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Aldose reductase inhibitors and nanodelivery of diabetic therapeutics

Mini reviews in medicinal chemistry, 2012-04, Vol.12 (4), p.326-336

2012

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Novel tricyclic pyrone compounds prevent intracellular APP C99-induced cell death

Journal of molecular neuroscience, 2002-08, Vol.19 (1-2), p.57-61

2002

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A synthetic triptycene bisquinone, which blocks nucleoside transport and induces DNA fragmentation, retains its cytotoxic efficacy in daunorubicin-resistant HL-60 cell lines

International journal of oncology, 2001-12, Vol.19 (6), p.1169

2001

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6,7,8,9-Tetrahydro-3-methyl-1H-pyrano[4,3-b]quinolin-1-one

Acta crystallographica. Section C, Crystal structure communications, 1999-10, Vol.55 (10), p.1698-1701

1999

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Anticancer activities of 2,5,8,9-substituted 6-oxo-1,2,3,4,5,6-hexahydrophenanthridines on multi-drug-resistant phenotype cells

Anticancer research, 1997-07, Vol.17 (4A), p.2435

1997

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Second-generation Substituted Quinolines as Anticancer Drugs for Breast Cancer

Anticancer research, 2010-10, Vol.30 (10), p.3927-3932

2010

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Epidemiological characterization and risk factors of allergic rhinitis in the general population in Guangzhou City in china

PloS one, 2014-12, Vol.9 (12), p.e114950-e114950

2014

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Antitumor activity of novel tricyclic pyrone analogs in murine leukemia cells in vitro

Anticancer research, 1997-07, Vol.17 (4A), p.2427

1997

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The effect of the PQ1 anti-breast cancer agent on normal tissues

Anti-cancer drugs, 2012-10, Vol.23 (9), p.897-905

2012

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(5aS,7S)-7-Isopropenyl-3-methyl-5a,6,8,9-tetrahydro-1H,7H-pyrano[4,3-b][1]benzopyran-1-one

Acta crystallographica. Section C, Crystal structure communications, 1997-12, Vol.53 (12), p.1995-1997

1997

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Combining the rapid MTT formazan exocytosis assay and the MC65 protection assay led to the discovery of carbazole analogs as small molecule inhibitors of Aβ oligomer-induced cytotoxicity

Brain research, 2007-01, Vol.1130 (1), p.223-234

2007

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1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro

Anti-cancer drugs, 2000-06, Vol.11 (5), p.339-352

2000

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Asymmetric Total Synthesis of (-)-Lupinine and (+)-Epilupinine via α-Sulfinyl Ketimine. Stereocontrolled Reduction of β-Sulfinyl Enamines

Synthesis (Stuttgart), 1991, Vol.1991 (11), p.970-974

1991

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Among substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetraones, the lead antitumor triptycene bisquinone TT24 blocks nucleoside transport, induces apoptotic DNA fragmentation and decreases the viability of L1210 leukemic cells in the nanomolar range of daunorubicin in vitro

Anti-cancer drugs, 2002-07, Vol.13 (6), p.567-581

2002

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cis-3,5a-Dimethyl-1-oxo-5a,6,8,9-tetrahydro-1H,7H-pyrano[4,3-b][1]benzopyran-6-yl Formate

Acta crystallographica. Section C, Crystal structure communications, 1997-11, Vol.53 (11), p.1642-1644

1997

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Triptycenes: a novel synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro

Anti-cancer drugs, 1999-09, Vol.10 (8), p.749-766

1999

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Protection of retinal cells from ischemia by a novel gap junction inhibitor

Biochemical and biophysical research communications, 2008-09, Vol.373 (4), p.504-508

2008

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(4aR,8R,SR)-8-(p-Tolylsulfinyl)-2,3,4,4a,5,6,7,8-octahydro-4a-quinolinol

Acta crystallographica. Section C, Crystal structure communications, 1994-03, Vol.50 (3), p.425-428

1994

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(SR,1R,2S)-1-(tert-Butylsulfinyl)2-(hydroxymethyl)ferrocene

Acta crystallographica. Section C, Crystal structure communications, 1997-04, Vol.53 (4), p.445-447

1997

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(4S,5S)-4-Methyl-5-phenyl-1,3-oxazolidin-2-one

Acta crystallographica. Section C, Crystal structure communications, 1993-06, Vol.49 (6), p.1238-1240

1993

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(SS,1S,2R)-1-(Hydroxymethyl)-2-(p-tolylsulfinyl)ferrocene

Acta crystallographica. Section C, Crystal structure communications, 1996-11, Vol.52 (11), p.2757-2760

1996

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Structure of sp-9-hydroxy-9-pivaloylfluorene, product of base-catalyzed autoxidation of ap-9-pivaloylfluorene

Acta crystallographica. Section C, Crystal structure communications, 1992-10, Vol.48 (10), p.1815-1818

1992

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Ethyl (2R,3R,SR)-3-(ethoxycarbonyloxy)-2-[1-(p-tolylsulfinyl)cyclopropyl]-1-pyrrolidinecarboxylate

Acta crystallographica. Section C, Crystal structure communications, 1992-11, Vol.48 (11), p.2088-2090

1992

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Effect of N-acetylation on the acidic solution stability and thermal and mechanical properties of membranes prepared from different chain flexibility chitosans

Journal of applied polymer science, 1996-08, Vol.61 (5), p.749-754

1996

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Structure of (+)-[S-(E)]-N-(α-methylbenzylidene)-p-toluenesulfinamide

Acta crystallographica. Section C, Crystal structure communications, 1991-03, Vol.47 (3), p.594-596

1991

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Aldose reductase inhibitors and nanodelivery of diabetic therapeutics

Novel tricyclic pyrone compounds prevent intracellular APP C99-induced cell death

A synthetic triptycene bisquinone, which blocks nucleoside transport and induces DNA fragmentation, retains its cytotoxic efficacy in daunorubicin-resistant HL-60 cell lines

6,7,8,9-Tetrahydro-3-methyl-1H-pyrano[4,3-b]quinolin-1-one

Anticancer activities of 2,5,8,9-substituted 6-oxo-1,2,3,4,5,6-hexahydrophenanthridines on multi-drug-resistant phenotype cells

Second-generation Substituted Quinolines as Anticancer Drugs for Breast Cancer

Epidemiological characterization and risk factors of allergic rhinitis in the general population in Guangzhou City in china

Antitumor activity of novel tricyclic pyrone analogs in murine leukemia cells in vitro

The effect of the PQ1 anti-breast cancer agent on normal tissues

(5aS,7S)-7-Isopropenyl-3-methyl-5a,6,8,9-tetrahydro-1H,7H-pyrano[4,3-b][1]benzopyran-1-one

Combining the rapid MTT formazan exocytosis assay and the MC65 protection assay led to the discovery of carbazole analogs as small molecule inhibitors of Aβ oligomer-induced cytotoxicity

1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro

Asymmetric Total Synthesis of (-)-Lupinine and (+)-Epilupinine via α-Sulfinyl Ketimine. Stereocontrolled Reduction of β-Sulfinyl Enamines

Among substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetraones, the lead antitumor triptycene bisquinone TT24 blocks nucleoside transport, induces apoptotic DNA fragmentation and decreases the viability of L1210 leukemic cells in the nanomolar range of daunorubicin in vitro

cis-3,5a-Dimethyl-1-oxo-5a,6,8,9-tetrahydro-1H,7H-pyrano[4,3-b][1]benzopyran-6-yl Formate

Triptycenes: a novel synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro

Protection of retinal cells from ischemia by a novel gap junction inhibitor

(4aR,8R,SR)-8-(p-Tolylsulfinyl)-2,3,4,4a,5,6,7,8-octahydro-4a-quinolinol

(SR,1R,2S)-1-(tert-Butylsulfinyl)2-(hydroxymethyl)ferrocene

(4S,5S)-4-Methyl-5-phenyl-1,3-oxazolidin-2-one

(SS,1S,2R)-1-(Hydroxymethyl)-2-(p-tolylsulfinyl)ferrocene

Structure of sp-9-hydroxy-9-pivaloylfluorene, product of base-catalyzed autoxidation of ap-9-pivaloylfluorene

Ethyl (2R,3R,SR)-3-(ethoxycarbonyloxy)-2-[1-(p-tolylsulfinyl)cyclopropyl]-1-pyrrolidinecarboxylate

Effect of N-acetylation on the acidic solution stability and thermal and mechanical properties of membranes prepared from different chain flexibility chitosans

Structure of (+)-[S-(E)]-N-(α-methylbenzylidene)-p-toluenesulfinamide

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