R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL


R Plus 3-BETA HYDROXYL
 
  1. R.Dixon, V.Vincent and N.Kase, Steroids 6:757 (1965)
2. E.-E.Baulieu and r.Emiliozzi, Bull. Soc. Chim. Biol. 44:823 (1962)
3. J.McKenna and A.E.Rippon, Biochem. J. 95:107 (1965)
4. E.Schapiro, Nature 142:1036 (1938)
5. E.Schapiro, Biochem. J. 33:385 (1939)
6. P.K.Siteri, Ph.D. Thesis, Columbia University, New York (1963)
7. P.K.Siteri, R.L.Vande Wiele and S.Lieberman, J. Clin. Endocrinol. and Metab. 23:588 (1963)
8. J.P.Joseph, J.P.Dusza and S.Bernstein, Steroids 7:577 (1966)
9. E.-E.Baulieu, Compt. rend. 248:1441 (1959)
10. S.Lieberman, L.B.Hariton and D.K.Fukushima, J.Am. Chem. Soc. 70:1427 (1948)
11. F.D'Alo, Farmace (Pavia) Ed. Sci. 11:477 (1956)
12. J.F.Becker, Biochem. Biophys. Acta 100:574 (1965)
13. R.Emiliozzi, Compt. rend. 258:3875 (1964)
14. R.Emiliozzi, Bull. Soc. Chim. France, 911 (1960)
15. S.Burstein and S.Lieberman, J. Am. Chem. Soc. 80:5235 (1958)
16. E.-E.Baulieu and R.Emiliozzi, Compt. rend. 251:3106 (1960)
17. E.-E.Baulieu, R.Emiliozzi and C. Corpechot, Experientia 17:110 (1961)
18. H.H.Wotiz, H.G.Sie and W.H.Fishman, J. Biol. Chem. 232:723 (1958)
19. R.Vihko, Acta endocrinol. Suppl. 52:109 (1966)
20. R.Zelnik, B.Desfosses and R.Emiliozzi, Compt. rend. 250:1671 (1960)
21. W.Klyne and G.F. Marrian, Biochem. J. 39:45p (1945)
22. R.A.Lucas,D.F.Dickel,R.L.Dzieman,M.J.Ceglowski,B.L.Hensie,H.B.MacPhillamy, J.Am.Chem.Soc. 82:5688 (1960)
23. H.I.Calvin and S.Lieberman, Biochemistry, 3:259 (1964)
24. K.D.Roberts, L.Bandi, H.I.Calvin, W.D.Drucker and S.Lieberman, Biochemistry 3:1983 (1964)

Steroid Glucuronides and Sulfates. A table of their physico-chemical constants, structures and nomenclature.
COPYRIGHT © Harry E. Hadd, Ph.D., 1969

The compounds are listed in the table first by the Number of the Carbon Atom of the Steroid bearing the Hydroxyl Group that is Conjuated and its Configuration, viz., 3-Alpha Hydroxyl: second by the Number of Carbon Atoms in the Steroid; third by the Glucuronide and Sulfate of that Steroid.

The Structural Formula of each Steroid Conjugate is that of the Free Acid. Listed are the Physical Constants of the Steroid Glucuronides: Free Acid (G), Sodium Salt (G-Na), acetylated methyl ester (GAc3); of the Steroid Sulfates: Sodium Salt (Na+), Potassium Salt (K+), Ammonium Salt (NH4+), Pyridinium Salt. The number in parenthesis is the Reference Number to the listed conjugate. If the conjugate or derivative have been made, the Melting Point and Optical Rotation are recorded. The Molecular Weight and Elemental Composition are shown by % Composition of the individual atoms, beneath which is the number of atoms in the molecule.

** M is Na or K