R. Bugianesi

发表

CELL-SPECIFIC LIGANDS FOR SELECTIVE DRUG DELIVERY TO TISSUES AND ORGANS

J. C. Robbins, T. Doebber, M. Ponpipom, 1982 .

Enhanced macrophage uptake of synthetically glycosylated human placental beta-glucocerebrosidase.

R. Brady, M. Wu, T. Doebber, 1982, The Journal of biological chemistry.

Metabolism of the platelet-activating factor antagonist (+/-)-trans-2-(3'-methoxy-5'-methylsulphonyl-4'-propoxyphenyl)-5-(3",4" ,5"- trimethoxyphenyl)tetrahydrofuran (L-659,989) in rhesus monkeys.

B. Arison, J. C. Chabala, M. Ponpipom, 1991, Xenobiotica; the fate of foreign compounds in biological systems.

Synthesis and biological activity of MK 287(L-680, 573) a potent specific and orally active PAF receptor antagonist.

Margaret S. Wu, T. Doebber, D. Macintyre, 1991 .

(+/-)-trans-2-(3-Methoxy-5-methylsulfonyl-4-propoxyphenyl)-5-(3,4,5- trimethoxyphenyl)tetrahydrofuran (L-659,989), a novel, potent PAF receptor antagonist.

T. Doebber, A. Alberts, J. C. Chabala, 1988, Biochemical and biophysical research communications.

Synthesis of azide and amide analogs of platelet-activating factor and related derivatives

M. Ponpipom, R. Bugianesi, 1984 .

Modified in vivo behavior of liposomes containing synthetic glycolipids.

J. C. Robbins, M. Wu, M. Ponpipom, 1981, Biochimica et biophysica acta.

Chemoselective removal and replacement of the C-4′ and C-6 acyl esters of zaragozic Acid A

W. Parsons, M. Ponpipom, R. Burk, 1993 .

Targeting of synthetically glycosylated human placental glucocerebrosidase.

R. Brady, M. Wu, T. Doebber, 1985, Biochemical medicine.

Synthesis and biological activity of the platelet-activating factor antagonist (±)-trans-2-(3-methoxy-4-phenylsulfonylethoxy-5-n-propylsulfonylphenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (L-671,284) and its analogs

Margaret S. Wu, T. Doebber, A. Alberts, 1992 .

Saccharide Receptor-Mediated Drug Delivery

J. C. Robbins, T. Doebber, M. Ponpipom, 1984 .

Synthesis of paragloboside analogs

M. Ponpipom, T. Shen, R. Bugianesi, 1978 .

Preparation of sepharose-bound poly (rI:rC).

T. Shen, R. Bugianesi, A. F. Wagner, 1971, Biochemical and biophysical research communications.

Biochemical and pharmacological characterization of L-659,989: an extremely potent, selective and competitive receptor antagonist of platelet-activating factor.

A. Alberts, J. C. Chabala, S. Hwang, 1988, The Journal of pharmacology and experimental therapeutics.

Bioactive carbohydrate derivatives

D. Ebel, R. Fecher, T. Shen, 1972 .

Development, synthesis, and biological evaluation of (-)-trans-(2S,5S)-2-[3-[(2-oxopropyl)sulfonyl]-4-n-propoxy-5-(3- hydroxypropoxy)-phenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, a potent orally active platelet-activating factor (PAF) antagonist and its water-soluble prodrug phosphate ester.

T. Bach, A. Alberts, J. C. Chabala, 1992, Journal of medicinal chemistry.

Synthesis of chiral β-methyl tryptamine-derived GnRH antagonists

M. Goulet, J. Simeone, M. Ponpipom, 2001 .

Synthesis of 1,4-diamino-1,4-dideoxy-6-O-(4-deoxy-4-propionamido-α- and β-d-glucopyranosyl)-d-glucitol

E. Walton, M. Ponpipom, T. Shen, 1978 .

Glycolipids as potential immunologic adjuvants.

M. Ponpipom, T. Shen, A. Friedman, 1980, Journal of medicinal chemistry.

Cell surface carbohydrates for targeting studies

M. Ponpipom, T. Shen, R. Bugianesi, 1980 .

Nucleosides. IV. Synthesis of 5-substituted-2′-deoxy-6-azauridines

W. V. Ruyle, T. Shen, R. Bugianesi, 1965 .

Novel analogs of glycopeptides

M. Ponpipom, T. Shen, R. Bugianesi, 1980 .

Structure-activity relationships of aminoalkyl and -aryl glycosides having insulin-like activity.

M. Glitzer, M. Cascieri, M. Ponpipom, 1978, Journal of medicinal chemistry.

Synthesis and carbon-13 n.m.r. spectroscopy of Man3 Lys2-raffinose conjugate

J. C. Robbins, M. Ponpipom, R. Bugianesi, 1982 .

Synthesis and SAR of 2,3-diarylpyrrole inhibitors of parasite cGMP-dependent protein kinase as novel anticoccidial agents.

D. Schmatz, P. Liberator, M. Fisher, 2005, Bioorganic & medicinal chemistry letters.

A chemical synthesis of I-O-indomethacin- -D-glucosyluronic acid.

T. Shen, R. Bugianesi, 1971, Carbohydrate research.

Synthetic glycopeptide substrates for receptor-mediated endocytosis by macrophages.

J. C. Robbins, M. Lam, M. Ponpipom, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Cell-specific ligands for selective drug delivery to tissues and organs.

J. C. Robbins, T. Doebber, M. Ponpipom, 1981, Journal of medicinal chemistry.

Inhibition of stromelysin-1 (MMP-3) by P1'-biphenylylethyl carboxyalkyl dipeptides.

M. Maccoss, J. W. Becker, W. Hagmann, 1997, Journal of medicinal chemistry.

Total synthesis of kadsurenone and its analogs

M. Ponpipom, T. Shen, R. Bugianesi, 1986 .

Synthesis of N-substituted D-mannosylamines and 1-(benzylamino)-1-deoxy-alditols for biological evaluation

M. Ponpipom, T. Shen, R. Bugianesi, 1980 .

Structure-activity relationships of C1 and C6 side chains of zaragozic acid A derivatives.

R. Marquis, K. Bartizal, W. Parsons, 1994, Journal of medicinal chemistry.

Modification of the pyridine moiety of non-peptidyl indole GnRH receptor antagonists.

M. Goulet, A. Mao, J. Cui, 2002, Bioorganic & Medicinal Chemistry Letters.

Steroidal androgen biosynthesis inhibitors.

A. Patchett, N. G. Brink, E. A. Ham, 1971, Journal of medicinal chemistry.