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Novel quinoline and naphthalene derivatives as potent antimycobacterial agents

European journal of medicinal chemistry, 2010-05, Vol.45 (5), p.1854-1867

2010

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Inhibiting β-Catenin by β-Carboline-Type MDM2 Inhibitor for Pancreatic Cancer Therapy

Frontiers in pharmacology, 2018-01, Vol.9, p.5-5

2018

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Targeting MDM2 for Neuroblastoma Therapy: In Vitro and In Vivo Anticancer Activity and Mechanism of Action

Cancers, 2020-12, Vol.12 (12), p.3651

2020

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Targeted Brain Tumor Therapy by Inhibiting the MDM2 Oncogene: In Vitro and In Vivo Antitumor Activity and Mechanism of Action

Cells (Basel, Switzerland), 2020-07, Vol.9 (7), p.1592

2020

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Pharmacophore generation and atom-based 3D-QSAR of novel 2-(4-methylsulfonylphenyl)pyrimidines as COX-2 inhibitors

Molecular diversity, 2010-08, Vol.14 (3), p.559-568

2010

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3D-QSAR of histone deacetylase inhibitors: hydroxamate analogues

Organic & biomolecular chemistry, 2006-08, Vol.4 (15), p.2858-2868

2006

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Integration of fingerprint-based similarity searching and kernel-based partial least squares analysis to predict inhibitory activity against CSK, HER2, JAK1, JAK2, and JAK3

Molecular diversity, 2024-04, Vol.28 (2), p.497-507

2024

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QSAR analysis of N-myristoyltransferase inhibitors: antifungal activity of benzofurans

Medicinal chemistry research, 2009-03, Vol.18 (3), p.206-220

2009

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SS-4 is a highly selective small molecule inhibitor of STAT3 tyrosine phosphorylation that potently inhibits GBM tumorigenesis in vitro and in vivo

Cancer letters, 2022-05, Vol.533, p.215614-215614, Article 215614

2022

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QSAR studies of new pyrido[3,4-b]indole derivatives as inhibitors of colon and pancreatic cancer cell proliferation

Medicinal chemistry research, 2018-12, Vol.27 (11-12), p.2466-2481

2018

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Inhibition of the Herpesvirus Fusion Protein Using Targeted Small Molecules

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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3D-QSAR of histone deacetylase inhibitors as anticancer agents by genetic function approximation

Indian journal of biochemistry & biophysics, 2006-12, Vol.43 (6), p.360-371

2006

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Inhibition of gastric tumor growth by a novel Hsp90 inhibitor

Biochemical pharmacology, 2013-05, Vol.85 (9), p.1246-1256

2013

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Abstract 4478: Biopharmaceutic studies of novel nucleoside transporter inhibitor prodrugs that can protect against nucleoside drug-induced mitochondrial toxicity

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.4478-4478

2014

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Synthesis and structure–activity relationship study of substituted caffeate esters as antinociceptive agents modulating the TREK-1 channel

European journal of medicinal chemistry, 2014-03, Vol.75, p.391-402

2014

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A quantitative LC-MS/MS method for determination of SP-141, a novel pyrido[b]indole anticancer agent, and its application to a mouse PK study

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2014-10, Vol.969, p.235-240

2014

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Synthesis and evaluation of bidentate ligands designed to interact with PDZ domains

Bioorganic & medicinal chemistry, 2011-07, Vol.19 (14), p.4346-4354

2011

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Identification of PDZ ligands by docking-based virtual screening for the development of novel analgesic agents

Bioorganic & medicinal chemistry letters, 2013-05, Vol.23 (9), p.2624-2627

2013

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Synthesis and structure-activity relationship study of substituted caffeateesters as antinociceptive agents modulating the TREK-1 channel

European journal of medicinal chemistry, 2014, Vol.75, p.391-402

2014

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NMR evaluation of interactions between substituted-indole and PDZ1 domain of PSD-95

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (11), p.3349-3353

2011

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Synthesis, Biological Evaluation and Modeling Studies of New Pyrido[3,4-b] indole Derivatives as Broad-Spectrum Potent Anticancer Agents

Drug designing (Los Angeles, CA, U.S.A.), 2017-03, Vol.6 (1)

2017

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Novel quinoline and naphthalene derivatives as potent antimycobacterial agents

Inhibiting β-Catenin by β-Carboline-Type MDM2 Inhibitor for Pancreatic Cancer Therapy

Targeting MDM2 for Neuroblastoma Therapy: In Vitro and In Vivo Anticancer Activity and Mechanism of Action

Targeted Brain Tumor Therapy by Inhibiting the MDM2 Oncogene: In Vitro and In Vivo Antitumor Activity and Mechanism of Action

Pharmacophore generation and atom-based 3D-QSAR of novel 2-(4-methylsulfonylphenyl)pyrimidines as COX-2 inhibitors

3D-QSAR of histone deacetylase inhibitors: hydroxamate analogues

Integration of fingerprint-based similarity searching and kernel-based partial least squares analysis to predict inhibitory activity against CSK, HER2, JAK1, JAK2, and JAK3

QSAR analysis of N-myristoyltransferase inhibitors: antifungal activity of benzofurans

SS-4 is a highly selective small molecule inhibitor of STAT3 tyrosine phosphorylation that potently inhibits GBM tumorigenesis in vitro and in vivo

QSAR studies of new pyrido[3,4-b]indole derivatives as inhibitors of colon and pancreatic cancer cell proliferation

Inhibition of the Herpesvirus Fusion Protein Using Targeted Small Molecules

3D-QSAR of histone deacetylase inhibitors as anticancer agents by genetic function approximation

Inhibition of gastric tumor growth by a novel Hsp90 inhibitor

Abstract 4478: Biopharmaceutic studies of novel nucleoside transporter inhibitor prodrugs that can protect against nucleoside drug-induced mitochondrial toxicity

Synthesis and structure–activity relationship study of substituted caffeate esters as antinociceptive agents modulating the TREK-1 channel

A quantitative LC-MS/MS method for determination of SP-141, a novel pyrido[b]indole anticancer agent, and its application to a mouse PK study

Synthesis and evaluation of bidentate ligands designed to interact with PDZ domains

Identification of PDZ ligands by docking-based virtual screening for the development of novel analgesic agents

Synthesis and structure-activity relationship study of substituted caffeateesters as antinociceptive agents modulating the TREK-1 channel

NMR evaluation of interactions between substituted-indole and PDZ1 domain of PSD-95

Synthesis, Biological Evaluation and Modeling Studies of New Pyrido[3,4-b] indole Derivatives as Broad-Spectrum Potent Anticancer Agents

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