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Correction: The HDAC inhibitor, MPT0E028, enhances erlotinib induced cell death in EGFR-TKI-resistant NSCLC cells

Cell death & disease, 2024-07, Vol.15 (7), p.490-4, Article 490

2024

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The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells

Cell death & disease, 2013-09, Vol.4 (9), p.e810-e810

2013

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Pharmaceutical design of antimitotic agents based on combretastatins

Current pharmaceutical design, 2005-05, Vol.11 (13), p.1655-1677

2005

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Preclinical anti-arthritic study and pharmacokinetic properties of a potent histone deacetylase inhibitor MPT0G009

Cell death & disease, 2014-04, Vol.5 (4), p.e1166-e1166

2014

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In vitro evaluation of the effect of haemodilution with dextran 40 on coagulation profile as measured by thromboelastometry and multiple electrode aggregometry

Anaesthesia and intensive care, 2017-09, Vol.45 (5), p.562-568

2017

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Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib

Cell death & disease, 2014-04, Vol.5 (4), p.e1162-e1162

2014

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Leak Detection—Transient Flow Simulation Approaches

Journal of energy resources technology, 1995-09, Vol.117 (3), p.243-248

1995

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C-Alkylated spiro[benzofuran-3(2H),4′-1′-methyl-piperidine-7-ols] as potent opioids: A conformation-activity study

Bioorganic & medicinal chemistry letters, 1998-07, Vol.8 (14), p.1813-1818

1998

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7-Aroyl-aminoindoline-1-sulfonamides as a Novel Class of Potent Antitubulin Agents

Journal of medicinal chemistry, 2006-11, Vol.49 (23), p.6656-6659

2006

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Concise Synthesis and Structure−Activity Relationships of Combretastatin A-4 Analogues, 1-Aroylindoles and 3-Aroylindoles, as Novel Classes of Potent Antitubulin Agents

Journal of medicinal chemistry, 2004-08, Vol.47 (17), p.4247-4257

2004

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Azatyrosinamides: novel RAS-related anticancer agents

Anticancer research, 2013-02, Vol.33 (2), p.425-432

2013

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Synthesis and Structure−Activity Relationships of 3-Aminobenzophenones as Antimitotic Agents

Journal of medicinal chemistry, 2004-05, Vol.47 (11), p.2897-2905

2004

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Synthesis and Structure−Activity Relationship of 2-Aminobenzophenone Derivatives as Antimitotic Agents

Journal of medicinal chemistry, 2002-06, Vol.45 (12), p.2556-2562

2002

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AUV hydrodynamics for survivability and controllability

OCEANS'11 MTS/IEEE KONA, 2011, p.1-9

Liou, J. C. P.

2011

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Structure–activity and crystallographic analysis of benzophenone derivatives—the potential anticancer agents

Bioorganic & medicinal chemistry letters, 2003-01, Vol.13 (1), p.101-105

2003

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A concise synthesis of denbinobin

Tetrahedron letters, 2005-11, Vol.46 (47), p.8103-8104

2005

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Total synthesis of (±)-desoxycodeine- d: a novel route to the morphine skeleton

Tetrahedron letters, 2000-02, Vol.41 (6), p.915-918

2000

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Concise Synthesis and Structure-Activity Relationships of Combretastatin A-4 Analogues, 1-Aroylindoles and 3-Aroylindoles, as Novel Classes of Potent Antitubulin Agents

Journal of medicinal chemistry, 2004-08, Vol.47 (17), p.4247-4257

2004

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A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells

Biochemical pharmacology, 2004-07, Vol.68 (2), p.293-303

2004

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Dual inhibition of topoisomerase I and tubulin polymerization by BPR0Y007, a novel cytotoxic agent

Biochemical pharmacology, 2003-06, Vol.65 (12), p.2009-2019

2003

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ChemInform Abstract: Synthesis of Morphine Fragments Spiro(benzofuran-3(2H),4′-piperidine) and Octahydro-1H-benzofuro(3,2-e)isoquinoline by Intramolecular Heck Reaction

ChemInform, 1997-09, Vol.28 (40), p.no-no

1997

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ChemInform Abstract: Novel Radical Synthesis of Morphine Fragments Spiro(benzofuran-3(2H),4′ -piperidine) and Octahydro-1H-benzofuro(3,2-e)isoquinoline

ChemInform, 1996-12, Vol.27 (50), p.no-no

1996

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Synthesis of morphine fragments spiro[benzofuran-3(2H),4′-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline by intramolecular Heck reaction

Tetrahedron letters, 1997-06, Vol.38 (26), p.4571-4574

1997

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Novel radical synthesis of morphine fragments spiro[benzofuran-3(2H),4′-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline

Tetrahedron, 1996-08, Vol.52 (33), p.10935-10944

1996

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On the solvability of water distribution networks with unknown pipe characteristics

Applied mathematical modelling, 1993, Vol.17 (7), p.380-387

1993

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Correction: The HDAC inhibitor, MPT0E028, enhances erlotinib induced cell death in EGFR-TKI-resistant NSCLC cells

The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells

Pharmaceutical design of antimitotic agents based on combretastatins

Preclinical anti-arthritic study and pharmacokinetic properties of a potent histone deacetylase inhibitor MPT0G009

In vitro evaluation of the effect of haemodilution with dextran 40 on coagulation profile as measured by thromboelastometry and multiple electrode aggregometry

Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib

Leak Detection—Transient Flow Simulation Approaches

C-Alkylated spiro[benzofuran-3(2H),4′-1′-methyl-piperidine-7-ols] as potent opioids: A conformation-activity study

7-Aroyl-aminoindoline-1-sulfonamides as a Novel Class of Potent Antitubulin Agents

Concise Synthesis and Structure−Activity Relationships of Combretastatin A-4 Analogues, 1-Aroylindoles and 3-Aroylindoles, as Novel Classes of Potent Antitubulin Agents

Azatyrosinamides: novel RAS-related anticancer agents

Synthesis and Structure−Activity Relationships of 3-Aminobenzophenones as Antimitotic Agents

Synthesis and Structure−Activity Relationship of 2-Aminobenzophenone Derivatives as Antimitotic Agents

AUV hydrodynamics for survivability and controllability

Structure–activity and crystallographic analysis of benzophenone derivatives—the potential anticancer agents

A concise synthesis of denbinobin

Total synthesis of (±)-desoxycodeine- d: a novel route to the morphine skeleton

Concise Synthesis and Structure-Activity Relationships of Combretastatin A-4 Analogues, 1-Aroylindoles and 3-Aroylindoles, as Novel Classes of Potent Antitubulin Agents

A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells

Dual inhibition of topoisomerase I and tubulin polymerization by BPR0Y007, a novel cytotoxic agent

ChemInform Abstract: Synthesis of Morphine Fragments Spiro(benzofuran-3(2H),4′-piperidine) and Octahydro-1H-benzofuro(3,2-e)isoquinoline by Intramolecular Heck Reaction

ChemInform Abstract: Novel Radical Synthesis of Morphine Fragments Spiro(benzofuran-3(2H),4′ -piperidine) and Octahydro-1H-benzofuro(3,2-e)isoquinoline

Synthesis of morphine fragments spiro[benzofuran-3(2H),4′-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline by intramolecular Heck reaction

Novel radical synthesis of morphine fragments spiro[benzofuran-3(2H),4′-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline

On the solvability of water distribution networks with unknown pipe characteristics

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