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1221189-11-2

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  • (2S)-2-aMino-6-((1-(6-nitrobenzo[d][1,3]dioxol-5-yl)ethoxy)carbonylaMino)hexanoic acid

    Cas No: 1221189-11-2

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  • (2S)-2-aMino-6-((1-(6-nitrobenzo[d][1,3]dioxol-5-yl)ethoxy)carbonylaMino)hexanoic acid

    Cas No: 1221189-11-2

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  • (2S)-2-aMino-6-((1-(6-nitrobenzo[d][1,3]dioxol-5-yl)ethoxy)carbonylaMino)hexanoic acid

    Cas No: 1221189-11-2

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1221189-11-2 Usage

General Description

The chemical compound " (2S)-2-Amino-6-((1-(6-nitrobenzo[d][1,3]dioxol-5-yl)ethoxy)carbonylaMino)hexanoic acid" is a complex amino acid derivative. It is composed of a six-carbon chain with an amino group at the 2-position and a carboxylic acid group at the 6-position. Additionally, the compound contains a nitrobenzodioxole ring linked to the carbon chain through an ether linkage. The presence of the nitro group in the benzodioxole ring contributes to the compound's potential pharmaceutical properties, making it of interest for further research in drug development. The compound's intricate structure and various functional groups provide a basis for potential biological activity and medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1221189-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,1,8 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1221189-11:
(9*1)+(8*2)+(7*2)+(6*1)+(5*1)+(4*8)+(3*9)+(2*1)+(1*1)=112
112 % 10 = 2
So 1221189-11-2 is a valid CAS Registry Number.

1221189-11-2Downstream Products

1221189-11-2Relevant articles and documents

Spatiotemporal Activation of Protein O-GlcNAcylation in Living Cells

Fan, Zhiya,He, Jiahui,Qin, Weijie,Tian, Yinping,Yang, Weiwei,Yi, Wen,Zhang, Wanjun,Zhou, Yichao,Zhu, Qiang

supporting information, (2022/02/23)

O-linked N-acetylglucosamine (O-GlcNAc) is a prevalent protein modification that plays fundamental roles in both cell physiology and pathology. O-GlcNAc is catalyzed solely by O-GlcNAc transferase (OGT). The study of protein O-GlcNAc function is limited by the lack of tools to control OGT activity with spatiotemporal resolution in cells. Here, we report light control of OGT activity in cells by replacing a catalytically essential lysine residue with a genetically encoded photocaged lysine. This enables the expression of a transiently inactivated form of OGT, which can be rapidly reactivated by photo-decaging. We demonstrate the activation of OGT activity by monitoring the time-dependent increase of cellular O-GlcNAc and profile glycoproteins using mass-spectrometry-based quantitative proteomics. We further apply this activation strategy to control the morphological contraction of fibroblasts. Furthermore, we achieved spatial activation of OGT activity predominantly in the cytosol. Thus, our approach provides a valuable chemical tool to control cellular O-GlcNAc with much needed spatiotemporal precision, which aids in a better understanding of O-GlcNAc function.

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