Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Davette L. Behrens"'
Autor:
Robert C. Bruckner, Andrew M. Stern, Anne Higley, Graciani Nilsa R, Sandya Mandlekar, Maria Rafalski, Melody Diamond, Ross L. Stein, Eddy W. Yue, Xiang Jiang, Pearl S. Huang, Randine Dowling, Dimeo Susan, Lisa C. Grimminger, Mingzhu Zhang, Zhihong Lai, Amy L. Musselman, Swamy Yeleswaram, Davette L. Behrens, Robert A. Copeland, Andrew P. Combs, Oliff Allen I, Wei Han, Shu-Yun Zhang, Rebecca Taub, Bruce Car, George L. Trainor, Charles F. Albright, Steve P. Seitz, Daniel Hu
Publikováno v:
Molecular Cancer Therapeutics. 4:751-760
Matrix metalloproteinase (MMP)–activated prodrugs were formed by coupling MMP-cleavable peptides to doxorubicin. The resulting conjugates were excellent in vitro substrates for MMP-2, -9, and -14. HT1080, a fibrosarcoma cell line, was used as a mod
Publikováno v:
Journal of Medicinal Chemistry. 37:2232-2237
A series of nitrocoumarin and nitrochromene derivatives have been prepared and shown to inhibit the phosphatidylinositol-specific phospholipase C(PLC)(IC50 < 10 micrograms/mL) isolated from human melanoma. The inhibition of PLC by nitrocoumarin 4a wa
Publikováno v:
ChemInform. 25
A series of nitrocoumarin and nitrochromene derivatives have been prepared and shown to inhibit the phosphatidylinositol-specific phospholipase C(PLC)(IC50 < 10 micrograms/mL) isolated from human melanoma. The inhibition of PLC by nitrocoumarin 4a wa
Publikováno v:
Journal of biomolecular screening. 4(1)
Impairment of G proteincoupled seven-transmembrane (7 TM) receptor function has been implicated in a variety of different pathologic conditions, suggesting that the discovery of specific antagonists may lead to the development of successful therape
Autor:
Barry Allen Stone, George L. Trainor, Siew Peng Ho, Davette L. Behrens, Dustin H. O. Britton, Lynn Leffet, Jeffrey Allan Miller, Frank W. Hobbs
Publikováno v:
Nucleic acids research. 24(10)
Antisense oligonucleotides can vary significantly and unpredictably in their ability to inhibit protein synthesis. Libraries of chimeric oligonucleotides and RNase H were used to cleave and thereby locate sites on human multidrug resistance-1 RNA tra
Autor:
Davette L. Behrens, Huey-Shin L. Shen, Charles C. Whitney, Daniel L. Dexter, Martin Forbes, Shih-Fong Chen
Publikováno v:
Cancer chemotherapy and pharmacology. 22(3)
The distribution of the novel anticancer drug candidate Brequinar Sodium (DuP 785, NSC 368390) was studied in control mice and mice implanted subcutaneously with human colon carcinoma xenografts. Mice were given radiolabeled 14C-Brequinar Sodium intr