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(2E)-5-(benzyloxy)-2-(2-nitrovinyl)-3'-(trifluoromethyl)-1,1'-biphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1382722-91-9

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1382722-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1382722-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,2,7,2 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1382722-91:
(9*1)+(8*3)+(7*8)+(6*2)+(5*7)+(4*2)+(3*2)+(2*9)+(1*1)=169
169 % 10 = 9
So 1382722-91-9 is a valid CAS Registry Number.

1382722-91-9Downstream Products

1382722-91-9Relevant academic research and scientific papers

C-TERMINAL HSP90 INHIBITORS

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Paragraph 00245; 00246; 00251, (2013/08/28)

Hsp90 C-terminal inhibitors and pharmaceutical compositions containing such compounds are provided. The compounds of the disclosure are useful for the treatment and/or prevention of neurodegenerative disorders such as diabetic peripheral neuropathy.

Synthesis and evaluation of novologues as C-terminal Hsp90 inhibitors with cytoprotective activity against sensory neuron glucotoxicity

Kusuma, Bhaskar Reddy,Zhang, Liang,Sundstrom, Teather,Peterson, Laura B.,Dobrowsky, Rick T.,Blagg, Brian S. J.

, p. 5797 - 5812 (2012/07/30)

Compound 2 (KU-32) is a first-generation novologue (a novobiocin-based, C-terminal, heat shock protein 90 (Hsp90) inhibitor) that decreases glucose-induced death of primary sensory neurons and reverses numerous clinical indices of diabetic peripheral neuropathy in mice. The current study sought to exploit the C-terminal binding site of Hsp90 to determine whether the optimization of hydrogen bonding and hydrophobic interactions of second-generation novologues could enhance neuroprotective activity. Using a series of substituted phenylboronic acids to replace the coumarin lactone of 2, we identified that electronegative atoms placed at the meta-position of the B-ring exhibit improved cytoprotective activity, which is believed to result from favorable interactions with Lys539 in the Hsp90 C-terminal binding pocket. Consistent with these results, a meta-3-fluorophenyl substituted novologue (13b) exhibited a 14-fold lower ED50 for protection against glucose-induced toxicity of primary sensory neurons compared to 2.

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