目录号 | 产品详情 | 靶点 | |
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T24661 | |||
Pridefine is an antidepressant drug. It acts as a balanced reuptake inhibitor of serotonin, dopamine, and norepinephrine. It also has some weak releasing activity. | |||
T19893 | Others | ||
Thozalinone 是一种精神兴奋剂,可诱导去甲肾上腺素和多巴胺的释放。 | |||
T28380 | Dopamine Receptor 5-HT Receptor | ||
PF-184298 是一种血清素和去甲肾上腺素单胺再摄取抑制剂(SNRI),抑制多巴胺再摄取。 | |||
T10758L | Dopamine Receptor Serotonin Transporter Adrenergic Receptor Norepinephrine | ||
Centanafadine hydrochloride (EB-1020 hydrochloride) 是一种去甲肾上腺素(NE)/多巴胺(DA)转运的双抑制剂,还能抑制5-羟色胺(serotonin)转运体。它对人 NE,DA 和5-羟色胺转运体的 IC50值分别为6 nM,38 nM 和 83 nM。 | |||
T34795 | Dopamine Receptor Serotonin Transporter | ||
Tedatioxetine (Lu AA24530) 是一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂(SNDRI),具有抗抑郁作用。Tedatioxetine 可作为 CYP2D6 底物。 | |||
T33711L | Dopamine Receptor Norepinephrine | ||
Nolomirole HCl(CHF 1035) 是一种具有口服活性的新型选择性多巴胺激动剂,对去甲肾上腺素的释放有抑制作用,可用于研究轻度慢性心力衰竭。 | |||
T1045 | Dopamine Receptor 5-HT Receptor Antibacterial Adrenergic Receptor Norepinephrine Histamine Receptor | ||
Trimipramine maleate (Surmontil maleate) 是一种 5-HT 受体拮抗剂,对 5-HT1C、5-HT2和 5-HT1A 受体的 pKi 值分别为 6.39、8.10和 4.66。 | |||
T7940 | Serotonin Transporter | ||
Milnacipran (1S-cis) hydrochloride (Levomilnacipran Hydrochloride) 是 5-羟色胺去甲肾上腺素再摄取抑制剂,用于研究纤维肌痛。 | |||
T7308 | Dopamine Receptor | ||
Nomifensine ((±)-Nomifensin) 是一种去甲肾上腺素-多巴胺再摄取抑制剂,可防止多巴胺再摄取进入突触体。 | |||
T0689 | Endogenous Metabolite Monocarboxylate transporter | ||
D-Phenylalanine 是一种苯丙氨酸的合成右旋异构体,可抑制Pseudoalteromonas sp.SC2014 的生物膜发育。 |
目录号 | 产品名/同用名 | 种属 | 表达系统 | ||
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TMPY-03852 | Dopamine beta-Hydroxylase Protein, Human, Recombinant (His) | Human | HEK293 | ||
DBH is a 29 kDa copper-containing oxygenase. It can be detected in noradrenergic nerve terminals of the central and peripheral nervous systems, and is also expressed in chromaffin cells of the adrenal medulla. DBH contains our identical subunits, and its activity requires ascorbate as a cofactor. It functions in in the synthesis of small-molecule neurotransmitters that is membrane-bound, making norepinephrine the only transmitter synthesized inside vesicles. DBH has been shown to be associated with decision making and addictive behaviors such as alcohol and smoking, attention deficit hyperactivity disorder, and also with neurological diseases such as Schizophrenia and Alzheimer's.
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TMPY-02948 | SULT1A3 Protein, Human, Recombinant (His) | Human | E. coli | ||
SULT1A3 belongs to the sulfotransferase 1 family. Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. They are different in their tissue distributions and substrate specificities while their gene structure (number and length of exons) is similar. SULT1A3 gene encodes a phenol sulfotransferase with thermolabile enzyme activity. Four sulfotransferase genes are located on the p arm of chromosome 16; this gene and SULT1A4 arose from a segmental duplication. It is the most centromeric of the four sulfotransferase genes. Exons of this gene overlap with exons of a gene that encodes a protein containing GIY-YIG domains (GIYD1). SULT1A3 is expressed in liver, colon, kidney, lung, brain, spleen, small intestine, placenta and leukocyte. SULT1A3 is a sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of phenolic monoamines (neurotransmitters such as dopamine, norepinephrine and serotonin) and phenolic and catechol drugs.
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