-
3
-
-
0035976575
-
Prostaglandins and leukotrienes: Advances in Eicosanoid biology
-
Funk C.D. Prostaglandins and leukotrienes: advances in Eicosanoid biology. Science. 294:2001;1871-1875
-
(2001)
Science
, vol.294
, pp. 1871-1875
-
-
Funk, C.D.1
-
4
-
-
0030736867
-
The structure of mammalian 15-lipoxygenase reveals similarity to the lipases and the determinants of substrate specificity
-
Gillmor S.A., Villasenor A., Fletterick R., Sigal E., Browner M.F. The structure of mammalian 15-lipoxygenase reveals similarity to the lipases and the determinants of substrate specificity. Nat. Struct. Biol. 4:1997;1003-1009
-
(1997)
Nat. Struct. Biol.
, vol.4
, pp. 1003-1009
-
-
Gillmor, S.A.1
Villasenor, A.2
Fletterick, R.3
Sigal, E.4
Browner, M.F.5
-
5
-
-
0029925883
-
Chiral acetals: Stereocontrolled syntheses of 16-, 17-, and 18-hydroxyeicosatetraenoic acids, cytochrome P-450 arachidonate metabolites
-
Heckmann B., Mioskowski C.H., Lumin S., Falck J.R., Wei S.H., Capdevila J.H. Chiral acetals: stereocontrolled syntheses of 16-, 17-, and 18-hydroxyeicosatetraenoic acids, cytochrome P-450 arachidonate metabolites. Tetrahedron Lett. 37:1996;1425-1428
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 1425-1428
-
-
Heckmann, B.1
Mioskowski, C.H.2
Lumin, S.3
Falck, J.R.4
Wei, S.H.5
Capdevila, J.H.6
-
6
-
-
0036235265
-
A simple method for the preparation of (5Z,8Z,11Z,14Z)-16-hydroxyeicosa- 5,8,11,14-tetraenoic acid enantiomers and the corresponding 14,15-dehydro analogues: Role of the 16-hydroxy group for the lipoxygenase reaction
-
Ivanov I.V., Romanov S.G., Groza N.V., Nigam S., Kuhn H., Myagkova G.I. A simple method for the preparation of (5Z, 8Z, 11Z, 14Z)-16-hydroxyeicosa-5, 8, 11, 14-tetraenoic acid enantiomers and the corresponding 14, 15-dehydro analogues: role of the 16-hydroxy group for the lipoxygenase reaction. Bioorg. Med. Chem. 10:2002;2335-2343
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 2335-2343
-
-
Ivanov, I.V.1
Romanov, S.G.2
Groza, N.V.3
Nigam, S.4
Kuhn, H.5
Myagkova, G.I.6
-
7
-
-
0030461132
-
Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents
-
Kurumbail R.G., Stevens A.M., Gierse J.K., McDonald J.J., Stegeman R.A., Pak J.Y., Gildehaus D., Iyashiro J.M., Penning T.D., Seibert K., Isakson P.C., Stallings W.C. Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents. Nature. 384:1996;644-648
-
(1996)
Nature
, vol.384
, pp. 644-648
-
-
Kurumbail, R.G.1
Stevens, A.M.2
Gierse, J.K.3
McDonald, J.J.4
Stegeman, R.A.5
Pak, J.Y.6
Gildehaus, D.7
Iyashiro, J.M.8
Penning, T.D.9
Seibert, K.10
Isakson, P.C.11
Stallings, W.C.12
-
8
-
-
0004713126
-
Fatty acids, part 31. the preparation and some physical properties of azido fatty esters
-
Lie Ken Jie M.S.F., Lao H.B. Fatty acids, part 31. The preparation and some physical properties of azido fatty esters. Chem. Phys. Lipids. 45:1987;65-74
-
(1987)
Chem. Phys. Lipids
, vol.45
, pp. 65-74
-
-
Lie Ken Jie, M.S.F.1
Lao, H.B.2
-
9
-
-
3042731405
-
Organocopper chemistry. Halo-, cyano-, and carbonyl-substituted ketones from the corresponding acyl chlorides and organocopper reagents
-
Posner G.H., Whitten C.E., McFarland P.E. Organocopper chemistry. Halo-, cyano-, and carbonyl-substituted ketones from the corresponding acyl chlorides and organocopper reagents. J. Am. Chem. Soc. 94:1972;5106-5108
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 5106-5108
-
-
Posner, G.H.1
Whitten, C.E.2
McFarland, P.E.3
-
10
-
-
0018227672
-
The lipoxygenase of reticulocytes. Purification, characterization and biological dynamics of the lipoxygenase its identity with the respiratory inhibitors of the reticulocyte
-
Rapoport S.M., Schewe T., Wiesner R., Halangk W., Ludwig P., Janicke-Höhne M., Tannert C., Hiebsch C., Klatt D. The lipoxygenase of reticulocytes. Purification, characterization and biological dynamics of the lipoxygenase its identity with the respiratory inhibitors of the reticulocyte. Eur. J. Biochem. 96:1979;545-561
-
(1979)
Eur. J. Biochem.
, vol.96
, pp. 545-561
-
-
Rapoport, S.M.1
Schewe, T.2
Wiesner, R.3
Halangk, W.4
Ludwig, P.5
Janicke-Höhne, M.6
Tannert, C.7
Hiebsch, C.8
Klatt, D.9
-
11
-
-
0037078271
-
Total synthesis of (5Z,8Z,11Z,14Z)-18- and 19-oxoeicosa-5,8,11,14- tetraenoic acids
-
Romanov S.G., Ivanov I.V., Groza N.V., Kuhn H., Myagkova G.I. Total synthesis of (5Z, 8Z, 11Z, 14Z)-18- and 19-oxoeicosa-5, 8, 11, 14-tetraenoic acids. Tetrahedron. 58:2002;8483-8487
-
(2002)
Tetrahedron
, vol.58
, pp. 8483-8487
-
-
Romanov, S.G.1
Ivanov, I.V.2
Groza, N.V.3
Kuhn, H.4
Myagkova, G.I.5
-
12
-
-
0032810754
-
2α
-
2α. J. Label. Comp. Radiopharm. 42:1999;663-672
-
(1999)
J. Label. Comp. Radiopharm.
, vol.42
, pp. 663-672
-
-
Shevchenko, V.P.1
Nagaev, I.Yu.2
Myasoedov, N.F.3
Guy, A.4
Durand, T.5
Vidal, A.6
Vidal, J.-P.7
Rossi, J.-C.8
Bezuglov, V.V.9
|