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2. Peptides (journal) - Wikipedia

   en.wikipedia.org/wiki/Peptides_(journal)

   Peptides is a monthly peer-reviewed scientific journal covering the biochemistry, neurochemistry, pharmacology, and biological functions of peptides. It was established in 1980 and is published by Elsevier. The editor-in-chief is Karl-Heinz Herzig (University of Oulu).

3. Journal of Peptide Science - Wikipedia

   en.wikipedia.org/wiki/Journal_of_Peptide_Science

   The Journal of Peptide Science is abstracted and indexed by Chemical Abstracts Service, MEDLINE/PubMed, Scopus, and the Science Citation Index.According to the Journal Citation Reports, the journal has a 2021impact factor of 2.408, ranking it 66th out of 87 journals in the category "Chemistry Analytical" [1] and 255th out of 297 journals in the category "Biochemistry & Molecular Biology".

4. CutePDF - Wikipedia

   en.wikipedia.org/wiki/CutePDF

   CutePDF is a proprietary Portable Document Format converter and editor for Microsoft Windows developed by Acro Software. [1] [2] CutePDF Writer can create PDF files, [3] and CutePDF Form Filler can edit simple PDF forms so that they can be sent without using more expensive PDF authoring software. [4] CutePDF can convert documents, images, and ...

5. Split-intein circular ligation of peptides and proteins

   en.wikipedia.org/wiki/Split-intein_circular...

   [3] Circular peptides tend to be resistant to protease activity, and may be suitable for use as orally administered drugs. Once a cyclic peptide is identified with a biological activity of interest, it may also be possible to identify the target of the peptide (a gene that encodes a protein with which it interacts) by functional complementation ...

6. Open Journal Systems - Wikipedia

   en.wikipedia.org/wiki/Open_Journal_Systems

   Open Journal Systems, also known as OJS, is an open source and free software for the management of peer-reviewed academic journals, created by the Public Knowledge Project, and released under the GNU General Public License.

7. Amino acid N-carboxyanhydride - Wikipedia

   en.wikipedia.org/wiki/Amino_acid_N-carboxyanhydride

   Glycine N-carboxyanhydride is the parent member of the amino acid N-carboxyanhydrides.. NCAs are typically prepared by phosgenation of amino acids: [4]. They were first synthesized by Hermann Leuchs by heating an N-ethoxycarbonyl or N-methoxycarbonyl amino acid chloride in a vacuum at 50-70 °C: [5] [6]