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The Journal of Organic Chemistry
|
September 10, 2005
Efficient solid-phase-based total synthesis of the bisintercalator TANDEM
John P Malkinson, Michael K Anim, Mire Zloh, et al.
Organic & Biomolecular Chemistry
|
September 21, 2005
Design and synthesis of a DNA-crosslinking azinomycin analogue
Maxwell A Casely-Hayford, Klaus Pors, Colin H James, et al.
Chemical Communications (Cambridge, England)
|
September 3, 2013
A rapid screen for molecules that form duplex to duplex crosslinks in DNA
María J Marín, Benjamin D Rackham, Andrew N Round, et al.
British Journal of Pharmacology
|
August 16, 2021
Taspine is a natural product that suppresses P2X4 receptor activity via phosphoinositide 3-kinase inhibition
Izzuddin Bin Nadzirin, Anna Fortuny-Gomez, Neville Ngum, et al.
Pharmacology Research & Perspectives
|
August 29, 2024
IS4-FAM, a fluorescent tool to study CXCR4 affinity and competitive antagonism in native cancer cells
Isabel Hamshaw, Marco M D Cominetti, Princess Nana-Akyin, et al.
Journal of Medicinal Chemistry
|
October 14, 2005
Development of nonsymmetrical 1,4-disubstituted anthraquinones that are potently active against cisplatin-resistant ovarian cancer cells
Klaus Pors, Jane A Plumb, Robert Brown, et al.
Experimental Parasitology
|
March 21, 2024
Suramin: Effectiveness of analogues reveals structural features that are important for the potent trypanocidal activity of the drug
Dietmar Steverding, Ryan A J Tinson, Monica Piras, et al.
Organic & Biomolecular Chemistry
|
June 21, 2024
Borylation <i>via</i> iridium catalysed C-H activation: a new concise route to duocarmycin derivatives
Marco M D Cominetti, Zoë R Goddard, Bethany R Hood, et al.
Journal of Medicinal Chemistry
|
November 28, 2006
Synthesis of DNA-directed pyrrolidinyl and piperidinyl confined alkylating chloroalkylaminoanthraquinones: potential for development of tumor-selective N-oxides
Klaus Pors, Steven D Shnyder, Paul H Teesdale-Spittle, et al.
Molecular Pharmacology
|
October 31, 2021
Structural Basis of the Negative Allosteric Modulation of 5-BDBD at Human P2X4 Receptors
Stefan Bidula, Izzuddin Bin Nadzirin, Marco Cominetti, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 55) with videos related to
Sort By:
Page
of 6
The Journal of Organic Chemistry
|
September 10, 2005
Efficient solid-phase-based total synthesis of the bisintercalator TANDEM
John P Malkinson, Michael K Anim, Mire Zloh, et al.
Organic & Biomolecular Chemistry
|
September 21, 2005
Design and synthesis of a DNA-crosslinking azinomycin analogue
Maxwell A Casely-Hayford, Klaus Pors, Colin H James, et al.
Chemical Communications (Cambridge, England)
|
September 3, 2013
A rapid screen for molecules that form duplex to duplex crosslinks in DNA
María J Marín, Benjamin D Rackham, Andrew N Round, et al.
British Journal of Pharmacology
|
August 16, 2021
Taspine is a natural product that suppresses P2X4 receptor activity via phosphoinositide 3-kinase inhibition
Izzuddin Bin Nadzirin, Anna Fortuny-Gomez, Neville Ngum, et al.
Pharmacology Research & Perspectives
|
August 29, 2024
IS4-FAM, a fluorescent tool to study CXCR4 affinity and competitive antagonism in native cancer cells
Isabel Hamshaw, Marco M D Cominetti, Princess Nana-Akyin, et al.
Journal of Medicinal Chemistry
|
October 14, 2005
Development of nonsymmetrical 1,4-disubstituted anthraquinones that are potently active against cisplatin-resistant ovarian cancer cells
Klaus Pors, Jane A Plumb, Robert Brown, et al.
Experimental Parasitology
|
March 21, 2024
Suramin: Effectiveness of analogues reveals structural features that are important for the potent trypanocidal activity of the drug
Dietmar Steverding, Ryan A J Tinson, Monica Piras, et al.
Organic & Biomolecular Chemistry
|
June 21, 2024
Borylation <i>via</i> iridium catalysed C-H activation: a new concise route to duocarmycin derivatives
Marco M D Cominetti, Zoë R Goddard, Bethany R Hood, et al.
Journal of Medicinal Chemistry
|
November 28, 2006
Synthesis of DNA-directed pyrrolidinyl and piperidinyl confined alkylating chloroalkylaminoanthraquinones: potential for development of tumor-selective N-oxides
Klaus Pors, Steven D Shnyder, Paul H Teesdale-Spittle, et al.
Molecular Pharmacology
|
October 31, 2021
Structural Basis of the Negative Allosteric Modulation of 5-BDBD at Human P2X4 Receptors
Stefan Bidula, Izzuddin Bin Nadzirin, Marco Cominetti, et al.
Page
of 6