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2-((2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosyl)oxy)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898283-68-6

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898283-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898283-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,2,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 898283-68:
(8*8)+(7*9)+(6*8)+(5*2)+(4*8)+(3*3)+(2*6)+(1*8)=246
246 % 10 = 6
So 898283-68-6 is a valid CAS Registry Number.

898283-68-6Relevant academic research and scientific papers

A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells

Peng, Lu,Gao, Meng,Cai, Xiaolei,Zhang, Ruoyu,Li, Kai,Feng, Guangxue,Tong, Aijun,Liu, Bin

, p. 9168 - 9172 (2015)

A novel fluorescent probe SA-βGal is reported here with light-up response to β-galactosidase. SA-βGal possesses the β-galactopyranoside group to react with β-galactosidase and releases the fluorescent salicylaldehyde azine with both aggregation induced emission (AIE) and excited-state intramolecular proton transfer (ESIPT) characteristics. The linear fluorescent response enables the in vitro quantification of β-galactosidase activity in a range of 0-0.1 U mL-1 with a detection limit of 0.014 U mL-1. The probe exhibits significant advantages, such as no self-quenching at high concentrations, a large Stokes shift (190 nm) and high specificity to β-galactosidase with an excellent light-up ratio of 820 fold. Moreover, thanks to its good retention in living cells, the application of SA-βGal for the imaging of cellular β-galactosidase was also achieved with high contrast.

COMPOUNDS COMPRISING CLEAVABLE LINKER AND USES THEREOF

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Page/Page column 142, (2020/09/03)

Provided are a compound including a cleavable linker, a use thereof, and an intermediate compound for preparing the same, and more particularly, the compound including a cleavable linker of the present invention may include an active agent (for example, a drug, a toxin, a ligand, a probe for detection, etc.) having a specific function or activity, a -S(=0)(=N-)- functional group which is capable of selectively releasing the active agent, and a functional group which triggers a chemical reaction, a physicochemical reaction and/or a biological reaction by external stimulation, and may further include a ligand (for example, oligopeptide, polypeptide, antibody, etc.) having binding specificity for a desired target receptor.

COMPOUNDS COMPRISING CLEAVABLE LINKER AND USES THEREOF

-

, (2020/07/21)

Provided are a compound including a cleavable linker, a use thereof, and an intermediate compound for preparing the same, and more particularly, the compound including a cleavable linker of the present invention may include an active agent (for example, a drug, a toxin, a ligand, a probe for detection, etc.) having a specific function or activity, a SO2 functional group which is capable of selectively releasing the active agent, and a functional group which triggers a chemical reaction, a physicochemical reaction and/or a biological reaction by external stimulation, and may further include a ligand (for example, oligopeptide, polypeptide, antibody, etc.) having binding specificity for a desired target receptor.

COMPOUNDS COMPRISING CLEAVABLE LINKER AND USES THEREOF

-

Page/Page column 137, (2019/01/21)

Provided are a compound including a cleavable linker, a use thereof, and an intermediate compound for preparing the same, and more particularly, the compound including a cleavable linker of the present invention may include an active agent (for example, a drug, a toxin, a ligand, a probe for detection, etc.) having a specific function or activity, a SO2 functional group which is capable of selectively releasing the active agent, and a functional group which triggers a chemical reaction, a physicochemical reaction and/or a biological reaction by external stimulation, and may further include a ligand (for example, oligopeptide, polypeptide, antibody, etc.) having binding specificity for a desired target receptor.

Ratiometric electrochemical detection of β-galactosidase

Spring, Sam A.,Goggins, Sean,Frost, Christopher G.

supporting information, p. 7122 - 7126 (2017/09/07)

A novel ferrocene-based substrate for the ratiometric electrochemical detection of β-galactosidase was designed and synthesised. It was demonstrated to be an excellent electrochemical substrate for β-Gal detection with sensitivity as low as 0.1 U mL-1.

Synthesis of Glycosylated Chrysin Derivatives Via Ester Linkers

Fei, Gaishun,Fan, Xiaofei,Ma, Huiping,Fan, Pengchang,Jia, Zhengping,Jing, Linlin

, p. 602 - 610 (2016/08/31)

A series of glycosylated chrysin derivatives have been synthesized in good yields with simple procedures and mild reaction conditions. Six different kinds of sugar moieties were introduced through each ester linker.

Synthesis and biological evaluation of glycosylated psoralen derivatives

Chen, Chao-Yue,Sun, Jian-Guo,Liu, Fei-Yan,Fung, Kwok-Pui,Wu, Ping,Huang, Zhi-Zhen

experimental part, p. 2598 - 2606 (2012/05/20)

A novel route for the efficient synthesis of a target psoralen moiety, 4,4′-dimethylxanthotoxol, has been developed, which need only four steps using cheap pyrogallol as a starting material. Subsequently, a range of new glycosylated psoralen derivatives w

Studies on the synthesis and antiproliferative activities of 13-cis-retinoyl sugar derivatives

Xiang, Jian-Nan,Jiang, Li-Hui,Chen, Chao-Yue,Fu, Zhi-Ying,Duan, Jun-Fei,He, Xiao-Xiao,Wang, Ke-Min

, p. 595 - 614 (2007/10/03)

New retinoyl sugar derivatives of 13-cis-retinoic acid were synthesized in three ways in this paper in order to enhance pharmacal effects, especially antiproliferative activities of 13-cis-retinoic acid. Their structures were confirmed by IR, 1H-NMR, 13C-NMR, and MS spectra and their antiproliferative activities were determined in vitro using human cancer lines. Results showed that some compounds possessed potential antitumor activities. Copyright Taylor & Francis Group, LLC.

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