BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 3486292)

  • 1. Inhibitors of dihydropteroate synthase: substituent effects in the side-chain aromatic ring of 6-[[3-(aryloxy)propyl]amino]-5-nitrosoisocytosines and synthesis and inhibitory potency of bridged 5-nitrosoisocytosine-p-aminobenzoic acid analogues.
    Lever OW; Bell LN; Hyman C; McGuire HM; Ferone R
    J Med Chem; 1986 May; 29(5):665-70. PubMed ID: 3486292
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Monocyclic pteridine analogues. Inhibition of Escherichia coli dihydropteroate synthase by 6-amino-5-nitrosoisocytosines.
    Lever OW; Bell LN; McGuire HM; Ferone R
    J Med Chem; 1985 Dec; 28(12):1870-4. PubMed ID: 3906132
    [TBL] [Abstract][Full Text] [Related]  

  • 3. P-Aminobenzoic acid derivatives as inhibitors of the cell-free H2-pteroate synthesizing system of Escherichia coli.
    Thijssen HH
    J Med Chem; 1977 Feb; 20(2):233-6. PubMed ID: 319235
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The effect of mafenide on dihydropteroate synthase.
    Eagon RG; McManus AT
    J Antimicrob Chemother; 1990 Jan; 25(1):25-9. PubMed ID: 2108114
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phosphanilic acid inhibits dihydropteroate synthase.
    Eagon RG; McManus AT
    Antimicrob Agents Chemother; 1989 Nov; 33(11):1936-8. PubMed ID: 2514624
    [TBL] [Abstract][Full Text] [Related]  

  • 6. P-Aminobenzoic acid derivatives. Mode of action and structure-activity relationships in a cell-free system (Escherichia coli).
    Seydel JK; Butte W
    J Med Chem; 1977 Mar; 20(3):439-47. PubMed ID: 321779
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cell-free dihydropteroate synthetase activity: its use to investigate the relationship between structure and activity of p-aminobenzoic derivatives.
    Thijssen HH
    Methods Enzymol; 1980; 66():570-6. PubMed ID: 6990197
    [No Abstract]   [Full Text] [Related]  

  • 8. Inhibition of Pneumocystis carinii dihydropteroate synthetase by para-acetamidobenzoic acid: possible mechanism of action of isoprinosine in human immunodeficiency virus infection.
    Kovacs JA; Powell F; Voeller D; Allegra CJ
    Antimicrob Agents Chemother; 1993 Jun; 37(6):1227-31. PubMed ID: 7687120
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Potential antiatherosclerotic agents. 4. [(Functionalized-alkyl)amino]benzoic acid analogues of cetaben.
    DeVries VG; Largis EE; Miner TG; Shepherd RG; Upeslacis J
    J Med Chem; 1983 Oct; 26(10):1411-21. PubMed ID: 6604818
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Potential antiatherosclerotic agents. 3. Substituted benzoic and non benzoic acid analogues of cetaben.
    Albright JD; DeVries VG; Du MT; Largis EE; Miner TG; Reich MF; Shepherd RG
    J Med Chem; 1983 Oct; 26(10):1393-411. PubMed ID: 6604817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of mutationally altered dihydropteroate synthase and its ability to form a sulfonamide-containing dihydrofolate analog.
    Swedberg G; Castensson S; Sköld O
    J Bacteriol; 1979 Jan; 137(1):129-36. PubMed ID: 368012
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PABA/NO as an anticancer lead: analogue synthesis, structure revision, solution chemistry, reactivity toward glutathione, and in vitro activity.
    Saavedra JE; Srinivasan A; Buzard GS; Davies KM; Waterhouse DJ; Inami K; Wilde TC; Citro ML; Cuellar M; Deschamps JR; Parrish D; Shami PJ; Findlay VJ; Townsend DM; Tew KD; Singh S; Jia L; Ji X; Keefer LK
    J Med Chem; 2006 Feb; 49(3):1157-64. PubMed ID: 16451080
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interaction of sulfonamide and sulfone compounds with Toxoplasma gondii dihydropteroate synthase.
    Allegra CJ; Boarman D; Kovacs JA; Morrison P; Beaver J; Chabner BA; Masur H
    J Clin Invest; 1990 Feb; 85(2):371-9. PubMed ID: 2298911
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantitative structure-activity relationships in dihydropteroate synthase inhibition by multisubstituted sulfones. Design and synthesis of some new derivatives with improved potency.
    De Benedetti PG; Iarossi D; Folli U; Frassineti C; Menziani MC; Cennamo C
    J Med Chem; 1989 Oct; 32(10):2396-9. PubMed ID: 2677378
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Potential antiatherosclerotic agents. 2. (Aralkylamino)- and (alkylamino) benzoic acid analogues of cetaben.
    Albright JD; DeVries VG; Largis EE; Miner TG; Reich MF; Schaffer SA; Shepherd RG; Upeslacis J
    J Med Chem; 1983 Oct; 26(10):1378-93. PubMed ID: 6604816
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeting methanopterin biosynthesis to inhibit methanogenesis.
    Dumitru R; Palencia H; Schroeder SD; DeMontigny BA; Takacs JM; Rasche ME; Miner JL; Ragsdale SW
    Appl Environ Microbiol; 2003 Dec; 69(12):7236-41. PubMed ID: 14660371
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Quantitative structure-activity analysis in dihydropteroate synthase inhibition by sulfones. Comparison with sulfanilamides.
    De Benedetti PG; Iarossi D; Menziani C; Caiolfa V; Frassineti C; Cennamo C
    J Med Chem; 1987 Mar; 30(3):459-64. PubMed ID: 3546688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structure-activity relationships in dihydropteroate synthase inhibition by sulfanilamides. Comparison with the antibacterial activity.
    De Benedetti PG; Rastelli A; Frassineti C; Cennamo C
    J Med Chem; 1981 Apr; 24(4):454-7. PubMed ID: 7021831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Arabidopsis dihydropteroate synthase: general properties and inhibition by reaction product and sulfonamides.
    Prabhu V; Lui H; King J
    Phytochemistry; 1997 May; 45(1):23-7. PubMed ID: 9127492
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Computational insights into factor affecting the potency of diaryl sulfone analogs as Escherichia coli dihydropteroate synthase inhibitors.
    Das BK; Pv P; Chakraborty D
    Comput Biol Chem; 2019 Feb; 78():37-52. PubMed ID: 30497019
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.