Zobrazeno 1 - 9
of 9
pro vyhledávání: '"L. G. Tensmeyer"'
Publikováno v:
Applied Spectroscopy. 48:1150-1155
FT-IR studies of the secondary structure of mt-PA6 and mt-PA6 treated with L-arginine, (+)-citrulline, and L-asparagine were carried out in aqueous buffer solution. Spectral subtraction was used to remove the interfering water bands in the amide abso
Publikováno v:
Advances in Chemical Physics: Chemical Dynamics: Papers in Honor of Henry Eyring, Volume 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38efcb0f24ade418b7df1fce305ebd97
https://doi.org/10.1002/9780470143698.ch52
https://doi.org/10.1002/9780470143698.ch52
Autor:
L. G. Tensmeyer, C. Ainsworth
Publikováno v:
The Journal of Organic Chemistry. 31:1878-1883
Publikováno v:
Journal of parenteral science and technology : a publication of the Parenteral Drug Association. 35(3)
Autor:
S. L. Briggs, B. Chao, G. A. .. Koppel, H. L. .. Hunter, J . B. Deeter, L. G. Tensmeyer, R. Nagarajan
Publikováno v:
SPIE Proceedings.
We report the successful quantitative determination of small molecules (haptens) to biomacromolecules. Results are shown for two such systems: 7-[4-chloro-3,5-dinitro-benzamido)-deacetoxycephalosporanic acid (CDNB-7-ADCA), coupled to bovine serum alb
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Publikováno v:
Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 26:1184-1184
In a previous study on the solution behavior of testosterone in aqueous media, conversion of the anhydrate form to a hydrate was reported (Thakkar & Hall, 1969). Since testosterone is a natural hormone and exists in an aqueous environment, characteri
Autor:
Michael H. Fisch, H. D. Pierce, A. L. Thakkar, L. G. Tensmeyer, R. B. Hermann, W. L. Wilham, P. Rigo, M. Bressian, B. Corain, A. Turco
Publikováno v:
Journal of the Chemical Society D: Chemical Communications. :1128
Publikováno v:
Journal of the Chemical Society D: Chemical Communications. :524
A possible mode of self-association of caffeine in aqueous solution is suggested on the basis of the concentration dependence of chemical shifts.