7729. Pregnan-3α-ol-20-one

Nomenclature

CAS number: 128-20-1
(3α,5β)-3-Hydroxypregnan-20-one; 3α-hydroxy-5β-pregnan-20-one; pregnanolone; eltanolone; KABI 2213.
C21H34O2; mol wt 318.49.
C 79.19%, H 10.76%, O 10.05%.

Description and references

Naturally occurring metabolite of progesterone, q.v. Isoln from urine of pregnant women: R. E. Marker, O. Kamm, J. Am. Chem. Soc. 59, 1373 (1937); from bile of pregnant cows: W. H. Pearlman, E. Cerceo, J. Biol. Chem. 176, 847 (1948). Prepn: R. E. Marker et al., J. Am. Chem. Soc. 59, 1841 (1937); L. Gyermek et al., J. Med. Chem. 11, 117 (1968); T. L. G. Lemos, J. D. McChesney, J. Nat. Prod. 53, 152 (1990). Pharmacokinetics and pharmacodynamics: P. Carl et al., Acta Anaesthesiol. Scand. 38, 734 (1994). Comparative clinical evaluation: J. Van Hemelrijck et al., Anesthesiology 80, 36 (1994); H. Eriksson et al., Acta Anaesthesiol. Scand. 39, 479 (1995). Hemodynamic effects in humans: J. W. Sear et al., J. Clin. Anesth. 7, 126 (1995).

Chemical structure

Properties

Needles from aq methanol, mp 148-148.5° (Pearlman, Cerceo); also reported as cryst from hexane, mp 131-132° (Lemos, McChesney). [α]D23 +59.6° (c = 0.3 in chloroform). [α]D26 +108.5 ±1° (c = 9.23 mg/1.23 ml abs ethanol). LD50 in mice, rats (mg/kg): 66 ± 10, 27.5 ± 2.4 i.v. (Gyermek).

Therapeutic Category

Anesthetic (local).