Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Rudiger D. Haugwitz"'
Autor:
Robert L. Geahlen, Jurjus Jurayj, Mark Cushman, Asit K. Chakraborti, Pennamuthiriar Chinnasamy, Rudiger D. Haugwitz
Publikováno v:
International Journal of Peptide and Protein Research. 36:538-543
An asymmetric synthesis of [beta-(4-pyridyl-1-oxide)-L-alanine4]-angiotensin I (1a), which is a potential suicide substrate (mechanism-based inhibitor) for protein-tyrosine kinases, has been performed. Deprotonation of 6 with n-butyllithium in THF ga
Autor:
Jeffrey A. Vroman, Rudiger D. Haugwitz, Mark Cushman, Melinda Hollingshead, Ankush B. Argade, Rajesh Devraj
Publikováno v:
Journal of Medicinal Chemistry. 41:3337-3346
The addition of a variety of thiols to the alpha,beta-unsaturated lactone functionality present in brefeldin A has been carried out, and the resulting sulfides have been oxidized to the corresponding sulfoxides. These sulfoxides have the potential to
Autor:
Ankush B. Argade, Mark Cushman, John F. Kozlowski, and Phillip E. Fanwick, Rajesh Devraj, Rudiger D. Haugwitz
Publikováno v:
The Journal of Organic Chemistry. 63:273-278
The Michael addition of thiols to brefeldin A occurs with high diastereoselectivity, affording ratios of major to minor diastereomers of at least 30:1. On the basis of the X-ray structure of a crystalline dibenzoyl derivative, the major diastereomers
Autor:
Mark Cushman, John F. Barrett, Rudiger D. Haugwitz, Kenneth D. Paull, Ravi K. Varma, Jurjus Jurayj
Publikováno v:
Journal of Medicinal Chemistry. 37:2190-2197
9-Methoxy-2-methylellipticinium acetate (6), along with the 9-methyl and 9-chloro derivatives (7, and 8, respectively) have shown remarkable selectivities in vitro against the NCI human CNS cancer subpanel. In order to target these types of compounds
Autor:
Kenneth D. Paull, John F. Barrett, Jurjus Jurayj, Ravi K. Varma, Mark Cushman, Rudiger D. Haugwitz
Publikováno v:
ChemInform. 25
9-Methoxy-2-methylellipticinium acetate (6), along with the 9-methyl and 9-chloro derivatives (7, and 8, respectively) have shown remarkable selectivities in vitro against the NCI human CNS cancer subpanel. In order to target these types of compounds
Autor:
John F. Kozlowski, Phillip E. Fanwick, Rajesh Devraj, Ankush B. Argade, Rudiger D. Haugwitz, Mark Cushman
Publikováno v:
ChemInform. 29
Publikováno v:
Biochemical and Biophysical Research Communications. 187:1409-1417
A simple synthesis of the sulfonated azo dye Quinobene ( 3 ) and its derivatives, as well as the results of their evaluation in anti-HIV screening have been described. Thus, reacting the diazonium salt of 4,4′-diaminostilbene-2,2′-disulfonic acid
Publikováno v:
Journal of medicinal chemistry. 38(17)
The potential therapeutic application of the naturally occurring, cytotoxic pseudoguaianolide sesquiterpene lactone ambrosin is limited by its aqueous insolubility. A number of water-soluble ambrosin derivatives have therefore been prepared for poten
Autor:
B. V. Maurer, Rudiger D. Haugwitz, Larry R. Cruthers, J. Szanto, G. A. Jacobs, R. G. Angel, V. L. Narayanan
Publikováno v:
Journal of Medicinal Chemistry. 25:969-974
The synthesis and antiparasitic properties of 22 isothiocyanato-2-pyridinylbenzoxazoles and benzothiazoles are described; the preparation and anthelmintic activities of 14 isothiocyanato-2-thienyl-, -furyl-, and -pyrrolylbenzoxazoles are outlined. In
Autor:
Ronald S. Michalak, David R. Myers, Rudiger D. Haugwitz, Prabhakar A. Risbood, Venkatachala L. Narayanan, Jack L. Parsons
Publikováno v:
Tetrahedron Letters. 30:4783-4786
Irisquinone 1 has been synthesized for the first time to investigate its use as a potential radiosensitizer. The key step in its synthesis involves the regioselective lithiation of a phenol ether. The cis-double bond has been confirmed via 1H NMR spe