Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Magda M. Gagliardi"'
Autor:
Lucia Herranz, Joanne E. Tomassini, Pia L. Graham, Donette S. Quamina, Deborah L. Zink, Russell B. Lingham, Ziqiang Guan, Magda M. Gagliardi, Renee Danzeisen, Sheo B. Singh, Hiranthi Jayasuriya, Olga Genilloud
Publikováno v:
Journal of Natural Products. 65:1091-1095
Tat is a small HIV protein essential for both viral replication and the progression of HIV disease. In our efforts to discover Tat inhibitors from natural product screening of microbial fermentation extracts, we discovered durhamycin A (1) as a poten
Autor:
Janet M. Sigmund, Isabel Martin, Olga Genilloud, Russell B. Lingham, Magda M. Gagliardi, Brian Heimbuch, Jackson B. Gibbs, Suzanne E. Gartner, Mary Nallin-Omstead, Gregory E. Koch, Sheo B. Singh, George M. Garrity, Carmen Cascales, Manuel Sanchez, Maria Teresa Diez, Charles F. Hirsch, Keith C. Silverman
Publikováno v:
Applied Microbiology and Biotechnology. 43:610-616
Actinoplanic acids A and B are macrocyclic polycarboxylic acids that are potent reversible inhibitors of farnesyl-protein transferase. Actinoplanic acids A and B were isolated from Actinoplanes sp. MA 7066 while actinoplanic acid B was isolated from
Autor:
Russell B. Lingham, George M. Garrity, Maria Teresa Diez, Olga Genilloud, Nancy N. Tsou, Suzanne E. Gartner, Charles F. Hirsch, D. L. Zink, Brian Heimbuch, Gregory E. Koch, Amy Hsu, Manuel Sanchez, Isabel Martin, Jerrold M. Liesch, Gino Salituro, Magda M. Gagliardi, Janet M. Sigmund, Julie A. O'Brien
Publikováno v:
ChemInform. 27
Autor:
H. Boyd Woodruff, Kristine A. Faust, Deborah L. Zink, Sara A. Currie, George M. Garrity, Raymond S.L. Chang, Debra Bogen, Otto D. Hensens, Magda M. Gagliardi, Loretta Zitano, Cheryl D. Schwartz, Y. K. Tony Lam
Publikováno v:
The Journal of Antibiotics. 44:613-625
The discovery and physico-chemical characterization of three novel and minor virginiamycin M1 analogs as potent gastrin antagonists from a culture of a strain of Streptomyces olivaceus are described. These analogs are L-156,586, L-156,587 and L-156,5
Autor:
George M. Garrity, Amy Hsu, Suzanne E. Gartner, Brian Heimbuch, Russell B. Lingham, Charles F. Hirsch, Magda M. Gagliardi, Gregory E. Koch, Manuel Sanchez, Julie A. O'Brien, Deborah L. Zink, Jerrold M. Liesch, Gino Salituro, Janet M. Sigmund, Olga Genilloud, Nancy N. Tsou, Isabel Martin, Maria Teresa Diez
Publikováno v:
The Journal of antibiotics. 49(3)
Quinoxapeptin A and B are novel chromodepsipeptides which were isolated from a nocardioform actinomycete with indeterminant morphology. Quinoxapeptins A and B are potent inhibitors of HIV-1 and HIV-2 reverse transcriptase and almost equally active ag
Autor:
Harri G. Ramjit, Laszlo R. Treiber, Steven M. Pitzenberger, George M. Garrity, Byron H. Arison, Magda M. Gagliardi, Frederick W. Hartner, Suresh K. Balani, Amy Hsu, Georgette Dezeny, Wayne J. Thompson, Joan S. Murphy, Lawerence F. Colwell, Edward S. Inamine, Paul L. Darke, Russell B. Lingham
Publikováno v:
Biochemical and biophysical research communications. 181(3)
L-689,502 is a potent inhibitor of HIV-1 protease activity in vitro. Microbial biotransformations of L-689,502 by cultures belonging to the genus Streptomyces sp. were performed. Extracts of culture broths were examined for the production of metaboli
Autor:
Jayasuriya H; Merck Research Laboratories, P.O. Box 2000, Rahway, New Jersey 07065, USA. hiranthi_jayasuriya@merck.com, Lingham RB, Graham P, Quamina D, Herranz L, Genilloud O, Gagliardi M, Danzeisen R, Tomassini JE, Zink DL, Guan Z, Singh SB
Publikováno v:
Journal of natural products [J Nat Prod] 2002 Aug; Vol. 65 (8), pp. 1091-5.