Detalhe da pesquisa
1.
Comparison of triazines as inhibitors of L1210 dihydrofolate reductase and of L1210 cells sensitive and resistant to methotrexate.
Cancer Res
; 46(2): 744-56, 1986 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-3940640
2.
Human placental alkaline phosphatase in benign and malignant ovarian neoplasia.
Cancer Res
; 45(2): 892-902, 1985 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-3967249
3.
The structure-activity relationship of the papain hydrolysis of N-benzoylglycine esters.
Biochim Biophys Acta
; 1038(2): 158-63, 1990 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-2331480
4.
Separation of electronic and hydrophobic effects for the papain hydrolysis of substituted N-benzoylglycine esters.
Biochim Biophys Acta
; 1079(1): 43-52, 1991 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-1888764
5.
Selective inhibition of Leishmania dihydrofolate reductase and Leishmania growth by 5-benzyl-2,4-diaminopyrimidines.
Mol Biochem Parasitol
; 31(1): 79-85, 1988 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-3185614
6.
On the structure of medicinal chemistry.
J Med Chem
; 19(1): 1-6, 1976 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-1246029
7.
Correlation analysis of Baker's studies on enzyme inhibition. 2. Chymotrypsin, trypsin, thymidine phosphorylase, uridine phosphorylase, thymidylate synthetase, cytosine nucleoside deaminase, dihydrofolate reductase, malate dehydrogenase, glutamate dehydrogenase, lactate dehydrogenase, and glyceraldehyde-phosphate dehydrogenase.
J Med Chem
; 19(1): 71-98, 1976 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-1107550
8.
Correlation analysis of Baker's studies on enzyme inhibition. 1. Guanine deaminase, xanthine oxidase, dihydrofolate reductase, and complement.
J Med Chem
; 19(1): 62-71, 1976 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-1246055
9.
Structure-activity relationships in antitumor aniline mustards.
J Med Chem
; 21(1): 16-26, 1978 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-619146
10.
Structure-activity relationship of aniline mustards acting against B-16 melanoma in mice.
J Med Chem
; 22(10): 1267-9, 1979 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-513075
11.
Structure-activity relationship of the ficin hydrolysis of phenyl hippurates. Comparison with papain, actinidin, and bromelain.
J Med Chem
; 27(11): 1427-31, 1984 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-6387120
12.
Mutagenicity of substituted (o-phenylenediamine)platinum dichloride in the Ames test. A quantitative structure-activity analysis.
J Med Chem
; 23(4): 459-61, 1980 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-6991694
13.
Structure-activity relationship in synthetic fibrinolytics. 2-Phenethynylcyclopropanecarboxylates.
J Med Chem
; 18(9): 950-1, 1975 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1159718
14.
A comparison of the inhibitory action of 5-(substituted-benzyl)-2,4-diaminopyrimidines on dihydrofolate reductase from chicken liver with that from bovine liver.
J Med Chem
; 25(4): 435-40, 1982 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-7069722
15.
Quantitative structure-selectivity relationships. Comparison of the inhibition of Escherichia coli and bovine liver dihydrofolate reductase by 5-(substituted-benzyl)-2,4-diaminopyrimidines.
J Med Chem
; 24(5): 538-44, 1981 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-7017146
16.
Structure-activity relationships of antineoplastic agents in multidrug resistance.
J Med Chem
; 33(7): 1914-9, 1990 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-2362268
17.
Quantitative structure-activity relationships of antimalarial and dihydrofolate reductase inhibition by quinazolines and 5-substituted benzyl-2,4-diaminopyrimidines.
J Med Chem
; 20(1): 96-102, 1977 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-319234
18.
Inhibition of dihydrofolate reductase. Structure-activity correlations of quinazolines.
J Med Chem
; 19(5): 605-11, 1976 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-1271401
19.
Dependence of hydrophobicity of apolar molecules on their molecular volume.
J Med Chem
; 19(5): 611-5, 1976 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-1271402
20.
Quantitative structure-activity relationship of chymotrypsin-ligand interactions.
J Med Chem
; 20(11): 1420-35, 1977 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-915902