Pub. Date : 2006 Jul
PMID : 16894785
11 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | A chiral stationary phase (CSP 1) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was applied to the resolution of N-(substituted benzoyl)-alpha-amino acid amides and esters. | 18-crown-6 2,3,11,12-tetracarboxylic acid | regulator of calcineurin 1 | Homo sapiens |
| 2 | A chiral stationary phase (CSP 1) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was applied to the resolution of N-(substituted benzoyl)-alpha-amino acid amides and esters. | n-(substituted benzoyl)-alpha-amino acid amides | regulator of calcineurin 1 | Homo sapiens |
| 3 | A chiral stationary phase (CSP 1) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was applied to the resolution of N-(substituted benzoyl)-alpha-amino acid amides and esters. | Esters | regulator of calcineurin 1 | Homo sapiens |
| 4 | Among the substituents on the benzoyl group of analytes, the nitro group was the best for good resolution of analytes on CSP 1. | nitro | regulator of calcineurin 1 | Homo sapiens |
| 5 | From these results, the two N-H hydrogens of the amide tethers of CSP 1, the carbonyl oxygen of the amide group of analytes, and the nitro group on the benzoyl group of analytes were concluded to play significant roles in chiral recognition. | Nitrogen | regulator of calcineurin 1 | Homo sapiens |
| 6 | From these results, the two N-H hydrogens of the amide tethers of CSP 1, the carbonyl oxygen of the amide group of analytes, and the nitro group on the benzoyl group of analytes were concluded to play significant roles in chiral recognition. | Hydrogen | regulator of calcineurin 1 | Homo sapiens |
| 7 | From these results, the two N-H hydrogens of the amide tethers of CSP 1, the carbonyl oxygen of the amide group of analytes, and the nitro group on the benzoyl group of analytes were concluded to play significant roles in chiral recognition. | Amides | regulator of calcineurin 1 | Homo sapiens |
| 8 | From these results, the two N-H hydrogens of the amide tethers of CSP 1, the carbonyl oxygen of the amide group of analytes, and the nitro group on the benzoyl group of analytes were concluded to play significant roles in chiral recognition. | Amides | regulator of calcineurin 1 | Homo sapiens |
| 9 | In addition, various N-(3,5-dinitrobenzoyl)leucine amides with different lengths of N-alkylamide chains were resolved on CSP 1 and N-(3,5-dinitrobenzoyl) leucine N-propylamide was found to show the best chiral recognition in terms of the separation (alpha = 1.30) and the resolution factor (Rs= 3.17). | n-(3,5-dinitrobenzoyl)leucine amides | regulator of calcineurin 1 | Homo sapiens |
| 10 | In addition, various N-(3,5-dinitrobenzoyl)leucine amides with different lengths of N-alkylamide chains were resolved on CSP 1 and N-(3,5-dinitrobenzoyl) leucine N-propylamide was found to show the best chiral recognition in terms of the separation (alpha = 1.30) and the resolution factor (Rs= 3.17). | n-alkylamide | regulator of calcineurin 1 | Homo sapiens |
| 11 | In addition, various N-(3,5-dinitrobenzoyl)leucine amides with different lengths of N-alkylamide chains were resolved on CSP 1 and N-(3,5-dinitrobenzoyl) leucine N-propylamide was found to show the best chiral recognition in terms of the separation (alpha = 1.30) and the resolution factor (Rs= 3.17). | n-(3,5-dinitrobenzoyl) leucine n-propylamide | regulator of calcineurin 1 | Homo sapiens |