Analogues of [3H] chloramphenicol for photoaffinity labeling

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Analogues of [3H] chloramphenicol for photoaffinity labeling. / Hansen, J B; Nielsen, Peter E.; Leick, V; Buchardt, O.

In: Hoppe-Seyler's Zeitschrift fur Physiologische Chemie, Vol. 360, No. 6, 06.1979, p. 721-4.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Hansen, JB, Nielsen, PE, Leick, V & Buchardt, O 1979, 'Analogues of [3H] chloramphenicol for photoaffinity labeling', Hoppe-Seyler's Zeitschrift fur Physiologische Chemie, vol. 360, no. 6, pp. 721-4. https://doi.org/10.1515/bchm2.1979.360.1.721

APA

Hansen, J. B., Nielsen, P. E., Leick, V., & Buchardt, O. (1979). Analogues of [3H] chloramphenicol for photoaffinity labeling. Hoppe-Seyler's Zeitschrift fur Physiologische Chemie, 360(6), 721-4. https://doi.org/10.1515/bchm2.1979.360.1.721

Vancouver

Hansen JB, Nielsen PE, Leick V, Buchardt O. Analogues of [3H] chloramphenicol for photoaffinity labeling. Hoppe-Seyler's Zeitschrift fur Physiologische Chemie. 1979 Jun;360(6):721-4. https://doi.org/10.1515/bchm2.1979.360.1.721

Author

Hansen, J B ; Nielsen, Peter E. ; Leick, V ; Buchardt, O. / Analogues of [3H] chloramphenicol for photoaffinity labeling. In: Hoppe-Seyler's Zeitschrift fur Physiologische Chemie. 1979 ; Vol. 360, No. 6. pp. 721-4.

Bibtex

@article{b97ea0f5e4c442adb71955a93de9c427,
title = "Analogues of [3H] chloramphenicol for photoaffinity labeling",
abstract = "The synthesis of [3H]chloramphenicol and its erythro-diastereoisomer with specific activities of 1.25 Ci/mmol, and the further transformation of the [3H]chloramphenicol to a series of azido and diazo-substituted derivatives are described. The antibiotic activity of the compounds was considered insufficient for their use as photoaffinity labels.",
keywords = "Affinity Labels, Chemical Phenomena, Chemistry, Chloramphenicol/analogs & derivatives, Escherichia coli/drug effects, Isotope Labeling/methods, Ribosomes/drug effects, Tritium",
author = "Hansen, {J B} and Nielsen, {Peter E.} and V Leick and O Buchardt",
year = "1979",
month = jun,
doi = "10.1515/bchm2.1979.360.1.721",
language = "English",
volume = "360",
pages = "721--4",
journal = "Biological Chemistry",
issn = "1431-6730",
publisher = "De Gruyter",
number = "6",

}

RIS

TY - JOUR

T1 - Analogues of [3H] chloramphenicol for photoaffinity labeling

AU - Hansen, J B

AU - Nielsen, Peter E.

AU - Leick, V

AU - Buchardt, O

PY - 1979/6

Y1 - 1979/6

N2 - The synthesis of [3H]chloramphenicol and its erythro-diastereoisomer with specific activities of 1.25 Ci/mmol, and the further transformation of the [3H]chloramphenicol to a series of azido and diazo-substituted derivatives are described. The antibiotic activity of the compounds was considered insufficient for their use as photoaffinity labels.

AB - The synthesis of [3H]chloramphenicol and its erythro-diastereoisomer with specific activities of 1.25 Ci/mmol, and the further transformation of the [3H]chloramphenicol to a series of azido and diazo-substituted derivatives are described. The antibiotic activity of the compounds was considered insufficient for their use as photoaffinity labels.

KW - Affinity Labels

KW - Chemical Phenomena

KW - Chemistry

KW - Chloramphenicol/analogs & derivatives

KW - Escherichia coli/drug effects

KW - Isotope Labeling/methods

KW - Ribosomes/drug effects

KW - Tritium

U2 - 10.1515/bchm2.1979.360.1.721

DO - 10.1515/bchm2.1979.360.1.721

M3 - Journal article

C2 - 381142

VL - 360

SP - 721

EP - 724

JO - Biological Chemistry

JF - Biological Chemistry

SN - 1431-6730

IS - 6

ER -

ID: 203631991