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Cholesterol progesterone

For all the calculations the parameter ki2 of the classical van der Waals mixing rules was fitted. It can be seen from Table 2 that the volume correction does not give a significant improvement slightly worst results are obtaned with SRK EOS while the PRmod shows a clear improvement at lower temperatures (as in the case of Cholesterol, Progesterone..). [Pg.266]

Progesterone can be manufactured from cholesterol, from certain steroid sapogenins and from stigmasierol. [Pg.327]

A direct, one-step aromatization of 19-substituted steroids has appeared in the Hterature, ie, cholesterol (3), dehydroisoandrosterone, androsterone, progesterone (1), and testosterone react with an electrophilic mthenium complex, C Ru , where Cp represents Tj -cyclopentadienyl, obtained through protonation of [Cp Ru(OCH2)]2 using triflic acid, to provide estrone (20) directly (46). [Pg.210]

FIGURE 25.43 The steroid hormones are synthesized from cholesterol, with intermediate formation of pregnenolone and progesterone. Testosterone, the principal male sex hormone steroid, is a precursor to /3-estradiol. Cortisol, a glucocorticoid, and aldosterone, a mineralocorticoid, are also derived from progesterone. [Pg.848]

BCRP (ABCG2) Cisplatin, folate, methotrexate, mitoxantrone, topotecan, irinotecan, steroids (cholesterol, testosterone, progesterone), certain chlorophyll metabolites, and others... [Pg.7]

Recently, Voogt et al. [91] have reported on the d5-pathway in steroid metabolism of Asterias rubens. These workers established the existence of the d5-pathway (Scheme 20), analogous to the pathway found in mammals this conclusion was based on the observation that radiolabeled cholesterol (1) was converted to pregnenolone (112), 17a-hydroxypregnenolone (141), and androstenediol (142). Labeled pregnenolone was converted additionally to progesterone (129). Androstenediol (142) was the main metabolite of de-hydroepiandrosterone (143), a reaction catalyzed by 17/i-hydroxysteroid dehydrogenase (17/1-HSD). The metabolic conversion of androstenedione (131) to testosterone (132) is also mediated by 17/J-HSD and is related to... [Pg.32]

FIGURE 4.44 Cytochrome P450-dependent oxidative conversion of cholesterol to progesterone... [Pg.70]

Figure 19.8 A brief summary of the pathways for formation and secretion of oestradiol and progesterone within the cells of the follicle. Cholesterol is taken up by thecal cells in a complex with low density lipoprotein. In the thecal cells, cholesterol is converted to testosterone which is released to be taken up by granulosa cells where it is converted into oestradiol. For synthesis of progesterone in the granulosa cells, cholesterol is synthesised de novo within the cells from acetyl-CoA. In the follicle the enzyme aromatase, which produces the aromab c ring in the female sex hormones, is restricted to the granulosa cells. The reacrions that are stimulated by LH and FSH increase synthesis and, therefore, secretion of testosterone and increased synthesis of oestrogens and progesterone. Figure 19.8 A brief summary of the pathways for formation and secretion of oestradiol and progesterone within the cells of the follicle. Cholesterol is taken up by thecal cells in a complex with low density lipoprotein. In the thecal cells, cholesterol is converted to testosterone which is released to be taken up by granulosa cells where it is converted into oestradiol. For synthesis of progesterone in the granulosa cells, cholesterol is synthesised de novo within the cells from acetyl-CoA. In the follicle the enzyme aromatase, which produces the aromab c ring in the female sex hormones, is restricted to the granulosa cells. The reacrions that are stimulated by LH and FSH increase synthesis and, therefore, secretion of testosterone and increased synthesis of oestrogens and progesterone.
The interaction between the adrenal cortex of the foetus and the placenta in production of steroid hormones is complex. In outline, the placenta produces progesterone from cholesterol (which is available from the maternal blood) whereas the foetal adrenal cortex produces corticosteroids and androgens from the progesterone produced in the placenta. The placenta then converts some of these androgens into oestrogens. The interplay between the placenta and the foetal adrenal cortex is acknowledged by the use of the term foeto-placental unit to describe steroido-... [Pg.444]

Examples are shown in Fig. 23.9. Stereochemistry is indicated by dotted lines (a-bonds, behind the plane) and solid lines (P-bonds, in front of the plane) of any substituents on the rings. The sex hormones are the molecules mainly responsible for differentiating the sexes. The difference between testosterone and progesterone is a hydroxy versus an acetyl group. The natural sex hormones are used to treat prostate cancer, to alleviate menopausal distress, and to correct menstrual disorders. Other common natural steroids are estradiol, cholesterol, and cortisone. Infamous... [Pg.445]


See other pages where Cholesterol progesterone is mentioned: [Pg.318]    [Pg.1096]    [Pg.2106]    [Pg.756]    [Pg.241]    [Pg.290]    [Pg.2751]    [Pg.318]    [Pg.1096]    [Pg.2106]    [Pg.756]    [Pg.241]    [Pg.290]    [Pg.2751]    [Pg.685]    [Pg.1100]    [Pg.95]    [Pg.207]    [Pg.174]    [Pg.685]    [Pg.1100]    [Pg.255]    [Pg.833]    [Pg.1113]    [Pg.1156]    [Pg.438]    [Pg.274]    [Pg.86]    [Pg.210]    [Pg.79]    [Pg.31]    [Pg.106]    [Pg.849]    [Pg.849]    [Pg.217]    [Pg.69]    [Pg.435]    [Pg.444]    [Pg.56]    [Pg.376]    [Pg.50]    [Pg.124]    [Pg.399]    [Pg.686]    [Pg.20]    [Pg.72]    [Pg.178]   
See also in sourсe #XX -- [ Pg.397 ]




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