Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Gordon O. Potts"'
Publikováno v:
Contraception. 24:289-299
Win 32,729 [(2 alpha, 4 alpha, 5 alpha, 17 beta)-4,5-epoxy-17-hydroxy-4,17-dimethyl-3-oxoandrostane-2-carbonitrile] is an orally active interceptive agent in rats and rhesus monkeys (M mulatta). A single oral dose of 48 mg/kg terminated gestation whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd598501da4b4db473d23aa2cb8d7f74
https://doi.org/10.1016/0010-7824(81)90042-1
https://doi.org/10.1016/0010-7824(81)90042-1
Publikováno v:
Fertility and Sterility. 25:367-372
A steroid danazol (17-alpha-Pregn-4-en-20-yno(23-d)-isoxazol-17-ol) possesses a marked separation of pituitary gonadotropin inhibitory activity from overt sex hormonal activities. The effect of danazol on fertility in the rat was determined. Danazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c16c1ef063603ea507bba307d005dd03
https://doi.org/10.1016/s0015-0282(16)40338-9
https://doi.org/10.1016/s0015-0282(16)40338-9
Autor:
Ludwig Kiesel, Josef Kellermann, Gordon O. Potts, Benno Runnebaum, Thomas Rabe, Klaus Weidenhammer
Publikováno v:
Fertility and Sterility. 39:829-835
The inhibitory effect in vitro of four synthetic steroids on enzyme systems of placental progesterone synthesis at term was analyzed. Cholesterol side chain cleavage enzyme (CSCC) was not influenced by azastene, trilostane, and WIN 32,729. A 50% inhi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::949ab417ab97b7308df67cabcd89e55f
https://doi.org/10.1016/s0015-0282(16)47125-6
https://doi.org/10.1016/s0015-0282(16)47125-6
Publikováno v:
Fertility and Sterility. 30:86-90
Azastene (4,4,17α-trimethylandrost-5-eno [2,3-d]isoxazol-17-ol), when given orally to rats at a dose of 12 mg/kg once on day 10 of pregnancy, induced resorption of all fetuses and a precipitous decline of circulating progesterone levels in all test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba6e7dcb6e4ba9b076aee76b7b51435
https://doi.org/10.1016/s0015-0282(16)43401-1
https://doi.org/10.1016/s0015-0282(16)43401-1
Publikováno v:
Fertility and Sterility. 30:343-347
Azastene is an orally effective "luteolytic" agent in rhesus monkeys. In nonpregnant monkeys it reverses the human chorionic gonadotropin-stimulated increase in progesterone production and delay in the onset of menstruation, and in inseminated monkey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::258bd4274eac43327228e039b81b682a
https://doi.org/10.1016/s0015-0282(16)43523-5
https://doi.org/10.1016/s0015-0282(16)43523-5
Publikováno v:
Endocrinology. 69:819-833
N,N′-4-Xylylene-bis(N-ethyldichloroacetamide), Compound I,and N,N′-bis (dichloroacetyl)-l,8-octamethylenediamine, Compound II, produced in rats marked testicular weight regression associated with complete arrest of spermatogenesis. Compound II wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e7b67a2e3a2fd682fbfedd9a5379612
https://doi.org/10.1210/endo-69-4-819
https://doi.org/10.1210/endo-69-4-819
Publikováno v:
Endocrinology. 67:849-854
The myotrophic and nitrogen retaining effects of five steroids (methyltestosterone; methylandrostenediol; 17α-methylandrosta-4,6-diene-17β-ol-3-one; 19-nor-17α-methylandrost-5 (10) eno-17β-ol-3-one and 17β-hydroxy-17α:-methylandrost-4-eno[3,2-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67b3c800b7b5f84aa4d702ddb905c7f2
https://doi.org/10.1210/endo-67-6-849
https://doi.org/10.1210/endo-67-6-849
Publikováno v:
Endocrinology. 88:427-432
Estrone and estradiol-17β were shown to displace 3H-estradiol-17β from binding sites in plasma of the pregnant rat. The ligand specificity of this plasma differed from that of human pregnancy plasma. In the rat preparation, neither testosterone nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8036a7f7b32b5ab9b8aa7b5544cff871
https://doi.org/10.1210/endo-88-2-427
https://doi.org/10.1210/endo-88-2-427
Autor:
K. F. Jennings, Franklyn W. Gubitz, Robert L. Clarke, Philip E. Shaw, Gordon O. Potts, A. L. Beyler
Publikováno v:
Journal of Medicinal Chemistry. 7:555-560
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::100f413f9b5d761e32a2fbaf640ec632
https://doi.org/10.1021/jm00334a034
https://doi.org/10.1021/jm00334a034
Publikováno v:
Journal of Medicinal Chemistry. 13:948-951
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::010f0c7d559ac5ff152e5ef33ef6d684
https://doi.org/10.1021/jm00299a034
https://doi.org/10.1021/jm00299a034