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pro vyhledávání: '"R. Blohm"'
Publikováno v:
IEEE Transactions on Power Systems. 18:406-413
The authors argue that the original paper ("Statistical and dynamic analysis of generation control performance standards", T. Sasaki et al., see ibid., vol.17, p.476-81, 2002) presents interesting research that contributes to the general understandin
Publikováno v:
Journal of Lipid Research, Vol 8, Iss 6, Pp 589-597 (1967)
Free fatty acids (FFA), the uranyl ion, and the basic dye Rhodamine B form colored complexes, which are extractable into toluene or benzene. Fatty acids of different chain lengths above C10 and different degrees of unsaturation gave constant molar yi
Externí odkaz:
https://doaj.org/article/e856778eab044a6b89bc9f3ebba4e383
Autor:
Angela L. Marquart, Marie E. Laughlin, Norton P. Peet, Cynthia A. Gates, Thomas R. Blohm, Philip M. Weintraub, Michael R. Angelastro
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:97-100
Androstenes bearing a cyclopropyl group attached to the C-17β position with a heteroatom linker, designed as mechanism-based inhibitors of steroid C 17(20) lyase, were found to be potent, time-dependent inhibitors of this enzyme.
Autor:
Ian A. McDonald, Cynthia A. Gates, Thomas R. Blohm, Daniel M. Muench, Philip M. Weintruab, Philip L. Nyce, Marie E. Laughlin
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:847-851
Modified steroids, in which the D-ring has been converted to a six-membered ring lactam, were designed as inverted (or backward-binding), competitive inhibitors of steroid 5α-reductase.
Autor:
Dennis M. Hoover, Thomas R. Blohm, Blake Lee Neubauer, Nancy B. Stamm, E. Barry Smalstig, Richard E. Toomey, Marie E. Laughlin, Kevin L. Best, Kenneth Steven Hirsch, Cynthia A. Gates, Robin L. Goode, Vladimir Petrow
Publikováno v:
The Prostate. 23:181-199
LY207320 is an in vitro inhibitor (estimated IC50 = 0.06 microM) of steroid 5 alpha-reductase that catalyzes the conversion of testosterone (T) to dihydrotestosterone (DHT). In contrast, LY207320 was only moderately active against rat prostatic 5 alp
Autor:
Marie E. Laughlin, Philip M. Weintraub, Angela L. Marquart, Thomas R. Blohm, Cynthia A. Gates, Norton P. Peet, Michael R. Angelastro
Publikováno v:
ChemInform. 27
Androstenes bearing a cyclopropyl group attached to the C-17β position with a heteroatom linker, designed as mechanism-based inhibitors of steroid C 17(20) lyase, were found to be potent, time-dependent inhibitors of this enzyme.
Autor:
R. Blohm
Publikováno v:
IEEE Transactions on Power Systems. 18:957-958
The author comments on the paper by T. Sasaki et al. (see ibid., vol.17, p.806-11, 2002). He points out that the paper serves to demonstrate the usefulness of dynamic simulation as a quasiempirical check on conclusions derived theoretically from a sm
Autor:
R. Blohm
Publikováno v:
IEEE Transactions on Power Systems. 18:408-409
The author comments on the original paper ("Statistical and dynamic analysis of generation control performance standards", T. Sasaki et al., see ibid., vol.17 p.476-81, 2002). He argues that the basic concepts of the paper are obscured because they a
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Publikováno v:
Biochemical and Biophysical Research Communications. 95:273-280
RMI 18,341 (5α,20-R)-4-diazo-21-hydroxy-20-methylpregnan-3-one, was designed to be an enzyme-activated irreversible inhibitor of testosterone 5α-reductase. It produced time-dependent, apparently first-order inactivation of the enzyme, which can be