617718-45-3Relevant articles and documents
Alcohol compound-based in-situ deoxygenation fluorination synthesis method and alcohol compound-based F radiolabeling method
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Paragraph 0043-0045; 0067-0069, (2020/02/14)
The invention discloses an alcohol compound-based in-situ deoxidation fluorination synthesis method and an alcohol compound-based F radiolabeling method. Alkyl alcohols such as 4-phenyl-1-butanol,which are used as raw materials, react with trifluorome
9-AMINOMETHYL SUBSTITUTED TETRACYCLINE COMPOUND
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Paragraph 0163-0164, (2014/06/24)
The present invention relates to 9-aminomethyl substituted tetracycline compounds represented by formula (I), or pharmaceutically acceptable salt, prodrug, solvate or isomer thereof, as well as a method for preparing these compounds and a pharmaceutical composition comprising the same. The present invention relates also to a use of these compounds in the preparation of a medicament for the treatment and/or prophylaxis of tetracycline drug-sensitive disease. wherein, R2a, R2b, R3, R4a, R4b, R5, R6a, R6b, R7, R8, R9a, R9b, R10, R11, R12, R13a and R13b are each independently as defined in the description.
Fluorinated lysine derivatives as dipeptidyl peptidase IV inhibitors
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Page/Page column 12, (2008/06/13)
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