Zobrazeno 1 - 10
of 37
pro vyhledávání: '"J. Strohmeier"'
Publikováno v:
Biopharmaceutics & Drug Disposition. 38:115-126
Background Induction or inhibition of drug transporting proteins by concomitantly administered drugs can cause serious drug–drug interactions (DDIs). However, in vitro assays currently available are mostly for studying the inhibitory potential of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59e71436052b491aba6b6c33443524f4
https://doi.org/10.1002/bdd.2025
https://doi.org/10.1002/bdd.2025
Publikováno v:
Biopharmaceuticsdrug disposition. 38(2)
Induction or inhibition of drug transporting proteins by concomitantly administered drugs can cause serious drug-drug interactions (DDIs). However, in vitro assays currently available are mostly for studying the inhibitory potential of drugs on intes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d2c24ff482cbf7de708dd412dc5902ac
https://pubmed.ncbi.nlm.nih.gov/27516347
https://pubmed.ncbi.nlm.nih.gov/27516347
Publikováno v:
American annals of the deaf. 139(2)
Criterion-related validity of Raven's Progressive Matrices (RPM) was investigated using a sample of 107 deaf residential adolescents. Data collection involved retrieval of psychoeducational test scores (RPM; WISC-R Performance IQ; VMI-R; Bender-Gesta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70bc349d96b303e87190e882ae9d0e6c
https://pubmed.ncbi.nlm.nih.gov/8037075
https://pubmed.ncbi.nlm.nih.gov/8037075
Akademický článek
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Autor:
J. Strohmeier, E. von Angerer
Publikováno v:
Archiv der Pharmazie. 320:407-417
2-Phenylindoles with aromatic substituents at C-3 and hydroxy functions at the aromatic rings were synthesized and tested for their binding affinity for the calf uterine estrogen receptor. Most of these indoles bind to the estrogen receptor. The high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec5a5e628e05322faf9a8ab7d971196
https://doi.org/10.1002/ardp.19873200506
https://doi.org/10.1002/ardp.19873200506
Autor:
E. von Angerer, J. Strohmeier
Publikováno v:
Archiv der Pharmazie. 318:421-431
Syntheses and estrogen receptor affinities of the 1,2-dialkyl(hydroxy)-3-(hydroxyphenyl)indoles 11b–19b are described. Derivatives 15b, 16b with a hydroxy group at position 6 of the indole and an ethyl group at C-2 show a strong binding affinity wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2790c166d1b8d14c4e9ca7ab016b82
https://doi.org/10.1002/ardp.19853180508
https://doi.org/10.1002/ardp.19853180508
Autor:
J. Strohmeier, E. von Angerer
Publikováno v:
Journal of Medicinal Chemistry. 30:131-136
Hydroxy-2-phenylindoles carrying substituted benzyl groups and similar substituents at the nitrogen were synthesized and tested for their ability to displace estradiol from its receptor. All of the derivatives tested exhibited high binding affinities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd2e5bbfd5362fb2b26d831170739376
https://doi.org/10.1021/jm00384a022
https://doi.org/10.1021/jm00384a022
Akademický článek
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Publikováno v:
Chemischer Informationsdienst. 16
A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized. In addition, different alkyl groups were introduced into pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::778e5051ed74ba255d566363e4b8876a
https://doi.org/10.1002/chin.198512186
https://doi.org/10.1002/chin.198512186
Publikováno v:
Journal of medicinal chemistry. 27(11)
A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized. In addition, different alkyl groups were introduced into pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59a660b9c956c3b850635a8b5ab3945b
https://pubmed.ncbi.nlm.nih.gov/6492074
https://pubmed.ncbi.nlm.nih.gov/6492074