D. Kalvin

发表

Potent and orally bioavailable noncysteine-containing inhibitors of protein farnesyltransferase.

S. Ng, D. Augeri, P. Kovar, 1999, Bioorganic & medicinal chemistry letters.

Novel antibacterial class: a series of tetracyclic derivatives.

N. Soni, Philip J. Merta, B. Beutel, 2006, Journal of medicinal chemistry.

DNA breakage activity of the methanol extract of auromomycin

S. Crooke, E. Peters, M. Lischwe, 2004, Cancer Chemotherapy and Pharmacology.

Alternate substrates and inhibitors of 1-aminocyclopropane-1-carboxylic acid synthase

R. Woodard, K. Ramalingam, D. Kalvin, 1987 .

Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 antagonists.

D. Donnelly-roberts, P. Honore, M. Jarvis, 2007, Bioorganic & medicinal chemistry letters.

Thrombospondin-1 mimetic peptide inhibitors of angiogenesis and tumor growth: design, synthesis, and optimization of pharmacokinetics and biological activities.

S. Badylak, F. Haviv, J. Henkin, 2005, Journal of medicinal chemistry.

Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties.

Scott A. Erickson, K. Comess, A. Vasudevan, 2006, Bioorganic & medicinal chemistry letters.

Scaffold oriented synthesis. Part 4: design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing heterocycle forming and multicomponent reactions.

Eric F. Johnson, I. Akritopoulou‐Zanze, P. Kovar, 2011, Bioorganic & medicinal chemistry letters.

Microwave-assisted synthesis utilizing supported reagents: a rapid and efficient acylation procedure.

D. Sauer, K. Phelan, D. Kalvin, 2003, Organic letters.

Microwave‐Assisted Synthesis Utilizing Supported Reagents: A Rapid and Efficient Acylation Procedure.

D. Sauer, K. Phelan, D. Kalvin, 2004 .

Novel inhibitors of bacterial protein synthesis: structure-activity relationships for 1,8-naphthyridine derivatives incorporating position 3 and 4 variants.

N. Soni, R. Clark, Y. Gu, 2004, Bioorganic & medicinal chemistry letters.

Discovery of a series of cyclohexylethylamine-containing protein farnesyltransferase inhibitors exhibiting potent cellular activity.

S. Ng, S. Rosenberg, H. Sham, 1999, Journal of medicinal chemistry.

Synthesis of (1S,2R)- and (1S,2S)-1-amino[2-2H]cyclopropane-1-carboxylic acids: The total 1H NMR assignment of cyclo[ACC-.alpha.-methyl-Phe]

R. Woodard, K. Ramalingam, D. Kalvin, 1989 .

A Facile Procedure for the Preparation of Alicyclic α-Amino Acids

R. Woodard, K. Ramalingam, D. Kalvin, 1985 .

Synthesis of deuterium-labeled 1-aminocyclopropane-1-carboxylic acid

R. Woodard, K. Ramalingam, D. Kalvin, 1984 .

Potent and selective non-cysteine-containing inhibitors of protein farnesyltransferase.

S. Ng, D. Augeri, S. Rosenberg, 1998, Journal of medicinal chemistry.

Preparation of 1-deuterioaldehydes via tub use of diisobutylaluminum deuteride (DIBAL-D)

R. Woodard, D. Kalvin, 1984 .

A practical large scale chemical synthesis of chiral glycines

R. Woodard, K. Ramalingam, D. Kalvin, 1988 .

Structure-activity relationship studies on N'-aryl carbohydrazide P2X7 antagonists.

D. Donnelly-roberts, P. Honore, M. Jarvis, 2008, Journal of medicinal chemistry.

Synthesis of potential antifilarial agents. 1-(5-Benzoylbenzimidazol-2-yl)-3-alkyl- and -arylureas.

D. Ortwine, J. Mccall, L. Townsend, 1984, Journal of Medicinal Chemistry.

SYNTHESIS OF POTENTIAL ANTIFILARIAL AGENTS. 1. 1-(5-BENZOYLBENZIMIDAZOL-2-YL)-3-ALKYL AND ARYL UREAS

D. Ortwine, J. Mccall, L. Townsend, 1984 .