A. Sandström

Christel A. S. Bergström, P. Artursson, A. Sandström, 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

An imidazole based H-Phe-Phe-NH2 peptidomimetic with anti-allodynic effect in spared nerve injury mice.

F. Gaugaz, F. Nyberg, A. Sandström, 2018, Bioorganic & medicinal chemistry letters.

Importance of N‐ and C‐terminal residues of substance P 1–7 for alleviating allodynia in mice after peripheral administration

G. Lindeberg, F. Gaugaz, F. Nyberg, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Constrained H-Phe-Phe-NH2 analogues with high affinity to the substance P 1-7 binding site and with improved metabolic stability and cell permeability.

Richard Svensson, Christian Sköld, Per Artursson, 2013, Journal of medicinal chemistry.

Discovery of dipeptides with high affinity to the specific binding site for substance P1-7.

G. Lindeberg, F. Nyberg, A. Sandström, 2010, Journal of medicinal chemistry.

Exploration and pharmacokinetic profiling of phenylalanine based carbamates as novel substance p 1-7 analogues.

P. Artursson, A. Sandström, M. Hallberg, 2014, ACS medicinal chemistry letters.

Discovery of achiral inhibitors of the hepatitis C virus NS3 protease based on 2(1H)-pyrazinones.

Aparna Vema, A. Karlén, M. Larhed, 2010, Bioorganic & medicinal chemistry.

P2-P1' macrocyclization of P2 phenylglycine based HCV NS3 protease inhibitors using ring-closing metathesis.

E. Åkerblom, G. Lindeberg, Aparna Vema, 2011, Bioorganic & medicinal chemistry.

Spectroscopic, kinetic and semiempirical molecular orbital studies on 8-amino-, 8-methylamino- & 8-dimethylamino-adenosines

J. Chattopadhyaya, A. Sandström, J. Hovinen, 1991 .

New stereocontrolled synthesis of isomeric C-branched-β-D nucleosides by intramolecular free-radical cyclization-opening reactions based on temporary silicon connection

J. Plavec, J. Chattopadhyaya, A. Sandström, 1992 .

Improved P2 phenylglycine-based hepatitis C virus NS3 protease inhibitors with alkenylic prime-side substituents.

G. Lindeberg, Aparna Vema, A. Karlén, 2010, Bioorganic & medicinal chemistry.

Phenylglycine as a novel P2 scaffold in hepatitis C virus NS3 protease inhibitors.

Yogesh Sabnis, G. Lindeberg, A. Karlén, 2007, Bioorganic & medicinal chemistry.

Synthesis of new 2',3'-dideoxy-2',3'-α-fused-heterocyclic uridines, & some 2', 3'-ene-2'-substituted uridines from easily accessible 2',3'- ene-3'phenylselenonyl uridine

J. Chattopadhyaya, A. Sandström, W. Tong, 1990 .

The tunable transmission of the aromatic character of the aglycone through the anomeric effect in C-nucleosides drives its own sugar conformation: A thermodynamic study

I. Luyten, A. Sandström, J. Chattopadhyaya, 1997 .

Beta-amino acid substitutions and structure-based CoMFA modeling of hepatitis C virus NS3 protease inhibitors.

Anders Karlén, Johanna Nurbo, Shane D Peterson, 2008, Bioorganic & medicinal chemistry.

Solution conformation of hexameric & heptameric lariat-RNAs and their self-cleavage reactions which give products mimicking those from some catalytic RNAs (ribozymes)

G. Viswanadham, J. Chattopadhyaya, A. Sandström, 1994 .

The interaction of the 2′-OH group with the vicinal phosphate in ribonucleoside 3′-ethylphosphate drives the sugar-phosphate backbone into unique (S,ω−) conformational state

J. Plavec, G. Viswanadham, J. Chattopadhyaya, 1995 .

Assessment of competing 2′«5′ versus 3′«5′ stackings in solution structure of branched-RNA by 1H- & 31 P-NMR spectroscopy

L. Koole, J. Chattopadhyaya, A. Sandström, 1992 .

The solution structure of a 3'-phenazinium (Pzn) tethered DNA-RNA duplex with a dangling adenosine: r(5'G-AUUGAA3'):d(5'TCAATC3'-Pzn).

A. Venyaminova, J. Chattopadhyaya, A. Sandström, 1994, Nucleic Acids Research.

New developments in the discovery of agents to treat hepatitis C.

A. Sandström, Robert Rönn, Anja Sandström, 2008, Current topics in medicinal chemistry.

Small constrained SP1–7 analogs bind to a unique site and promote anti-allodynic effects following systemic injection in mice

H. Watanabe, E. Brolin, F. Nyberg, 2015, Neuroscience.

Chemical synthesis of a pentaribonucleoside tetraphosphate constituting the 3'-acceptor stem sequence of E. coli tRNAIle using 2'-O-(3-methoxy-1,5-dicarbomethoxypentan-3-yl)-ribonucleoside building blocks. Application of a new achiral and acid-labile 2'-hydroxyl protecting group in tRNA synthesis.

J. Chattopadhyaya, A. Sandström, M. Kwiatkowski, 1985, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry.

Use of reverse phase ion pair chromatography to fractionate and purify DNA fragments and monomeric components of RNA.

J. Chattopadhyaya, A. Sandström, M. Kwiatkowski, 1984, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry.

The Synthesis of Lariat-RNAs and their Conformational Analysis by NMR Spectroscopy: The Study of their Unique Self-Cleavage Reaction Modelling Some Catalytic RNAs (Ribozymes)

G. Viswanadham, J. Chattopadhyaya, A. Sandström, 2010 .

The NMR structure of 31mer RNA domain of Escherichia coli RNase P RNA using its non-uniformly deuterium labelled counterpart [the 'NMR-window' concept].

J. Kufel, J. Chattopadhyaya, A. Sandström, 1996, Nucleic acids research.

Solution structure of branched U3′p5′A2′p5′G3′p5′C and its comparison with A2′p5′G3′p5′U by 500 MHz NMR spectroscopy

L. Koole, J. Chattopadhyaya, A. Sandström, 1991 .

Temperature-dependent 31P n.m.r. shifts to assess the conformations of branched tri- and tetra-nucleotides which are formed as lariats in the splicing reactions

X.-X. Zhou, J. Chattopadhyaya, A. Sandström, 1988 .

Determination of The Solution Conformation of A Non-Uniformly Deuterium Labelled (Uppsala ‘Nmr-Window’) 21Mer Rna Hairpin by Nmr Spectroscopy And Computational Methods.

J. Chattopadhyaya, A. Sandström, T. Maltseva, 1997 .

The NMR structure of estrone (Es)-tethered tandem DNA duplex: [d(5'pCAGCp3')-Es] + [Es-d(5'pTCCA3')]: d(5'pTGGAGCTG3').

D. Pyshnyi, J. Chattopadhyaya, A. Sandström, 1997, Journal of biomolecular structure & dynamics.

Targeting the NS2B-NS3 protease of tick-borne encephalitis virus with pan-flaviviral protease inhibitors.

J. Lennerstrand, Å. Lundkvist, J. Järhult, 2021, Antiviral research.

Resistance Profiling of Hepatitis C Virus Protease Inhibitors using Full-Length NS3

E. Åkerblom, A. Sandström, U. Danielson, 2007, Antiviral therapy.

Structural studies of the 5'-phenazinium-tethered matched and G-A-mismatched DNA duplexes by NMR spectroscopy.

J. Chattopadhyaya, A. Sandström, V. Zarytova, 1993, Journal of biochemical and biophysical methods.

Impact of N‐methylation of the substance P 1–7 amide on anti‐allodynic effect in mice after peripheral administration

G. Lindeberg, F. Gaugaz, F. Nyberg, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Ultralarge Virtual Screening Identifies SARS-CoV-2 Main Protease Inhibitors with Broad-Spectrum Activity against Coronaviruses

J. Lennerstrand, J. Kihlberg, Å. Lundkvist, 2022, Journal of the American Chemical Society.

The C-terminal amidated analogue of the substance P (SP) fragment SP1–7 attenuates the expression of naloxone-precipitated withdrawal in morphine dependent rats

T. Gordh, F. Nyberg, A. Sandström, 2009, Peptides.

Structure–activity relationships of HCV NS3 protease inhibitors evaluated on the drug-resistant variants A156T and D168V

E. Åkerblom, Aparna Vema, A. Karlén, 2010, Antiviral therapy.

The effect of substance P1–7 amide on nociceptive threshold in diabetic mice

M. Ohsawa, J. Kamei, F. Nyberg, 2011, Peptides.

Mechanistic studies of electrophilic protease inhibitors of full length hepatic C virus (HCV) NS3

A. Poliakov, A. Sandström, U. Helena Danielson, 2007, Journal of enzyme inhibition and medicinal chemistry.

Novel Peptidomimetic Hepatitis C Virus NS3/4A Protease Inhibitors Spanning the P2-P1' Region.

E. Åkerblom, G. Lindeberg, P. Artursson, 2014, ACS medicinal chemistry letters.

Effects on protease inhibition by modifying of helicase residues in hepatitis C virus nonstructural protein 3

E. Åkerblom, A. Sandström, U. Danielson, 2007, The FEBS journal.

Structural studies of anti-HIV 3′-(α-fluorothymidine & 3′-(α-azidothymidine by 500 MHz 1H-NMR spectroscopy & molecular mechanics (MM2) calculations

J. Plavec, L. Koole, J. Chattopadhyaya, 1991 .

Antibacterial sulfonimidamide-based oligopeptides as type I signal peptidase inhibitors: Synthesis and biological evaluation.

A. Karlén, S. Mowbray, D. Hughes, 2021, European journal of medicinal chemistry.