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1. Ripka, WC; Barker, G; Krakover, J
   High-throughput purification of compound libraries
   DRUG DISCOVERY TODAY
   
   W.C. Ripka et al., "High-throughput purification of compound libraries", DRUG DISC T, 6(9), 2001, pp. 471-477
2. Slee, DH; Romano, SJ; Yu, JH; Nguyen, TN; John, JK; Raheja, NK; Axe, FU; Jones, TK; Ripka, WC
   Development of potent non-carbohydrate imidazole-based small molecule selectin inhibitors with antiinflammatory activity
   JOURNAL OF MEDICINAL CHEMISTRY
   
   D.H. Slee et al., "Development of potent non-carbohydrate imidazole-based small molecule selectin inhibitors with antiinflammatory activity", J MED CHEM, 44(13), 2001, pp. 2094-2107
3. Ripka, WC
   Protein tyrosine phosphatase inhibition
   ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 35
   
   W.C. Ripka, "Protein tyrosine phosphatase inhibition", ANNU REP M, 35, 2000, pp. 231-250
4. RIPKA WC
   NEW THROMBIN INHIBITORS IN CARDIOVASCULAR-DISEASE
   CURRENT OPINION IN CHEMICAL BIOLOGY
   
   W.C. Ripka, "NEW THROMBIN INHIBITORS IN CARDIOVASCULAR-DISEASE", CURRENT OPINION IN CHEMICAL BIOLOGY, 1(2), 1997, pp. 242-253
5. SEMPLE JE; ROWLEY DC; BRUNCK TK; RIPKA WC
   SYNTHESIS AND BIOLOGICAL-ACTIVITY OF P-2-P-4 AZAPEPTIDOMIMETIC P-1-ARGININAL AND P-1-KETOARGININAMIDE DERIVATIVES - A NOVEL CLASS OF SERINE-PROTEASE INHIBITORS
   Bioorganic & medicinal chemistry letters
   
   J.E. Semple et al., "SYNTHESIS AND BIOLOGICAL-ACTIVITY OF P-2-P-4 AZAPEPTIDOMIMETIC P-1-ARGININAL AND P-1-KETOARGININAMIDE DERIVATIVES - A NOVEL CLASS OF SERINE-PROTEASE INHIBITORS", Bioorganic & medicinal chemistry letters, 7(3), 1997, pp. 315-320
6. TAMURA SY; GOLDMAN EA; BRUNCK TK; RIPKA WC; SEMPLE JE
   RATIONAL DESIGN, SYNTHESIS, AND SERINE-PROTEASE INHIBITORY ACTIVITY OF A NOVEL P-1-ARGININAL DERIVATIVE FEATURING A CONFORMATIONALLY CONSTRAINED P-2-P-3-BICYCLIC LACTAM MOIETY
   Bioorganic & medicinal chemistry letters
   
   S.Y. Tamura et al., "RATIONAL DESIGN, SYNTHESIS, AND SERINE-PROTEASE INHIBITORY ACTIVITY OF A NOVEL P-1-ARGININAL DERIVATIVE FEATURING A CONFORMATIONALLY CONSTRAINED P-2-P-3-BICYCLIC LACTAM MOIETY", Bioorganic & medicinal chemistry letters, 7(3), 1997, pp. 331-336
7. SEMPLE JE; MINAMI NK; TAMURA SY; BRUNCK TK; NUTT RF; RIPKA WC
   RATIONAL DESIGN AND SYNTHESIS OF A NOVEL, SELECTIVE CLASS OF THROMBININHIBITORS - P-1-ARGININAL DERIVATIVES INCORPORATING P-3-P-4 QUATERNARY LACTAM DIPEPTIDE SURROGATES
   Bioorganic & medicinal chemistry letters
   
   J.E. Semple et al., "RATIONAL DESIGN AND SYNTHESIS OF A NOVEL, SELECTIVE CLASS OF THROMBININHIBITORS - P-1-ARGININAL DERIVATIVES INCORPORATING P-3-P-4 QUATERNARY LACTAM DIPEPTIDE SURROGATES", Bioorganic & medicinal chemistry letters, 7(18), 1997, pp. 2421-2426
8. TAMURA SY; SEMPLE JE; REINER JE; GOLDMAN EA; BRUNCK TK; LIMWILBY MS; CARPENTER SH; ROTE WE; OLDESHULTE GL; RICHARD BM; NUTT RF; RIPKA WC
   DESIGN AND SYNTHESIS OF A NOVEL CLASS OF THROMBIN INHIBITORS INCORPORATING HETEROCYCLIC DIPEPTIDE SURROGATES
   Bioorganic & medicinal chemistry letters
   
   S.Y. Tamura et al., "DESIGN AND SYNTHESIS OF A NOVEL CLASS OF THROMBIN INHIBITORS INCORPORATING HETEROCYCLIC DIPEPTIDE SURROGATES", Bioorganic & medicinal chemistry letters, 7(12), 1997, pp. 1543-1548
9. TAMURA SY; SHAMBLIN BM; BRUNCK TK; RIPKA WC
   RATIONAL DESIGN, SYNTHESIS, AND SERINE-PROTEASE INHIBITORY ACTIVITY OF NOVEL P-1-ARGININOYL HETEROCYCLES
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   S.Y. Tamura et al., "RATIONAL DESIGN, SYNTHESIS, AND SERINE-PROTEASE INHIBITORY ACTIVITY OF NOVEL P-1-ARGININOYL HETEROCYCLES", Bioorganic & medicinal chemistry letters, 7(10), 1997, pp. 1359-1364
10. KRISHNAN R; TULINSKY A; VLASUK GP; PEARSON D; VALLAR P; BERGUM P; BRUNCK TK; RIPKA WC
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    R. Krishnan et al., "SYNTHESIS, STRUCTURE, AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF DIVALENT THROMBIN INHIBITORS CONTA AN ALPHA-KETO-AMIDE TRANSITION-STATE MIMETIC", Protein science, 5(3), 1996, pp. 422-433
11. LEVY OE; SEMPLE JE; LIM ML; REINER J; ROTE WE; DEMPSEY E; RICHARD BM; ZHANG E; TULINSKY A; RIPKA WC; NUTT RF
    POTENT AND SELECTIVE THROMBIN INHIBITORS INCORPORATING THE CONSTRAINED ARGININE MIMIC L-3-PIPERIDYL(N-GUANIDINO)ALANINE AT P-1
    Journal of medicinal chemistry
    
    O.E. Levy et al., "POTENT AND SELECTIVE THROMBIN INHIBITORS INCORPORATING THE CONSTRAINED ARGININE MIMIC L-3-PIPERIDYL(N-GUANIDINO)ALANINE AT P-1", Journal of medicinal chemistry, 39(23), 1996, pp. 4527-4530
12. SEMPLE JE; ROWLEY DC; BRUNCK TK; HAUONG T; MINAMI NK; OWENS TD; TAMURA SY; GOLDMAN EA; SIEV DV; ARDECKY RJ; CARPENTER SH; GE Y; RICHARD BM; NOLAN TG; HAKANSON K; TULINSKY A; NUTT RF; RIPKA WC
    DESIGN, SYNTHESIS, AND EVOLUTION OF A NOVEL, SELECTIVE, AND ORALLY BIOAVAILABLE CLASS OF THROMBIN INHIBITORS - P1-ARGININAL DERIVATIVES INCORPORATING P3-P4 LACTAM SULFONAMIDE MOIETIES
    Journal of medicinal chemistry
    
    J.E. Semple et al., "DESIGN, SYNTHESIS, AND EVOLUTION OF A NOVEL, SELECTIVE, AND ORALLY BIOAVAILABLE CLASS OF THROMBIN INHIBITORS - P1-ARGININAL DERIVATIVES INCORPORATING P3-P4 LACTAM SULFONAMIDE MOIETIES", Journal of medicinal chemistry, 39(23), 1996, pp. 4531-4536
13. RIPKA WC
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    W.C. Ripka, "DESIGN STRATEGIES FOR SERINE-PROTEASE INHIBITORS", The FASEB journal, 9(6), 1995, pp. 1253-1253
14. STASSEN JM; LAMBEIR AM; MATTHYSSENS G; RIPKA WC; NYSTROM A; SIXMA JJ; VERMYLEN J
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    J.M. Stassen et al., "CHARACTERIZATION OF A NOVEL SERIES OF APROTININ-DERIVED ANTICOAGULANTS .1. IN-VITRO AND PHARMACOLOGICAL PROPERTIES", Thrombosis and haemostasis, 74(2), 1995, pp. 646-654
15. RIPKA WC; DELUCCA GV; BACH AC; POTTORF RS; BLANEY JM
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16. RIPKA WC; DELUCCA GV; BACH AC; POTTORF RS; BLANEY JM
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