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Quantitative Comparison of Enrichment from DNA-Encoded Chemical Library Selections

ACS combinatorial science, 2019-02, Vol.21 (2), p.75-82

2019

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Quinolone Signaling in the Cell-to-Cell Communication System of Pseudomonas aeruginosa

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (20), p.11229-11234

1999

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Synthesis and Evaluation of Stable Bidentate Transition Metal Complexes of 1-(Chloromethyl)-5-hydroxy-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1H-pyrrolo[3,2-f]quinoline (seco-6-azaCBI-TMI) as Hypoxia Selective Cytotoxins

Journal of medicinal chemistry, 2009-11, Vol.52 (21), p.6822-6834

2009

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First Total Synthesis of (±)-Stemonamide and (±)-Isostemonamide

Organic letters, 2001-08, Vol.3 (16), p.2505-2508

2001

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Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists

Bioorganic & medicinal chemistry, 2007-12, Vol.17 (23), p.6525-6528

2007

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Rational design of 7-arylquinolines as non-competitive metabotropic glutamate receptor subtype 5 antagonists

Bioorganic & medicinal chemistry letters, 2007-08, Vol.17 (16), p.4415-4418

2007

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4-Anilino-5-carboxamido-2-pyridone Derivatives as Noncompetitive Inhibitors of Mitogen-Activated Protein Kinase Kinase

Journal of medicinal chemistry, 2007-10, Vol.50 (21), p.5090-5102

2007

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Synthesis of 1-Substituted 3-(Chloromethyl)-6-aminoindoline (6-Amino-seco-CI) DNA Minor Groove Alkylating Agents and Structure−Activity Relationships for Their Cytotoxicity

Journal of medicinal chemistry, 1999-02, Vol.42 (4), p.649-658

1999

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5-Amino-1-(chloromethyl)-1,2-dihydro-3H-benz[e]indoles: Relationships between Structure and Cytotoxicity for Analogues Bearing Different DNA Minor Groove Binding Subunits

Journal of medicinal chemistry, 1999-08, Vol.42 (17), p.3400-3411

1999

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Synthesis and Biological Evaluation of Prostaglandin-F Alkylphosphinic Acid Derivatives as Bone Anabolic Agents for the Treatment of Osteoporosis

Journal of medicinal chemistry, 2001-11, Vol.44 (24), p.4157-4169

2001

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Cytotoxicity and DNA Interaction of the Enantiomers of 6-Amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)carbonyl]indoline (Amino-seco-CI-TMI)

Chemical research in toxicology, 1999-08, Vol.12 (8), p.700-706

1999

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Synthesis and Biological Evaluation of Prostaglandin-F Alkylphosphinic Acid Derivatives as Bone Anabolic Agents for the Treatment of Osteoporosis

Journal of medicinal chemistry, 2001-11, Vol.44 (24), p.4307-4307

2001

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Experiments Directed Towards the Synthesis of Anthracyclinones. XXXI. Reductive Claisen Rearrangements of Bis(allyloxy)anthraquinones

Australian journal of chemistry, 1997, Vol.50 (4), p.379

1997

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11-(2-Chloro-2-propenyl)-5,11-dihydroxy-2-methylanthra[1,2-b]furan-6(11H)-one

Acta crystallographica. Section C, Crystal structure communications, 1997-08, Vol.53 (8), p.1102-1103

1997

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Synthesis and Evaluation of Stable Bidentate Transition Metal Complexes of 1-(Chloromethyl)-5-hydroxy-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1 H -pyrrolo[3,2- f ]quinoline ( seco -6-azaCBI-TMI) as Hypoxia Selective Cytotoxins

Journal of medicinal chemistry, 2009-11, Vol.52 (21), p.6822-6834

2009

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Cytotoxicity and DNA interaction of the enantiomers of 6-amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)carbonyl]indo- line (amino-seco-CI-TMI)

Chemical research in toxicology, 1999-08, Vol.12 (8), p.700

1999

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5-Amino-1-(chloromethyl)-1,2-dihydro-3 H -benz[ e ]indoles: Relationships between Structure and Cytotoxicity for Analogues Bearing Different DNA Minor Groove Binding Subunits

Journal of medicinal chemistry, 1999-08, Vol.42 (17), p.3400-3411

1999

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REDUCTIVE CLAISEN REARRANGEMENTS OF ALLYLOXYANTHRAQUINONES. A REVIEW

Organic preparations and procedures international, 1997-08, Vol.29 (4), p.365-407

1997

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Sodium metabisulfite, a reagent for reductive claisen rearrangements

Synthetic communications, 1996-02, Vol.26 (4), p.715-720

1996

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Quinolone signaling in the cell-to-cell communication system of Pseudomonasaeruginosa

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (20), p.11229

1999

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ChemInform Abstract: Reductive Claisen Rearrangements of Allyloxyanthraquinones

ChemInform, 1997-10, Vol.28 (43), p.no-no

1997

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ChemInform Abstract: Experiments Directed Towards the Synthesis of Anthracyclinones. Part 30. Formation and Use of an Anthraquinone Formyl Ester

ChemInform, 1997-04, Vol.28 (17), p.no-no

1997

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ChemInform Abstract: Sodium Metabisulfite, a Reagent for Reductive Claisen Rearrangements

ChemInform, 1996-06, Vol.27 (24), p.no-no

1996

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ChemInform Abstract: Total Synthesis of (.+-.)-Stemonamide and (.+-.)-Isostemonamide

ChemInform, 2002-06, Vol.33 (24), p.no-no

2002

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ChemInform Abstract: First Total Synthesis of (.+-.)-Stemonamide and (.+-.)-Isostemonamide

ChemInform, 2001-11, Vol.32 (46), p.no-no

2001

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Quantitative Comparison of Enrichment from DNA-Encoded Chemical Library Selections

Quinolone Signaling in the Cell-to-Cell Communication System of Pseudomonas aeruginosa

Synthesis and Evaluation of Stable Bidentate Transition Metal Complexes of 1-(Chloromethyl)-5-hydroxy-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1H-pyrrolo[3,2-f]quinoline (seco-6-azaCBI-TMI) as Hypoxia Selective Cytotoxins

First Total Synthesis of (±)-Stemonamide and (±)-Isostemonamide

Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists

Rational design of 7-arylquinolines as non-competitive metabotropic glutamate receptor subtype 5 antagonists

4-Anilino-5-carboxamido-2-pyridone Derivatives as Noncompetitive Inhibitors of Mitogen-Activated Protein Kinase Kinase

Synthesis of 1-Substituted 3-(Chloromethyl)-6-aminoindoline (6-Amino-seco-CI) DNA Minor Groove Alkylating Agents and Structure−Activity Relationships for Their Cytotoxicity

5-Amino-1-(chloromethyl)-1,2-dihydro-3H-benz[e]indoles: Relationships between Structure and Cytotoxicity for Analogues Bearing Different DNA Minor Groove Binding Subunits

Synthesis and Biological Evaluation of Prostaglandin-F Alkylphosphinic Acid Derivatives as Bone Anabolic Agents for the Treatment of Osteoporosis

Cytotoxicity and DNA Interaction of the Enantiomers of 6-Amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)carbonyl]indoline (Amino-seco-CI-TMI)

Synthesis and Biological Evaluation of Prostaglandin-F Alkylphosphinic Acid Derivatives as Bone Anabolic Agents for the Treatment of Osteoporosis

Experiments Directed Towards the Synthesis of Anthracyclinones. XXXI. Reductive Claisen Rearrangements of Bis(allyloxy)anthraquinones

11-(2-Chloro-2-propenyl)-5,11-dihydroxy-2-methylanthra[1,2-b]furan-6(11H)-one

Synthesis and Evaluation of Stable Bidentate Transition Metal Complexes of 1-(Chloromethyl)-5-hydroxy-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1 H -pyrrolo[3,2- f ]quinoline ( seco -6-azaCBI-TMI) as Hypoxia Selective Cytotoxins

Cytotoxicity and DNA interaction of the enantiomers of 6-amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)carbonyl]indo- line (amino-seco-CI-TMI)

5-Amino-1-(chloromethyl)-1,2-dihydro-3 H -benz[ e ]indoles: Relationships between Structure and Cytotoxicity for Analogues Bearing Different DNA Minor Groove Binding Subunits

REDUCTIVE CLAISEN REARRANGEMENTS OF ALLYLOXYANTHRAQUINONES. A REVIEW

Sodium metabisulfite, a reagent for reductive claisen rearrangements

Quinolone signaling in the cell-to-cell communication system of Pseudomonasaeruginosa

ChemInform Abstract: Reductive Claisen Rearrangements of Allyloxyanthraquinones

ChemInform Abstract: Experiments Directed Towards the Synthesis of Anthracyclinones. Part 30. Formation and Use of an Anthraquinone Formyl Ester

ChemInform Abstract: Sodium Metabisulfite, a Reagent for Reductive Claisen Rearrangements

ChemInform Abstract: Total Synthesis of (.+-.)-Stemonamide and (.+-.)-Isostemonamide

ChemInform Abstract: First Total Synthesis of (.+-.)-Stemonamide and (.+-.)-Isostemonamide

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