1972
DOI: 10.1016/s0039-128x(72)80019-9
|View full text |Cite
|
Sign up to set email alerts
|

Pattern of estetrol conjugation in the human

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
5
0

Year Published

1976
1976
2021
2021

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(6 citation statements)
references
References 16 publications
1
5
0
Order By: Relevance
“…Although [19]; (9) YoungLai et al [20]. not calculated in that study, the data are consistent with a metabolic half-life of 12-15 h. Further analysis of the excretion products from that study indicated that E 4 was predominantly glucuronidated on Ring D [22].…”
Section: Excretion Of Estetrolsupporting
confidence: 72%
“…Although [19]; (9) YoungLai et al [20]. not calculated in that study, the data are consistent with a metabolic half-life of 12-15 h. Further analysis of the excretion products from that study indicated that E 4 was predominantly glucuronidated on Ring D [22].…”
Section: Excretion Of Estetrolsupporting
confidence: 72%
“…The solvent systems are shown in Table I. The preparation of alumina and Sephadex columns has been described previously (Emerman et al, 1967;Jirku and Levitz, 1969). Thin-layer chromatography was carried out on silica gel G. The solvent system was chloroform-ethanol (7:4, v/v), the plate being developed twice to effect the separation of 15a-OHEiGNAc from 15a-OHEi-3 sulfate.…”
Section: Methodsmentioning
confidence: 99%
“…To characterize the product the aqueous phase was centrifuged and the supernatant was flash evaporated. The residue was chromatographed on Sephadex (Jirku and Levitz, 1969). Additional characterization of the N-acetylglucosaminide was obtained from chromatography in system 8 (HBV 2) and 9 (HBV 2-3).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The hepatic metabolism of E4 is slow in both humans and rodents and is similar across the two species. E4 metabolites are produced through conjugation, mainly methylation, (de) hydroxylation, glucuronidation and sulfation, they are inactive [32,38] and are rapidly excreted in urine [32,[38][39][40]. The principal urine metabolite is the Ring D-monoglucuronide, but E4 can also be excreted in an unconjugated form that cannot be reciprocally converted back into E2 or E3 [35,36].…”
Section: Estetrol Biologymentioning
confidence: 99%