RS 8359
CAS No. 105365-76-2
RS 8359( —— )
Catalog No. M26814 CAS No. 105365-76-2
RS 8359 is a reversible inhibitor of monoamine oxidase A (MAO-A) with a selectivity ratio of about 2200 for the A:B enzyme types.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 188 | In Stock |
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| 5MG | 170 | In Stock |
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| 10MG | 275 | In Stock |
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| 25MG | 550 | In Stock |
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| 50MG | 867 | In Stock |
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| 100MG | 1386 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameRS 8359
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NoteResearch use only, not for human use.
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Brief DescriptionRS 8359 is a reversible inhibitor of monoamine oxidase A (MAO-A) with a selectivity ratio of about 2200 for the A:B enzyme types.
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DescriptionRS 8359 is a reversible inhibitor of monoamine oxidase A (MAO-A) with a selectivity ratio of about 2200 for the A:B enzyme types. RS 8359 has antidepressant activity.(In Vivo):RS 8359 shows relatively little effect upon blood pressure when administered together with tyramine, thus effectively eliminating the 'cheese' effect which has contributed to the limited clinical use of the classical monoamine oxidase inhibitors. RS 8359 shows little affinity for the common central nervous system receptors and little anticholinergic effect.
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In Vitro——
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In VivoRS 8359 shows relatively little effect upon blood pressure when administered together with tyramine. RS-8359 shows little affinity for the common central nervous system receptors and little anticholinergic effect.
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Synonyms——
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PathwayMetabolic Enzyme/Protease
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TargetMAO
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RecptorWnt| β-catenin
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Research Area——
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Indication——
Chemical Information
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CAS Number105365-76-2
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Formula Weight252.277
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Molecular FormulaC14H12N4O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (198.20 mM)
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SMILESOC1CCc2c1ncnc2Nc1ccc(cc1)C#N
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.1. Waaler J, et al. Novel synthetic antagonists of canonical Wnt signaling inhibit colorectal cancer cell growth. Cancer Res. 2011;71(1):197-205.
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