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The Generation of Indole-2,3-quinodimethanes from the Deamination of 1,2,3,4-Tetrahydropyrrolo[3,4- b ]indoles

Molecules (Basel, Switzerland), 2020-01, Vol.25 (2), p.261

2020

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New Approaches to Synthetic Organic Chemistry

2023

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N-quinoline-benzenesulfonamide derivatives exert potent anti-lymphoma effect by targeting NF-κB

iScience, 2020-12, Vol.23 (12), p.101884-101884, Article 101884

2020

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Discovery of potent non-urea inhibitors of soluble epoxide hydrolase

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (8), p.2354-2359

2009

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Synthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors

Bioorganic & medicinal chemistry letters, 2013-01, Vol.23 (2), p.417-421

2013

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Chloride channel blockade relaxes airway smooth muscle and potentiates relaxation by β-agonists

American journal of physiology. Lung cellular and molecular physiology, 2014-08, Vol.307 (3), p.L273-L282

2014

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DT‐01‐01: Plasma Membrane Monoamine Transporter Modulates Bace1 Activity

Alzheimer's & dementia, 2016-07, Vol.12 (7S_Part_23), p.P1134-P1134

2016

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PLASMA MEMBRANE MONOAMINE TRANSPORTER MODULATES BACE1 ACTIVITY

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P1134-P1134

2016

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Targeting NF-κB with First in Class N-Quinoline Benzenesulfonamides (NQBS) Reveals Potent Activity in Models of Diffuse Large B-Cell Lymphoma (DLBCL)

Blood, 2015-12, Vol.126 (23), p.4435-4435

2015

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Six-Membered Ring Systems: Diazines and Benzo Derivatives

Progress in Heterocyclic Chemistry, 2020, Vol.31, p.465-504

Rinderspacher, K. Alison

2020

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Chloride channel blockade relaxes airway smooth muscle and potentiates relaxation by [Beta]-agonists

American journal of physiology. Lung cellular and molecular physiology, 2014-08, Vol.307 (3), p.L273

2014

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Yeast-Based High-Throughput Screen Identifies Plasmodium falciparum Equilibrative Nucleoside Transporter 1 Inhibitors That Kill Malaria Parasites

ACS chemical biology, 2015-03, Vol.10 (3), p.775-783

2015

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Inhibition of Lymphoid Tyrosine Phosphatase by Benzofuran Salicylic Acids

Journal of medicinal chemistry, 2011-01, Vol.54 (2), p.562-571

2011

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Convenient preparation of N-8-quinolinyl benzenesultams as novel NF-κB inhibitors

Tetrahedron letters, 2008-03, Vol.49 (14), p.2320-2323

2008

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Synthesis and structureaactivity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors

Bioorganic & medicinal chemistry letters, 2013-01, Vol.23 (2), p.417-421

2013

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Six-Membered Ring Systems: Diazines and Benzo Derivatives

Progress in Heterocyclic Chemistry, 2013, Vol.25, p.357-390

Rinderspacher, Alison

2013

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Discovery of a novel submicromolar inhibitor of the lymphoid specific tyrosine phosphatase

Bioorganic & medicinal chemistry, 2008-05, Vol.18 (9), p.2840-2844

2008

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Structures of Three New (Phenylsulfonyl)Indole Derivatives

Journal of chemical crystallography, 2010, Vol.40 (1), p.40-47

2010

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ChemInform Abstract: Six-Membered Ring Systems: Diazines and Benzo Derivatives

ChemInform, 2014-09, Vol.45 (38), p.no-no

Rinderspacher, Alison

2014

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Discovery of novel small molecule cell type-specific enhancers of NF-κB nuclear translocation

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (4), p.1191-1194

2009

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Distinct functional and conformational states of the human lymphoid tyrosine phosphatase catalytic domain can be targeted by choice of the inhibitor chemotype

Journal of computer-aided molecular design, 2011-09, Vol.25 (9), p.873-883

2011

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Potent inhibitors of Huntingtin protein aggregation in a cell-based assay

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (6), p.1715-1717

2009

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Identification of N-(quinolin-8-yl)benzenesulfonamides as agents capable of down-regulating NFκB activity within two separate high-throughput screens of NFκB activation

Bioorganic & medicinal chemistry letters, 2008-01, Vol.18 (1), p.329-335

2008

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Discovery of novel small molecule cell type-specific enhancers of NF- mu B nuclear translocation

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (4), p.1191-1194

2009

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Identification of N-(quinolin-8-yl)benzenesulfonamides as agents capable of down-regulating NF[kappa]B activity within two separate high-throughput screens of NF[kappa]B activation

Bioorganic & medicinal chemistry, 2008-01, Vol.18 (1), p.329-335

2008

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The Generation of Indole-2,3-quinodimethanes from the Deamination of 1,2,3,4-Tetrahydropyrrolo[3,4- b ]indoles

New Approaches to Synthetic Organic Chemistry

N-quinoline-benzenesulfonamide derivatives exert potent anti-lymphoma effect by targeting NF-κB

Discovery of potent non-urea inhibitors of soluble epoxide hydrolase

Synthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors

Chloride channel blockade relaxes airway smooth muscle and potentiates relaxation by β-agonists

DT‐01‐01: Plasma Membrane Monoamine Transporter Modulates Bace1 Activity

PLASMA MEMBRANE MONOAMINE TRANSPORTER MODULATES BACE1 ACTIVITY

Targeting NF-κB with First in Class N-Quinoline Benzenesulfonamides (NQBS) Reveals Potent Activity in Models of Diffuse Large B-Cell Lymphoma (DLBCL)

Six-Membered Ring Systems: Diazines and Benzo Derivatives

Chloride channel blockade relaxes airway smooth muscle and potentiates relaxation by [Beta]-agonists

Yeast-Based High-Throughput Screen Identifies Plasmodium falciparum Equilibrative Nucleoside Transporter 1 Inhibitors That Kill Malaria Parasites

Inhibition of Lymphoid Tyrosine Phosphatase by Benzofuran Salicylic Acids

Convenient preparation of N-8-quinolinyl benzenesultams as novel NF-κB inhibitors

Synthesis and structureaactivity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors

Six-Membered Ring Systems: Diazines and Benzo Derivatives

Discovery of a novel submicromolar inhibitor of the lymphoid specific tyrosine phosphatase

Structures of Three New (Phenylsulfonyl)Indole Derivatives

ChemInform Abstract: Six-Membered Ring Systems: Diazines and Benzo Derivatives

Discovery of novel small molecule cell type-specific enhancers of NF-κB nuclear translocation

Distinct functional and conformational states of the human lymphoid tyrosine phosphatase catalytic domain can be targeted by choice of the inhibitor chemotype

Potent inhibitors of Huntingtin protein aggregation in a cell-based assay

Identification of N-(quinolin-8-yl)benzenesulfonamides as agents capable of down-regulating NFκB activity within two separate high-throughput screens of NFκB activation

Discovery of novel small molecule cell type-specific enhancers of NF- mu B nuclear translocation

Identification of N-(quinolin-8-yl)benzenesulfonamides as agents capable of down-regulating NF[kappa]B activity within two separate high-throughput screens of NF[kappa]B activation

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