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6,6'-diazido-2,2',3,3',4,4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-D-trehalose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18933-87-4

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18933-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18933-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,3 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18933-87:
(7*1)+(6*8)+(5*9)+(4*3)+(3*3)+(2*8)+(1*7)=144
144 % 10 = 4
So 18933-87-4 is a valid CAS Registry Number.

18933-87-4Relevant academic research and scientific papers

Design of Trehalose-Based Amide/Sulfonamide C-type Lectin Receptor Signaling Compounds

Rasheed, Omer K.,Buhl, Cassandra,Evans, Jay T.,Ryter, Kendal T.

, p. 1246 - 1251 (2021)

Mincle agonists have been shown to induce inflammatory cytokine production, such as tumor necrosis factor-alpha (TNF) and promote the development of a Th1/Th17 immune response that might be crucial to development of effective vaccination against pathogens

DIARYL TREHALOSE COMPOUNDS AND USES THEREOF

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Paragraph 00273, (2019/09/12)

Disclosed herein are diaryl trehalose compounds and methods of use thereof, for example as vaccine adjuvants.

Synthesis and biological evaluation of trehalose analogs as potential inhibitors of mycobacterial cell wall biosynthesis

Rose, Jerry D.,Maddry, Joseph A.,Comber, Robert N.,Suling, William J.,Wilson, Larry N.,Reynolds, Robert C.

, p. 105 - 120 (2007/10/03)

Analogs of trehalose are reported that were designed to interfere with mycolylation pathways in the mycobacterial cell wall. Several derivatives of 6,6′-dideoxytrehalose, including N,N′-dialkylamino and 6,6′-bis(sulfonamido) analogs, were prepared and evaluated for antimycobacterial activity against Mycobacterium tuberculosis H37Ra and a panel of clinical isolates of Mycobacterium avium. 6,6′-Diaminotrehalose and its diazido precursor were both inactive, but significant activity apparently related to aliphatic chain length was found among the sulfonamides, N-alkylamines, and one of the amidines.

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