| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
A new class of angiotensin-converting enzyme inhibitors.
|
Nature
|
1980
|
3.03
|
|
2
|
Enalapril maleate and a lysine analogue (MK-521): disposition in man.
|
Br J Clin Pharmacol
|
1982
|
2.49
|
|
3
|
Enalapril maleate and a lysine analogue (MK-521) in normal volunteers; relationship between plasma drug levels and the renin angiotensin system.
|
Br J Clin Pharmacol
|
1982
|
1.95
|
|
4
|
The physiological disposition and metabolism of enalapril maleate in laboratory animals.
|
Drug Metab Dispos
|
1982
|
1.79
|
|
5
|
Alpha-isopropylmalate synthase from yeast: purification, kinetic studies, and effect of ligands on stability.
|
J Bacteriol
|
1972
|
1.66
|
|
6
|
Effect of N-[(S)-1-carboxy-3-phenylpropyl]-L-Ala-L-Pro and its ethyl ester (MK-421) on angiotensin converting enzyme in vitro and angiotensin I pressor responses in vivo.
|
J Pharmacol Exp Ther
|
1981
|
1.44
|
|
7
|
Effect of experimental diabetes on elimination kinetics of diflunisal in rats.
|
Drug Metab Dispos
|
1989
|
1.14
|
|
8
|
Enalapril maleate (MK-421), a potent, nonsulfhydryl angiotensin-converting enzyme inhibitor: absorption, disposition, and metabolism in man.
|
Drug Metab Rev
|
1983
|
1.04
|
|
9
|
Role of oleate in the regulation of "neutral" rabbit liver fructose 1,6-diphosphatase activity.
|
J Biol Chem
|
1973
|
0.99
|
|
10
|
Differential renal handling of angiotensin-converting enzyme inhibitors enalaprilat and lisinopril in rats.
|
Drug Metab Dispos
|
1988
|
0.97
|
|
11
|
Bexarotene metabolism in rat, dog, and human, synthesis of oxidative metabolites, and in vitro activity at retinoid receptors.
|
Drug Metab Dispos
|
2001
|
0.94
|
|
12
|
A Phase I study of LGD1069 in adults with advanced cancer.
|
Clin Cancer Res
|
1999
|
0.94
|
|
13
|
Novel renin inhibitors containing the amino acid statine.
|
Nature
|
1983
|
0.93
|
|
14
|
Phosphorus-containing inhibitors of angiotensin-converting enzyme.
|
Proc Natl Acad Sci U S A
|
1982
|
0.93
|
|
15
|
Inhibitors of glycolic acid oxidase. 4-Substituted 3-hydroxy-1H-pyrrole-2,5-dione derivatives.
|
J Med Chem
|
1983
|
0.92
|
|
16
|
The reaction of PGA1 with sulfhydryl groups; a component in the binding of A-type prostaglandins to proteins.
|
Prostaglandins
|
1975
|
0.88
|
|
17
|
Urinary excretion kinetics of famotidine in rats.
|
Drug Metab Dispos
|
1987
|
0.88
|
|
18
|
Effects of retinoid treatment of rats on hepatic microsomal metabolism and cytochromes P450. Correlation between retinoic acid receptor/retinoid x receptor selectivity and effects on metabolic enzymes.
|
Drug Metab Dispos
|
1998
|
0.86
|
|
19
|
Biotransformation of lovastatin. I. Structure elucidation of in vitro and in vivo metabolites in the rat and mouse.
|
Drug Metab Dispos
|
1990
|
0.85
|
|
20
|
Initial clinical trial of the retinoid receptor pan agonist 9-cis retinoic acid.
|
Clin Cancer Res
|
1996
|
0.84
|
|
21
|
Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analogue inhibitors containing a novel analogue of statine.
|
J Med Chem
|
1985
|
0.84
|
|
22
|
Oxidative and reductive metabolism of 9-cis-retinoic acid in the rat. Identification of 13,14-dihydro-9-cis-retinoic acid and its taurine conjugate.
|
Drug Metab Dispos
|
1996
|
0.83
|
|
23
|
Biotransformation of lovastatin. V. Species differences in in vivo metabolite profiles of mouse, rat, dog, and human.
|
Drug Metab Dispos
|
1994
|
0.83
|
|
24
|
Fructose-1, 6-diphosphatase from rabbit liver.
|
Methods Enzymol
|
1975
|
0.82
|
|
25
|
Kinetic studies on the competition between famotidine and cimetidine in rats. Evidence of multiple renal secretory systems for organic cations.
|
Drug Metab Dispos
|
1988
|
0.81
|
|
26
|
Conformationally restricted inhibitors of angiotensin converting enzyme: synthesis and computations.
|
J Med Chem
|
1986
|
0.81
|
|
27
|
Benzolactams. A new class of converting enzyme inhibitors.
|
Biochem Biophys Res Commun
|
1983
|
0.81
|
|
28
|
Renin inhibitors. Statine-containing tetrapeptides with varied hydrophobic carboxy termini.
|
J Med Chem
|
1987
|
0.80
|
|
29
|
Phase I study of 9-cis-retinoic acid (ALRT1057 capsules) in adults with advanced cancer.
|
Clin Cancer Res
|
1998
|
0.80
|
|
30
|
Total serum angiotensin converting enzyme activity in rats and dogs after enalapril maleate (MK-421).
|
Life Sci
|
1982
|
0.79
|
|
31
|
Disposition of enalapril and its diacid metabolite, enalaprilat, in a perfused rat liver preparation. Presence of a diffusional barrier for enalaprilat into hepatocytes.
|
Drug Metab Dispos
|
1984
|
0.79
|
|
32
|
A 15-hydroxyprostaglandin dehydrogenase specific for prostaglandin A in rabbit kidney.
|
Proc Natl Acad Sci U S A
|
1976
|
0.78
|
|
33
|
A uniquely potent renin inhibitor and its unanticipated plasma binding component.
|
J Med Chem
|
1985
|
0.78
|
|
34
|
Possible mechanisms for reduced plasma clearance of diflunisal in rat experimental renal failure.
|
J Pharmacol Exp Ther
|
1986
|
0.78
|
|
35
|
Disposition of enalapril in the perfused rat intestine-liver preparation: absorption, metabolism and first-pass effect.
|
J Pharmacol Exp Ther
|
1985
|
0.78
|
|
36
|
Pharmacokinetics of 9-cis-retinoic acid in the rhesus monkey.
|
Cancer Res
|
1995
|
0.77
|
|
37
|
Renal effects of enalapril in dogs.
|
Kidney Int Suppl
|
1987
|
0.75
|
|
38
|
Antihypertensive activity of metyrosine in spontaneously hypertensive rats and its enhancement by carbidopa.
|
Clin Sci Mol Med Suppl
|
1978
|
0.75
|
|
39
|
Azapeptides: a new class of angiotensin-converting enzyme inhibitors.
|
Biochem Biophys Res Commun
|
1984
|
0.75
|
|
40
|
Quantitative determination of L-364,718, a novel cholecystokinin antagonist, by solid-phase extraction and high-performance liquid chromatography.
|
J Chromatogr
|
1988
|
0.75
|
|
41
|
Species-dependent enantioselective plasma protein binding of MK-571, a potent leukotriene D4 antagonist.
|
Drug Metab Dispos
|
1990
|
0.75
|
|
42
|
Dose-dependent pharmacokinetics of MK-417, a potent carbonic anhydrase inhibitor, in rabbits following single and multiple doses.
|
Drug Metab Dispos
|
1991
|
0.75
|
|
43
|
Differential effects of phenobarbital on ester and ether glucuronidation of diflunisal in rats.
|
J Pharmacol Exp Ther
|
1987
|
0.75
|
|
44
|
Dipeptide mimics. Conformationally restricted inhibitors of angiotensin-converting enzyme.
|
Biochem Biophys Res Commun
|
1983
|
0.75
|
|
45
|
Involvement of cytosol proteins in oleate activation of rabbit liver fructose-1,6-diphosphatase.
|
J Biol Chem
|
1975
|
0.75
|
|
46
|
Antihypertensive activity of some novel pyridinylidene arylurea derivatives in spontaneously hypertensive rats.
|
Experientia
|
1979
|
0.75
|
|
47
|
Renin inhibitors containing 2-substituted statine.
|
Biochem Soc Trans
|
1984
|
0.75
|
|
48
|
Renin inhibitors containing hydrophilic groups. Tetrapeptides with enhanced aqueous solubility and nanomolar potency.
|
J Med Chem
|
1988
|
0.75
|
|
49
|
Design of proteolytically-stable, peptidal renin inhibitors and determination of their fate in vivo.
|
Regul Pept Suppl
|
1985
|
0.75
|
|
50
|
Angiotensin-converting enzyme inhibitors: synthesis and biological activity of acyl tripeptide analogues of enalapril.
|
J Med Chem
|
1985
|
0.75
|
|
51
|
Dose-dependent stereopharmacokinetics of 5,6-dihydro-4H-4(isobutylamino)thieno(2,3-B)thiopyran-2-sulfonamide-7,7 -dioxide , a potent carbonic anhydrase inhibitor, in rats.
|
Drug Metab Dispos
|
1991
|
0.75
|
|
52
|
Dose-dependent kinetics of cilastatin in laboratory animals.
|
Drug Metab Dispos
|
1989
|
0.75
|