K. Pankiewicz

发表

Comparative metabolism of 2-[bis(2-chloroethyl)amino]tetrahydro-2-H-1,3,2-oxazaphosphorine-2-oxide (cyclophosphamide) and its enantiomers in humans.

W. Stec, J. Smyth, M. Jarman, 1979, Cancer research.

Selective inhibition of nicotinamide adenine dinucleotide kinases by dinucleoside disulfide mimics of nicotinamide adenine dinucleotide analogues.

Y. Sham, G. Magni, M. Di Stefano, 2009, Bioorganic & medicinal chemistry.

Synthesis of 2′-β-fluoro-substituted nucleosides by a direct approach

Kyoichi A. Watanabe, K. Pankiewicz, 1993 .

Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis.

P. Tonge, Taesoo Kim, L. Bonnac, 2007, Bioorganic & medicinal chemistry letters.

Inhibitors of the IMPDH Enzyme as Potential Anti-Bovine Viral Diarrhoea Virus Agents

M. Otto, L. Stuyver, S. Patterson, 2002, Antiviral chemistry & chemotherapy.

The Chemistry of Nucleoside and Dinucleotide Inhibitors of Inosine Monophosphate Dehydrogenase (IMPDH)1

K. Pankiewicz, B. Goldstein, 2002 .

The practical synthesis of a methylenebisphosphonate analogue of benzamide adenine dinucleotide: inhibition of human inosine monophosphate dehydrogenase (type I and II).

A. Zatorski, K. Watanabe, Kyoichi A. Watanabe, 1997, Journal of medicinal chemistry.

NAD-analogues as potential anticancer agents: conformational restrictions as basis for selectivity.

A. Zatorski, K. Watanabe, K. Pankiewicz, 1996, Acta biochimica Polonica.

Chemical synthesis of benzamide adenine dinucleotide: inhibition of inosine monophosphate dehydrogenase (types I and II).

A. Zatorski, K. Watanabe, K. Pankiewicz, 1996, Journal of medicinal chemistry.

Dynamics of Subgenomic Hepatitis C Virus Replicon RNA Levels in Huh-7 Cells after Exposure to Nucleoside Antimetabolites

M. Otto, L. Stuyver, R. Schinazi, 2003, Journal of Virology.

NAD-based inhibitors with anticancer potential.

K. Pankiewicz, K. Felczak, R. Vince, 2014, Bioorganic & medicinal chemistry letters.

Novel nicotinamide adenine dinucleotide analogues as potential anticancer agents: quest for specific inhibition of inosine monophosphate dehydrogenase.

K. Pankiewicz, 1997, Pharmacology & therapeutics.

Synthesis of oligodeoxynucleotides containing the c-nucleoside and 2- deoxy-2’-fluoro-ara-nucleoside moieties by the h-phosphonate method.1.2

Kyoichi A. Watanabe, K. Pankiewicz, I. Rosenberg, 1993 .

A second target of benzamide riboside

D. Banerjee, J. Bertino, K. Scotto, 2012, Cancer biology & therapy.

Mycophenolic acid potently inhibits rotavirus infection with a high barrier to resistance development.

M. Koopmans, M. Peppelenbosch, L. J. van der Laan, 2016, Antiviral research.

SYNTHESIS OF N3,5′-CYCLO-4-(β-D-RIBOFURANOSYL)-VIC-TRIAZOLO[4,5-b]PYRIDIN-5-ONE AND ITS 3′-DEOXYSUGAR ANALOGUE AS POTENTIAL ANTI-HEPATITIS C VIRUS AGENTS

M. Otto, L. Stuyver, R. Schinazi, 2005, Nucleosides, nucleotides & nucleic acids.

Multivalent glycocluster design through directed evolution.

L. Hedstrom, Sevan Habeshian, K. Pankiewicz, 2011, Angewandte Chemie.

Inhibitors of inosine monophosphate dehydrogenase as potential chemotherapeutic agents

K. Pankiewicz, 1999 .

Synthesis of Methylenebis(Phosphonate) Analogues of 2-, 4-, and 6-Pyridones of Nicotinamide Adenine Dinucleotide

K. Pankiewicz, K. Felczak, 2011, Nucleosides, nucleotides & nucleic acids.

Prodrug Activation by Cryptosporidium Thymidine Kinase*

P. Rathod, L. Hedstrom, B. Striepen, 2010, The Journal of Biological Chemistry.

Technical aspects of imaging and transfemoral arterial treatment of N1-S1 tumors in rats: an appropriate model to test the biology and therapeutic response to transarterial treatments of liver cancers.

Yun Liang, L. Bonnac, S. Ju, 2009, Journal of vascular and interventional radiology : JVIR.

Methylenebis(sulfonamide) linked nicotinamide adenine dinucleotide analogue as an inosine monophosphate dehydrogenase inhibitor.

L. Bonnac, Daniel J. Wilson, E. Bennett, 2007, Bioorganic & medicinal chemistry letters.

Design, synthesis, and antiviral activity of 2'-deoxy-2'-fluoro-2'-C-methylcytidine, a potent inhibitor of hepatitis C virus replication.

W. Stec, M. Otto, L. Stuyver, 2005, Journal of medicinal chemistry.

Synthesis of Methylenebis(phosphonate) Analogs of Dinucleotide Pyrophosphates

S. Patterson, K. Pankiewicz, G. Gao, 2006, Current protocols in nucleic acid chemistry.

SYNTHESIS OF METHYLENEBIS(PHOSPHONATE) ANALOGUES OF NUCLEOTIDE COENZYMES. A NOVEL COUPLING MECHANISM

Kyoichi A. Watanabe, K. Pankiewicz, K. Lesiak, 1999 .

Synthesis of a methylenebis(phosphonate) analogue of mycophenolic adenine dinucleotide: a glucuronidation-resistant MAD analogue of NAD.

K. Watanabe, K. Pankiewicz, B. Goldstein, 1998, Journal of medicinal chemistry.

Suppression of Hepatocellular Carcinoma by Mycophenolic Acid in Experimental Models and in Patients

M. Peppelenbosch, P. Boor, J. Kwekkeboom, 2019, Transplantation.

Novel mycophenolic adenine bis(phosphonate)s as potent anticancer agents and inducers of cells differentiation.

K. Pankiewicz, K. Lesiak-watanabe, 1999, Nucleosides & nucleotides.

Potent inhibitors of human inosine monophosphate dehydrogenase type II. Fluorine-substituted analogues of thiazole-4-carboxamide adenine dinucleotide.

A. Zatorski, J. Jones, T. Colby, 1995, Journal of medicinal chemistry.

Nicotinamide adenine dinucleotide based therapeutics.

L. Bonnac, R. Petrelli, G. Gao, 2008, Current medicinal chemistry.

Kinetic mechanism of damage site recognition and uracil flipping by Escherichia coli uracil DNA glycosylase.

J. Stivers, K. Watanabe, K. Pankiewicz, 1999, Biochemistry.

Crystallographic studies of isosteric NAD analogues bound to alcohol dehydrogenase: specificity and substrate binding in two ternary complexes.

H. Li, K. Watanabe, K. Pankiewicz, 1995, Biochemistry.

CNAD: a potent and specific inhibitor of alcohol dehydrogenase.

H. Li, J. Jones, K. Watanabe, 1994, Journal of medicinal chemistry.

Synthesis of isosteric analogues of nicotinamide adenine dinucleotide containing C-nucleotide of nicotinamide or picolinamide.

K. Watanabe, J. E. Bell, K. Pankiewicz, 1993, Journal of medicinal chemistry.

Nucleosides. Part 151. Efficient Synthesis of 5-(β-D-Ribofuranosyl)nicotinamide and Its α-Isomer.

K. Watanabe, E. Sochacka, K. Pankiewicz, 1989 .

Efficient synthesis of 5-(β-D-ribofuranosyl)nicotinamide and its α-isomer

E. Sochacka, Kyoichi A. Watanabe, K. Pankiewicz, 1988 .

EFFICIENT SYNTHESIS OF METHYLENEBIS(PHOSPHONATE) ANALOGUES OF P1,P2-DISUBSTITUTED PYROPHOSPHATES OF BIOLOGICAL INTEREST. A NOVEL PLAUSIBLE MECHANISM

Kyoichi A. Watanabe, K. Pankiewicz, K. Lesiak, 1997 .

Cofactor mimics as selective inhibitors of NAD-dependent inosine monophosphate dehydrogenase (IMPDH)--the major therapeutic target.

L. Stuyver, R. Schinazi, S. Patterson, 2004, Current medicinal chemistry.

Crystallographic studies of two alcohol dehydrogenase-bound analogues of thiazole-4-carboxamide adenine dinucleotide (TAD), the active anabolite of the antitumor agent tiazofurin.

H L Carrell, H. L. Carrell, H. Li, 1994, Biochemistry.

Nucleosides. 130. Synthesis of 2′-Deoxy-2′-substituted- and 5′-Deoxy-5′-substituted-ψ-uridine Derivatives. Crystalline and Molecular Structure of 2′-Chloro-2′-deoxy-1,3-dimethyl-ψ-uridine. Studies Directed Toward the Synthesis of 2′-Deoxy-2′-substituted-arabino-Nucleosides. 1†

H. Ogura, Kyoichi A. Watanabe, K. Pankiewicz, 1985 .

Fluorinated nucleosides.

K. Pankiewicz, 2000, Carbohydrate research.

Synthesis of 3-methylpseudouridine and 2'-deoxy-3-methyl-pseudouridine.

A. Matsuda, K. Watanabe, K. Pankiewicz, 1982, Carbohydrate research.

Phosphonoxins: rational design and discovery of a potent nucleotide anti-Giardia agent.

R. Pohl, S. Patterson, C. Dykstra, 2007, Bioorganic & medicinal chemistry letters.

Synthesis of N3,5'-cyclo-4-(beta-D-ribofuranosyl)-vic-triazolo[4,5-b]pyridin-5-one, a novel compound with anti-hepatitis C virus activity.

M. Otto, L. Stuyver, R. Schinazi, 2004, Journal of medicinal chemistry.

A single-amino acid substitution in West Nile virus 2K peptide between NS4A and NS4B confers resistance to lycorine, a flavivirus inhibitor

B. Zhang, P. Shi, Bo Zhang, 2008, Virology.

Triazole-linked inhibitors of inosine monophosphate dehydrogenase from human and Mycobacterium tuberculosis.

Y. Sham, C. Aldrich, Daniel J. Wilson, 2010, Journal of medicinal chemistry.

Inhibition of Calcineurin or IMP Dehydrogenase Exerts Moderate to Potent Antiviral Activity against Norovirus Replication

M. Koopmans, M. Peppelenbosch, H. Metselaar, 2017, Antimicrobial Agents and Chemotherapy.

Rational design and synthesis of novel nucleotide anti-Giardia agents.

L. Bonnac, S. Patterson, C. Dykstra, 2007, Bioorganic & medicinal chemistry letters.

A single-amino acid substitution in West Nile virus 2K peptide between NS4A and NS4B confers resistance to lycorine, a flavivirus inhibitor

P. Shi, Bo Zhang, Zhiming Yuan, 2008, Virology.

Synthesis and absolute configuration of the optically active forms of 2-(bis(2-chloroethyl)amino)-4-methyltetrahydro-2h-1,3,2-oxazaphosphorine 2-oxide (4-methylcyclophosphamide).

W. Stec, K. Pankiewicz, R. Kinas, 1977, The Journal of organic chemistry.

Synthesis of 9-(2-Deoxy-2-Fukuoro-β-D- Abinoruranosyl)Hypoxhine. The First Direct Introduction of A 2′-β-Fldoro Substituent in Ppepormed Purine Nucleosides. Studies Directed Toward the Synthesis of 2′-DEOXY-2′-Substituted Arabppmocebosides. 8.1

B. Nawrot, Kyoichi A. Watanabe, K. Pankiewicz, 1991 .

Synthesis of a novel C-nucleoside, 2-amino-7-(2-deoxy-beta-D-erythro- pentofuranosyl)-3H,5H-pyrrolo-[3,2-d]pyrimidin-4-one (2'-deoxy-9-deazaguanosine).

L. Gudas, K. Watanabe, K. Pankiewicz, 1999, Nucleosides & nucleotides.

Nucleosides. 121. Improved and General Synthesis of 2′-Deoxy C-Nucleosides. Synthesis of 5-(2-Deoxy-β-D-erythro-pentofuranosyl)uracil, -1-methyluracil, -1,3-dimethyluracil, and -isocytosine

A. Matsuda, Kyoichi A. Watanabe, K. Pankiewicz, 1982 .

From ribavirin to NAD analogues and back to ribavirin in search for anticancer agents

K. Pankiewicz, K. Felczak, 2015 .

SYNTHESIS AND IN VITRO ANTI-HCV ACTIVITY OF β-D- and L-2′-DEOXY-2′-FLUORORIBONUCLEOSIDES

M. Otto, L. Stuyver, R. Schinazi, 2005 .

Synthesis and anti-viral activity of a series of d- and l-2'-deoxy-2'-fluororibonucleosides in the subgenomic HCV replicon system.

M. Otto, L. Stuyver, R. Schinazi, 2005, Bioorganic & medicinal chemistry.

Nucleosides. CXLIV. Some reactions of 2'-O-triflyl-2,3'-anhydroxylosyluracil with nucleophilic reagents. Synthesis of 2'-chloro-2',3'-dideoxyuridinene. Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides. (5).

K. Watanabe, K. Pankiewicz, 1987, Chemical & pharmaceutical bulletin.

SYNTHESIS OF METHYLENE-BRIDGED ANALOGUES OF NICOTINAMIDE RIBOSIDE, NICOTINAMIDE, MONONUCLEOTIDE AND NICOTINAMIDE ADENINE DINUCLEOTIDE

K. Watanabe, K. Pankiewicz, P. Lipka, 1996 .

Synthesis of 2,2′-Anhydro-2-Hydroxy- and 6,2′-Anhydro-6-Hydroxy-1-β-D-Arabindfuranosylnicotinamide as Conformationally Restricted Nicotinamide Nucleoside Analogs1

K. Pankiewicz, A. Ptak, L. Ciszewski, 1991 .

Nucleosides. 145. Synthesis of 2,5′-Anhydro-2-Thiouridine and its Conversion to 3′-O-Acetyl-2,2′-Anhydro-5′-Chloro-5′-Deoxy-2-Thiouridine. Studies Directed Toward the Synthesis of 2′-Deoxy-2′-Substituted arabino Nucleosides (7)

Kyoichi A. Watanabe, K. Pankiewicz, T. Su, 1989 .

Nucleosides. 146. 1-Methyl-5-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil, the C-nucleoside isostere of the potent antiviral agent 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)thymine (FMAU). Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides. 6.

B. Nawrot, K. Watanabe, K. Pankiewicz, 1987, Journal of medicinal chemistry.

The chemistry of nicotinamide adenine dinucleotide (NAD) analogues containing C-nucleosides related to nicotinamide riboside.

Kyoichi A. Watanabe, K. Pankiewicz, H. Jayaram, 2002, Current medicinal chemistry.

Nucleosides. 131. The Synthesis of 5-(2-Chloro-2-Deoxy-β-D-arabino-Furanosyl)Uracil. Reinterpretation of Reaction of ψ-Uridine With α-Acetoxyisobutyryl Chloride. Studies Directed Toward the Synthesis of 2′-Deoxy-2′-Substituted Arabino-Nucleosides. 2

Kyoichi A. Watanabe, K. Pankiewicz, 1985 .

Efficient Synthesis of Benzamide Riboside, a Potential Anticancer Agent

L. Bonnac, S. Patterson, Liqiang Chen, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis and in vitro anti-HCV activity of beta-D- and 1-2'-deoxy-2'-fluororibonucleosides.

M. Otto, L. Stuyver, R. Schinazi, 2005, Nucleosides, Nucleotides & Nucleic Acids.

Synthesis of 1-methyl-5-(3-azido-2,3-dideoxy-beta-D-erythro-pentofuranosyl)uracil and 1-methyl-5-(3-azido-2,3-dideoxy-2-fluoro-beta-D-arabinofuranosyl)uracil. The C-nucleoside isostere of 3'-azido-3'-deoxythymidine and its 2'-"up"-fluoro analogue.

B. Nawrot, K. Watanabe, E. Sochacka, 1990, Journal of Medicinal Chemistry.

Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides.

B. Nawrot, K. Watanabe, E. Sochacka, 1987, Nucleic Acids Symposium Series.

A Synthesis of 2’-Fluoro- and 3’-Fluoro-Substituted Purine Nucleosides via a Direct Approach

Kyoichi A. Watanabe, K. Pankiewicz, 1993 .

A synthesis of 9-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)adenine and -hypoxanthine. An effect of C3'-endo to C2'-endo conformational shift on the reaction course of 2'-hydroxyl group with DAST

Kyoichi A. Watanabe, K. Pankiewicz, J. Krzemiński, 1992 .

Synthesis of thiazole-4-carboxamide-adenine difluoromethylenediphosphonates substituted with fluorine at C-2' of the adenosine.

A. Zatorski, K. Watanabe, K. Pankiewicz, 1993, Carbohydrate research.

Nucleosides. 164. Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides. 10. Synthesis of 2'-.beta.-fluoro- and 3'-.alpha.-fluoro-substituted guanine nucleosides. Effect of sugar conformational shifts on nucleophilic displacement of the 2'-hydroxy and 3'-hydroxy group

Kyoichi A. Watanabe, K. Pankiewicz, J. Krzemiński, 1992 .

Cytotoxicity and cellular differentiation activity of methylenebis(phosphonate) analogs of tiazofurin and mycophenolic acid adenine dinucleotide in human cancer cell lines.

Steven E Patterson, S. Patterson, Joel A Yalowitz, 2002, Cancer letters.

C-Nucleoside Analogues of Nicotinamide Mononucleotide (NMN)

E. Sochacka, Kyoichi A. Watanabe, K. Pankiewicz, 1988 .

Nucleosides. CXLVIII. Synthesis of 6-(beta-D-ribofuranosyl)picolinamide. A novel C-nucleoside from D-ribonolactone.

K. Watanabe, E. Sochacka, K. Pankiewicz, 1988, Chemical & pharmaceutical bulletin.

Synthesis of 5-beta-D-ribofuranosylnicotinamide and its N-methyl derivative. The isosteric and isoelectronic analogues of nicotinamide nucleoside.

K. Watanabe, K. Pankiewicz, M. Kabat, 1987, Journal of medicinal chemistry.

Synthesis of nonhydrolyzable analogues of thiazole-4-carboxamide and benzamide adenine dinucleotide containing fluorine atom at the C2' of adenine nucleoside: induction of K562 differentiation and inosine monophosphate dehydrogenase inhibitory activity.

K. Watanabe, K. Pankiewicz, B. Goldstein, 1997, Journal of medicinal chemistry.

Nucleosides. CXLIII. Synthesis of 5'-deoxy-5'-substituted-2,2'-anhydro-1-(beta-D-arabinofuranosyl) uracils. A new 2,5'- to 2,2'-anhydro-nucleoside transformation. Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides. (4).

K. Watanabe, K. Pankiewicz, K. Watanabe, 1987, Chemical & pharmaceutical bulletin.

Nucleosides. 137. (Trifluoromethyl)sulfonyl (triflyl) migration. Synthesis of 6,3'-anhydro-3-benzyl-1-(5-chloro-5-deoxy-.beta.-D-xylofuranosyl)barbituric acid from the 2'-trifluoromethanesulfonate (triflate) of 6,5'-anhydro-3-benzyl-1-.beta.-D-ribofuranosylbarbituric acid

B. Nawrot, Kyoichi A. Watanabe, K. Pankiewicz, 1986 .

Nucleosides. 132. Synthesis of 5-(2'-substituted-2'-deoxy-.beta.-D-arabinofuranosyl)-1-methyluracils from 1-methyl-.psi.-uridine. The first direct introduction of the 2'-substituent to C-2' in the "up" configuration by nucleophilic reactions. Studies directed toward the synthesis of 2'-deoxy-2'-subs

J. Kim, Kyoichi A. Watanabe, K. Pankiewicz, 1985 .

Cytotoxic and non-cytotoxic N-alkyl derivatives of putrescine: effect on polyamine uptake and growth of prostatic cancer cells in vitro.

K. Watanabe, W. Heston, D. Covey, 1987, Biochemical pharmacology.

Synthesis and Reactivity of Benzyl 2-O-Trifluoromethyl-Sulfonyl- and Benzyl 3-O-Trifluoromethylsulfonyl-β-D-Ribofuranoside - The first Evidence of Trifluoromethyl-Sulfonyl (Triflyl) Migration in Carbohydrates

B. Nawrot, Kyoichi A. Watanabe, K. Pankiewicz, 1988 .

Nucleosides. 120. Syntheses of 2'-deoxy-.psi.-isocytidine and 2'-deoxy-1-methyl-.psi.-uridine from .psi.-uridine

A. Matsuda, C. K. Chu, Kyoichi A. Watanabe, 1981 .

Nucleosides. Part 153. Synthesis of 1-Methyl-5-(3-azido-2,3-dideoxy-. beta.-D-erythro-pentofuranosyl)uracil and 1-Methyl-5-(3-azido-2,3- dideoxy-2-fluoro-β-D-arabinofuranosyl)uracil. The C-Nucleoside Isostere of 3′-Azido-3′-deoxythymidine and Its 2′-“Up”-Fluoro Analogue.

K. Watanabe, E. Sochacka, K. Pankiewicz, 1991 .

Heteronuclear NMR and crystallographic studies of wild-type and H187Q Escherichia coli uracil DNA glycosylase: electrophilic catalysis of uracil expulsion by a neutral histidine 187.

G. Gilliland, G. Xiao, J. Stivers, 1999, Biochemistry.

Mycophenolic acid analogs with a modified metabolic profile.

Daniel J. Wilson, Liqiang Chen, K. Pankiewicz, 2008, Bioorganic & medicinal chemistry.

Cross Talk between Nucleotide Synthesis Pathways with Cellular Immunity in Constraining Hepatitis E Virus Replication

M. Peppelenbosch, Lei Xu, H. Metselaar, 2016, Antimicrobial Agents and Chemotherapy.

Synthesis and absolute configuration assignments of enantiomeric forms of ifosphamide, sulfosphamide, and trofosphamide

W. Stec, M. Jarman, K. Pankiewicz, 1979 .

Cofactor-type inhibitors of inosine monophosphate dehydrogenase via modular approach: targeting the pyrophosphate binding sub-domain.

R. Petrelli, P. Kusumanchi, Daniel J. Wilson, 2011, Bioorganic & medicinal chemistry.

Recent development of IMP dehydrogenase inhibitors for the treatment of cancer.

Liqiang Chen, K. Pankiewicz, Liqiang Chen, 2007, Current opinion in drug discovery & development.

Inosine monophosphate dehydrogenase : a major therapeutic target

K. Pankiewicz, B. Goldstein, 2003 .

Raman spectroscopy of uracil DNA glycosylase-DNA complexes: insights into DNA damage recognition and catalysis.

P. Carey, J. Stivers, J. Dong, 2000, Biochemistry.

Stereospecific synthesis of chiral metabolites of ifosfamide and their determination in the urine.

W. Stec, K. Misiura, K. Pankiewicz, 1983, Journal of medicinal chemistry.

STEREOSPECIFIC SYNTHESIS OF CHIRAL METABOLITES OF IFOSFAMIDE AND THEIR DETERMINATION IN THE URINE

W. Stec, K. Misiura, K. Pankiewicz, 1983 .

Application of deuterium labelling mass spectrometry in a study of the metabolism of the enantiomers of cyclophosphamide.

W. Stec, P. Farmer, P. Cox, 1977, Biomedical mass spectrometry.

THE SYNTHESIS OF THE OPTICAL ISOMERS OF 2-(2-CHLOROETHYLAMINO)-3-(2-CHLOROETHYL)TETRAHYDRO-2H-1,3,2-OXAZAPHOSPHORINE 2-OXIDE (ISOPHOSPHAMIDE)

W. Stec, P. Farmer, M. Jarman, 1978 .

The synthesis of enantiomers of 4-ketocyclophosphamide

W. Stec, M. Jarman, K. Misiura, 1981, Experientia.

Bis(sulfonamide) isosters of mycophenolic adenine dinucleotide analogues: inhibition of inosine monophosphate dehydrogenase.

R. Petrelli, M. Olesiak, Daniel J. Wilson, 2008, Bioorganic & medicinal chemistry.

Novel mycophenolic adenine bis(phosphonate)s as potential immunosuppressants.

K. Pankiewicz, K. Malinowski, K. Lesiak-watanabe, 1999, Current medicinal chemistry.

ABSOLUTE CONFIGURATION OF THE CANCEROSTATIC S(-)-CYCLOPHOSPHAMIDE

W. Stec, M. Gdaniec, K. Pankiewicz, 1977 .

Rehab of NAD(P)-dependent enzymes with NAD(P)-based inhibitors.

K. Pankiewicz, K. Felczak, 2011, Current medicinal chemistry.

Inosine Monophosphate Dehydrogenase and Its Inhibitors: An Overview

K. Pankiewicz, B. Goldstein, 2003 .

Inhibition of Calcineurin or IMP Dehydrogenase Exerts Moderate to Potent Antiviral Activity against Norovirus Replication

M. Koopmans, M. Peppelenbosch, H. Metselaar, 2017, Antimicrobial Agents and Chemotherapy.

The metabolism and antitumour activity of the enantiomers of cis- and trans-4-methylcyclophosphamide.

W. Stec, P. Farmer, M. Jarman, 1977, Chemico-biological interactions.

Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylase based on a cinnamic hydroxamic acid core structure.

Y. Sham, R. Petrelli, Daniel J. Wilson, 2010, Bioorganic & medicinal chemistry.

Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylases for cancer treatment.

Daniel J. Wilson, Liqiang Chen, K. Pankiewicz, 2007, Journal of Medicinal Chemistry.