N-Acetyl-L-tyrosine
CAS No. 537-55-3
N-Acetyl-L-tyrosine( Ac-Tyr-OH )
Catalog No. M19989 CAS No. 537-55-3
Acetyltyrosine is a side chain reaction of tyrosine. It converts to tyrosine and then can be used in neurotransmitter treatment as a precursor of cathecholamine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 37 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameN-Acetyl-L-tyrosine
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NoteResearch use only, not for human use.
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Brief DescriptionAcetyltyrosine is a side chain reaction of tyrosine. It converts to tyrosine and then can be used in neurotransmitter treatment as a precursor of cathecholamine.
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DescriptionAcetyltyrosine is a side chain reaction of tyrosine. It converts to tyrosine and then can be used in neurotransmitter treatment as a precursor of cathecholamine.
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In Vitro——
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In Vivo——
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SynonymsAc-Tyr-OH
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research AreaOthers
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Indicationnutrition support
Chemical Information
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CAS Number537-55-3
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Formula Weight223.23
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Molecular FormulaC11H13NO4
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Purity>98% (HPLC)
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SolubilityDMSO:200 mM
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SMILESCC(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O
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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
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Barbadin
Barbadin is a novel and specific inhibitor of β-arrestin/β2-adaptin interaction with an IC50 value of 19.1 μM for β-arestin1 and 15.6 μM for β-arestin2.
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Carboxyatractyloside...
Carboxyatractyloside is a natural product. It acts as an inhibitor of ADP/ATP carrier inhibits mitochondrial ADP/ATP transport.
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Neuropeptide W-30 (r...
Neuropeptide W-30 (rat) is an important stress mediator in the central nervous system that modulates the hypothalamus-pituitary-adrenal (HPA) axis and sympathetic outflow. Neuropeptide W-30 (rat) is an endogenous ligand for the two structurally related orphan G-protein-coupled receptors (GPCRs) GPR7 and GPR8. NPW-30 activates and binds to both GPR7 and GPR8 at similar effective doses.
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