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Results: 1-12 |
Results: 12
PREGNANES THAT BIND TO THE DIGITALIS RECEPTOR
Authors: LABELLA FS TEMPLETON JF
Citation: Fs. Labella et Jf. Templeton, PREGNANES THAT BIND TO THE DIGITALIS RECEPTOR, Clinical and experimental hypertension, 20(5-6), 1998, pp. 601-609
SYNTHESIS OF 4-HYDROXYESTROGENS FROM STEROID 4,5-EPOXIDES - THERMAL REARRANGEMENT OF 4-CHLORO-4,5-EPOXIDES
Authors: MAJGIERBARANOWSKA H BRIDSON JN MARAT K TEMPLETON JF
Citation: H. Majgierbaranowska et al., SYNTHESIS OF 4-HYDROXYESTROGENS FROM STEROID 4,5-EPOXIDES - THERMAL REARRANGEMENT OF 4-CHLORO-4,5-EPOXIDES, Journal of the Chemical Society. Perkin transactions. I (Print), (12), 1998, pp. 1967-1972
BINDING OF [H-3]PALMITATE TO BSA
Authors: ELMADHOUN BM WANG GQ TEMPLETON JF BURZCZYNSKI FJ
Citation: Bm. Elmadhoun et al., BINDING OF [H-3]PALMITATE TO BSA, American journal of physiology: Gastrointestinal and liver physiology, 38(4), 1998, pp. 638-644
SYNTHESIS OF 19-HYDROXY-1-BETA,19-CYCLOSTEROIDS
Authors: TEMPLETON JF LIN WY LING YZ MAJGIERBARANOWSKA H MARAT K
Citation: Jf. Templeton et al., SYNTHESIS OF 19-HYDROXY-1-BETA,19-CYCLOSTEROIDS, Journal of the Chemical Society. Perkin transactions. I, (14), 1997, pp. 2037-2043
19-HYDROXY-5-BETA,19-CYCLOSTEROIDS - SYNTHESIS, ISOMERIZATION AND RING-OPENING
Authors: TEMPLETON JF LING YZ LIN WY MAJGIERBARANOWSKA H MARAT K
Citation: Jf. Templeton et al., 19-HYDROXY-5-BETA,19-CYCLOSTEROIDS - SYNTHESIS, ISOMERIZATION AND RING-OPENING, Journal of the Chemical Society. Perkin transactions. I, (12), 1997, pp. 1895-1904
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 17-BETA-SUBSTITUTED14-BETA-3-HYDROXYSTEROID 3-(ALPHA-L-RHAMNOPYRANOSIDE)S - STEROIDS THAT BIND TO THE DIGITALIS RECEPTOR
Authors: TEMPLETON JF LING YZ MARAT K LABELLA FS
Citation: Jf. Templeton et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 17-BETA-SUBSTITUTED14-BETA-3-HYDROXYSTEROID 3-(ALPHA-L-RHAMNOPYRANOSIDE)S - STEROIDS THAT BIND TO THE DIGITALIS RECEPTOR, Journal of medicinal chemistry, 40(10), 1997, pp. 1439-1446
RING-A CONFORMATION IN STEROIDS .3. CYCLOSTEROIDS AND CYCLOPROPANOSTEROIDS
Authors: MARAT K TEMPLETON JF LING YZ LIN WY GUPTA RK
Citation: K. Marat et al., RING-A CONFORMATION IN STEROIDS .3. CYCLOSTEROIDS AND CYCLOPROPANOSTEROIDS, Magnetic resonance in chemistry, 33(7), 1995, pp. 529-540
NOVEL INSERTION, REARRANGEMENT AND ADDITION-PRODUCTS FROM DIHALOGENOCARBENE REACTIONS WITH 5(10)-UNSATURATED STEROIDS
Authors: TEMPLETON JF LING YZ LIN WY PITURA RJ MARAT K BRIDSON JN
Citation: Jf. Templeton et al., NOVEL INSERTION, REARRANGEMENT AND ADDITION-PRODUCTS FROM DIHALOGENOCARBENE REACTIONS WITH 5(10)-UNSATURATED STEROIDS, Journal of the Chemical Society. Perkin transactions. I, (9), 1994, pp. 1149-1158
SYNTHESIS OF 20-HYDROXY-17,21-CYCLOPREGNANE DERIVATIVES - POTENTIAL C-20 OXO STEROID OXIDOREDUCTASE INHIBITORS
Authors: ORR JC TEMPLETON JF MAJGIERBARANOWSKA H MARAT K
Citation: Jc. Orr et al., SYNTHESIS OF 20-HYDROXY-17,21-CYCLOPREGNANE DERIVATIVES - POTENTIAL C-20 OXO STEROID OXIDOREDUCTASE INHIBITORS, Journal of the Chemical Society. Perkin transactions. I, (18), 1994, pp. 2667-2670
PREGNANE AND 21-NORPREGNANE DERIVATIVES OF OUABAIN THAT BIND TO THE DIGITALIS RECEPTOR
Authors: TEMPLETON JF LING Y ZEGLAM TH MARAT K LABELLA FS
Citation: Jf. Templeton et al., PREGNANE AND 21-NORPREGNANE DERIVATIVES OF OUABAIN THAT BIND TO THE DIGITALIS RECEPTOR, European journal of medicinal chemistry, 29(10), 1994, pp. 799-804
SYNTHESIS AND ISOMERIZATION OF 19-HYDROXY-5-BETA,19-CYCLOSTEROIDS
Authors: TEMPLETON JF LIN WY LING YZ MARAT K
Citation: Jf. Templeton et al., SYNTHESIS AND ISOMERIZATION OF 19-HYDROXY-5-BETA,19-CYCLOSTEROIDS, Tetrahedron letters, 35(32), 1994, pp. 5755-5758
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 14-BETA-HYDROXY-5-ALPHA-PREGNANES - PREGNANES THAT BIND TO THE CARDIAC GLYCOSIDE RECEPTOR
Authors: TEMPLETON JF LING YZ KUMAR VPS LABELLA FS
Citation: Jf. Templeton et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 14-BETA-HYDROXY-5-ALPHA-PREGNANES - PREGNANES THAT BIND TO THE CARDIAC GLYCOSIDE RECEPTOR, Steroids, 58(11), 1993, pp. 518-523
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