1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
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NMR structure of the single QALGGH zinc finger domain from the Arabidopsis thaliana SUPERMAN proteinConformational restriction through C alpha i C alpha i cyclization: Ac12c, the largest cycloaliphatic C alpha,alpha- disubstituted glycine knownScreening and Development of New Inhibitors of FtsZ from M. TuberculosisThe effect of leaving groups on binding and reactivity in enzyme-free copying of DNA and RNAEnergy transport in peptide helicesSpectroscopically labeled peptaibiotic analogs: the 4-nitrophenylalanine infrared absorption probe inserted at different positions into trichogin GA IV.Functional and structural characterization of synthetic HIV-1 Vpr that transduces cells, localizes to the nucleus, and induces G2 cell cycle arrest.Design and characterization of a membrane permeable N-methyl amino acid-containing peptide that inhibits Abeta1-40 fibrillogenesis.Convergent strategies for the attachment of fluorescing reporter groups to peptide nucleic acids in solution and on solid phase.Conformational features of human melanin-concentrating hormone: an NMR and computational analysis.Screening of N-alkyl-cyanoacetamido oximes as substitutes for N-hydroxysuccinimideHomologs of 1,2,5-hexahydro-3-one-1H-1,4-diazepine (DAP) as novel dipeptidomimetics and molecular scaffolds: efficient preparation of synthons.Purification and characterization of active recombinant human napsin A.Synthesis and phorbol ester binding of the cysteine-rich domains of diacylglycerol kinase (DGK) isozymes. DGKgamma and DGKbeta are new targets of tumor-promoting phorbol esters.Preferred conformation of peptides based on cycloaliphatic C(alpha,alpha)-disubstituted glycines: 1-amino-cycloundecane-1-carboxylic acid (Ac11c).Peptide-bond modification for metal coordination: peptides containing two hydroxamate groups.T-cell receptor ligation by peptide/MHC induces activation of a caspase in immature thymocytes: the molecular basis of negative selection.Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures.Challenges for protein chemical synthesis in the 21st century: bridging genomics and proteomics.Large-scale synthesis of peptides.Concise total synthesis of sintokamides A, B, and E by a unified, protecting-group-free strategy.Accelerated chemical synthesis of peptides and small proteinsTotal synthesis of the putative structure of the proposed Banyasin A.Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.Anthranilic acid-containing cyclic tetrapeptides: at the crossroads of conformational rigidity and synthetic accessibilityImproving the Fmoc Solid Phase Synthesis of the Cyclic Hexapeptide Complement C5a Antagonist, PMX205.Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.Identification and Optimization of the First Highly Selective GLUT1 Inhibitor BAY-876.Rapid kit-based (68)Ga-labelling and PET imaging with THP-Tyr(3)-octreotate: a preliminary comparison with DOTA-Tyr(3)-octreotateBivalency as a principle for proteasome inhibitionSynthesis of hemopressin peptides by classical solution phase fragment condensationPiperazic acid-containing natural products: isolation, biological relevance and total synthesis.Peptides and proteins as a continuing exciting source of inspiration for peptidomimetics.Microwave heating in solid-phase peptide synthesis.Phosphino-carboxamides: the inconspicuous gems.Cu-mediated enamide formation in the total synthesis of complex peptide natural products.Total synthesis of oxazolomycins.Ester coupling reactions--an enduring challenge in the chemical synthesis of bioactive natural products.Evaluation of combined use of Oxyma and HATU in aggregating peptide sequences.Induction of Antibodies Directed Against Branched Core O-Mannosyl Glycopeptides-Selectivity Complimentary to the ConA Lectin.
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P2860
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
description
im Mai 1993 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в травні 1993
@uk
name
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@en
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@nl
type
label
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@en
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@nl
prefLabel
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@en
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@nl
P356
P1476
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
@en
P304
P356
10.1021/JA00063A082
P407
P577
1993-05-01T00:00:00Z