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Induction of enantio-selective apoptosis in human leukemia HL-60 cells by (S)-erypoegin K, an isoflavone isolated from Erythrina poeppigiana

Bioorganic & medicinal chemistry, 2020-06, Vol.28 (11), p.115490-115490, Article 115490

2020

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Preparation of conophylline affinity nano-beads and identification of a target protein

Bioorganic & medicinal chemistry, 2009-09, Vol.17 (17), p.6188-6195

2009

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Reversal of anticancer drug resistance by COTC based on intracellular glutathione and glyoxalase I

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (4), p.1111-1114

2005

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(S)-Erypoegin K, an isoflavone isolated from Erythrina poeppigiana, is a novel inhibitor of topoisomerase IIα: Induction of G2 phase arrest in human gastric cancer cells

Bioorganic & medicinal chemistry, 2021-01, Vol.30, p.115904-115904, Article 115904

2021

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Rational design, synthesis and in vitro evaluation of novel exo-methylene butyrolactone salicyloylamide as NF-κB inhibitor

Bioorganic & medicinal chemistry letters, 2017-02, Vol.27 (3), p.562-566

2017

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Reversal of Anticancer Drug Resistance Targetting Intracellular Glutathione and Glyoxalase I

Yūki gōsei kagaku kyōkaishi, 2012-03, Vol.70 (3), p.240-249

2012

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Design, synthesis, and biological evaluation of novel estradiol–bisphosphonate conjugates as bone-specific estrogens

Bioorganic & medicinal chemistry, 2010-02, Vol.18 (3), p.1143-1148

2010

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Unusual intramolecular N→ O acyl group migration occurring during conjugation of (−)-DHMEQ with cysteine

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (18), p.5380-5382

2009

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Advance in Synthesis of Sugar-Modified Nucleosides in Past 10 Years

Journal of Synthetic Organic Chemistry, Japan, 2001/04/01, Vol.59(4), pp.331-345

2001

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Syntheses of Oxetanocin A and Related Unusual Nucleosides with Bis(hydroxymethyl)-branched Sugars

Synthesis (Stuttgart), 2002-01, Vol.2002 (1)

2002

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Synthesis and Structure–Activity Relationship of Dehydroxymethylepoxyquinomicin Analogues as Inhibitors of NF-κB Functions

Bioorganic & medicinal chemistry, 2002-12, Vol.10 (12), p.3933-3939

2002

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Synthesis of enantiomerically pure 9[(1′ R,2′ R,3′ S)-bis(hydroxymethyl)thietan-1′-yl]adenine, 3′-thio analog of oxetanocin A

Tetrahedron letters, 1999-10, Vol.40 (41), p.7385-7388

1999

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Synthesis of 2′,3′-dideoxy-3′- C-(hydroxymethyl)-4′-thiopentofuranosyl nucleosides as potential antiviral agent

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1113-1114

1999

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Synthesis of carbocyclic nucleosides: synthesis of (±)-2,2-bis(hydroxymethyl)cyclopropyl nucleosides

J. Chem. Soc., Perkin Trans. 1, 1992 (19), p.2519-2525

1992

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Synthesis of cleonine, amino(1-hydroxycyclopropyl)acetic acid, a novel amino acid contained in cleomycin

Tetrahedron letters, 1980, Vol.21 (51), p.4925-4926

1980

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Synthesis and structure-activity relationship of ribofuranosyl echiguanine analogs as inhibitors of phosphatidylinositol 4-kinase

Tetrahedron, 1998-04, Vol.54 (17), p.4251-4266

1998

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Synthesis of [(2′ S, 3′ S)-bis(hydroxylmethyl)pyrrolidin-1-yl] purine and pyrimidine nucleosides as potential antiviral agents

Bioorganic & medicinal chemistry letters, 1998-05, Vol.8 (10), p.1187-1188

1998

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Design and synthesis of an antitumor prodrug released by the reaction with sulfhydryl compounds

Bioorganic & medicinal chemistry letters, 1995-03, Vol.5 (6), p.593-596

1995

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Synthesis of echiguanine analogs and their ribofuranosyl glycosides that inhibit phosphatidylinositol 4-kinase

Bioorganic & medicinal chemistry letters, 1997-04, Vol.7 (7), p.861-864

1997

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Synthesis of ribofuranosyl glycosides of echiguanines A and B, inhibitors of phosphatidylinositol 4-kinase

Bioorganic & medicinal chemistry letters, 1996-11, Vol.6 (21), p.2487-2490

1996

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Enantiomerically pure synthesis and antiviral evaluation of [(2′ S, 3′ S)-bis(hydroxymethyl)azetidin-1-yl] purine nucleosides: Analogs of oxetanocin-A

Bioorganic & medicinal chemistry letters, 1995-10, Vol.5 (19), p.2273-2276

1995

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Synthesis and antiviral evaluation of [(2′ S, 3′ S)-bis(hydroxymethyl)azeitidin-1-yl]pyrimidine nucleosides: analogs of oxetanocin-A

Bioorganic & medicinal chemistry letters, 1994-09, Vol.4 (17), p.2083-2086

1994

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Synthesis of C-oxetanosyl-thiazole and its carbocyclic analog nucleosides as potential chemotherapeutic agents

Bioorganic & medicinal chemistry letters, 1996-08, Vol.6 (16), p.1897-1900

1996

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Enantiospecific synthesis of [(2′ S, 3′ S)-bis(hydroxymethyl)azetidin-1-yl] pyrimidine nucleosides as potential antiviral agents

Tetrahedron, 1994, Vol.50 (47), p.13335-13346

1994

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A total synthesis of oxetanocin, a novel nucleoside with an oxetane ring

Tetrahedron letters, 1988, Vol.29 (37), p.4743-4746

1988

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Induction of enantio-selective apoptosis in human leukemia HL-60 cells by (S)-erypoegin K, an isoflavone isolated from Erythrina poeppigiana

Preparation of conophylline affinity nano-beads and identification of a target protein

Reversal of anticancer drug resistance by COTC based on intracellular glutathione and glyoxalase I

(S)-Erypoegin K, an isoflavone isolated from Erythrina poeppigiana, is a novel inhibitor of topoisomerase IIα: Induction of G2 phase arrest in human gastric cancer cells

Rational design, synthesis and in vitro evaluation of novel exo-methylene butyrolactone salicyloylamide as NF-κB inhibitor

Reversal of Anticancer Drug Resistance Targetting Intracellular Glutathione and Glyoxalase I

Design, synthesis, and biological evaluation of novel estradiol–bisphosphonate conjugates as bone-specific estrogens

Unusual intramolecular N→ O acyl group migration occurring during conjugation of (−)-DHMEQ with cysteine

Advance in Synthesis of Sugar-Modified Nucleosides in Past 10 Years

Syntheses of Oxetanocin A and Related Unusual Nucleosides with Bis(hydroxymethyl)-branched Sugars

Synthesis and Structure–Activity Relationship of Dehydroxymethylepoxyquinomicin Analogues as Inhibitors of NF-κB Functions

Synthesis of enantiomerically pure 9[(1′ R,2′ R,3′ S)-bis(hydroxymethyl)thietan-1′-yl]adenine, 3′-thio analog of oxetanocin A

Synthesis of 2′,3′-dideoxy-3′- C-(hydroxymethyl)-4′-thiopentofuranosyl nucleosides as potential antiviral agent

Synthesis of carbocyclic nucleosides: synthesis of (±)-2,2-bis(hydroxymethyl)cyclopropyl nucleosides

Synthesis of cleonine, amino(1-hydroxycyclopropyl)acetic acid, a novel amino acid contained in cleomycin

Synthesis and structure-activity relationship of ribofuranosyl echiguanine analogs as inhibitors of phosphatidylinositol 4-kinase

Synthesis of [(2′ S, 3′ S)-bis(hydroxylmethyl)pyrrolidin-1-yl] purine and pyrimidine nucleosides as potential antiviral agents

Design and synthesis of an antitumor prodrug released by the reaction with sulfhydryl compounds

Synthesis of echiguanine analogs and their ribofuranosyl glycosides that inhibit phosphatidylinositol 4-kinase

Synthesis of ribofuranosyl glycosides of echiguanines A and B, inhibitors of phosphatidylinositol 4-kinase

Enantiomerically pure synthesis and antiviral evaluation of [(2′ S, 3′ S)-bis(hydroxymethyl)azetidin-1-yl] purine nucleosides: Analogs of oxetanocin-A

Synthesis and antiviral evaluation of [(2′ S, 3′ S)-bis(hydroxymethyl)azeitidin-1-yl]pyrimidine nucleosides: analogs of oxetanocin-A

Synthesis of C-oxetanosyl-thiazole and its carbocyclic analog nucleosides as potential chemotherapeutic agents

Enantiospecific synthesis of [(2′ S, 3′ S)-bis(hydroxymethyl)azetidin-1-yl] pyrimidine nucleosides as potential antiviral agents

A total synthesis of oxetanocin, a novel nucleoside with an oxetane ring

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