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Search Results for " noradrenergic "

20

抑制剂 & 化合物

1

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T13664	DSP-4 hydrochloride Neurotoxin DSP 4 (hydrochloride)	Others	Others
	DSP-4 hydrochloride (Neurotoxin DSP 4 (hydrochloride)) 是一种高选择性的神经毒素，主要是来自蓝斑 (LC) 的神经元，容易通过血脑屏障。它对成年和发育中大鼠去甲肾上腺素能神经元具有神经毒性作用，可用于中枢和外周去甲肾上腺素能神经元的暂时选择性降解。
T2150	Guanfacine hydrochloride 盐酸胍法辛,Tenex,Intuniv,Guanfacine	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Guanfacine hydrochloride (Intuniv) 是一种 α2A 肾上腺素受体激动剂，Kd=31 nM，具有抗高血压作用。
T0137	Mirtazapine 米氮平,6-Azamianserin,Org3770	Dopamine Receptor; 5-HT Receptor; Opioid Receptor; Adrenergic Receptor; Histamine Receptor	Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Mirtazapine (6-Azamianserin) 是一种有效的具有口服活性的去甲肾上腺素能和特异性血清素能抗抑郁剂 (NaSSA)。它也是一种5-HT2、5-HT3、组胺 H1 受体和 α2-肾上腺素受体拮抗剂，pKi 值分别为 8.05、8.1、9.3 和 6.95。
T60325	Viloxazine Emovit,Viloxazin	5-HT Receptor; Norepinephrine	GPCR/G Protein; Neuroscience
	Viloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2B receptors, with respective potency values of EC 50 = 32 μM and IC 50 = 27 μM. Its primary mechanism of action involves the modulation of serotonergic and noradrenergic pathways. Viloxazine is commonly employed in depression research [1] [2].
T7065	Tizanidine	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Tizanidine 是一种 α2-肾上腺素受体激动剂，能够抑制神经递质从CNS 去甲肾上腺素激活的神经元中释放。
T0290	Tizanidine hydrochloride 盐酸替扎尼定,Tizanidine HCl,DS 103-282	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Tizanidine hydrochloride (Tizanidine HCl) 是一种 α2-肾上腺素受体激动剂，可抑制神经递质从 CNS 去甲肾上腺素激活的神经元中释放。
T31582	DSP 4 DSP4,UNII-PQ1P7JP5C1,DSP-4,az-Dsp 4
	DSP 4 is a selective neurotoxin selective for noradrenergic neurons in the locus coeruleus noradrenergic system and capable of crossing the blood–brain barrier and cyclizes to a reactive aziridinium derivative that is accumulated into the noradrenergic ne
TP2058	Catestatin
	Non-competitive nicotinic cholinergic antagonist; selectively inhibits nicotinic-stimulated catecholamine secretion from chromaffin cells and noradrenergic neurons (IC50 ~ 200 nM). Blocks nicotinic-induced cationic signaling (IC50 ~ 200 - 250 nM) and inhi
T27523	H77-77 H77/77
	H77-77, a monoamine oxidase (MAO) inhibitor, produces a pronounced protection against phenelzine within the serotonergic and noradrenergic neurons in rats.
T26759	BE 2254 BE-2254,BE2254
	BE 2254 is an antagonist of central noradrenergic receptor.
T37391	PSEM 308 hydrochloride
	PSAM (pharmacologically selective actuator module) agonist. Activates PSAML141F-GlyR chimeric ion channels. Inhibits activity of neurons expressing PSAML141F-GlyR in vivo and activates locus coeruleus noradrenergic neurons expressing PSAML141F,Y115F-5-HT3 ion channels. Recommended concentration for use in mice is 5 mg/kg or lower. Plasmid vectors for the transfection of cells with PSAML141F-GlyR and PSAML141F,Y115F-5-HT3 are available from Addgene. Lovett-Barron et al (2012) Regulation of neu...
T1769	Pardoprunox 帕多芦诺,SLV-308,DU-126891	Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Pardoprunox (SLV-308) 是多巴胺受体D2、D3部分激动剂和5-HT1A 激动剂，pEC50分别为 8、9.2 和 6.3。
T41193	FFN 270
	FFN 270 is a fluorescent false neurotransmitter (FFN). Fluorescent substrate for NET and VMAT2. Labels noradrenergic neurons and their synaptic vesicles, and enables imaging of synaptic vesicle content release from specific axonal sitesin vivo. Selectively labels NA neurons over other monoamine and CNS targets. Exhibits two resolved absorption/excitation maxima depending on solvent pH (excitation maxima: 320 nm or 365 nm, emission maxima: 475 nm).
T40869	Moxonidine hydrochloride BDF5895hydrochloride,盐酸莫索尼定
	Moxonidine Hydrochloride is a selective agonist at the imidazoline receptor subtype 1, used as antihypertensive agent. Target: I1-R Moxonidine Hydrochloride is a centrally acting antihypertensive agent. Mixed Nischarin (I1 imidazoline receptor) and α2-AR (adrenergic) agonist; displays 40-fold higher affinity for I1 receptors versus α2-adrenoceptors. Moxonidine reduced stimulated NE overflow (log EC50: -6.15 +/- 0.14). AGN192403, a selective ligand at I1-R, had no influence on the dose-response...
T16393	ONO-2952	Others	Others
	ONO-2952 is more selective for TSPO than other receptors, transporters, ion channels, and enzymes. ONO-2952 is a potent and selective translocator protein 18 kDa (TSPO) antagonist (Ki: 0.33-9.30 nM for rat and human TSPO). ONO-2952 has the potential for i
T15455	RGH-5526 GYKI-11679	Others	Others
	RGH-5526是一种新型的抗高血压药。它引起下丘脑去甲肾上腺素（NA）周转（利用）增加，下丘脑去甲肾上腺素能神经元活性的增加可能导致外周交感神经活性的降低，从而显著降低血压。
T75898	CART(62-76)(human,rat) TFA
	CART(62-76)(human,rat) TFA 是一种类似神经递质的神经肽，由CART肽的62至76残基组成。该化合物能够调控纹状体去甲肾上腺素能、皮质纹状体及下丘脑在5-羟色胺能(5-HT)系统中的活性。
T71356	Lanperisone HCl
	Lanperisone, also known as NK433, is a muscle relaxant. NK433 inhibited the facilitation of the flexor reflex mediated by group II afferent fibers that was induced by intrathecal administration of noradrenaline-HCl. NK433 had effects more than three times stronger and tending to be longer-lasting than those of eperisone-HCl. These results suggest that NK433 exerts a non-selective inhibition on spinal reflexes and that inhibition of the descending noradrenergic tonic facilitation within the spina...
T28495	R-84760 hydrochloride R84760,R 84760,R 86436,R-86436,R86436
	R-84760 is a κ-opioid receptor agonist. R-84760 produces an extremely potent antinociceptive effect against tonic pain through the kappa-opioid receptors; the sites of action of subcutaneously administered R-84760 are the supraspinal and spinal loci in th
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

DSP-4 hydrochloride

Cat.No: T13664

Synonym: Neurotoxin DSP 4 (hydrochloride)

Target: Others

Guanfacine hydrochloride

Cat.No: T2150

Synonym: 盐酸胍法辛,Tenex,Intuniv,Guanfacine

Target: Adrenergic Receptor

Cat.No: T0137

Synonym: 米氮平,6-Azamianserin,Org3770

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

Cat.No: T60325

Synonym: Emovit,Viloxazin

Target: 5-HT Receptor, Norepinephrine

Cat.No: T7065

Target: Adrenergic Receptor

Tizanidine hydrochloride

Cat.No: T0290

Synonym: 盐酸替扎尼定,Tizanidine HCl,DS 103-282

Target: Adrenergic Receptor

Cat.No: T31582

Synonym: DSP4,UNII-PQ1P7JP5C1,DSP-4,az-Dsp 4

Cat.No: TP2058

Cat.No: T27523

Synonym: H77/77

Cat.No: T26759

Synonym: BE-2254,BE2254

PSEM 308 hydrochloride

Cat.No: T37391

Cat.No: T1769

Synonym: 帕多芦诺,SLV-308,DU-126891

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

Cat.No: T41193

Moxonidine hydrochloride

Cat.No: T40869

Synonym: BDF5895hydrochloride,盐酸莫索尼定

Cat.No: T16393

Target: Others

Cat.No: T15455

Synonym: GYKI-11679

Target: Others

CART(62-76)(human,rat) TFA

Cat.No: T75898

Lanperisone HCl

Cat.No: T71356

R-84760 hydrochloride

Cat.No: T28495

Synonym: R84760,R 84760,R 86436,R-86436,R86436

Cat.No: T78126

Synonym: Dosulepin,Dothep

Target: Histamine Receptor

Cat. No.	Product Name	Target	Signaling Pathways
T4S1990	Carvacrol 香荆芥酚,Karvakrol,O-Thymol,cymophenol,香芹酚	Apoptosis; Others; Gamma-secretase; Endogenous Metabolite; Antifungal	Apoptosis; Metabolism; Microbiology/Virology; Neuroscience; Others; Proteases/Proteasome; Stem Cells
	Carvacrol (O-Thymol) 是唇形科植物中的一种单萜酚类天然产物，具有镇痛、抗焦虑、抗抑郁、抗氧化、抗炎和抗癌作用。

天然产物

Cat.No: T4S1990

Synonym: 香荆芥酚,Karvakrol,O-Thymol,cymophenol,香芹酚

Target: Apoptosis, Others, Gamma-secretase, Endogenous Metabolite, Antifungal

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