Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Vinod K. Naithani"'
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 357:751-758
Antisera to the C-peptide of human proinsulin were obtained by immunizing guinea pigs with synthetic benzyloxycarbonyl-C-peptide conjugated to human albumin with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide. In three series of 10, the animals were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326accbfb6229f6c70f51e7e5fca003b
https://doi.org/10.1515/bchm2.1976.357.1.751
https://doi.org/10.1515/bchm2.1976.357.1.751
Autor:
Erika E. Büllesbach, Vinod K. Naithani
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 361:723-734
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ea61e3dedc25b3c4b3a40f660516b89
https://doi.org/10.1515/bchm2.1980.361.1.723
https://doi.org/10.1515/bchm2.1980.361.1.723
Autor:
Josef Föhles, Vinod K. Naithani
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 359:1173-1182
The synthesis of the C-terminal decapeptide derivative B21--30 of the B-chain of human insulin (benzyloxycarbonyl-gamma-t-butoxyglutamyl-arginyl-glycyl-phenylalanyl-phenylalanyl-O-t-butyltyrosyl-O-t-butylthreonyl-prolyl-Nepsilon-t-butyl-oxycarbonylly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0871ae77851339a8dda860deff7fdd2e
https://doi.org/10.1515/bchm2.1978.359.2.1173
https://doi.org/10.1515/bchm2.1978.359.2.1173
Autor:
Heinz Berndt, André N. Sasaki, Zahn H, Erika E. Büllesbach, Waleed Danho, Vinod K. Naithani, Josef Föhles
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 361:857-864
The synthesis of two protected large peptides 1--45, and 46--86 covering the entire amino acid sequence of human proinsulin is described. Peptide 1--45, was synthesized from two intermediate fragments 1--23 and 24--45 and purified by countercurrent d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0661583316f89cde25874e29fa1a06c7
https://doi.org/10.1515/bchm2.1980.361.1.857
https://doi.org/10.1515/bchm2.1980.361.1.857
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 356:1305-1312
The synthesis of tyrosyl human C-peptide, a sequence of 32 amino acids, by the fragment condensation of the N-terminal octapeptide and C-terminal tetracosapeptide is described. The t-butyl protecting groups were removed by trifluoroacetic acid to obt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea76ad9fbb47daa973e3f0c23b3eeefb
https://doi.org/10.1515/bchm2.1975.356.2.1305
https://doi.org/10.1515/bchm2.1975.356.2.1305
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 356:997-1010
An improved synthesis of human C-peptide is described. Five fragments: 33-39, 40-46, 47-49, 50-54 and 55-63 were used in the total synthesis. In the fully protected C-peptide the N-terminal alpha-amino function was blocked by a benzyloxycarbonyl grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5243c4dcb27dd1787133ffc7b2f96ad
https://doi.org/10.1515/bchm2.1975.356.s1.997
https://doi.org/10.1515/bchm2.1975.356.s1.997
Autor:
Vinod K. Naithani
Publikováno v:
Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 354:141-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8c7932f1793332500b25bce1fe14432
https://doi.org/10.1515/bchm2.1973.354.1.141
https://doi.org/10.1515/bchm2.1973.354.1.141
Publikováno v:
Angewandte Chemie International Edition in English. 19:394-396
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba39ee3cbfd902696ec73245b8ea9108
https://doi.org/10.1002/anie.198003941
https://doi.org/10.1002/anie.198003941
Autor:
Hans-Gregor Gattner, Vinod K. Naithani
Publikováno v:
Hoppe-Seyler's Zeitschrift fur physiologische Chemie. 363(12)
Acylation of insulin with citraconic anhydride was studied at different pH values. The controlled acylation at pH 8.5 and 7 yielded mainly A1-citraconylinsulin (41%) and A1,B1-dicitraconylinsulin (39%), respectively. Acylation with excess reagent at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b312700275aea3b88b6e4d42b6731f77
https://pubmed.ncbi.nlm.nih.gov/6761261
https://pubmed.ncbi.nlm.nih.gov/6761261
Autor:
Vinod K. Naithani, Hans-Gregor Gattner
Publikováno v:
Hoppe-Seyler's Zeitschrift fur physiologische Chemie. 362(6)
The semisynthesis of Arg-A-(SS)2 is described by the following chemical and enzymatic procedures: 1) A-(SSO theta 3)4 was acylated with arginine N-carboxyanhydride by the known method. Arg-A-(SSO theta 3)4 was purified, reduced and oxidized to Arg-A(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c79c523aab0de34bdb3d1b2dd15693
https://pubmed.ncbi.nlm.nih.gov/7275005
https://pubmed.ncbi.nlm.nih.gov/7275005