Scientific Reviews
Product Guides
Blogs
Topics
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
121 Results for "
catecholamines
" in MedChemExpress (MCE) Product Catalog:
Products (121)
121 Results for "catecholamines" in MCE Product Catalog:
Cat. No.: HY-118406A
CAS No.: 26598-44-7
Synonyms: Ponalid hydrochloride; UK 738 hydrochloride
Target:
Research Areas:
Ethybenztropine hydrochloride (Ponalid hydrochloride) is an anticholinergic drug with antiparkinsonian activity. Ethybenztropine hydrochloride may also have dopamine reuptake inhibitory effects. Ethybenztropine hydrochloride is used to improve motor symptoms in patients with Parkinson's disease. Ethybenztropine hydrochloride exerts its inhibitory effects by regulating the balance of neurotransmitters .
Cat. No.: HY-118406B
CAS No.: 24815-25-6
Synonyms: Ponalid hydrobromide; UK 738 hydrobromide
Target:
Research Areas:
Ethybenztropine hydrobromide (Ponalid hydrobromide) is an anticholinergic drug with antiparkinsonian activity. Ethybenztropine hydrobromide may also act as a dopamine reuptake inhibitor. Ethybenztropine hydrobromide is commonly used to suppress Parkinson's disease .
Cat. No.: HY-128446
CAS No.: 1210360-87-4
Target:
Research Areas:
CAY10781 (Compound 11) is an inhibitor of the neuropilin-1 (NRP-1) and VEGF-A interaction. CAY10781 inhibits VEGF-A-induced phosphorylation of VEGFR2 in Catecholamine A-differentiated (CAD) cells [1]< sup>.
Research Areas:
Cat. No.: HY-121578
CAS No.: 58298-77-4
Synonyms: GDHB
Target:
Research Areas:
Agaridoxin (GDHB) is a blocker of catecholamine and adrenergic alpha-type receptors isolated from mushrooms. Agaridoxin activates adenylyl cyclase in rat hypothalamic membrane granules in the presence of guanosyl imide diphosphate (Gpp(NH)p) .
Category:
Cat. No.: HY-P3064
CAS No.: 142948-19-4
Synonyms: Leiurotoxin I
Target:
Research Areas:
Cat. No.: HY-16256
CAS No.: 75898-90-7
Target:
Research Areas:
Amrinone lactate is a positive inotropic-vasodilator agent. Amrinone lactate is a selective phosphodiesterase III inhibitor that increases cyclic adenosine monophosphate by preventing its breakdown. Amrinone lactate is also an orally active, non-glycosidic and non-catecholamine cardiotonic agent .
Cat. No.: HY-A0171
CAS No.: 17243-39-9
Synonyms: Ba-30803 free base
Target:
Research Areas:
Benzoctamine is an orally active and potent psychoactive agent which possesses tranquillizing properties. Benzoctamine increases the turnover rate of catecholamines. Benzoctamine enhances the [3H]noradrenaline uptake in the rat heart. Benzoctamine also accelerated the disappearance of intracisternally injected [3H]noradrenaline .
Cat. No.: HY-W002110R
CAS No.: 1131-94-8
Synonyms: 3-Hydroxy-4-methoxyphenylacetic acid (Standard); iso-HVA (Standard); Homoisovanillic acid (Standard)
Target:
Cat. No.: HY-B1294R
CAS No.: 60719-84-8
Synonyms: Inamrinone (Standard)
Research Areas:
Amrinone (Standard) is the analytical standard of Amrinone. This product is intended for research and analytical applications. Amrinone (Inamrinone) is a positive inotropic-vasodilator agent. Amrinone is a selective phosphodiesterase III inhibitor that increases cyclic adenosine monophosphate by preventing its breakdown. Amrinone is also an orally active, non-glycosidic and non-catecholamine cardiotonic agent .
Cat. No.: HY-W015007R
CAS No.: 672-87-7
Target:
Research Areas:
Metyrosine (Standard) is the analytical standard of Metyrosine. This product is intended for research and analytical applications. Metyrosine is a selective tyrosine hydroxylase enzyme inhibitor. Metyrosine exerts anti-inflammatory and anti-ulcerative effects. Metyrosine significantly inhibits high COX-2 activity . Metyrosine is a very effective agent for blood pressure control .
Cat. No.: HY-B0158S8
Synonyms: Cytosine β-D-riboside-d13; Cytosine-1-β-D-ribofuranoside-d13
Cat. No.: HY-101775
CAS No.: 51131-85-2
Target:
Research Areas:
9-hydroxyellipticine is an inhibitor of Topo II and RyR, exhibiting high affinity for DNA with a Pka value of 9.8 at pH 7.4. It has antitumor, antioxidant, and catecholamine-releasing activities, with IC50 values of 1.6 μM and 1.2 μM for Hela S-3 and 293T cells, respectively. It also demonstrates anticancer effects in L1210 leukemia mice .
Cat. No.: HY-116222
CAS No.: 115103-48-5
Target:
Research Areas:
A 53693 is a rigid catecholamine with selective adrenergic agonist activity. A 53693 has affinity for certain rat alpha-2 receptor subtypes. A 53693 shows high selectivity for alpha-2 receptors and, in contrast, has low affinity for alpha-1 receptors. A 53693 is used as a probe in biological studies to explore the molecular interactions of alpha agonist compounds .
Cat. No.: HY-P1544
CAS No.: 94071-26-8
Research Areas:
Cat. No.: HY-W778608R
CAS No.: 38934-20-2
Synonyms: Quercetin 7-O-β-glucuronide (Standard)
Target:
Cat. No.: HY-101775AR
CAS No.: 52238-35-4
Category:
Target:
Cat. No.: HY-P3419A
Research Areas:
Cat. No.: HY-100959R
CAS No.: 7659-29-2
Synonyms: OR-486 (Standard); 3,5-Dinitropyrocatechol (Standard)
Target:
3,5-Dinitrocatechol (Standard) (OR-486 (Standard); 3,5-Dinitropyrocatechol (Standard)) is the analytical standard of 3,5-Dinitrocatechol (HY-100959). This product is intended for research and analytical applications. 3,5-Dinitrocatechol (OR-486) is an orally active, blood-brain barrier-permeable selective catechol-O-methyltransferase (COMT) inhibitor. 3,5-Dinitrocatechol can be used in research related to Parkinson's disease, pheochromocytoma and adult cataract .
-
-
Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
