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Chemical Compound Review

Acetylpyridine     1-pyridin-2-ylethanone

Synonyms: PubChem13363, CHEMBL11945, SureCN55127, AGN-PC-00G6BY, SureCN149590, ...
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Disease relevance of NSC15043


High impact information on NSC15043


Chemical compound and disease context of NSC15043


Anatomical context of NSC15043


Associations of NSC15043 with other chemical compounds


  1. Antiviral activity of 2-acetylpyridine thiosemicarbazones against herpes simplex virus. Shipman, C., Smith, S.H., Drach, J.C., Klayman, D.L. Antimicrob. Agents Chemother. (1981) [Pubmed]
  2. In vitro susceptibility of Neisseria gonorrhoeae to 2-acetylpyridine thiosemicarbazones. Christenson, B., Rodríguez, J.R., Gorbea, H.F., Ramírez-Rond, C.H. Antimicrob. Agents Chemother. (1985) [Pubmed]
  3. 2-Acetylpyridine 5-[(dimethylamino)thiocarbonyl]-thiocarbonohydrazone (1110U81) potently inhibits human cytomegalovirus replication and potentiates the antiviral effects of ganciclovir. Hamzeh, F.M., Spector, T., Lietman, P.S. Antimicrob. Agents Chemother. (1993) [Pubmed]
  4. Structural chemistry and In vitro antitubercular activity of acetylpyridine benzoyl hydrazone and its copper complex against Mycobacterium smegmatis. Patole, J., Sandbhor, U., Padhye, S., Deobagkar, D.N., Anson, C.E., Powell, A. Bioorg. Med. Chem. Lett. (2003) [Pubmed]
  5. Thiosemicarbazones of 2-acetylpyridine, 2-acetylquinoline, 1-acetylisoquinoline, and related compounds as inhibitors of herpes simplex virus in vitro and in a cutaneous herpes guinea pig model. Shipman, C., Smith, S.H., Drach, J.C., Klayman, D.L. Antiviral Res. (1986) [Pubmed]
  6. Redox state of peroxy and ferryl intermediates in cytochrome c oxidase catalysis. Fabian, M., Palmer, G. Biochemistry (1999) [Pubmed]
  7. In vitro assessment of 2-acetylpyridine thiosemicarbazones against chloroquine-resistant Plasmodium falciparum. Lambros, C., Childs, G.E., Notsch, J.D., Scovill, J.P., Klayman, D.L., Davidson, D.E. Antimicrob. Agents Chemother. (1982) [Pubmed]
  8. 2-Acetylpyridine thiosemicarbazones. 2. N4,N4-Disubstituted derivatives as potential antimalarial agents. Klaymann, D.L., Scovill, J.P., Bartosevich, J.F., Mason, C.J. J. Med. Chem. (1979) [Pubmed]
  9. Synthesis and antiamoebic activity of new oxime ether derivatives containing 2-acetylpyridine/2-acetylfuran. Abid, M., Husain, K., Azam, A. Bioorg. Med. Chem. Lett. (2005) [Pubmed]
  10. 2-Acetylpyridine thiosemicarbazones. 6.2-Acetylpyridine and 2-butyrylpyridine thiosemicarbazones as antileukemic agents. Klayman, D.L., Scovill, J.P., Mason, C.J., Bartosevich, J.F., Bruce, J., Lin, A.J. Arzneimittel-Forschung. (1983) [Pubmed]
  11. Coupling of "malic" enzyme and NADPH:NAD transhydrogenase in the energetics of Hymenolepis diminuta (Cestoda). McKelvey, J.R., Fioravanti, C.F. Comp. Biochem. Physiol., B (1984) [Pubmed]
  12. Synthesis and biological activity of conformationally controlled 2-PAM derivatives. Jahng, Y., Park, J.G., Yoo, J.W., Kim, S.Y., Kim, T., Yang, J.H. Arch. Pharm. Res. (2000) [Pubmed]
  13. Activation of human placental 5-pregnene-3,20-dione isomerase activity by pyridine nucleotides. Blomquist, C.H., Kotts, C.E., Hakanson, E.Y. J. Steroid Biochem. (1988) [Pubmed]
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