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Journal Abstract Search

166 related items for PubMed ID: 25022879

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  • 3. Synthesis of 4'-modified noraristeromycins to clarify the effect of the 4'-hydroxyl groups for inhibitory activity against S-adenosyl-L-homocysteine hydrolase.
    Ando T, Kojima K, Chahota P, Kozaki A, Milind ND, Kitade Y.
    Bioorg Med Chem Lett; 2008 Apr 15; 18(8):2615-8. PubMed ID: 18374570
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  • 4. Discovery and structural analyses of S-adenosyl-L-homocysteine hydrolase inhibitors based on non-adenosine analogs.
    Nakao A, Suzuki H, Ueno H, Iwasaki H, Setsuta T, Kashima A, Sunada S.
    Bioorg Med Chem; 2015 Aug 01; 23(15):4952-4969. PubMed ID: 26037610
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  • 5. Open-chain carbocyclic analogs of adenosine with dihalovinyl unit as potential inhibitors of S-adenosyl-L-homocysteine hydrolase.
    Lewandowska E, Lalama J, Yuan CS, Wnuk SF.
    Nucleosides Nucleotides Nucleic Acids; 2003 Sep 01; 22(9):1747-55. PubMed ID: 14533879
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  • 8. Inhibition of S-adenosyl-L-homocysteine hydrolase induces immunosuppression.
    Wu QL, Fu YF, Zhou WL, Wang JX, Feng YH, Liu J, Xu JY, He PL, Zhou R, Tang W, Wang GF, Zhou Y, Yang YF, Ding J, Li XY, Chen XR, Yuan C, Lawson BR, Zuo JP.
    J Pharmacol Exp Ther; 2005 May 01; 313(2):705-11. PubMed ID: 15640397
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  • 11. Are L-adenosine and its derivatives substrates for S-adenosyl-L-homocysteine hydrolase?
    Wang M, Zhang J, Andrei D, Kuczera K, Borchardt RT, Wnuk SF.
    J Med Chem; 2005 May 19; 48(10):3649-53. PubMed ID: 15887973
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  • 12. Synthesis and biological activity of novel S-adenosyl-L-homocysteine hydrolase inhibitors.
    Steere JA, Honek JF.
    Bioorg Med Chem; 2003 Jul 31; 11(15):3229-36. PubMed ID: 12837532
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  • 13. Targeting "hydrolytic" activity of the S-adenosyl-L-homocysteine hydrolase.
    Wnuk SF.
    Mini Rev Med Chem; 2001 Sep 31; 1(3):307-16. PubMed ID: 12369977
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  • 14. Identification of novel S-adenosyl-L-homocysteine hydrolase inhibitors through homology-model-based virtual screening, synthesis, and biological evaluation.
    Khare P, Gupta AK, Gajula PK, Sunkari KY, Jaiswal AK, Das S, Bajpai P, Chakraborty TK, Dube A, Saxena AK.
    J Chem Inf Model; 2012 Mar 26; 52(3):777-91. PubMed ID: 22324915
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  • 16. Structure-based optimization of potent 4- and 6-azaindole-3-carboxamides as renin inhibitors.
    Scheiper B, Matter H, Steinhagen H, Böcskei Z, Fleury V, McCort G.
    Bioorg Med Chem Lett; 2011 Sep 15; 21(18):5480-6. PubMed ID: 21840218
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  • 18. The antiviral drug ribavirin is a selective inhibitor of S-adenosyl-L-homocysteine hydrolase from Trypanosoma cruzi.
    Cai S, Li QS, Borchardt RT, Kuczera K, Schowen RL.
    Bioorg Med Chem; 2007 Dec 01; 15(23):7281-7. PubMed ID: 17845853
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  • 19. Discovery of aminoheterocycles as potent and brain penetrant prolylcarboxypeptidase inhibitors.
    Wu Z, Yang C, Graham TH, Verras A, Chabin RM, Xu S, Tong X, Xie D, Lassman ME, Bhatt UR, Garcia-Calvo MM, Shen Z, Chen Q, Bleasby K, Sinharoy R, Hale JJ, Tata JR, Pinto S, Colletti SL, Shen DM.
    Bioorg Med Chem Lett; 2012 Feb 15; 22(4):1727-30. PubMed ID: 22290078
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  • 20. Synthesis of halogenated 9-(dihydroxycyclopent-4'-enyl) adenines and their inhibitory activities against S-adenosylhomocysteine hydrolase.
    Jeong LS, Park JG, Choi WJ, Moon HR, Lee KM, Kim HO, Kim HD, Chun MW, Park HY, Kim K, Sheen YY.
    Nucleosides Nucleotides Nucleic Acids; 2003 Feb 15; 22(5-8):919-21. PubMed ID: 14565311
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