Discover the magic of the 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carboxamide

The result showed that such a combination of chemo- and biocatalysis improved the catalytic yield more than two times compared with that of sole metal catalysis.I hope my blog about 3564-73-6 is helpful to your research. Name: 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carboxamide.

You could be based in a university, combining chemical research with teaching; or in a public-sector research center, helping to ensure national healthcare provision keeps pace with new discoveries. Like 3564-73-6, Name is 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carboxamide. In a document, author is Brown, GR, introducing its new discovery. Name: 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carboxamide.

Optimised quinuclidine squalene synthase (SQS) inhibitors are reported; 3-[2-(2-allyl-4-(2-ethoxy carbonylethyl)phenyl)ethynyl]quinuclidin-3-ol 1c, is a potent inhibitor of rat (KI = 6 nM) and human (KI = 43 nM) microsomal SQS; the oral ED(50) of 1c, for the inhibition of rat cholesterol biosynthesis was 1.3+/-0.45 mg/kg and for the R-enantiomer 1m, 0.8+/-0.2 mg/kg, with the corresponding R-carboxylic acid 6a, being 0.9+/-0.25 mg/kg. (C) 1997 Elsevier Science Ltd. All rights reserved.

The result showed that such a combination of chemo- and biocatalysis improved the catalytic yield more than two times compared with that of sole metal catalysis.I hope my blog about 3564-73-6 is helpful to your research. Name: 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carboxamide.

Reference:
Quinuclidine – Wikipedia,
,Quinuclidine | C7H13N | ChemSpider