Zobrazeno 1 - 10
of 14
pro vyhledávání: '"N. A. Krit"'
Autor:
L. Kh. Vinograd, S. F. Dugin, E. A. Dukhanina, Yu. N. Tribunskaya, M. P. Filatova, O. V. Dolgun, M. D. Mashkovskii, N. A. Krit, S. D. Yuzhakov
Publikováno v:
Pharmaceutical Chemistry Journal. 27:683-688
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30d2f5792b0d5e4032497796013f753e
https://doi.org/10.1007/bf00780544
https://doi.org/10.1007/bf00780544
Publikováno v:
Pharmaceutical Chemistry Journal. 25:482-485
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db2bc88f70112118cae2d544985f520e
https://doi.org/10.1007/bf00772004
https://doi.org/10.1007/bf00772004
Publikováno v:
Die Pharmazie. 47(7)
Inhibitors of the angiotensin converting enzyme (ACE, EC 3.4.15.1) are important in the treatment of the high blood pressure. The therapeutically used drugs captopril, enalapril and ramipril are enzymatic stable short pseudo-peptides. They are stabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::68694de16a0b8cf94e41ec76450ebed3
https://pubmed.ncbi.nlm.nih.gov/1381510
https://pubmed.ncbi.nlm.nih.gov/1381510
Publikováno v:
Bioorganicheskaia khimiia. 17(5)
Inhibitors of the angiotensin-converting enzyme were synthesized by substituting N-and C-terminal amino acid residues of tripeptide Bz-Phe-Ala-Pro by the residues of 8-methoxy-5-sulphoquinoline and carboxy-1,2,3,4-tetrahydroquinoline, respectively, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0bccbe1ae834b21e7eb14ee7321d0020
https://pubmed.ncbi.nlm.nih.gov/1662954
https://pubmed.ncbi.nlm.nih.gov/1662954
Publikováno v:
Chemistry of Natural Compounds. 11:45-54
A pentapeptide and undecapeptide possessing bradykinin-potentiating action have been synthesized, and they have been subjected to comparative pharmacological investigation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e68698753f94cc9d868ae0edae97637
https://doi.org/10.1007/bf00567029
https://doi.org/10.1007/bf00567029
Publikováno v:
Bulletin of the Academy of Sciences, USSR Division of Chemical Science. 14:1954-1957
Depsipeptides containing α-hydroxy α-amino acid residues as hydroxy-acid component were synthesized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c12eb9ea435533ea05c6c54cad811f7
https://doi.org/10.1007/bf00845888
https://doi.org/10.1007/bf00845888
Publikováno v:
Chemistry of Natural Compounds. 8:499-501
The reaction of Nα-benzyloxycarbonyl-Nδ-formyl-L-ornithine with α-hydroxy esters has been studied and conditions have been found under which aminoacylation takes place in high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d26419da840533b96f0c984cb3d7693
https://doi.org/10.1007/bf00563680
https://doi.org/10.1007/bf00563680
Publikováno v:
Безопасность информационных технологий, Vol 18, Iss 2, Pp 17-20 (2011)
The algorithm of the full search of the arguments for the conditional optimization of the multi-dimensional criterion is suggested. Determination consists of the serial numerical optimization several coefficients with the own numeration of the each s
Externí odkaz:
https://doaj.org/article/d5babf72c5c644ef9f5803fa246acd2d
Publikováno v:
Безопасность информационных технологий, Vol 17, Iss 3, Pp 47-52 (2010)
Volume reduction of storing the data is one of the ways to increase the safety of information streams storage. Thus arising problem of formal representation of the data flow is shown in the form of a problem of identification of a time row with the n
Externí odkaz:
https://doaj.org/article/9293cf42508f4723a180033415a36e89
Publikováno v:
Voprosy meditsinskoi khimii. 30(3)
Properties of the carboxycathepsin inhibitors teprotide, captopryl, enalacryl are considered. Presence of low molecular thermo- and acid stable carboxycathepsin inhibitors of peptide nature in blood serum and lymphocytes is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da3809149e633996a1d2e5d0b6d0dbbd
https://pubmed.ncbi.nlm.nih.gov/6206649
https://pubmed.ncbi.nlm.nih.gov/6206649