Zobrazeno 1 - 10
of 50
pro vyhledávání: '"M.Ya. Karpeisky"'
Publikováno v:
FEBS Letters. 162:167-170
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95ffae16a8966e3b9076f25d4affc51
https://doi.org/10.1016/0014-5793(83)81071-0
https://doi.org/10.1016/0014-5793(83)81071-0
Autor:
Sergey N. Mikhailov, M.Ya. Karpeisky, O.N. Kartasheva, Ramamurthy Charubala, A.V. Itkes, Gennady I. Yakovlev, Wolfgang Pfleiderer, G. P. Moiseyev
Publikováno v:
Scopus-Elsevier
The rates of enzymatic hydrolysis of 2′,5′-oligoadenylates and their synthetic analogs have been measured. These compounds were treated with either NIH 3T3 cell lysates, mouse liver homogenates or snake venom phosphodiesterase. All analogs with 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3096c42a3f71f3f993c71c4a1fc867c1
https://doi.org/10.1016/0014-5793(88)80048-6
https://doi.org/10.1016/0014-5793(88)80048-6
Autor:
V.L. Florentiev, N.D. Doktorova, K. F. Turchin, M.Ya. Karpeisky, N. Sh. Padyukova, L. V. Ionova
Publikováno v:
Tetrahedron. 25:3527-3553
Pyridoxine analogues have been synthesized via a Diels—Alder reaction of 5-ethoxyoxazoles with dimethyl maleate followed by reduction. The products on oxidation with manganese dioxide yielded pyridoxal analogues. Pyridoxamine derivatives were obtai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c92f5ff14e362d1c7b4b9b2c15b0dfc
https://doi.org/10.1016/s0040-4020(01)82888-x
https://doi.org/10.1016/s0040-4020(01)82888-x
Autor:
S.M. Dudkin, I.I. Chervin, S.V. Shliapnikov, M.Ya. Karpeisky, Vladimir F. Bystrov, V.G. Sacharovsky, Gennady I. Yakovlev
Publikováno v:
FEBS Letters. 33:323-326
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::824b7af3205afafa080166edd5c35a10
https://doi.org/10.1016/0014-5793(73)80221-2
https://doi.org/10.1016/0014-5793(73)80221-2
Publikováno v:
Tetrahedron. 26:3083-3090
3-Deoxypyridoxal phosphate and 3-O-methylpyridoxal phosphate have been synthesized by transamination of the corresponding pyridoxamine phosphate analogues. The amine phosphates were obtained by reduction of oximes of pyridoxal analogues followed by p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ca8350cf5902193c151018737854f81
https://doi.org/10.1016/s0040-4020(01)92891-1
https://doi.org/10.1016/s0040-4020(01)92891-1
Publikováno v:
FEBS Letters. (3):177-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aef5155dc0f8cb4647f691dafe06e74
Autor:
M.Ya. Karpeisky, L.V. Karabachyan, T.G. Geidarov, S.N. Borisova, S.V. Shlyapnikov, S.M. Dudkin
Publikováno v:
Biochimica et biophysica acta. 386(1)
We have studied the spectral properties of RNAase A containing a phosphopyridoxyl residue at the e-NH2 group of Lys7 or Lys14. The overall conformations of the native and modified enzymes were shown to be rather similar. All three proteins have simil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa58e571bb55ee2155c3b10574e8a420
https://pubmed.ncbi.nlm.nih.gov/236023
https://pubmed.ncbi.nlm.nih.gov/236023
Autor:
Gennady I. Yakovlev, M.Ya. Karpeisky
Publikováno v:
FEBS letters. 75(1)
NOE nuclear Overhauser effect, RNAase A bovine pancreatic ribonuclease, PMR proton magnetic resonance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11c9523f1272f6f7aed3755fd1467646
https://pubmed.ncbi.nlm.nih.gov/558118
https://pubmed.ncbi.nlm.nih.gov/558118
Publikováno v:
Biochemical and biophysical research communications. 30(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70d2557a65fde9b41f87df0dadb9cb9f
https://pubmed.ncbi.nlm.nih.gov/5645431
https://pubmed.ncbi.nlm.nih.gov/5645431
Publikováno v:
Biochimica et biophysica acta. 92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470a384f89d8c2d1ada89fab0c3eff4e
https://pubmed.ncbi.nlm.nih.gov/14249127
https://pubmed.ncbi.nlm.nih.gov/14249127