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Search Results for " serotonin uptake "

35

抑制剂 & 化合物

8

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T8702	SKF-83566	Dopamine Receptor; 5-HT Receptor; AChR	GPCR/G Protein; Neuroscience
	SKF-83566 是一种具有血脑渗透性和口服活性的 D1 样多巴胺受体拮抗剂和一种较弱的竞争性 5-HT2 受体拮抗剂，Ki 为 11 nM。它是竞争性多巴胺转运蛋白抑制剂，可用于研究帕金森氏症和对尼古丁渴望的缓解的相关研究。
T0031L	Ziprasidone hydrochloride 盐酸齐拉西酮,齐拉西酮盐酸盐,CP-88059 hydrochloride,CP-88059,Ziprasidone HCl	Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Norepinephrine; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Ziprasidone hydrochloride (CP-88059 hydrochloride) 是一种联合 5-HT（5-羟色胺）和多巴胺受体拮抗剂，具有抗精神病活性的强效作用。它也是去甲肾上腺素再摄取抑制剂。
T7341	Diclofensine Ro 8-4650,(+/-)-双氮奋兴	Dopamine Receptor; Monoamine Transporter	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Diclofensine (Ro 8-4650) 是一种高效单胺再摄取抑制剂，在大鼠脑突触体中能够阻断多巴胺 (IC50=0.74 nM)、去甲肾上腺素 (IC50=2.3 nM) 和 5-羟色胺 (IC50=3.7 nM)。
T1636	Paroxetine hydrochloride Paroxetine HCl,BRL29060 hydrochloride,FG-7051,BRL29060A,盐酸帕罗西汀	5-HT Receptor; Serotonin Transporter; GRK; AChR; Autophagy	Autophagy; GPCR/G Protein; Neuroscience
	Paroxetine hydrochloride (Paroxetine HCl) 是一种血清素摄取抑制剂，能抑制 GRK2 活性，IC50值为 14 μM。它可研究抑郁症。
T8708	Paroxetine	Serotonin Transporter	Neuroscience
	Paroxetine 是选择性血清素再摄取抑制剂，是苯基哌啶的衍生物。它对于甲肾上腺素摄取抑制功能较弱，但比该位点其他SSRIs 更有效。
T0450	Fluoxetine 氟西汀,LY-110140	5-HT Receptor; Serotonin Transporter; MRP; Autophagy	Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Fluoxetine (LY-110140) 是一种高度特异性的血清素摄取抑制剂，是选择性 5-羟色胺 (5-HT) 再吸收抑制剂。Fluoxetine 具有抗抑郁活性。
T0482	Sertraline hydrochloride Sertraline HCl,CP-51974-1 HCl,盐酸舍曲林	5-HT Receptor; Serotonin Transporter	GPCR/G Protein; Neuroscience
	Sertraline hydrochloride (Sertraline HCl) 是选择性 5- 羟色胺再吸收抑制剂类的抗抑郁剂，可用于多种疾病的研究，如重度抑郁症和强迫症。
T0255	Clomipramine hydrochloride Clomipramine HCl,Anafranil,盐酸氯米帕明	Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Norepinephrine; GST	GPCR/G Protein; Neuroscience; oxidation-reduction
	Clomipramine hydrochloride (Anafranil) 是一种5-羟色胺转运体(Ki:0.14 nM)、去甲肾上腺素转运体(Ki:54 nM)和多巴胺转运体(Ki:3 nM)阻断剂。
T1471	Duloxetine hydrochloride Duloxetine HCl,盐酸度洛西汀,LY-248686 hydrochloride,(S)-Duloxetine hydrochloride,LY-248686 HCl	Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Norepinephrine	GPCR/G Protein; Neuroscience
	Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) 是一种 5-羟色胺-去甲肾上腺素重吸收 (serotonin-norepinephrine reuptake) 抑制剂 (SNRI)，Ki=4.6 nM，可用于广泛性焦虑症的研究。
T1619	Trazodone hydrochloride KB-831,盐酸曲唑酮,Trazodone HCl,AF-1161	5-HT Receptor; Adrenergic Receptor; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Trazodone hydrochloride (Trazodone HCl) 是5 羟色胺受体拮抗剂和重吸收抑制剂，用作抗抑郁药，可治疗失眠和焦虑。
T0450L	Fluoxetine hydrochloride Fluoxetine HCl,盐酸氟西汀,LY-110140,Lilly110140	5-HT Receptor; Serotonin Transporter; Autophagy	Autophagy; GPCR/G Protein; Neuroscience
	Fluoxetine hydrochloride (Lilly110140) 是一种高度特异性血清素摄取抑制剂。它被用作抗抑郁药，并且通常比传统的抗抑郁药具有更可接受的副作用特征。
T21013	Clomipramine Chlorimipramine,Anafranil,Clomicalm,Anafranil (free base),Clomipramina,氯米帕明	5-HT Receptor	GPCR/G Protein; Neuroscience
	Clomipramine (Clomicalm) 是一种三环类抗抑郁药，能够有效阻断 5-HT 再摄取 (IC50:1.5 nM) ，可用于研究强迫症 (OCD) 及抑郁症。
T1568	Amoxapine 阿莫沙平,CL-67772	GlyT	Neuroscience
	Amoxapine (CL-67772) 是一种dibenzoxazepine 家族的四环抗抑郁药，常被归类为仲胺三环类抗抑郁药。
T0991	Desipramine hydrochloride NSC-114901,Desmethylimipramine,盐酸去甲咪嗪,JB-8181,EX-4355,Norimipramine,G-35020	Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Desipramine hydrochloride (Norimipramine) 是一种二苯并氮杂类衍生物三环类抗抑郁药，可作为选择性去甲肾上腺素再摄取抑制剂。它还显示出较弱的 5-羟色胺再摄取抑制、α1 阻断、抗组胺和抗胆碱能作用。
T41194	FFN 102 mesylate	Others	Others
	FFN 102 mesylate 是pH 响应型荧光假神经递质(FFN)，作为选择性多巴胺转运蛋白(DAT)和VMAT2底物。FFN 102 mesylate 与38个中枢神经系统受体(包括多巴胺和血清素受体)无明显结合。它的Ex-max在pH 值5时为340 nm，在pH 值7.5时为370 nm，在pH 值为5和7.5时，Em-max为435 nm。
Fr13587	7-Chloro-4-(piperazin-1-yl)quinoline
	7-Chloro-4-(piperazin-1-yl)quinolone 结构是药物化学中的重要支架，它单独或与其他活性药效团混合显示出多种药理特性。7-Chloro-4-（piperazin-1-yl）quinolone 是有效的sirtuin 抑制剂，并且抑制 5-羟色胺的摄取，IC50值为 50 μM。7-Chloro-4-(piperazin-1-yl)quinolone 对恶性疟原虫 D10 和 K1 菌株表现出抗疟疾活性，IC50分别为 1.18 μM 和 0.97 μM。
T68949	Chlorocitalopram hydrobromide
	Chlorocitalopram hydrobromide is an internal standard of Citalopram -- an inhibitor of serotonin (5-HT) uptake.
T71463	MCN-5652W68 perchlorate
	MCN-5652W68 perchlorate is a serotonin uptake inhibitor.
T68210	MCN-5652 perchlorate
	MCN-5652 perchlorate is a serotonin uptake inhibitor.
T27156	Dexnafenodone Hydrochloride LU43706,LU 43706,Dexnafenodone HCl,LU-43706
	Dexnafenodone Hydrochloride is an adrenergic receptor antagonist and serotonin uptake inhibitor.
T25248	Cianopramine Ro 112465,Ro-112465,Ro112465
	Cianopramine is a tricyclic antidepressant and a potent neuronal serotonin (5-HT) uptake inhibitor in animals.
T26765	Beloxepin ORG-4428,ADL6906,ADL-6906,ORG4428,ORG 4428,ADL 6906
	Beloxepin is an oral dual selective inhibitor of serotonin and norepinephrine uptake.
T27589	Ifoxetine sulfate CGP-15210G,CGP15210G,CGP 15210G
	Ifoxetine sulfate, a 5-HT uptake inhibitor with atypical effects on serotonin uptake, may exhibit a therapeutic and/or side-effect profile which differs from that of classical 5-HT uptake inhibitors.
T70261	Amitriptyline Embonate
	Amitriptyline Embonate is an inhibitor of the re-uptake of norepinephrine and serotonin, thereby inhibiting N-methyl-D-aspartate (NMDA) receptors.
T26184	Seproxetine HCl (S)-Norfluoxetine hydrochloride,Seproxetine hydrochloride,(S)-Desmethylfluoxetine Hydrochloride
	Seproxetine HCl, a more active enantiomer of N-desmethyl metabolite fluoxetine, works by selectively inhibiting the serotonin uptake carrier.
T29216	Zimelidine A23140,A 23140,A-23140
	Zimelidine is a serotonin uptake inhibitor formerly used for depression, but was withdrawn worldwide because of the risk of Gullain-Barre syndrome associated with its use.
T69002	Zimeldine hydrochloride hydrate
	Zimeldine hydrochloride hydrate is a serotonin uptake inhibitor that was formerly used for depression but was withdrawn worldwide in September 1983 because of the risk of Guillain-Barre Syndrome associated with its use.
T69943	Citalopram oxalate
	Citalopram oxalate is a furancarbonitrile that is one of the SEROTONIN UPTAKE INHIBITORS used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patients who also suffer from tardive dyskinesia in preference to tricyclic antidepressants, which aggravate this condition.
T37212	5-hydroxy-Nω-methyl Tryptamine (oxalate)
	5-hydroxy-Nω-methyl Tryptamine is a metabolite of serotonin in humans that has also been found in plants. It is an agonist of the 5-HT receptor subtype 5-HT7 (IC50 = 23 pM in a radioligand binding assay). 5-hydroxy-Nω-methyl Tryptamine increases intracellular cyclic AMP production in HEK293 cells expressing 5-HT7 (EC50 = 22 nM). It inhibits serotonin uptake in HEK293 cells expressing human serotonin transporters (IC50 = 490 nM). Elevated levels of urinary 5-hydroxy-Nω-methyl tryptamine have been...
T27689	JNJ-7925476 HCl JNJ-7925476,JNJ7925476,JNJ 7925476
	JNJ-7925476 HCl is a triple monoamine uptake inhibitor. JNJ-7925476 Salt blocks the dopamine transporter (DAT), norepinephrine transporter (NET) and serotonin transporter (SERT) in the central nervous system. The ED(50) values for JNJ-7925476 occupancy of
T35920	N-methyl Paroxetine
	N-methyl Paroxetine is a derivative of the selective serotonin reuptake inhibitor (SSRI) antidepressant paroxetine that inhibits [3H]paroxetine binding to rat cortical membranes (Ki = 4.3 nM). It inhibits serotonin uptake in rat brain synaptosomes with an IC50 value of 22 nM. N-methyl Paroxetine has been used as a precursor in the synthesis of paroxetine and is a potential impurity in commercial preparations of paroxetine.
T0204	Protriptyline hydrochloride 盐酸普罗替林,Protriptyline HCl	5-HT Receptor; AChE	GPCR/G Protein; Neuroscience
	Protriptyline hydrochloride (Protriptyline HCl) 是一种含有一个仲胺的三环结构抗抑郁试剂，可以用于抑郁和 ADHD 的相关研究。它使动物精力充沛起激励作用，并且有时用于嗜睡症的相关研究。
T28349	PD-89211 PD89211
	PD 89211 is a selective dopamine D4 receptor antagonist with high selectivity for the DA D4.2 receptor (> 800-fold) as compared to other hDA receptor subtypes, rat brain serotonin, and adrenergic receptors. In vitro, PD 89211 reverses quinpirole-induced [
T71302	Norfluoxetine-d5 HCl
	Norfluoxetine-d5 is intended for use as an internal standard for the quantification of norfluoxetine by GC- or LC-MS. Norfluoxetine is an active metabolite of the antidepressant fluoxetine. It is formed from fluoxetine by the cytochrome P450 (CYP) isoforms CYP2C9, CYP2C19, and CYP3A. Norfluoxetine inhibits serotonin (5-HT) uptake in rat brain synaptosomal membrane preparations (Ki = 44.7 nM) and isolated human platelets (IC50 = ~15 nM). It has been found in the tissues of fish exposed to wastewa...
T78126	Dothiepin Dosulepin,Dothep	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Dothiepin（Dosulepin; Dothep）是一种具备镇静/抗焦虑作用的抗抑郁药物。该化合物主要通过抑制去甲肾上腺素的再摄取，而非血清素，以增强去肾上腺素能神经传递。同时，Dothiepin作为组胺H1受体的拮抗剂，具备显著的镇痛活性，适用于治疗心因性面部疼痛、特发性纤维肌痛综合征或类风湿关节炎，并且不具有心脏毒性。

化合物

Cat.No: T8702

Target: Dopamine Receptor, 5-HT Receptor, AChR

Ziprasidone hydrochloride

Cat.No: T0031L

Synonym: 盐酸齐拉西酮,齐拉西酮盐酸盐,CP-88059 hydrochloride,CP-88059,Ziprasidone HCl

Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor, Norepinephrine, Histamine Receptor

Cat.No: T7341

Synonym: Ro 8-4650,(+/-)-双氮奋兴

Target: Dopamine Receptor, Monoamine Transporter

Paroxetine hydrochloride

Cat.No: T1636

Synonym: Paroxetine HCl,BRL29060 hydrochloride,FG-7051,BRL29060A,盐酸帕罗西汀

Target: 5-HT Receptor, Serotonin Transporter, GRK, AChR, Autophagy

Cat.No: T8708

Target: Serotonin Transporter

Cat.No: T0450

Synonym: 氟西汀,LY-110140

Target: 5-HT Receptor, Serotonin Transporter, MRP, Autophagy

Sertraline hydrochloride

Cat.No: T0482

Synonym: Sertraline HCl,CP-51974-1 HCl,盐酸舍曲林

Target: 5-HT Receptor, Serotonin Transporter

Clomipramine hydrochloride

Cat.No: T0255

Synonym: Clomipramine HCl,Anafranil,盐酸氯米帕明

Target: Dopamine Receptor, 5-HT Receptor, Serotonin Transporter, Norepinephrine, GST

Duloxetine hydrochloride

Cat.No: T1471

Synonym: Duloxetine HCl,盐酸度洛西汀,LY-248686 hydrochloride,(S)-Duloxetine hydrochloride,LY-248686 HCl

Target: Dopamine Receptor, 5-HT Receptor, Serotonin Transporter, Norepinephrine

Trazodone hydrochloride

Cat.No: T1619

Synonym: KB-831,盐酸曲唑酮,Trazodone HCl,AF-1161

Target: 5-HT Receptor, Adrenergic Receptor, Histamine Receptor

Fluoxetine hydrochloride

Cat.No: T0450L

Synonym: Fluoxetine HCl,盐酸氟西汀,LY-110140,Lilly110140

Target: 5-HT Receptor, Serotonin Transporter, Autophagy

Cat.No: T21013

Synonym: Chlorimipramine,Anafranil,Clomicalm,Anafranil (free base),Clomipramina,氯米帕明

Target: 5-HT Receptor

Cat.No: T1568

Synonym: 阿莫沙平,CL-67772

Target: GlyT

Desipramine hydrochloride

Cat.No: T0991

Synonym: NSC-114901,Desmethylimipramine,盐酸去甲咪嗪,JB-8181,EX-4355,Norimipramine,G-35020

Target: Dopamine Receptor, 5-HT Receptor, Serotonin Transporter, Adrenergic Receptor

FFN 102 mesylate

Cat.No: T41194

Target: Others

7-Chloro-4-(piperazin-1-yl)quinoline

Cat.No: Fr13587

Chlorocitalopram hydrobromide

Cat.No: T68949

MCN-5652W68 perchlorate

Cat.No: T71463

MCN-5652 perchlorate

Cat.No: T68210

Dexnafenodone Hydrochloride

Cat.No: T27156

Synonym: LU43706,LU 43706,Dexnafenodone HCl,LU-43706

Cat.No: T25248

Synonym: Ro 112465,Ro-112465,Ro112465

Cat.No: T26765

Synonym: ORG-4428,ADL6906,ADL-6906,ORG4428,ORG 4428,ADL 6906

Ifoxetine sulfate

Cat.No: T27589

Synonym: CGP-15210G,CGP15210G,CGP 15210G

Amitriptyline Embonate

Cat.No: T70261

Seproxetine HCl

Cat.No: T26184

Synonym: (S)-Norfluoxetine hydrochloride,Seproxetine hydrochloride,(S)-Desmethylfluoxetine Hydrochloride

Cat.No: T29216

Synonym: A23140,A 23140,A-23140

Zimeldine hydrochloride hydrate

Cat.No: T69002

Citalopram oxalate

Cat.No: T69943

5-hydroxy-Nω-methyl Tryptamine (oxalate)

Cat.No: T37212

JNJ-7925476 HCl

Cat.No: T27689

Synonym: JNJ-7925476,JNJ7925476,JNJ 7925476

N-methyl Paroxetine

Cat.No: T35920

Protriptyline hydrochloride

Cat.No: T0204

Synonym: 盐酸普罗替林,Protriptyline HCl

Target: 5-HT Receptor, AChE

Cat.No: T28349

Synonym: PD89211

Norfluoxetine-d5 HCl

Cat.No: T71302

Cat.No: T78126

Synonym: Dosulepin,Dothep

Target: Histamine Receptor

Cat. No.	Product Name	Target	Signaling Pathways
T19931	Gentisein NSC 329491,NSC329491,NSC-329491	Serotonin Transporter	Neuroscience
	Gentisein (NSC-329491) 是 Mangiferin 的主要代谢物，有效抑制 5-HT 的摄取，IC50为 4.7 µM。
T0185	Escitalopram Seroplex,依他普仑,S-(+)-Citalopram,艾司西酞普兰,(S)-Citalopram	Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Adrenergic Receptor; AChR; Norepinephrine; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Escitalopram (Seroplex) 是一种外消旋 Citalopram 的 S-对映体，是一种选择性 5-羟色胺再摄取抑制剂，Ki=0.89 nM，比 R(-)-enantiomer 结合亲和力高 30 倍。它对多巴胺转运体和去甲肾上腺素转运体均有选择性，是一种研究抑郁症的抗抑郁药。
T1045	Trimipramine maleate Surmontil maleate,马来酸三甲丙咪嗪,三甲丙咪嗪马来酸盐	Dopamine Receptor; 5-HT Receptor; Antibacterial; Adrenergic Receptor; Norepinephrine; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience
	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。
TN1740	Homoeriodictyol 高胜草酚,高圣草酚	5-HT Receptor; transporter; Sodium Channel; Drug Metabolite	GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Homoeriodictyol 是 Eriocitrin 的代谢物，属于黄酮类。Eriocitrin 是强效抗氧化剂。
T0791	Reserpine 利血平,Serpalan,Serpasil,Serpivite	Others; Potassium Channel; MRP; Monoamine Transporter; Autophagy	Autophagy; Immunology/Inflammation; Membrane transporter/Ion channel; Others
	Reserpine (Serpalan) 是一种从催吐萝芙木的根中发现的生物碱。它抑制去甲肾上腺素吸收到储存囊泡中，导致中枢和外周轴突末端的儿茶酚胺和血清素耗尽。它可作为抗高血压药和抗精神病药以及研究工具。
T1311	4-aminobenzoic acid PABA,Vitamin H1,Vitamin Bx,para-Aminobenzoic acid,对氨基苯甲酸	Endogenous Metabolite	Metabolism
	4-aminobenzoic acid (para-Aminobenzoic acid) 是一种具有紫外线吸收和抗纤维化特性的有机酸。当暴露在光线下时，4-aminobenzoic acid 吸收紫外线并通过光化学反应释放多余的能量，这可能会对DNA造成损害。4-aminobenzoic acid 还可以增加组织水平的摄氧量，并可能增强单胺氧化酶(MAO)活性以促进血清素的降解，过量可能导致纤维化变化。
T21772	Reserpine hydrochloride
	Reserpine hydrochloride 是一种从催吐萝芙木的根中发现的生物碱。它抑制去甲肾上腺素吸收到储存囊泡中，导致中枢和外周轴突末端的儿茶酚胺和血清素耗尽。它可作为抗高血压药和抗精神病药以及研究工具。
T75436	Jatrorrhizine hydroxide
	Jatrorrhizine hydroxide, 一种从黄连中提取的生物碱，展现了神经保护、抗菌、抗疟原虫及抗氧化的活性。作为一种高效的乙酰胆碱酯酶(AChE)抑制剂(IC50=872 nM)，其对BuChE的选择性高达115倍。此外，Jatrorrhizine hydroxide还能通过抑制uptake-2 transporter活性来减少血清素(5-HT)和去甲肾上腺素(NE)的摄取，表现出口服活性。

天然产物

Cat.No: T19931

Synonym: NSC 329491,NSC329491,NSC-329491

Target: Serotonin Transporter

Cat.No: T0185

Synonym: Seroplex,依他普仑,S-(+)-Citalopram,艾司西酞普兰,(S)-Citalopram

Target: Dopamine Receptor, 5-HT Receptor, Serotonin Transporter, Adrenergic Receptor, AChR, Norepinephrine, Histamine Receptor

Trimipramine maleate

Cat.No: T1045

Synonym: Surmontil maleate,马来酸三甲丙咪嗪,三甲丙咪嗪马来酸盐

Target: Dopamine Receptor, 5-HT Receptor, Antibacterial, Adrenergic Receptor, Norepinephrine, Histamine Receptor

Homoeriodictyol

Cat.No: TN1740

Synonym: 高胜草酚,高圣草酚

Target: 5-HT Receptor, transporter, Sodium Channel, Drug Metabolite

Cat.No: T0791

Synonym: 利血平,Serpalan,Serpasil,Serpivite

Target: Others, Potassium Channel, MRP, Monoamine Transporter, Autophagy

4-aminobenzoic acid

Cat.No: T1311

Synonym: PABA,Vitamin H1,Vitamin Bx,para-Aminobenzoic acid,对氨基苯甲酸

Target: Endogenous Metabolite

Reserpine hydrochloride

Cat.No: T21772

Jatrorrhizine hydroxide

Cat.No: T75436

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