Inhibition of phosphatidylinositol kinase by toyocamycin.
H Nishioka, T Sawa, M Hamada, N Shimura, M Imoto, K Umezawa
Index: J. Antibiot. 43 , 1586-1589, (1990)
Full Text: HTML
Abstract
We have screened toyocamycin as an inhibitor of phosphatidylinositol kinase. It inhibited the enzyme of A431 cell membrane with an IC50 of 3.3 micrograms/ml. Adenosine and formycin A also inhibited the enzyme, but other 6 related nucleosides did not. Although orobol and 2,3-dihydroxybenzaldehyde that inhibit phosphatidylinositol kinase inhibited in situ phosphatidylinositol turnover, toyocamycin did not.
Related Compounds
Related Articles:
Self-activating nuclease activity of copper (II) complexes of hydroxyl-rich ligands.
2006-01-01
[J. Inorg. Biochem. 100(1) , 51-7, (2006)]
1996-08-01
[Chem. Pharm. Bull. 44(8) , 1484-92, (1996)]
2016-01-01
[Photochem. Photobiol. Sci. 15 , 86-98, (2016)]
[Studies on chemical constituents from Elaeocarpus sylvestris].
2008-10-01
[Zhong Yao Cai 31(10) , 1503-5, (2008)]
Characterization of the effects of oxygen on xanthine oxidase-mediated nitric oxide formation.
2004-04-23
[J. Biol. Chem. 279(17) , 16939-46, (2004)]