Zobrazeno 1 - 8
of 8
pro vyhledávání: '"K. D. Bingham"'
Autor:
K. D. Bingham
Publikováno v:
International journal of cosmetic science. 3(1)
Synopsis The studies carried out on the metabolism of testosterone and other circulating androgens in human scalp skin and hair follicles have been reviewed with the aim of understanding the role of these androgens in male pattern alopecia (baldness)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a305973e05ebb8bc44203578c5f9e720
https://pubmed.ncbi.nlm.nih.gov/19469921
https://pubmed.ncbi.nlm.nih.gov/19469921
Autor:
J M, Beazley, K D, Bingham
Publikováno v:
The British journal of clinical practice. 27(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df712d54e9a9460a72093e74a0c11156
https://pubmed.ncbi.nlm.nih.gov/4804273
https://pubmed.ncbi.nlm.nih.gov/4804273
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eabb209c66a8060f5d0f512b072a034
https://doi.org/10.1002/chin.197103253
https://doi.org/10.1002/chin.197103253
Autor:
K. D. Bingham, D. A. Shaw
Publikováno v:
The Journal of endocrinology. 57(1)
SUMMARY [4-14C]Testosterone was incubated with human male scalp skin and the metabolites identified as 5α-androstane-3α, 17β-diol, androsterone, epiandrosterone, dihydrotestosterone, androstenedione and androstanedione. A metabolite not previously
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab0c7e604d0e8b0c8471e0e9ffafe6ac
https://pubmed.ncbi.nlm.nih.gov/4701164
https://pubmed.ncbi.nlm.nih.gov/4701164
Publikováno v:
J. Chem. Soc. C. :674-675
Condensations of 5β-lumista-7,22-dien-3-one and 5β-lumist-7-en-3-one with ethyl formate, and of 5β-lumista-7,22-dien-3-one with benzaldehyde occur at position 2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::061a16068dd9db8664dc9f866e68e2f7
https://doi.org/10.1039/j39690000674
https://doi.org/10.1039/j39690000674
Publikováno v:
Journal of the Chemical Society C: Organic. :510
Oxidation of lumisterol with perbenzoic and peroxylauric acids, and of lumisteryl acetate and lumisteryl 3,5-di-nitrobenzoate with peroxylauric acid gives 5β,6β-epoxides in high yields. The second-order rate constants (l. mole–1 sec.–1) are res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36b1c4e6e14c4c19789ce3551d528bc5
https://doi.org/10.1039/j39690000510
https://doi.org/10.1039/j39690000510
Publikováno v:
Journal of the Chemical Society C: Organic. :671
At 175°, lumistyeryl acetate and maleic anhydride gave a Diels–Alder type product (35%) represented as 3β-acetoxy-5β,8β-ethenolumist-22-ene-6β,7β-dicarboxylic anhydride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca23ed604fe0805b3c282c0d23670e5
https://doi.org/10.1039/j39690000671
https://doi.org/10.1039/j39690000671
Publikováno v:
Journal of the Chemical Society C: Organic. :2330
Examination of the conversion of 3-substituted cholest-5-enes into 5α,6β- and 5β,6β-epoxides by various peroxyacid–solvent combinations gives values for the ratios of isomers produced and the rate constants of the reactions. Peroxylauric acid i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c523628dd34695cd493ec9ff23534c1
https://doi.org/10.1039/j39700002330
https://doi.org/10.1039/j39700002330