Search Results - "Lattmann, Rene"
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Development of tridentate iron chelators: from desferrithiocin to ICL670
Published in Current medicinal chemistry (01-06-2003)“…Successful treatment of beta-thalassemia requires two key elements: blood transfusion and iron chelation. Regular blood transfusions considerably expand the…”
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Decomposing the effects of α-tACS on brain oscillations and aperiodic 1/f activity
Published in Brain stimulation (01-05-2024)“…•Effects of tACS are decomposed onto periodic and aperiodic activity.•Removing 1/f brain activity does not change the effect of tACS on α-oscillations.•1/f…”
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Design and Synthesis of Inhibitors of the E3 Ligase SMAD Specific E3 Ubiquitin Protein Ligase 1 as a Treatment for Lung Remodeling in Pulmonary Arterial Hypertension
Published in Journal of medicinal chemistry (22-06-2023)“…Pulmonary arterial hypertension (PAH) is a devastating rare disease, which despite currently available treatments, still represents a high unmet medical need…”
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2-Cyano-pyrimidines: A New Chemotype for Inhibitors of the Cysteine Protease Cathepsin K
Published in Journal of medicinal chemistry (22-02-2007)“…Starting from the purine lead structure 1, a new series of cathepsin K inhibitors based on a pyrimidine scaffold have been explored. Investigations of P3 and…”
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Novel scaffold for cathepsin K inhibitors
Published in Bioorganic & medicinal chemistry (15-11-2007)“…Pyrrolopyrimidine, a novel scaffold, allows to adjust interactions within the S3 subsite of cathepsin K. The core intermediate 10 facilitated the P3…”
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Crystal Structure of Human Estrogen-related Receptor α in Complex with a Synthetic Inverse Agonist Reveals Its Novel Molecular Mechanism
Published in The Journal of biological chemistry (10-08-2007)“…Inverse agonists of the constitutively active human estrogen-related receptorα (ERRα, NR3B1) are of potential interest for several disease indications (e.g…”
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Dipeptide nitrile inhibitors of cathepsin K
Published in Bioorganic & medicinal chemistry letters (01-05-2006)“…A series of dipeptidyl nitriles as inhibitors of cathepsin K have been explored starting from lead structure 1 (Cbz–Leu–NH–CH 2–CN, IC 50 = 39 nM). Attachment…”
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Preparation of 10,11-Epoxy-carbamazepine and 10,11-Dihydro-10-hydroxy-carbamazepine by Microbial Epoxidation and Hydroxylation
Published in Bioscience, biotechnology, and biochemistry (1993)“…Within a microbial screening two bacterial strains were identified that epoxidize carbamazepine (CBZ) to 10,11-epoxy-CBZ. Ten strains could hydroxylate…”
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4-[3,5-Bis(2-hydroxyphenyl)-1,2,4-triazol-1-yl]- benzoic Acid: A Novel Efficient and Selective Iron(III) Complexing Agent
Published in Angewandte Chemie International Edition (03-09-1999)Get full text
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10
Crystal Structure of Human Estrogen-related Receptor α in Complex with a Synthetic Inverse Agonist Reveals Its Novel Molecular Mechanism
Published in The Journal of biological chemistry (10-08-2007)“…Inverse agonists of the constitutively active human estrogen-related receptorα (ERRα, NR3B1) are of potential interest for several disease indications ( e.g…”
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11
ICL670A: preclinical profile
Published in Advances in experimental medicine and biology (2002)Get more information
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4‐[3,5‐Bis(2‐hydroxyphenyl)‐1,2,4‐triazol‐1‐yl]‐ benzoic Acid: A Novel Efficient and Selective Iron(III) Complexing Agent
Published in Angewandte Chemie International Edition (03-09-1999)“…An exceptionally stable 1:2 complex [FeL2]3− is formed from the ligand H3L and FeIII. In contrast, the affinity of this ligand for other biometals is…”
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4-[3,5-Bis(2-hydroxyphenyl)-1,2,4-triazol-1-yl]benzoesäure: ein neuartiger, effizienter und selektiver Eisen(III)-Komplexbildner
Published in Angewandte Chemie (03-09-1999)Get full text
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4‐[3,5‐Bis(2‐hydroxyphenyl)‐1,2,4‐triazol‐1‐yl]benzoesäure: ein neuartiger, effizienter und selektiver Eisen(III)‐Komplexbildner
Published in Angewandte Chemie (03-09-1999)“…Einen außerordentlich stabilen 1:2‐Komplex [FeL2]3− bildet der Ligand H3L (siehe Formel) mit FeIII. Seine Affinität für andere Biometalle ist dagegen…”
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15
D-Ribulokinase from Klebsiella pneumoniae for continuous production of D-(-)-ribulose-5-phosphate
Published in Applied microbiology and biotechnology (01-03-1990)“…The production of D-ribulose-5-phosphate in an enzyme membrane reactor was examined. Phosphoryl transfer from ATP to D-ribulose was catalysed by D-ribulokinase…”
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