catecholamine

Dopamine hydrochloride (ASL279) 是在脑黑质、脑腹侧被盖区和下丘脑中产生的一种天然儿茶酚胺，由二羟基苯丙氨酸脱羧形成，是去甲肾上腺素和肾上腺素的前体。它通过 D2 多巴胺受体来诱导 VEGFR2 的内吞作用，有促进血管生成活性。

Metyrosine (α-Methyltyrosine) 是一种选择性酪氨酸羟化酶抑制剂，可显著抑制高 COX-2 活性和有效控制血压，具有抗炎和抗溃疡作用。

napitane（A 75200）是一种新型儿茶酚胺摄取抑制剂，对α-肾上腺素能受体具有抑制作用且具有潜在的抗抑郁活性，可用于研究抑郁症。

Racemetirosine 是一种酪氨酸 3-单加氧酶抑制剂，因此会抑制儿茶酚胺的合成。

Felypressin (Octapressin) 是一种加压素 1 激动剂，也是血管收缩剂，可用于牙科手术中。

Felypressin acetate (PLV-2) 是加压素 1 的激动剂，作用于所有精氨酸加压素受体 1AS。 Felypressin acetate 可用于牙科手术。

GP2-114 是一种儿茶酚胺运动模拟剂 ，在通过透皮离子电渗疗法给药时均产生电流依赖性心血管作用，可用于研究冠状动脉疾病 （CAD）。

9-Hydroxyellipticine hydrochloride 是 Topo II 和 RyR 的抑制剂，具有抗肿瘤、抗氧化、抗心血管和抗白血病活性，抑制角叉菜胶诱导的水肿，可用于研究神经系统疾病和心血管疾病。

Vanilpyruvic acid is a metabolite of catecholamine and precursor of vanillactic acid.

Pyrilamine hydrochloride 抑制由尼古丁引发的儿茶酚胺分泌。

Levadopa Related Compound A is the 6-hydroxy derivative of the amino acid L-DOPA with neurotoxic properties. Exogenously administered 6-Hydroxy-L-DOPA is biotransformed by an amino acid decarboxylase to the highly potent and catecholamine-selective neurot

Prenylamine lactate is a drug formerly used in the treatment of angina pectoris. Prenylamine depletes myocardial catecholamine stores and has some calcium channel blocking activity.

A 53693 is a rigid catecholamine and a selective adrenergic agonist. A 53693 has affinity to certain alpha receptor subtypes in rat alpha-2 receptors.

Arbutamine hydrochloride is a catecholamine which acts as a cardiac stimulant.

Butopamine differs from dobutamine in location of only one hydroxyl group, but is no longer a catecholamine.

DPBX-L-Dopa is a boron-containing dopa-derivative, acting as a bladder relaxant through non-catecholamine receptors.

L-Tyrosine-13C9,15N is intended for use as an internal standard for the quantification of L-tyrosine by GC- or LC-MS. L-Tyrosine is a non-essential amino acid.1It is produced by hydroxylation of phenylalanine by phenylalanine hydroxylase but can also be obtained from dietary sources or degradation of endogenous proteins, resulting in L-tyrosine release.1,2L-Tyrosine is a precursor in the biosynthesis of catecholamine neurotransmitters, melanins, and thyroid hormones.3Plasma, skeletal muscle, and erythrocyte levels of L-tyrosine are decreased in patients with chronic kidney disease.1 1.Kopple, J.D.Phenylalanine and tyrosine metabolism in chronic kidney failureJ. Nutr.137(6 Suppl 1)1586S-1590S(2007) 2.Webster, D., and Wildgoose, J.Tyrosine supplementation for phenylketonuriaCochrane DB Syst. Rev.2013(6)CD001507(2013) 3.Slominski, A., and Paus, R.Towards defining receptors for L-tyrosine and L-DOPAMol. Cell Endocrinol.99(2)C7-C11(1994)

CAY10781 是一种神经纤毛蛋白-1 (NRP-1) 和 VEGF-A.1 之间蛋白质-蛋白质相互作用的抑制剂。当使用浓度为 12.5 μM 时，它可抑制 43% 的相互作用。 当以相同浓度使用时，CAY10781 还抑制 VEGF-A 诱导的儿茶酚胺 A 分化 (CAD) 细胞中 VEGFR2 的磷酸化。

Pirepemat (IRL752) is a cortical-preferring catecholamine agent that enhances cognition. It is utilized in the investigation of Parkinson's disease.

N-acetyldopamine (NADA) is a catecholamine utilized by insects as a precursor for sclerotization, a process that strengthens their cuticle.

L-Cytidine 是Cytidine 的 L-构型形式。L-Cytidine 是一种嘧啶核苷，是RNA 的组成部分。Cytidine 可控制神经胶质谷氨酸循环，影响脑磷脂代谢，儿茶酚胺的合成和线粒体功能。

Dobutamine 是合成儿茶酚胺，可增加心排血量，矫正低灌注。Dobutamine 作用于α1-AR,β1-AR 和β2-AR（α-1、β-1和β-2肾上腺素能受体），是 β1-AR 受体的选择性激动剂，对 α1-AR 和 β2-AR 活性相对较弱。

Pirepemat (IRL752) fumarate 可用于研究帕金森病。Pireemat fumarate 是一种偏向皮质的儿茶酚胺传递剂和认知促进剂。

Detomidine hydrochloride (MPV-253 AII) 是咪唑衍生物，是有效的 α2-肾上腺素能 (α2-adrenergic) 激动剂，可用于促进安定、缓解疼痛的研究。