Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Larry W, Hertel"'
Autor:
Kumiko, Takeuchi, Todd J, Kohn, Nicholas A, Honigschmidt, Vincent P, Rocco, Patrick G, Spinazze, Daniel J, Koch, Steven T, Atkinson, Larry W, Hertel, David L, Nelson, D Bradley, Wainscott, Laura J, Ahmad, Janice, Shaw, Penny G, Threlkeld, David T, Wong
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 13:2393-2397
Potent 5-HT1A/SSRIs at low nanomolar and subnanomolar concentrations were identified in a series of 1-(1H-indol-4-yloxy)-3-(4-benzo[b]thiophen-2-ylpiperidinyl)propan-2-ols. Incorporation of an alpha-Me group in the piperidine ring with its specific s
Publikováno v:
Journal of Enzyme Inhibition. 8:243-253
The enzyme S-adenosylhomocysteine hydrolase (E.C.3.3.1.1) occurs in two forms in bovine liver: Type A, which carries four moles of NAD+ per mole of enzyme tetramer, and Type B, which carries two moles of NAD+ per mole of tetramer.1 The inhibition of
Autor:
Kumiko Takeuchi, Todd J Kohn, Nicholas A Honigschmidt, Vincent P Rocco, Patrick G Spinazze, Steven T Atkinson, Larry W Hertel, David L Nelson, D.Bradley Wainscott, Laura J Ahmad, Janice Shaw, Penny G Threlkeld, David T Wong
Publikováno v:
Bioorganicmedicinal chemistry letters. 13(22)
A series of 1-aryloxy-3-piperidinylpropan-2-ols possessing potent dual 5-HT(1A) receptor antagonism and serotonin reuptake inhibition was discovered. Modification of potential metabolic sites of 1-(1H-indol-4-yloxy)-3-(4-benzo[b]thiophen-2-ylpiperidi
Publikováno v:
International journal of radiation oncology, biology, physics. 34(4)
Purpose We have reported that the deoxycytidine analog 2',2'difluoro-2'-deoxycytidine (dFdCyd) is a potent radiosensitizer of HT29 human colon cancer cells probably through its effects on intracellular deoxyribonucleotide (dNTP) pools. Because dFdCyd
Autor:
Rolf Gleiter, Leo A. Paquette, Mark A. Beno, Michael C. Boehm, Larry W. Hertel, Gary G. Christoph
Publikováno v:
Journal of the American Chemical Society. 103:7106-7121
Publikováno v:
The Journal of Organic Chemistry. 46:4403-4413
Autor:
Leo A. Paquette, Larry W. Hertel
Publikováno v:
Journal of the American Chemical Society. 101:7620-7622
Publikováno v:
Journal of the American Chemical Society. 100:6510-6512
Bei Photooxidationen der Isopropylidennorbornene (I) bestimmen wahrscheinlich hauptsachlich zwei Mechanismen das anti:syn-Verhaltnis im Produktgemisch.
Publikováno v:
Chemischer Informationsdienst. 10
Bei Photooxidationen der Isopropylidennorbornene (I) bestimmen wahrscheinlich hauptsachlich zwei Mechanismen das anti:syn-Verhaltnis im Produktgemisch.