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Development of HDAC Inhibitors Exhibiting Therapeutic Potential in T‑Cell Prolymphocytic Leukemia
Development of HDAC Inhibitors Exhibiting Therapeutic Potential in T‑Cell Prolymphocytic Leukemia
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Development of HDAC Inhibitors Exhibiting Therapeutic Potential in T‑Cell Prolymphocytic Leukemia

Toutah, Krimo ; Nawar, Nabanita ; Timonen, Sanna ; Sorger, Helena ; Raouf, Yasir S ; Bukhari, Shazreh ; von Jan, Jana ; Ianevski, Aleksandr ; Gawel, Justyna M ; Olaoye, Olasunkanmi O ; Geletu, Mulu ; Abdeldayem, Ayah ; Israelian, Johan ; Radu, Tudor B ; Sedighi, Abootaleb ; Bhatti, Muzaffar N ; Hassan, Muhammad Murtaza ; Manaswiyoungkul, Pimyupa ; Shouksmith, Andrew E ; Neubauer, Heidi A ; de Araujo, Elvin D ; Aittokallio, Tero ; Krämer, Oliver H ; Moriggl, Richard ; Mustjoki, Satu ; Herling, Marco ; Gunning, Patrick T

Journal of medicinal chemistry, 2021-06, Vol.64 (12), p.8486-8509 [Periódico revisado por pares]

United States: American Chemical Society

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New Iminodiacetate–Thiosemicarbazone Hybrids and Their Copper(II) Complexes Are Potential Ribonucleotide Reductase R2 Inhibitors with High Antiproliferative Activity
New Iminodiacetate–Thiosemicarbazone Hybrids and Their Copper(II) Complexes Are Potential Ribonucleotide Reductase R2 Inhibitors with High Antiproliferative Activity
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New Iminodiacetate–Thiosemicarbazone Hybrids and Their Copper(II) Complexes Are Potential Ribonucleotide Reductase R2 Inhibitors with High Antiproliferative Activity

Zaltariov, Mirela F ; Hammerstad, Marta ; Arabshahi, Homayon J ; Jovanović, Katarina ; Richter, Klaus W ; Cazacu, Maria ; Shova, Sergiu ; Balan, Mihaela ; Andersen, Niels H ; Radulović, Siniša ; Reynisson, Jóhannes ; Andersson, K. Kristoffer ; Arion, Vladimir B

Inorganic chemistry, 2017-03, Vol.56 (6), p.3532-3549 [Periódico revisado por pares]

United States: American Chemical Society

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3
Condensed Supramolecular Helices: The Twisted Sisters of DNA
Condensed Supramolecular Helices: The Twisted Sisters of DNA
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Condensed Supramolecular Helices: The Twisted Sisters of DNA

Du, Guanqun ; Belić, Domagoj ; Del Giudice, Alessandra ; Alfredsson, Viveka ; Carnerup, Anna M. ; Zhu, Kaizheng ; Nyström, Bo ; Wang, Yilin ; Galantini, Luciano ; Schillén, Karin

Angewandte Chemie (International ed.), 2022-01, Vol.61 (4), p.e202113279-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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Scaffold Modifications in Erythromycin Macrolide Antibiotics. A Chemical Minireview
Scaffold Modifications in Erythromycin Macrolide Antibiotics. A Chemical Minireview
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Scaffold Modifications in Erythromycin Macrolide Antibiotics. A Chemical Minireview

Undheim, Kjell

Molecules (Basel, Switzerland), 2020-08, Vol.25 (17), p.3941 [Periódico revisado por pares]

Switzerland: MDPI AG

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5
Synthetic brominated furanone F202 prevents biofilm formation by potentially human pathogenic Escherichia coli O103:H2 and Salmonella ser. Agona on abiotic surfaces
Synthetic brominated furanone F202 prevents biofilm formation by potentially human pathogenic Escherichia coli O103:H2 and Salmonella ser. Agona on abiotic surfaces
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Synthetic brominated furanone F202 prevents biofilm formation by potentially human pathogenic Escherichia coli O103:H2 and Salmonella ser. Agona on abiotic surfaces

Vestby, L.K ; Johannesen, K.C.S ; Witsø, I.L ; Habimana, O ; Scheie, A.A ; Urdahl, A.M ; Benneche, T ; Langsrud, S ; Nesse, L.L

Journal of applied microbiology, 2014-02, Vol.116 (2), p.258-268 [Periódico revisado por pares]

England: Published for the Society for Applied Bacteriology by Blackwell Science

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6
Regioselective monoalkylation of 17β-estradiol for the synthesis of cytotoxic estrogens
Regioselective monoalkylation of 17β-estradiol for the synthesis of cytotoxic estrogens
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Regioselective monoalkylation of 17β-estradiol for the synthesis of cytotoxic estrogens

Gansbeke, Koen Van ; Solum, Eirik Johansson ; Liekens, Sandra ; Vik, Anders ; Hansen, Trond Vidar

Steroids, 2017-08, Vol.124, p.54-59 [Periódico revisado por pares]

United States: Elsevier Inc

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7
tmQM DatasetQuantum Geometries and Properties of 86k Transition Metal Complexes
tmQM DatasetQuantum Geometries and Properties of 86k Transition Metal Complexes
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tmQM DatasetQuantum Geometries and Properties of 86k Transition Metal Complexes

Balcells, David ; Skjelstad, Bastian Bjerkem

Journal of chemical information and modeling, 2020-12, Vol.60 (12), p.6135-6146 [Periódico revisado por pares]

United States: American Chemical Society

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8
Catching a SPY: Using the SpyCatcher-SpyTag and Related Systems for Labeling and Localizing Bacterial Proteins
Catching a SPY: Using the SpyCatcher-SpyTag and Related Systems for Labeling and Localizing Bacterial Proteins
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Catching a SPY: Using the SpyCatcher-SpyTag and Related Systems for Labeling and Localizing Bacterial Proteins

Hatlem, Daniel ; Trunk, Thomas ; Linke, Dirk ; Leo, Jack C

International journal of molecular sciences, 2019-04, Vol.20 (9), p.2129 [Periódico revisado por pares]

Switzerland: MDPI AG

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9
The cystine‐glutamate exchanger (xCT, Slc7a11) is expressed in significant concentrations in a subpopulation of astrocytes in the mouse brain
The cystine‐glutamate exchanger (xCT, Slc7a11) is expressed in significant concentrations in a subpopulation of astrocytes in the mouse brain
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The cystine‐glutamate exchanger (xCT, Slc7a11) is expressed in significant concentrations in a subpopulation of astrocytes in the mouse brain

Ottestad‐Hansen, Sigrid ; Hu, Qiu Xiang ; Follin‐Arbelet, Virgine Veronique ; Bentea, Eduard ; Sato, Hideyo ; Massie, Ann ; Zhou, Yun ; Danbolt, Niels Christian

Glia, 2018-05, Vol.66 (5), p.951-970 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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10
Bicycloaromaticity and Baird-type bicycloaromaticity of dithienothiophene-bridged [34]octaphyrins
Bicycloaromaticity and Baird-type bicycloaromaticity of dithienothiophene-bridged [34]octaphyrins
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Bicycloaromaticity and Baird-type bicycloaromaticity of dithienothiophene-bridged [34]octaphyrins

Valiev, Rashid R ; Fliegl, Heike ; Sundholm, Dage

Physical chemistry chemical physics : PCCP, 2018, Vol.20 (26), p.17705-17713 [Periódico revisado por pares]

England: Royal Society of Chemistry

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