M. Chun

发表

Xylocydine, a Novel Inhibitor of Cyclin-Dependent Kinases, Prevents the Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand-Induced Apoptotic Cell Death of SK-HEP-1 Cells

Young-Mi Ham, Kyoung-Jin Choi, S. Song, 2004, Journal of Pharmacology and Experimental Therapeutics.

Synthesis of N 6-Substituted 3′-Ureidoadenosine Derivatives as Highly Potent Agonists at the Mutant A3 Adenosine Receptor

K. Jacobson, Zhang-Guo Gao, H. Moon, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis of 3′-Acetamidoadenosine Derivatives as Potential A3 Adenosine Receptor Agonists

K. Jacobson, Zhang-Guo Gao, M. Chun, 2008, Nucleosides, nucleotides & nucleic acids.

Design, synthesis, and biological activity of N6-substituted-4'-thioadenosines at the human A3 adenosine receptor.

K. Jacobson, Zhang-Guo Gao, H. Moon, 2006, Bioorganic & medicinal chemistry.

Design and synthesis of 3'-ureidoadenosine-5'-uronamides: effects of the 3'-ureido group on binding to the A3 adenosine receptor.

K. Jacobson, Zhang-Guo Gao, M. Chun, 2004, Bioorganic & medicinal chemistry letters.

Asymmetric Synthesis of Cyclopropyl-fused 2′- C -Methylcarbanucleosides as Potential Anti-HCV Agents

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Nucleosides. 123. Synthesis of antiviral nucleosides: 5-substituted 1-(2-deoxy-2-halogeno-beta-D-arabinofuranosyl)cytosines and -uracils. Some structure-activity relationships.

A. Matsuda, M. Chun, C. K. Chu, 1983, Journal of medicinal chemistry.

SYNTHESIS AND ANTIVIRAL ACTIVITY OF D- AND L-2′-AZIDO-2′,3′-DIDEOXY-4′-THIOPYRIMIDINE AND PURINE NUCLEOSIDES

M. Chun, L. Jeong, H. Kim, 2001, Nucleosides, nucleotides & nucleic acids.

Synthesis and antiviral activity of apio dideoxy nucleosides with azido or amino substituent.

H. Moon, M. Chun, L. Jeong, 1998, Nucleosides & nucleotides.

Methionine analogues as inhibitors of methionyl-tRNA synthetase.

M. Chun, S. Kim, J. Lee, 1998, Bioorganic & medicinal chemistry letters.

A synthetic study on cyclic phosphate derivatives of seconucleosides as potential antiviral agents (I): Synthesis of 3′,5′-cyclic phosphates of 2′-substituted secouridines and secoribavirins

M. Chun, S. Chun, J. Kim, 1991, Archives of pharmacal research.

STEREOSELECTIVE SYNTHESIS OF CONFORMATIONALLY RIGID APIO CARBANUCLEOSIDES AS POTENTIAL ANTIVIRAL AGENTS

H. Moon, M. Chun, L. Jeong, 2005, Nucleosides, nucleotides & nucleic acids.

Design, Synthesis, and In Vitro Evaluation of APIO Analogue of Neplanocin A

H. Moon, M. Chun, L. Jeong, 2003, Nucleosides, nucleotides & nucleic acids.

Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor.

H. Moon, M. Chun, L. Jeong, 2002, Organic letters.

Synthesis of D- and L-apio nucleoside analogues with 2'-hydroxyl group as potential anti-HIV agents.

H. Moon, M. Chun, L. Jeong, 2004, Bioorganic & medicinal chemistry.

Synthesis and Biological Evaluation of Novel Isonucleosides with 1,2,4‐Triazole‐3‐Carboxamide

M. Chun, Myong-Jung Kim, S. Y. Chung, 2005 .

Synthesis of 5'-substituted fluoro-neplanocin A analogues: importance of a hydrogen bonding donor at 5'-position for the inhibitory activity of S-adenosylhomocysteine hydrolase.

H. Moon, Sang Kook Lee, M. Chun, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of fluorinated cyclopentenyladenine as potent inhibitor of S-adenosylhomocysteine hydrolase.

H. Moon, M. Chun, W. J. Choi, 2004, Bioorganic & medicinal chemistry letters.

Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase.

H. Moon, Sang Kook Lee, M. Chun, 2003, Journal of medicinal chemistry.

Syntheses of D- and L-cyclopentenone derivatives using ring-closing metathesis: versatile intermediates for the synthesis of D- and L-carbocyclic nucleosides.

H. Moon, M. Chun, W. J. Choi, 2001, The Journal of organic chemistry.

Highly stereoselective intramolecular alkylation of ester enolate: An approach to trans-hydrindane system

M. Chun, Deukjoon Kim, W. Chung, 1986 .

Synthesis and biological activity of 5-hydroxy-4-quinolones and 5-methoxy-4-quinolones as truncated acridones

Jeewoo Lee, M. Chun, Chong-kyo Lee, 1998, Archives of pharmacal research.

Improved synthesis of D-1,3-oxathiolanyl acetate from D-mannose and D-galactose

M. Chun, J. Kim, S. Shin, 1994 .

Thiocyanation of indoles

M. Chun, Y. Tamura, Sundo Kwon, 1978 .

Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect

M. Chun, W. J. Choi, L. Jeong, 2002 .

Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents

Jeewoo Lee, H. Moon, M. Chun, 1997 .

Improved synthesis of L-1,3-dioxolanyl and L-1,3-oxathiolanyl acetate from L-gulose

Ji Yeon Song, M. Chun, J. Kim, 1994 .

Asymmetric synthesis of homo-apioneplanocin A from D-ribose

Jin-hee Kim, H. Moon, M. Chun, 2006 .

Synthesis of novel D-2'-deoxy-2'-C-difluoromethylene-4'-thiocytidine as a potential antitumor agent.

H. Moon, M. Chun, L. Jeong, 2002, Organic letters.

Participation of sulfur occurred during the Mitsunobu reaction: synthesis of novel isodideoxythionucleosides

H. Moon, M. Chun, L. Jeong, 1998 .

Methionyl adenylate analogues as inhibitors of methionyl-tRNA synthetase.

M. Chun, S. Kim, J. Lee, 1999, Bioorganic & medicinal chemistry letters.

SYNTHESIS OF NOVEL 3′-DEOXY-3′-C-HYDROXYMETHYL NUCLEOSIDES WITH CONFORMATIONALLY RIGID SUGAR MOIETY AS POTENTIAL ANTIVIRAL AGENTS

M. Chun, L. Jeong, J. Kim, 2001, Nucleosides, nucleotides & nucleic acids.

Synthesis and antiviral activity of fluoro sugar nucleosides 2: Synthesis and biological evaluations of 2′, 3′-dideoxy-2′-fluoro-3′-C-hydroxymethyl-β-D-arabinofuranosyl nucleosides

Jeewoo Lee, M. Chun, Chong-kyo Lee, 1996 .

Synthesis and biological activities of truncated acridone: Structure-activity relationship studies of cytotoxic 5-hydroxy-4-quinolone

Jeewoo Lee, M. Chun, Chong-kyo Lee, 1997 .

N6-substituted D-4'-thioadenosine-5'-methyluronamides: potent and selective agonists at the human A3 adenosine receptor.

K. Jacobson, Zhang-Guo Gao, H. Moon, 2003, Journal of medicinal chemistry.

Ring contraction and rearrangement of 4-thiofuranose derivatives observed during DAST fluorination in the synthesis of l-2′-“up”-fluoro-4′-thiothymidine

H. Moon, Y. Lim, M. Chun, 1998 .

A Short and Efficient Synthesis of l-Thioarabinose Derivative: A Versatile Synthon for the Synthesis of l-2‘-Deoxy- 2‘,2‘-disubstituted-4‘-thionucleosides

H. Moon, M. Chun, L. Jeong, 1998 .

SYNTHESIS OF NOVEL D- AND L-3′-DEOXY-3′-C-HYDROXYMETHYL NUCLEOSIDE WITH EXOCYCLIC METHYLENE AS POTENTIAL RIBONUCLEOTIDE REDUCTASE INHIBITOR

M. Chun, L. Jeong, J. Kim, 2001, Nucleosides, nucleotides & nucleic acids.

Syntheses and structure--activity relationships of novel apio and thioapio dideoxydidehydronucleosides as anti-HCMV agents.

H. Moon, M. Chun, W. J. Choi, 2001, Journal of Medicinal Chemistry.

Synthesis of Enantiopure Pseudo-l-Vinylcyclopropyl Nucleosides Bearing Quaternary Carbon as Potential Anti-Herpesvirus Agent

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Asymmetric Synthesis of Novel Apio Carbocyclic Nucleoside Analogues as Potential Antiviral and Antitumor Agent

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis and biological evaluation of novel thioapio dideoxynucleosides.

H. Moon, M. Chun, W. J. Choi, 2002, Bioorganic & medicinal chemistry.

Syntheses and Structure—Activity Relationships of Novel Apio and Thioapio Dideoxydidehydronucleosides as Anti-HCMV Agents.

H. Moon, M. Chun, W. J. Choi, 2001 .

Synthesis of novel L-N-MCd4T as a potent anti-HIV agent.

H. Moon, M. Chun, L. Jeong, 2006, Organic & biomolecular chemistry.

Stereoselective Synthesis Of Homo-Apioneplanocin A As Potential Inhibitor Of S-Adenosylhomocysteine Hydrolase

Jin-hee Kim, H. Moon, M. Chun, 2007, Nucleosides, nucleotides & nucleic acids.

Asymmetric Synthesis of Apio Fluoroneplanocin a Analogs as Potential AdoHcy Hydrolase Inhibitor

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis and Antitumor Activity of Fluorocyclopentenyl-Pyrimidines

H. Moon, M. Chun, W. J. Choi, 2007, Nucleosides, nucleotides & nucleic acids.

STEREOSELECTIVE SYNTHESIS OF 3-HYDROXYMETHYL-D-CYCLOPENTENONE, THE VERSATILE INTERMEDIATE FOR THE SYNTHESIS OF CARBOCYCLIC NUCLEOSIDES

H. Moon, M. Chun, W. J. Choi, 2005, Nucleosides, nucleotides & nucleic acids.

Synthesis of Halogenated 9-(Dihydroxycyclopent-4′-enyl) Adenines and Their Inhibitory Activities Against S-Adenosylhomocysteine Hydrolase

H. Moon, M. Chun, W. J. Choi, 2003, Nucleosides, nucleotides & nucleic acids.

Enantioselective synthesis of cyclopropyl carbocyclic L-nucleosides

M. Chun, C. K. Chu, Yufen Zhao, 1995 .

Design, Enantiopure Synthesis, and Biological Evaluation of Novel ISO-D-2′,3′-Dideoxy-3′-Fluorothianucleoside Derivatives as a bioisostere of Lamivudine

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives

H. Moon, M. Chun, L. Jeong, 2006, Bioorganic & Medicinal Chemistry.

Synthesis and biological evaluation of thymine nucleosides fused with 3',4'-tetrahydrofuran ring.

M. Chun, L. Jeong, J. Kim, 2003, Bioorganic & medicinal chemistry letters.

SYNTHESIS OF 3′-DEOXY-3′-C-HYDROXYMETHYL ANALOGUES OF TIAZOFURIN AND RIBAVIRIN

M. Chun, L. Jeong, Myong-Jung Kim, 2005, Nucleosides, nucleotides & nucleic acids.

Synthesis and antiviral activity of fluoro sugar nucleosides 1: Studies on 4′-azido-2′-deoxy-2′-fluoro-arabinofuranosyl nucleosides

M. Chun, J. Kim, Y. Byun, 1995 .

Asymmetric Synthesis of Novel Pseudo-d-Vinylcyclopropyl Nucleosides Bearing Quaternary Carbon as Potential Anti-Herpesvirus Agent

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Dioxolane cytosine nucleosides as anti-hepatitis B agents

M. Chun, C. K. Chu, S. Pai, 1995 .

Synthesis of a Novel Bicyclic Nucleoside with a 3,7-Anhydrooctofuranosyl Skeleton

M. Chun, Myong-Jung Kim, 2007 .

Synthesis and Biological Evaluation of Thymine Nucleosides Fused with 3′,4′-Tetrahydrofuran Ring.

H. Moon, M. Chun, L. Jeong, 2004 .

Synthesis and Anti-HIV Activity of Carbocyclic Ring-Enlarged 4′,1′a-Methano Oxetanocin Analogues

M. Chun, L. Jeong, V. Marquez, 1997 .

Synthesis of Cyclopropyl-Fused Carbocyclic Nucleosides via the Regioselective Opening of Cyclic Sulfites.

Victor E. Marquez, H. Moon, M. Chun, 1999, The Journal of organic chemistry.

Synthesis of novel apio carbocyclic nucleoside analogues as selective a(3) adenosine receptor agonists.

K. Jacobson, H. Moon, M. Chun, 2005, Journal of Organic Chemistry.

Structure-activity relationships of beta-D-(2S,5R)- and alpha-D-(2S,5S)-1,3-oxathiolanyl nucleosides as potential anti-HIV agents.

R. Schinazi, M. Chun, C. K. Chu, 1993, Journal of medicinal chemistry.

Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as highly potent and selective agonists at the human A3 adenosine receptor.

K. Jacobson, Zhang-Guo Gao, H. Moon, 2006, Journal of medicinal chemistry.

Synthesis and Biological Evaluation of Novel Apio Nucleosides with Thiazole‐4‐carboxamide and 1,2,4‐Triazole‐3‐carboxamide

M. Chun, L. Jeong, J. Kim, 2004, Nucleosides, Nucleotides & Nucleic Acids.

STRUCTURE-ACTIVITY RELATIONSHIPS OF APIO NUCLEOSIDES AS POTENTIAL ANTIVIRAL AGENTS

H. Moon, M. Chun, W. J. Choi, 2001, Nucleosides, Nucleotides & Nucleic Acids.

STEREOSELECTIVE SYNTHESIS OF NOVEL THIOISO DIDEOXY NUCLEOSIDES WITH EXOCYCLIC METHYLENE AS POTENTIAL ANTIVIRAL AGENTS

M. Chun, L. Jeong, P. Gunaga, 2005, Nucleosides, Nucleotides & Nucleic Acids.

Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides

M. Chun, L. Jeong, H. Kim, 1998, Archives of pharmacal research.

Synthesis and antiviral activity of D- and L-isodideoxy nucleosides with exocyclic-methylene.

H. Moon, M. Chun, L. Jeong, 1999, Nucleosides and Nucleotides.

A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents

H. Moon, M. Chun, L. Jeong, 2000 .

NUCLEOSIDES. 123. SYNTHESIS OF ANTIVIRAL NUCLEOSIDES: 5-SUBSTITUTED 1-(2-DEOXY-2-HALOGENO-β-D-ARABINOFURANOSYL)CYTOSINES AND -URACILS. SOME STRUCTURE-ACTIVITY RELATIONSHIPS

A. Matsuda, M. Chun, C. K. Chu, 1983 .

Nucleosides. 124. 3-Amino-3-deoxyhexopyranosyl Nucleosides. 7. 1-(3-Deoxy-3-Nitro-β-D-glucopyranosyl) Uracil and Its Galactopyranosyl Isomer1

A. Matsuda, M. Chun, Kyoichi A. Watanabe, 1982 .

Synthesis and Biological Evaluation of Pyrimidine Nucleosides Fused with 3′,4′-Tetrahydrofuran Ring

H. Moon, M. Chun, L. Jeong, 2003, Nucleosides, nucleotides & nucleic acids.

Synthesis of a Novel Bicyclic Nucleoside with a 3,7‐Anhydrooctofuranosyl Skeleton.

M. Chun, Myong-Jung Kim, 2007 .

Synthesis and anti-HIV Activity of Carbocyclic Ring-Enlarged 4′,1′a-Methano Oxetanocin Analogues.

M. Chun, L. Jeong, V. Marquez, 1998 .

STRUCTURE-ACTIVITY RELATIONSHIP OF 5′-SUBSTITUTED FLUORO-NEPLANOCIN A ANALOGUES AS POTENT INHIBITORS OF S-ADENOSYLHOMOCYSTEINE HYDROLASE

H. Moon, M. Chun, L. Jeong, 2005, Nucleosides, nucleotides & nucleic acids.

Design, synthesis and binding affinity of 3'-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands.

K. Jacobson, Zhang-Guo Gao, H. Moon, 2003, Bioorganic & medicinal chemistry letters.

Synthesis of L-Sangivamycin and Toyocamycin Analogues and Their Inhibitory Activities of SER/THR Protein Kinases

S. Song, M. Chun, L. Jeong, 1999 .

Induction of apoptosis in human leukemia cells by MCS-C2 via caspase-dependent Bid cleavage and cytochrome c release.

Jung Mogg Kim, Y. Lim, M. Chun, 2005, Cancer letters.

SYNTHESIS OF 3′-UREIDOADENOSINE ANALOGUES AND THEIR BINDING AFFINITY TO THE A3 ADENOSINE RECEPTOR

K. Jacobson, Zhang-Guo Gao, M. Chun, 2005, Nucleosides, nucleotides & nucleic acids.

Synthesis and antiviral activities of 1,3-oxathiolanyl nucleosides with 5-hydroxymethyl substituent.

H. Moon, M. Chun, L. Jeong, 1999, Nucleosides & nucleotides.

Structure-Activity Relationships of β-D-(2S,5R)- and α-D-( 2S,5S)-1,3-Oxathiolanyl Nucleosides as Potential Anti-HIV Agents.

R. Schinazi, M. Chun, C. K. Chu, 1993 .

Synthesis and biological evaluation of novel tert-azido or tert-amino substituted penciclovir analogs.

H. Moon, M. Chun, L. Jeong, 2004, Organic & biomolecular chemistry.

Stereoselective Synthesis of 1′-Functionalized-4′-Thionucleosides

K. Jacobson, Zhang-Guo Gao, H. Moon, 2007, Nucleosides, nucleotides & nucleic acids.

Design, Synthesis, and Anti-Tumor Activity of 4′-Thionucleosides as Potent and Selective Agonists at the Human A3 Adenosine Receptor

K. Jacobson, Zhang-Guo Gao, H. Moon, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis and Biological Evaluation of Novel Apio Nucleosides with Thiazole-4-carboxamide and 1,2,4-Triazole-3-carboxamide.

M. Chun, L. Jeong, J. Kim, 2004 .

A Short and Efficient Synthesis of L-Thioarabinose Derivative: A Versatile Synthon for the Synthesis of L-2′-Deoxy-2′,2′-disubstituted-4′-thionucleosides.

H. Moon, M. Chun, L. Jeong, 1998 .

Synthesis and Antiviral Activity of D- and L-Isodideoxy Nucleosides with Exocyclic Methylene

H. Moon, M. Chun, L. Jeong, 1999 .

A Highly Efficient Synthesis of L‐β‐2′‐Deoxy‐4′‐thio‐1′‐purine Nucleosides as Potential Antiviral Agents.

H. Moon, M. Chun, L. Jeong, 2000 .

NOVEL NUCLEOSIDES WITH VINYL FLUORIDE OR VINYL BROMIDE MOIETY AS OPEN-CHAIN ANALOGS OF NEPLANOCIN A

M. Chun, L. Jeong, Chong-kyo Lee, 2001, Nucleosides, nucleotides & nucleic acids.

N-Alkoxysulfamide, N-hydroxysulfamide, and sulfamate analogues of methionyl and isoleucyl adenylates as inhibitors of methionyl-tRNA and isoleucyl-tRNA synthetases.

S. Y. Kim, Taehee Kang, Jeewoo Lee, 2003, Bioorganic & medicinal chemistry letters.

Synthesis and Antitumor Activity of Fluorocyclopentenyl‐pyrimidines

H. Moon, M. Chun, W. J. Choi, 2008 .

Synthesis of the acridone alkaloids glyfoline and congeners. Structure-activity relationship studies of cytotoxic acridones.

T. Chou, M. Chun, K. Watanabe, 1992, Journal of medicinal chemistry.

Reaction of benzo[b]furan and 1-acylindoles with iodine azide.

M. Chun, T. Okada, Muhammad Said, 1978 .

Synthesis of (Z)-(1-Fluoro-2-hydroxymethyl-cyclopropylmethyl)purines

Ju-Hyun Park, M. Chun, L. Jeong, 2003, Nucleosides, nucleotides & nucleic acids.

DESIGN AND SYNTHESIS OF NOVEL FLUOROCYCLOPROPANOID NUCLEOSIDES

M. Chun, L. Jeong, R. Jeon, 2001, Nucleosides, nucleotides & nucleic acids.

Synthesis of [1′-Fluoro-2′,2′-bis-(hydroxymethyl)-cyclopropylmethyl]purines as Antiviral Agents

Ju-Hyun Park, M. Chun, L. Jeong, 2003, Nucleosides, nucleotides & nucleic acids.

Synthesis of (Z)-(1-Fluoro-2-hydroxymethylcyclopropylmethyl)purines

Ju-Hyun Park, M. Chun, L. Jeong, 2004 .

Synthesis of [1′-Fluoro-2′,2′-bis-(hydroxymethyl)cyclopropylmethyl]purines as Antiviral Agents

Ju-Hyun Park, M. Chun, L. Jeong, 2004 .

Asymmetric Synthesis and Biological Activity of l-Bicyclocarba-d4T

H. Moon, M. Chun, L. Jeong, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis and Some Chemical Transformations of 2-Azidomethylindoles

M. Chun, Y. Tamura, M. Ikeda, 1978 .

SYNTHESIS AND SOME CHEMICAL TRANSFORMATIONS OF 2‐AZIDOMETHYLINDOLES

M. Chun, Y. Tamura, M. Ikeda, 1979 .

Development of potent and selective human A3 adenosine receptor agonists.

K. Jacobson, M. Chun, L. Jeong, 2005, Nucleic acids symposium series.

Design and Synthesis of A3 Adenosine Receptor Ligands, 3′-Fluoro Analogues of Cl-IB-MECA

K. Jacobson, H. Moon, M. Chun, 2003, Nucleosides, nucleotides & nucleic acids.

SYNTHESIS OF HOMO-N-NUCLEOSIDE WITH 1,2,4-TRIAZOLE-3-CARBOXAMIDE

M. Chun, L. Jeong, B. Kim, 2005, Nucleosides, nucleotides & nucleic acids.

A synthetic study on cyclic phosphate derivatives of seconucleosides as potential antiviral agents (II): Synthesis of 3′, 5′-cyclic phosphates of 6-aza-2′-azido-secouridine

M. Chun, Chong-kyo Lee, J. Kim, 1992 .