The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
8360884 |
134 |
Three-dimensional quantitative structure-activity relationship of angiotesin-converting enzyme and thermolysin inhibitors. II. A comparison of CoMFA models incorporating molecular orbital fields and desolvation free energies based on active-analog and complementary-receptor-field alignment rules. |
Washington University |
22541393 |
1 |
A variant peptide of buffalo colostrumß-lactoglobulin inhibits angiotensin I-converting enzyme activity. |
University of Mysore |
12852763 |
20 |
Computer-aided selection of potential antihypertensive compounds with dual mechanism of action. |
Institute of Biomedical Chemistry of Russian Academy of Medical Sciences |
10753476 |
84 |
Phosphinic derivatives as new dual enkephalin-degrading enzyme inhibitors: synthesis, biological properties, and antinociceptive activities. |
University of Paris |
10602705 |
82 |
Investigation of subsite preferences in aminopeptidase A (EC 3.4.11.7) led to the design of the first highly potent and selective inhibitors of this enzyme. |
University of Paris |
8632427 |
80 |
Optimal recognition of neutral endopeptidase and angiotensin-converting enzyme active sites by mercaptoacyldipeptides as a means to design potent dual inhibitors. |
University of Paris |
8691458 |
60 |
Design of orally active dual inhibitors of neutral endopeptidase and angiotensin-converting enzyme with long duration of action. |
University of Paris |
8459398 |
36 |
1,2-Cyclomethylenecarboxylic monoamide hydroxamic derivatives. A novel class of non-amino acid angiotensin converting enzyme inhibitors. |
Laboratori Guidotti |
2342054 |
19 |
Angiotensin-converting enzyme inhibitors. 9. Novel [[N-(1-carboxy-3-phenylpropyl)amino]acyl]glycine derivatives with diuretic activity. |
Rorer Central Research |
2544729 |
8 |
Angiotensin converting enzyme inhibitors: spirapril and related compounds. |
Schering-Plough |
3035180 |
44 |
Synthesis and structure-activity relationships of potent new angiotensin converting enzyme inhibitors containing saturated bicyclic amino acids. |
TBA |
3005576 |
27 |
Angiotensin converting enzyme inhibitors as antihypertensive agents: 1-[(2-mercaptocycloalkyl)carbonyl]-L-prolines. |
TBA |
3906131 |
61 |
Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analogue inhibitors containing a novel analogue of statine. |
TBA |
2999394 |
21 |
Angiotensin converting enzyme inhibitors: structure-activity profile of 1-benzazepin-2-one derivatives. |
TBA |
2995670 |
12 |
Angiotensin converting enzyme inhibitors: 1,5-benzothiazepine derivatives. |
TBA |
6298429 |
31 |
(Mercaptopropanoyl)indoline-2-carboxylic acids and related compounds as potent angiotensin converting enzyme inhibitors and antihypertensive agents. |
TBA |
6298428 |
28 |
Antihypertensive agents: angiotensin converting enzyme inhibitors. 1-[3-(Acylthio)-3-aroylpropionyl]-L-prolines. |
TBA |
| 22 |
Design and synthesis of phosphinic acids that triply inhibit endothelin converting enzyme, angiotensin converting enzyme and neutral endopeptidase 24.11 |
TBA |
| 8 |
Studies on the structural feature of S'1 subsite of neprilysin (EC.3.4.24.11): Stereochemical requirement for the enzyme-inhibitor docking process |
TBA |
12113828 |
63 |
N-[2-(Indan-1-yl)-3-mercapto-propionyl] amino acids as highly potent inhibitors of the three vasopeptidases (NEP, ACE, ECE): In vitro and In vivo activities. |
University of Paris |
8360886 |
4 |
A mechanism-based inactivation study of neutral endopeptidase 24.11. |
Salk Biotechnology/Industrial Associates |
7562931 |
41 |
Peptidyl alpha-ketoheterocyclic inhibitors of human neutrophil elastase. 3. In vitro and in vivo potency of a series of peptidyl alpha-ketobenzoxazoles. |
Zeneca Pharmaceuticals |
3430165 |
2 |
Inhibitory effects of various flavonoids isolated from leaves of persimmon on angiotensin-converting enzyme activity. |
Ehime University |
2522989 |
14 |
Carboxyalkyl dipeptides with atrial natriuretic factor potentiating and antihypertensive activity. |
Schering-Plough Research Institute |
28810191 |
4 |
Structure-function studies of BPP-BrachyNH |
Universidade Federal Do Piau£ |
1992145 |
5 |
Design, synthesis, and physicochemical properties of a novel, conformationally restricted 2,3-dihydro-1,3,4-thiadiazole-containing angiotensin converting enzyme inhibitor which is preferentially eliminated by the biliary route in rats. |
Research and Development Laboratories |
28442252 |
62 |
Approaches towards the development of chimeric DPP4/ACE inhibitors for treating metabolic syndrome. |
Ranbaxy Laboratories |