Neurological Disease
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Neurological Disease Related Products (19446)
Related Products (19446)
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Antibodies (42)
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Related Compound Screening Libraries (7)
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AD-35 free base
0 ImagesCat. No.: HY-117710ACAS No.: 1531586-58-9AD-35 free base is an orally active, blood-brain barrier-permeable acetylcholinesterase inhibitor with an IC50 of 793 nM. AD-35 free base inhibits metal-induced amyloid-β aggregation and disassembles preformed amyloid-β aggregates. In rat models of cognitive impairment, AD-35 free base attenuates Aβ25-35-induced astrocyte activation, TNF-α and IL-1β release, inhibits ERK phosphorylation, and alleviates learning and memory deficits. AD-35 free base can be used for research on Alzheimer's disease.
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Myristic acid-13C2
0 ImagesCat. No.: HY-N2041S8CAS No.: 287111-20-0Myristic acid-13C2 is the 13C-labeled Myristic acid (HY-N2041). Myristic acid is an orally active saturated 14-carbon fatty acid found in most animal and plant fats, especially milk fat coconut oil, palm oil and nutmeg oil. Myristic acid exerts anti-inflammatory activity through the NF-κB pathway. Myristic acid has antibacterial, anti-inflammatory and analgesic properties.
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Vadenersen
0 ImagesCat. No.: HY-185935CAS No.: 3027256-85-2Vadenersen is an inhibitor of MECP2 protein expression. Vadenersen has potential for research into Rett syndrome.
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Pramiracetam (Standard)
0 ImagesCat. No.: HY-17455RCAS No.: 68497-62-1Synonyms: CI-879 free base (Standard)Pramiracetam (Standard) is the analytical standard of Pramiracetam. This product is intended for research and analytical applications. Pramiracetam (CI-879 free base) is a PREP (prolyl endopeptidase) inhibitor. Pramiracetam improves cognitive impairment caused by traumatic brain injury. Pramiracetam can be used in the study of neurodegenerative diseases.
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MB327
0 ImagesCat. No.: HY-161118CAS No.: 61368-98-7MB327 is a bipyridine nonoxime compound that restores neuromuscular function. MB327 restores the activity of nicotinamide acetylcholine receptors (nAChRs) for carbachol desensitization in a typical type II PAM manner. MB327 can neutralize nerve agent poisoning.
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Dibucaine hydrochloride (Standard)
0 ImagesSynonyms: Cinchocaine hydrochloride (Standard)Dibucaine (hydrochloride) (Standard) is the analytical standard of Dibucaine (hydrochloride). This product is intended for research and analytical applications. Dibucaine hydrochloride (Cinchocaine hydrochloride) is a sodium channel inhibitor. Dibucaine hydrochloride is a potent SChE inhibitor.
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PB-22 7-Hydroxyisoquinoline isomer
0 ImagesCat. No.: HY-172052CAS No.: 2365471-61-8PB-22 7-Hydroxyisoquinoline isomer is a structural isomer of PB-22. PB-22 is a cannabinoid.
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4BP-TQS (Standard)
0 ImagesCat. No.: HY-110087RCAS No.: 360791-49-7 -
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Pimavanserin hemitartrate (Standard)
0 ImagesSynonyms: ACP-103 hemitartrate (Standard)Pimavanserin hemitartrate (Standard) is the analytical standard of Pimavanserin hemitartrate. This product is intended for research and analytical applications. Pimavanserin (ACP-103) hemitartrate is a potent and brain-penetrant 5-HT 2A receptor inverse agonist with pIC50 and pKi of 8.73 and 9.3, respectively.
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Dexpramipexole-d3 dihydrochloride
0 ImagesCat. No.: HY-17355BSCAS No.: 1432230-09-5Synonyms: (R)-Pramipexole-d3 dihydrochloride; R-(+)-Pramipexole-d3 dihydrochloride; KNS-760704-d3 dihydrochlorideDexpramipexole-d3 ((R)-Pramipexole-d3) dihydrochloride is the deuterium labeled Dexpramipexole. Dexpramipexole ((R)-Pramipexole) dihydrochloride is an orally active, blood-brain barrier permeable mitochondrial protective agent. Dexpramipexole dihydrochloride upregulates the expression of Parkin, PINK1, GPX4 and FSP1; binds to mitochondrial F1/Fo-ATP synthase; blocks the Nav1.8 sodium channel; and inhibits the activation of the NLRP3 inflammasome. Dexpramipexole dihydrochloride induces mitophagy, inhibits ferroptosis, pyroptosis, apoptosis, neuroinflammation and eosinophilopoiesis; maintains mitochondrial function and redox homeostasis; reduces reactive oxygen species production; and decreases myocardial infarct size. Dexpramipexole dihydrochloride is applicable to studies on eosinophilic asthma, myocardial ischemia/reperfusion injury, sepsis-associated encephalopathy, analgesia, and more.
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Methyllycaconitine citrate (Standard)
0 ImagesCat. No.: HY-N2332ARCAS No.: 351344-10-0Synonyms: MLA citrate (Standard)Methyllycaconitine citrate (Standard) is the analytical standard of Methyllycaconitine citrate (HY-N2332A). This product is intended for research and analytical applications. Methyllycaconitine (MLA) citrate is a blood-brain barrier-permeable antagonist of α7 nicotinic acetylcholine receptor (α7nAChR) with an IC50 of 2 nM. Methyllycaconitine citrate inhibits Aβ25-35-induced autophagy by restoring the mTOR pathway, and prevents reactive oxygen species (ROS) production, microglial activation, reduced dopamine uptake, loss of dopaminergic terminals and catecholamine secretion. Methyllycaconitine citrate induces hippocampal glutamate efflux, enhances long-term potentiation, and improves memory acquisition. Methyllycaconitine citrate can be used in research related to Alzheimer's disease, cerebral palsy, ParKinson's disease and schizophrenia.
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Vasopressin (Standard)
0 ImagesSynonyms: Arginine vasopressin (Standard); Antidiuretic hormone (Standard)Vasopressin (Standard) is the analytical standard of Vasopressin. This product is intended for research and analytical applications. Vasopressin is a cyclic nonapeptide that is synthesized centrally in the hypothalamus. Vasopressin participates in the hypothalamic-pituitary-adrenal axis, and regulates pituitary corticotropin secretion by potentiating the stimulatory effects of corticotropin releasing factor. Vasopressin also can act as a neurotransmitter, exerting its action by binding to specific G protein-coupled receptors.
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M4K2009 hydrochloride
0 ImagesCat. No.: HY-149591ACAS No.: 2772902-12-0M4K2009 hydrochloride is an orally active, blood-brain barrier permeable type I ALK2 inhibitor, with an IC50 value of 8-13 nM against human ALK2. M4K2009 hydrochloride exhibits moderate off-target inhibitory activity against hERG potassium channels (Potassium Channel), with an IC50 of 8 μM against the human channel. M4K2009 hydrochloride can be used in studies related to diffuse intrinsic pontine glioma.
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N,N-Dimethyl-3,4-DMA hydrochloride
0 ImagesCat. No.: HY-170742CAS No.: 70932-19-3Synonyms: 3,4-Dimethoxydimethylamphetamine hydrochlorideN,N-Dimethyl-3,4-DMA (3,4-Dimethoxydimethylamphetamine) hydrochloride is an amphetamine.
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5-Fluoro PB-22 N-(3-fluoropentyl) isomer
0 ImagesCat. No.: HY-172044CAS No.: 2365471-07-25-Fluoro PB-22 N-(3-fluoropentyl) isomer is a structural isomer of 5-Fluoro PB-22.
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3,4-EDMC hydrochloride
0 ImagesCat. No.: HY-172061CAS No.: 30253-44-23,4-EDMC hydrochloride is a drug derivative.
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8(R)-Hydroxy-9(R)-hexahydrocannabinol
0 ImagesCat. No.: HY-168789CAS No.: 42793-11-38(R)-Hydroxy-9(R)-hexahydrocannabinol, a phytocannabinoid compound, is a metabolite of 9(R)-Hexahydrocannabinol.
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3-Pyr-Cytisine
0 ImagesCat. No.: HY-107680CAS No.: 948027-43-8Synonyms: 3-Pyr-Cyt3-Pyr-Cytisine (3-Pyr-Cyt) is a cytisine derivative. 3-Pyr-Cytisine is a very weak α4β2 nAChR partial agonist that has been studied as an antidepressant.
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CAY10404 (Standard)
0 ImagesCat. No.: HY-121537RCAS No.: 340267-36-9CAY10404 (Standard) is the analytical standard of CAY10404. This product is intended for research and analytical applications. CAY10404 is a potent and selective cyclooxygenase-2 (COX-2) inhibitor with an IC50 of 1 nM and a selectivity index (SI; COX-1 IC50/COX-2 IC50) of >500000. CAY10404 is a potent PKB/Akt and MAPK signaling pathways inhibitor and induces apoptosis in non-small cell lung cancer (NSCLC) cells. CAY10404, a diarylisoxazole, has good analgesic, anti-inflammatory, and anti-cancer activities.
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UCM 608 (Standard)
0 ImagesSynonyms: 2-Phenylmelatonin (Standard) -
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0 ImagesCat. No.:Synonyms:-
Host:
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Application:
Human,
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Isotype:
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Reactivity:
,
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Neurotransmitter Compound Library
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