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N-(1-(4-cyanophenyl)-3-methyl-1-oxobutan-2-yl)-5-isopropyl-3-methylisoxazole-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1394017-41-4

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1394017-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394017-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,0,1 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1394017-41:
(9*1)+(8*3)+(7*9)+(6*4)+(5*0)+(4*1)+(3*7)+(2*4)+(1*1)=154
154 % 10 = 4
So 1394017-41-4 is a valid CAS Registry Number.

1394017-41-4Downstream Products

1394017-41-4Relevant academic research and scientific papers

BENZAMIDE TRPA1 ANTAGONISTS

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Page/Page column 83, (2014/12/12)

Compounds of formula I, pharmaceutically acceptable salts thereof, diastereomers, enantiomers, or mixtures thereof: wherein R, X, Y, Z, n and A are as defined in the specification, as well as pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.

N-1-Alkyl-2-oxo-2-aryl amides as novel antagonists of the TRPA1 receptor

Vallin, Karl S.A.,Sterky, Karin J.,Nyman, Eva,Bernstroem, Jenny,From, Rebecka,Linde, Christian,Minidis, Alexander B.E.,Nolting, Andreas,Naerhi, Katja,Santangelo, Ellen M.,Sehgelmeble, Fernando W.,Sohn, Daniel,Strindlund, Jennie,Weigelt, Dirk

supporting information; experimental part, p. 5485 - 5492 (2012/09/22)

A series of potent antagonists of the ion channel transient receptor potential A1 (TRPA1) was developed by modifying lead structure 16 that was discovered by high-throughput screening. Based on lead compound 16, a SAR was established, showing a narrow region at the nitro-aromatic R1 moiety and at the warhead, while the R2 side had a much wider scope including ureas and carbamates. Compound 16 inhibits Ca2+-activated TRPA1 currents reversibly in whole cell patch clamp experiments, indicating that under in vivo conditions, it does not react covalently, despite its potentially electrophilic ketone.

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