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Journal Abstract Search

126 related items for PubMed ID: 6038494

  • 1. Adenosine aminohydrolase. Binding and hydrolysis of 2-and 6-substituted purine ribonucleosides and 9-substituted adenine nucleosides.
    Chassy BM, Suhadolnik RJ.
    J Biol Chem; 1967 Aug 25; 242(16):3655-8. PubMed ID: 6038494
    [No Abstract] [Full Text] [Related]

  • 2. On the rate-determining step in the action of adenosine deaminase.
    Wolfenden R.
    Biochemistry; 1969 Jun 25; 8(6):2409-12. PubMed ID: 5816377
    [No Abstract] [Full Text] [Related]

  • 3. Substrate properties of cycloadenosines with adenosine aminohydrolase as evidence for the conformation of enzyme-bound adenosine.
    Hampton A, Harper PJ, Sasaki T.
    Biochemistry; 1972 Dec 05; 11(25):4736-9. PubMed ID: 4676271
    [No Abstract] [Full Text] [Related]

  • 4. Substrate binding by adenosine deaminase. Specificity, pH dependence, and competition by mercurials.
    Wolfenden R, Sharpless TK, Allan R.
    J Biol Chem; 1967 Mar 10; 242(5):977-83. PubMed ID: 5335916
    [No Abstract] [Full Text] [Related]

  • 5. On the mechanism of adenosine deaminase action.
    Bär HP, Drummond GI.
    Biochem Biophys Res Commun; 1966 Aug 23; 24(4):584-7. PubMed ID: 5967246
    [No Abstract] [Full Text] [Related]

  • 6. Alkylation of adenosine deaminase by benzylbromoacetate and 9-(p-bromoacetamidobenzyl)adenine.
    Ronca G, Saettone MF, Lucacchini A.
    Biochim Biophys Acta; 1970 Jun 10; 206(3):414-25. PubMed ID: 5459550
    [No Abstract] [Full Text] [Related]

  • 7. Ring-modified substrates of adenosine deaminases.
    Wolfenden R, Kaufman J, Macon JB.
    Biochemistry; 1969 Jun 10; 8(6):2412-5. PubMed ID: 5816378
    [No Abstract] [Full Text] [Related]

  • 8.
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  • 9. Enzyme inhibitors. XX. Studies on the hydrophobic and hydroxyl binding regions of adenosine deaminase. 9-(2-m-Bromoacetamidophenethyl)adenine, a new irreversible inhibitor of adenosine deaminase.
    Schaeffer HJ, Johnson RN.
    J Med Chem; 1968 Jan 10; 11(1):21-6. PubMed ID: 5637186
    [No Abstract] [Full Text] [Related]

  • 10. N6-(delta 2-isopentenyl)adenosine: its conversion to inosine, catalyzed by adenosine aminohydrolases from chicken bone marrow and calf intestinal mucosa.
    Hall RH, Alam SN, McLennan BD.
    Can J Biochem; 1971 Jun 10; 49(6):623-30. PubMed ID: 5315139
    [No Abstract] [Full Text] [Related]

  • 11. Deamination of purine antibiotics by adenosine deaminase.
    Fukagawa Y, Sawa T, Takeuchi T, Umezawa H.
    J Antibiot (Tokyo); 1965 Jul 10; 18(4):191. PubMed ID: 5898336
    [No Abstract] [Full Text] [Related]

  • 12. Novel substrate of adenosine deaminase.
    Ogilvie KK, Slotin L, Rheault P.
    Biochem Biophys Res Commun; 1971 Oct 15; 45(2):297-300. PubMed ID: 5168598
    [No Abstract] [Full Text] [Related]

  • 13. Enzyme inhibitors. XVI. Mode of binding of some 9-(2-hydroxyalkyl)-6-(substituted)purines to adenosine deaminase.
    Schaeffer HJ, Schwender CF.
    J Pharm Sci; 1967 Feb 15; 56(2):207-11. PubMed ID: 6025775
    [No Abstract] [Full Text] [Related]

  • 14. Binding specificities of adenosine aminohydrolase from calf intestinal mucosa with dialdehydes derived from hexofuranosyladenine nucleosides.
    Grant AJ, Lerner LM.
    J Med Chem; 1980 Jan 15; 23(1):39-42. PubMed ID: 6965728
    [Abstract] [Full Text] [Related]

  • 15. Enzymatic and chemical deamination of 3-(beta-D-ribofuranosyl)adenine.
    Wolfenden R, Sharpless TK, Ragade IS, Leonard NJ.
    J Am Chem Soc; 1966 Jan 05; 88(1):185-6. PubMed ID: 5900391
    [No Abstract] [Full Text] [Related]

  • 16. Dialdehydes derived from adenine nucleosides as substrates and inhibitors of adenosine aminohydrolase.
    Grant AJ, Lerner LM.
    Biochemistry; 1979 Jun 26; 18(13):2838-42. PubMed ID: 476055
    [Abstract] [Full Text] [Related]

  • 17.
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  • 18. 6-18-O-PURINE NUCLEOTIDES. SYNTHESIS AND INFRARED BAND ASSIGNMENT.
    HOWARD FB, MILES HT.
    J Biol Chem; 1965 Feb 26; 240():801-5. PubMed ID: 14275138
    [No Abstract] [Full Text] [Related]

  • 19. Inhibitors of adenosine deaminase. Studies in combining high-affinity enzyme-binding structural units. erythro-1,6-Dihydro-6-(hydroxymethyl)-9-(2-hydroxy-3-nonyl)purine and erythro-9-(2-hydroxy-3-nonyl)purine.
    Woo PW, Baker DC.
    J Med Chem; 1982 May 26; 25(5):603-5. PubMed ID: 7086847
    [Abstract] [Full Text] [Related]

  • 20.
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