D2DR inhibitor. Promazine Hydrochloride has been employed in studies investigating dopamine-stimulated glycosylation of brain proteins in vitro. It has actions similar to chlorpromazine but with less antipsychotic activity.
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