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1.
Chempluschem ; 89(8): e202400152, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38693599

ABSTRACT

Protein engineering techniques have vastly expanded their domain of impact, notably following the success of antibodies. Likewise, smaller peptide therapeutics have carved an increasingly significant niche for themselves in the pharmaceutical landscape. The concept of grafting such peptides onto larger protein scaffolds, thus harvesting the advantages of both, has given rise to a variety of protein engineering strategies that are reviewed herein. We also describe our own "Lasso-Grafting" approach, which combines traditional grafting concepts with mRNA display to streamline the production of multiple grafted drug candidates for virtually any target.


Subject(s)
Epitopes , Peptides , Protein Engineering , Peptides/chemistry , Epitopes/chemistry , Protein Engineering/methods , Humans , Proteins/chemistry
2.
Chemistry ; 28(9): e202200295, 2022 Feb 16.
Article in English | MEDLINE | ID: mdl-35142410

ABSTRACT

Invited for the cover of this issue is the group of Abraham Mendoza at Stockholm University. The image depicts a Grignard reagent "turbo-charged" with a magnesium anilide additive. Read the full text of the article at 10.1002/chem.202104053.

3.
Chemistry ; 28(9): e202104053, 2022 Feb 16.
Article in English | MEDLINE | ID: mdl-35084063

ABSTRACT

The synthesis of ketones through addition of organometallic reagents to aliphatic carboxylic acids is a straightforward strategy that is limited to organolithium reagents. More desirable Grignard reagents can be activated and controlled with a bulky aniline-derived turbo-Hauser base. This operationally simple procedure allows the straightforward preparation of a variety of aliphatic and perfluoroalkyl ketones alike from functionalized alkyl, aryl and heteroaryl Grignard reagents.


Subject(s)
Carboxylic Acids , Organometallic Compounds , Anilides , Indicators and Reagents , Molecular Structure
4.
RSC Adv ; 11(39): 23960-23967, 2021 Jul 06.
Article in English | MEDLINE | ID: mdl-35479010

ABSTRACT

We present an extensive photophysical study of a series of fluorescent indolylbenzothiadiazole derivatives and their ability to specifically image lipid droplets in astrocytes and glioblastoma cells. All compounds in the series displayed positive solvatochromism together with large Stokes shifts, and π-extended derivatives exhibited elevated brightness. It was shown that the fluorescence properties were highly tunable by varying the electronic character or size of the N-substituent on the indole motif. Three compounds proved capable as probes for detecting small quantities of lipid deposits in healthy and cancerous brain cells. In addition, all twelve compounds in the series were predicted to cross the blood-brain barrier, which raises the prospect for future in vivo studies for exploring the role of lipid droplets in the central nervous system.

5.
Org Lett ; 21(19): 7908-7913, 2019 10 04.
Article in English | MEDLINE | ID: mdl-31513423

ABSTRACT

The direct preparation of ketones from carboxylate anions is greatly limited by the required use of organolithium reagents or activated acyl sources that need to be independently prepared. Herein, a specific magnesium amide additive is used to activate and control the addition of more tolerant Grignard reagents to carboxylate anions. This strategy enables the modular synthesis of ketones from CO2 and the preparation of isotopically labeled pharmaceutical building blocks in a single operation.

6.
Angew Chem Int Ed Engl ; 56(50): 16042-16046, 2017 12 11.
Article in English | MEDLINE | ID: mdl-29053208

ABSTRACT

A new Pummerer-type C-C coupling protocol is introduced based on turbo-organomagnesium amides, which unlike traditional Pummerer reactions, does not require strong electrophilic activators, engages a broad range of C(sp3 )-, C(sp2 )-, and C(sp)-nucleophiles, and seamlessly integrates with C-H and C-X magnesiation. Given the central character of sulfur compounds in organic chemistry, this protocol allows access to unrelated carbonyls, olefins, organometallics, halides, and boronic esters through a single strategy.

8.
J Med Chem ; 59(23): 10661-10675, 2016 12 08.
Article in English | MEDLINE | ID: mdl-27933950

ABSTRACT

Despite the availability of numerous antiepileptic drugs, 20-30% of epileptic patients are pharmacoresistant with seizures not appropriately controlled. Consequently, new strategies to address this unmet medical need are required. T-type calcium channels play a key role in neuronal excitability and burst firing, and selective triple T-type calcium channel blockers could offer a new way to treat various CNS disorders, in particular epilepsy. Herein we describe the identification of new 1,4-benzodiazepines as brain penetrant and selective triple T-type calcium channel blockers. From racemic hit 4, optimization work led to the preparation of pyridodiazepine 31c with improved physicochemical properties, solubility, and metabolic stability. The racemic mixture was separated by chiral preparative HPLC, and the resulting lead compound (3R,5S)-31c showed promising efficacy in the WAG/Rij-rat model of generalized nonconvulsive absence-like epilepsy.


Subject(s)
Brain/drug effects , Calcium Channel Blockers/pharmacology , Calcium Channels, T-Type/metabolism , Animals , Brain/metabolism , Calcium Channel Blockers/chemistry , Calcium Channel Blockers/metabolism , Dose-Response Relationship, Drug , HEK293 Cells , Humans , Male , Microsomes, Liver/chemistry , Microsomes, Liver/metabolism , Molecular Structure , Rats , Rats, Inbred Strains , Seizures/drug therapy , Structure-Activity Relationship
9.
Angew Chem Int Ed Engl ; 54(47): 14094-8, 2015 Nov 16.
Article in English | MEDLINE | ID: mdl-26337253

ABSTRACT

The development of more active C-H oxidation catalysts has inspired a rapid, scalable, and stereoselective assembly of multifunctional piperazines through a [3+3] coupling of azomethine ylides. A combination of visible-light irradiation and aluminum organometallics is essential to promote this transformation, which introduces visible-light photochemistry of main-group organometallics and sets the basis for new and promising catalysts.

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