Zobrazeno 1 - 10
of 26
pro vyhledávání: '"J. M. KARLE"'
Autor:
Ai. J. Lin, J. M. Karle
Publikováno v:
Acta Crystallographica Section B Structural Science. 51:1063-1068
Large differences were observed in the 1 H NMR chemical shift pattern of the protons adjacent to the ether linkages of two diastereomeric artemisinin derivatives. These differences can be explained by the shielding/deshielding effects of the nitrophe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::444e1a6a4aa5dbb3e3d00cb27409eeb6
https://doi.org/10.1107/s0108768195005581
https://doi.org/10.1107/s0108768195005581
Autor:
J. M. Karle, I. L. Karle
Publikováno v:
ChemInform. 22
C 7 H 19 N 2 O 3 PS•2H 2 O cristallise dans P1 avec a=6,314, b=9,616, c=12,277 A, α=84,73, β=75,69, γ=73,73 o , Z=2; affinement jusqu'a R=0,065. La molecule cristallise sous forme d'ion amphotere double avec les deux atomes H des groupes phospha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b13ab9f259541689b05c4adf3902baa1
https://doi.org/10.1002/chin.199138054
https://doi.org/10.1002/chin.199138054
Autor:
J. M. Karle, I. L. Karle
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 47:1242-1245
C 7 H 19 N 2 O 3 PS•2H 2 O cristallise dans P1 avec a=6,314, b=9,616, c=12,277 A, α=84,73, β=75,69, γ=73,73 o , Z=2; affinement jusqu'a R=0,065. La molecule cristallise sous forme d'ion amphotere double avec les deux atomes H des groupes phospha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae27f8580b4e3ca4158bc3ba75604dd4
https://doi.org/10.1107/s0108270190010745
https://doi.org/10.1107/s0108270190010745
Publikováno v:
Journal of molecular recognition : JMR. 13(4)
Molecular similarity analysis of stereoelectronic properties between natural insect juvenile hormone (JH), -a synthetic insect juvenile hormone mimic (JH-mimic, undecen-2-yl carbamate), and N, N-diethyl-m-toluamide (DEET) and its analogs reveals simi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29650a18ed77e087bca606faa6a4e4b9
https://pubmed.ncbi.nlm.nih.gov/10931558
https://pubmed.ncbi.nlm.nih.gov/10931558
Autor:
A. J. Lin, J. M. Karle
Publikováno v:
Acta Crystallographica Section A Foundations of Crystallography. 58:c125-c125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5127eb05dc1c1e8c676a4cd8141bf0c
https://doi.org/10.1107/s0108767302090013
https://doi.org/10.1107/s0108767302090013
Autor:
J. M. Karle
Publikováno v:
Acta Crystallographica Section A Foundations of Crystallography. 52:C251-C251
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61344aa76be87ad289081d5ba98f0ca3
https://doi.org/10.1107/s0108767396089416
https://doi.org/10.1107/s0108767396089416
Publikováno v:
Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 36:3012-3016
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40cb39d0fcaf7c444411a2ebcf6c860b
https://doi.org/10.1107/s0567740880010709
https://doi.org/10.1107/s0567740880010709
Autor:
J. M. Karle
Publikováno v:
Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 33:185-188
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c20786d3f6d4ff552c2abbfd8935006b
https://doi.org/10.1107/s0567740877003008
https://doi.org/10.1107/s0567740877003008
Publikováno v:
Journal of Biological Chemistry. 259:67-72
The concentration of uridine in the media of cultured L1210 cells was maintained within the concentration range found in plasma (1 to 10 microM) to determine if such concentrations are sufficient to satisfy the pyrimidine requirements of a population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea9739e26d76aaa8d85b510be09165d6
https://doi.org/10.1016/s0021-9258(17)43622-2
https://doi.org/10.1016/s0021-9258(17)43622-2
Autor:
Alexander W. Wood, Haruhiko Yagi, B. Kedzierski, Dhiren R. Thakker, Derek R. Boyd, J. M. Karle, Richard N. Armstrong, Thomas J. Slaga, Allan H. Conney, M. K. Buening, Guru S. Gadaginamath, Wayne Levin, D M Jerina, R. L. Chang
Publikováno v:
Journal of Biological Chemistry. 255:9067-9074
The (+)- and (-)-enantiomers of benzo[a]pyrene 7,8-oxide are hydrated stereospecifically at C-8 to (-)- and (+)-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene, respectively, by rat hepatic epoxide hydrolase. The (-)-enantiomer of benzo[a]pyrene 7,8-ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d595dad7cfdcf8c15b440a8b74c028b
https://doi.org/10.1016/s0021-9258(19)70528-6
https://doi.org/10.1016/s0021-9258(19)70528-6