Search Results - "Lenz, Dirk H."
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Picomolar Inhibitors as Transition-State Probes of 5′-Methylthioadenosine Nucleosidases
Published in ACS chemical biology (01-11-2007)“…Transition states can be predicted from an enzyme’s affinity to related transition-state analogues. 5′-Methylthioadenosine nucleosidases (MTANs) are involved…”
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2
Energetic Mapping of Transition State Analogue Interactions with Human and Plasmodium falciparum Purine Nucleoside Phosphorylases
Published in The Journal of biological chemistry (26-08-2005)“…Human purine nucleoside phosphorylase (huPNP) is essential for human T-cell division by removing deoxyguanosine and preventing dGTP imbalance. Plasmodium…”
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3
Femtomolar Transition State Analogue Inhibitors of 5′-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase from Escherichia coli
Published in The Journal of biological chemistry (06-05-2005)“…Escherichia coli 5′-methylthioadenosine/S-adenosyl-homocysteine nucleosidase (MTAN) hydrolyzes its substrates to form adenine and 5-methylthioribose (MTR) or…”
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4
Synthesis, Formulation, and Adjuvanticity of Monodesmosidic Saponins with Olenanolic Acid, Hederagenin and Gypsogenin Aglycones, and some C‐28 Ester Derivatives
Published in ChemistryOpen (Weinheim) (01-12-2015)“…In an attempt to discover a new synthetic vaccine adjuvant, the glycosylation of hederagenin, gypsogenin, and oleanolic acid acceptors with di‐ and…”
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5
Structure and Inhibition of a Quorum Sensing Target from Streptococcus pneumoniae
Published in Biochemistry (Easton) (31-10-2006)“…Streptococcus pneumoniae 5‘-methylthioadenosine/S-adenosylhomocysteine hydrolase (MTAN) catalyzes the hydrolytic deadenylation of its substrates to form…”
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6
Syntheses and bio-activities of the L-enantiomers of two potent transition state analogue inhibitors of purine nucleoside phosphorylases
Published in Organic & biomolecular chemistry (01-01-2006)“…(1R)-1-(9-Deazahypoxanthin-9-yl)-1,4-dideoxy-1,4-imino-L-ribitol [(+)-5] and (3S,4S)-1-[(9-deazahypoxanthin-9-yl)methyl]-4-(hydroxymethyl)pyrrolidin-3-ol…”
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7
Second Generation Transition State Analogue Inhibitors of Human 5‘-Methylthioadenosine Phosphorylase
Published in Journal of medicinal chemistry (14-07-2005)“…The polyamine biosynthetic pathway is a therapeutic target for proliferative diseases because cellular proliferation requires elevated levels of polyamines. A…”
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A practical synthesis of (3R,4R)-N-tert-butoxycarbonyl-4-hydroxymethylpyrrolidin-3-ol
Published in Organic & biomolecular chemistry (01-01-2007)“…The title compound (+)-, required for production of transition state analogue inhibitors of enzymes involved in T-cell-dependent disorders, was synthesized in…”
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9
One-pot transformation of glycopyranosylcyanides to N-( t-butoxycarbonyl)methylamines
Published in Tetrahedron letters (02-07-2001)“…Protected glycopyranosylcyanides were transformed into the corresponding N- tert-butoxycarbonyl-glycopyranosyl methylamines in a one-pot transformation in high…”
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10
Femtomolar Transition State Analogue Inhibitors of 5â²-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase from Escherichia coli
Published in The Journal of biological chemistry (06-05-2005)“…Escherichia coli 5â²-methylthioadenosine/S-adenosyl-homocysteine nucleosidase (MTAN) hydrolyzes its substrates to form adenine and 5-methylthioribose (MTR) or…”
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