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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
13 Results for "
ergoline
" in MedChemExpress (MCE) Product Catalog:
Products (13)
13 Results for "ergoline" in MCE Product Catalog:
1
1 Cited Publications
Synonyms: Pergolide methanesulfonate; LY127809
Target:
Research Areas:
Cardiovascular Disease Neurological Disease Metabolic Disease
Pergolide mesylate (Pergolide methanesulfonate), an Ergoline derivative, is a potent and orally active dopamine D1 and D2 receptors agonist. Pergolide mesylate can be used for Parkinson's disease and hyperprolactinaemia research .
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Target:
Research Areas:
Cardiovascular Disease Neurological Disease Metabolic Disease
Pergolide (LY127809 free base), an Ergoline derivative, is a potent and orally active dopamine D1 and D2 receptor agonist. Pergolide can be used for Parkinson's disease and hyperprolactinaemia research .
Cat. No.: HY-B0702
CAS No.: 27848-84-6
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Research Areas:
Nicergoline, an ergoline derivative ester of bromonicotinic acid, is a potent, selective and orally active antagonist of α1A-adrenoceptor. Nicergoline has vasodilator effects. Nicergoline also has ameliorative effects on cognitive function in mouse models of Alzheimer's disease .
Cat. No.: HY-W783771
CAS No.: 2230715-45-2
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(8β)-N,N,6-Triethyl-9,10-didehydro-1-(1-oxopropyl)ergoline-8-carboxamide is a lysergamide.
Cat. No.: HY-13720AR
CAS No.: 66104-23-2
Synonyms: Pergolide methanesulfonate (Standard); LY127809 (Standard)
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Research Areas:
Pergolide (mesylate) (Standard) is the analytical standard of Pergolide (mesylate). This product is intended for research and analytical applications. Pergolide mesylate (Pergolide methanesulfonate), an Ergoline derivative, is a potent and orally active dopamine D1 and D2 receptors agonist. Pergolide mesylate can be used for Parkinson's disease and hyperprolactinaemia research .
Cat. No.: HY-123567
CAS No.: 148966-66-9
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LY86057 is an ergoline derivative without N1 substituents. It has higher affinity for porcine, squirrel monkey and human 5-HT2 receptors than rats and is an antagonist of 5-HT2 receptors. When studying the differences in recognition of a series of ergolines between species, LY86057 was found to be more selective for 5-HT2 receptors. Compared with LY53857, LY108742 resulted in a higher affinity for rat 5-HT2 receptors even when the N1 substituent was only methyl.
Cat. No.: HY-13720AS
CAS No.: 3026226-90-1
Synonyms: Pergolide methanesulfonate-d7; LY127809-d7
Cat. No.: HY-106512
CAS No.: 74627-35-3
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Cianergoline is a ergoline derivative with the activity of reducing intraocular pressure (IOP). Its primary regulatory mechanism involves the inhibition of sympathetic nervous function, achieved through actions on both prejunctional (DA2) and postjunctional (α1) adrenergic receptors. Cianergoline can be used for research in the field of glaucoma .
Cat. No.: HY-B0702R
CAS No.: 27848-84-6
Research Areas:
Nicergoline (Standard) is the analytical standard of Nicergoline. This product is intended for research and analytical applications. Nicergoline, an ergoline derivative ester of bromonicotinic acid, is a potent, selective and orally active antagonist of α1A-adrenoceptor. Nicergoline has vasodilator effects. Nicergoline also has ameliorative effects on cognitive function in mouse models of Alzheimer's disease .
Cat. No.: HY-B0702S
Cat. No.: HY-W743952
Cat. No.: HY-171798
CAS No.: 115178-28-4
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Research Areas:
BAM-2101 is an ergoline derivative with antihypertensive activity. BAM-2101 is orally active and lowers blood pressure in spontaneously hypertensive rats .
Cat. No.: HY-129481
CAS No.: 114943-19-0
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LY 178210 (Compound 24) is a selective partial agonist of the 5-HT1A receptor, with Ki values of 0.67 and 380 nM for the 5-HT1A and 5-HT1D receptors, respectively. LY 178210 has almost no activity against α₂-adrenergic receptors, 5-HT₂, and other neurotransmitter receptors. LY 178210 inhibits Foscolin-stimulated cyclase activity, but its maximum potency is lower than that of the full agonist 8-OH-DPAT (HY-112061). LY 178210 significantly reduces 5-hydroxyindoleacetic acid (5-HIAA) levels in the greater hypothalamus and increases serum corticosterone concentrations .
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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
