N-Acetyltyramine
CAS No. 1202-66-0
N-Acetyltyramine ( —— )
Catalog No. M28125 CAS No. 1202-66-0
N-Acetyltyramine is the active compound extracted from a fermentation broth of strain M3-10 which produces quorum-sensing inhibitor (QSI) compound. N-Acetyltyramine inhibits Chromobacterium violaceum ATCC 12472 violacein production and virulence factors, such as pyoverdine production, as well as swarming and twitching motilities, produced by Pseudomonas aeruginosa PAO1.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 46 | In Stock |
|
10MG | 72 | In Stock |
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25MG | 120 | In Stock |
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50MG | 177 | In Stock |
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100MG | 264 | In Stock |
|
200MG | 394 | In Stock |
|
500MG | 626 | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameN-Acetyltyramine
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NoteResearch use only, not for human use.
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Brief DescriptionN-Acetyltyramine is the active compound extracted from a fermentation broth of strain M3-10 which produces quorum-sensing inhibitor (QSI) compound. N-Acetyltyramine inhibits Chromobacterium violaceum ATCC 12472 violacein production and virulence factors, such as pyoverdine production, as well as swarming and twitching motilities, produced by Pseudomonas aeruginosa PAO1.
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DescriptionN-Acetyltyramine is the active compound extracted from a fermentation broth of strain M3-10 which produces quorum-sensing inhibitor (QSI) compound. N-Acetyltyramine inhibits Chromobacterium violaceum ATCC 12472 violacein production and virulence factors, such as pyoverdine production, as well as swarming and twitching motilities, produced by Pseudomonas aeruginosa PAO1.(In Vitro):N-Acetyltyramine enhances cytotoxicity of doxorubicin in resistant P388 murine leukemia cells (IC50 = 0.13 μg/ml).
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Synonyms——
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorWee1
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Research Area——
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Indication——
Chemical Information
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CAS Number1202-66-0
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Formula Weight179.2
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Molecular FormulaC10H13NO2
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(=O)NCCc1ccc(O)cc1
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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.Huang PQ, et al. Discovery of ZN-c3, a Highly Potent and Selective Wee1 Inhibitor Undergoing Evaluation in Clinical Trials for the Treatment of Cancer. J Med Chem. 2021 Sep 9;64(17):13004-13024.
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