Michaela Vallin

About me
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About me

I am a staff scientist chemistry and project manager at the national research
infrastructure for chemical biology at SciLifeLab, the Chemical Biology
Consortium Sweden [1] (CBCS).
During three years (2020–2022), I held additional sustainability
assignments at the KI President’s office of former President Ole Petter
Ottersen, in roles as UN Agenda 2030 Coordinator (2020–2021) and
Sustainability Liaison (2022).
I have research experience from both academic and industrial settings:
https://www.linkedin.com/in/michaelavallin
[1] https://www.scilifelab.se/units/cbcs/

Articles

Article: AUTOPHAGY. 2022;18(7):1486-1502
Identification of a novel compound that simultaneously impairs the ubiquitin-proteasome system and autophagy
Giovannucci TA; Salomons FA; Stoy H; Herzog LK; Xu S; Qian W; Merino LG; Gierisch ME; Haraldsson M; Lystad AH; Uvell H; Simonsen A; Gustavsson A-L; Vallin M; Dantuma NP
Article: BIOORGANIC AND MEDICINAL CHEMISTRY. 2021;30:115898
A FabG inhibitor targeting an allosteric binding site inhibits several orthologs from Gram-negative ESKAPE pathogens
Vella P; Rudraraju RS; Lundback T; Axelsson H; Almqvist H; Vallin M; Schneider G; Schnell R
Article: ACS CHEMICAL BIOLOGY. 2018;13(4):942-950
In Situ Target Engagement Studies in Adherent Cells
Axelsson H; Almqvist H; Otrocka M; Vallin M; Lundqvist S; Hansson P; Karlsson U; Lundback T; Seashore-Ludlow B
Article: JOURNAL OF MEDICINAL CHEMISTRY. 2016;59(14):6848-6859
Inhibitors of the Cysteine Synthase CysM with Antibacterial Potency against Dormant Mycobacterium tuberculosis
Brunner K; Maric S; Reshma RS; Almqvist H; Seashore-Ludlow B; Gustavsson A-L; Poyraz O; Yogeeswari P; Lundback T; Vallin M; Sriram D; Schnell R; Schneider G
Article: TETRAHEDRON. 2012;68(37):7613-7618
Kinetic resolution of diarylmethanols using a mutated variant of lipase CALB
Engstrom K; Vallin M; Hult K; Backvall J-E
Article: ORGANIC & BIOMOLECULAR CHEMISTRY. 2011;9(1):81-82
Mutated variant of Candida antarctica lipase B in (S)-selective dynamic kinetic resolution of secondary alcohols
Engstrom K; Vallin M; Syren P-O; Hult K; Backvall J-E
Article: BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS. 2010;20(6):1976-1980
Synthesis and evaluation of 2-pyridylbenzothiazole, 2-pyridylbenzoxazole and 2-pyridylbenzofuran derivatives as ¹¹C-PET imaging agents for β-amyloid plaques
Swahn B-M; Wensbo D; Sandell J; Sohn D; Slivo C; Pyring D; Malmstrom J; Arzel E; Vallin M; Bergh M; Jeppsson F; Johnson AE; Jureus A; Neelissen J; Svensson S
Article: CHEMBIOCHEM. 2010;11(3):411-416
Mutant Lipase-Catalyzed Kinetic Resolution of Bulky Phenyl Alkyl sec-Alcohols: A Thermodynamic Analysis of Enantioselectivity
Vallin M; Syren P-O; Hult K
Article: CHEMISTRY - A EUROPEAN JOURNAL. 2007;13(21):6063-6072
Racemization of secondary alcohols catalyzed by cyclopentadienylruthenium complexes:: Evidence for an alkoxide pathway by fast β-hydride elimination -: Readdition
Martin-Matute B; Aberg JB; Edin M; Backvall J-E
Article: TETRAHEDRON ASYMMETRY. 2006;17(4):708-715
Ruthenium- and lipase-catalyzed DYKAT of 1,2-diols:: an enantioselective synthesis of syn-1,2-diacetates
Edin M; Martín-Matute B; Bäckvall JE
Article: CHEMISTRY - A EUROPEAN JOURNAL. 2005;11(20):5832-5842
Highly efficient redox isomerization of allylic alcohols at ambient temperature catalyzed by novel ruthenium-cyclopentadienyl complexes-new insight into the mechanism
Martín-Matute B; Bogár K; Edin M; Kaynak FB; Bäckvall JE
Article: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. 2005;127(24):8817-8825
Combined ruthenium(II) and lipase catalysis for efficient dynamic kinetic resolution of secondary alcohols.: Insight into the racemization mechanism
Martín-Matute B; Edin M; Bogár K; Kaynak FB; Bäckvall JE
Article: ANGEWANDTE CHEMIE INTERNATIONAL EDITION. 2004;43(47):6535-6539
Highly compatible metal and enzyme catalysts for efficient dynamic kinetic resolution of alcohols at ambient temperature
Martín-Matute B; Edin M; Bogár K; Bäckvall JE
Article: TETRAHEDRON LETTERS. 2004;45(41):7697-7701
Tandem enantioselective organo- and biocatalysis:: a direct entry for the synthesis of enantiomerically pure aldols
Edin M; Bäckvall JE; Córdova A
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2004;101(16):5761-5766
One-pot synthesis of enantiopure syn-1,3-diacetates from racemic syn/anti mixtures of 1,3-diols by dynamic kinetic asymmetric transformation
Edin M; Steinreiber J; Bäckvall JE
Article: JOURNAL OF ORGANIC CHEMISTRY. 2003;68(6):2216-2222
On the mechanism of the unexpected facile formation of meso-diacetate products in enzymatic acetylation of alkanediols
Edin M; Bäckvall JE
Article: ARKIVOC. 2001;2:1033-1042
On the preparation of 1,2,5-selenadiazolo [3,4-e]indole and its [3,4-f] and [3,4-g] isomers through the Batcho-Leimgruber indole synthesis
Edin M; Grivas S

All other publications

Editorial comment: GLOBAL HEALTH ACTION. 2024;17(1):2330758
Life Science 2.0: reframing the life science sector for 'the benefit on mankind'
Vallin M; Tomson G; Kampmann B; Engebretsen E; Peterson SS; Wanyenze RK; Ottersen OP
Editorial comment: EUROPEAN JOURNAL OF PUBLIC HEALTH. 2021;31(5):929-930
Europe and the world: boosting international academic cooperation in a time of geopolitical tension and polarization
Vallin M; Gaunt A; Tomson G; Ottersen OP
Published conference paper: CHEMISTRY - A EUROPEAN JOURNAL. 2006;12(23):6053-6061
Highly efficient synthesis of enantiopure diacetylated C₂-symmetric diols by ruthenium- and enzyme-catalyzed dynamic kinetic asymmetric transformation (DYKAT)
Martin-Matute B; Edin M; Backvall J-E

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