Neurological Disease
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Neurological Disease Related Products (19440)
Related Products (19440)
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Antibodies (42)
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Related Compound Screening Libraries (7)
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Thiocolchicoside (Standard)
0 ImagesThiocolchicoside (Standard) is the analytical standard of Thiocolchicoside. This product is intended for research and analytical applications. Thiocolchicoside is a competitive γ-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist in the central nervous system. Thiocolchicoside is a semisynthetic sulfur derivative of colchicoside. Thiocolchicoside is a muscle relaxant and has anti-inflammatory, and analgesic properties.
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LY-411575 (isomer 3)
0 ImagesLY-411575 isomer 3 is an isomer of LY411575, which is a potent γ-secretase inhibitor.
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SCH772984 (Standard)
0 ImagesCat. No.: HY-50846RCAS No.: 942183-80-4SCH772984 (Standard) is the analytical standard of SCH772984 (HY-50846). This product is intended for research and analytical applications. SCH772984 is a highly selective and ATP-competitive ERK inhibitor, with IC50s of 4 and 1 nM for ERK1 and ERK2, respectively. SCH772984 has antitumor activity in MAPK inhibitor-naive and MAPK inhibitor-resistant cells containing BRAF or RAS mutations.
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6-APDB
0 ImagesCat. No.: HY-W680886CAS No.: 152623-93-36-APDB is a class of monoamine neurotransmitter releaser and Monoamine Transporter modulator that exerts selective effects on human monoamine transporters and acts as a partial agonist at 5-HT2 family receptors. For NET, 6-APDB has an IC50 of 0.56 μM and a Ki of 18 μM; for SERT, it has an IC50 of 2.3 μM and a Ki of 23 μM; for DAT, it has an IC50 of 33 μM and a Ki of >30 μM, and affinity for rat and mouse TAAR1, with Ki values of 1.0 μM and 0.21 μM, respectively. 6-APDB inhibits norepinephrine and 5-HT reuptake, mediates the release of three types of monoamine neurotransmitters, shows a dose-dependent biphasic locomotor effect in mice, and fully substitutes the discriminative stimulus effect of MDMA. 6-APDB shows no significant cytotoxicity at high concentrations, and possesses empathogenic psychoactivity, potential hallucinogenic effects, and behavioral effects associated with intermittent abuse.
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β-Methoxy 2C-D hydrochloride
0 ImagesCat. No.: HY-W722177CAS No.: 98537-38-3β-Methoxy 2C-D hydrochloride is a phenethylamine.
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- ε-Rhodomycinone
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8-Hydroxyguanosine (Standard)
0 ImagesCat. No.: HY-113262RCAS No.: 3868-31-38-Hydroxyguanosine (Standard) is the analytical standard of 8-Hydroxyguanosine. This product is intended for research and analytical applications. 8-Hydroxyguanosine, an oxidized nucleoside, is a marker of RNA oxidative damage and oxidative stress. 8-Hydroxyguanosine stimulates proliferation and differentiation of murine B cells with immunostimulatory activity. 8-Hydroxyguanosine is promising for research of Alzheimer’s disease and Down’s syndrome.
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Adaptaquin (Standard)
0 ImagesAdaptaquin (Standard) is the analytical standard of Adaptaquin (HY-101449). This product is intended for research and analytical applications. Adaptaquin is a BBB-penetrable HIF-PHDs inhibitor. Adaptaquin has anti-inflammatory and neuroprotective effects. Adaptaquin can effectively inhibit lipid peroxidation, maintain mitochondrial function, and reduce neuronal death. Adaptaquin can be used in the research of nervous system diseases such as Parkinson's disease.
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Isopaynantheine
0 ImagesCat. No.: HY-N13293CAS No.: 22032-51-5Synonyms: 3-IsopaynantheineIsopaynantheine (3-Isopaynantheine), an alkaloid, is an opioid. Isopaynantheine has antinociceptive activity in mice.
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Arisugacin F
0 ImagesCat. No.: HY-N13926CAS No.: 261951-44-4Arisugacin F, a microbial metabolite, is a structural analog of Arisugacin A (HY-N13901). Arisugacin F shows no activity against AChE.
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Protein kinase inhibitor 12
0 ImagesCat. No.: HY-W844543CAS No.: 721964-48-3Protein Kinase Inhibitor 12 (compound 1-91) is a triazolopyridazine derivative and protein kinase inhibitor that can be utilized in research related to diseases associated with protein kinases.
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- Cropropamide
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PD-147693
0 ImagesCat. No.: HY-169837CAS No.: 163239-24-5PD-147693 (compound II) is an active metabolite of the presynaptic dopamine autoreceptor agonist CI-1007 and has antipsychotic activity similar to CI-1007.
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Axillaridine A
0 ImagesCat. No.: HY-N2912CAS No.: 128255-16-3Axillaridine A can be isolated from Sarcococca hookeriana var. digyna. Axillaridine A inhibits the catalytic activity of AChE.
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PF-04701475
0 ImagesCat. No.: HY-120811CAS No.: 1488407-52-8PF-04701475 is a potent AMPA receptor potentiator with an EC50 of 123 nM. PF-04701475 can be used for the study of neurological disorders.
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Phenglutarimid hydrochloride
0 ImagesCat. No.: HY-U00001ACAS No.: 1674-96-0Synonyms: Ciba 10870 hydrochloride; Phenglutarimide hydrochloridePhenglutarimid hydrochloride is an anticholinergic used as an antiparkinsonian agent.
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Setiptiline-d3
0 ImagesCat. No.: HY-32329SCAS No.: 1795024-97-3Setiptiline-d3 is the deuterium labeled Setiptiline. Setiptiline (Org-8282) is a serotonin receptor antagonist. Setiptiline is a tetracyclic antidepressant (TeCA) which acts as a noradrenergic and specific serotonergic antidepressant (NaSSA). Setiptiline acts as a norepinephrine reuptake inhibitor, α2-adrenergic receptor antagonist, and serotonin receptor antagonist, likely at the 5-HT2A, 5-HT2C, and/or 5-HT3 subtypes, as well as an H1 receptor inverse agonist/antihistamine.
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Spirendolol
0 ImagesCat. No.: HY-101817CAS No.: 81840-58-6Synonyms: Li 32-468; S 32-468; Substance 32468Spirendolol is a β adrenergic receptor antagonist.
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BIP-135 (Standard)
0 ImagesCat. No.: HY-111055RCAS No.: 941575-71-9BIP-135 (Standard) is the analytical standard of BIP-135 (HY-111055). This product is intended for research and analytical applications. BIP-135 is a potent and selective ATP-competitive GSK-3 inhibitor, with IC50s of 16 nM and 21 nM for GSK-3α and GSK-3β, respectively. BIP 135 exhibits neuroprotective effect.
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JH-I-25
0 ImagesCat. No.: HY-138834CAS No.: 1042673-20-0JH-I-25 is an orally active IRAK1 and IRAK4 inhibitor. JH-I-25 inhibits LPS-induced IRAK4 phosphorylation, IRAK1 degradation, MAPK activation, and the expression of proinflammatory cytokines TNF-α and IL-6 in lung tissues. JH-I-25 improves the survival rate of LPS-induced septic mice and serves as an IRAK4 recruiter in the design of proteolysis-targeting chimeric molecules. JH-I-25 can be used in research related to diffuse large B-cell lymphoma, Waldenström's macroglobulinemia, septic shock, rheumatoid arthritis, atherosclerosis, Alzheimer's disease, acute lung injury, sepsis, and psoriasis.
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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
54 compoundsHY-L186 -
Neurotransmitter Receptor Compound Library
2,593 compoundsHY-L062 -
Neurodegenerative Disease-related Compound Library
3,759 compoundsHY-L086 -
Anti-Alzheimer's Disease Compound Library
2,174 compoundsHY-L069 -
Anti-Parkinson's Disease Compound Library
2,199 compoundsHY-L085 -
Neuroprotective Compound Library
1,851 compoundsHY-L070 -
Antidepressant Compound Library
3,059 compoundsHY-L108