Rifamycin antibiotics—new compounds and synthetic methods. Part 1: Study of the reaction of 3-formylrifamycin SV with primary alkylamines or ammonia
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference37 articles.
1. Ansamycine, eine neuartige Klasse von mikrobiellen Stoffwechselprodukten
2. Über die Konstitution und die Konfiguration der Rifamycine B, O, S und SV
3. Rifampidn inhibition of RNA synthesis by destabilisation of DNA-RNA polymerase-oligonucleotide-complexes
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1. Approved antibacterial drugs in the last 10 years: from the bench to the clinic;Exploration of Drug Science;2023-06-30
2. Structure–activity relationship studies of new rifamycins containing l -amino acid esters as inhibitors of bacterial RNA polymerases;European Journal of Medicinal Chemistry;2016-06
3. Semi-synthetic zwitterionic rifamycins: a promising class of antibiotics; survey of their chemistry and biological activities;RSC Advances;2016
4. The effect of complexation of 3-formylrifamycin SV macrocyclic ether derivatives with metal cations and small nitrogen-containing organic molecules on antibacterial activity against S. aureus and S. epidermidis;Bioorganic & Medicinal Chemistry Letters;2015-09
5. Rifamycin antibiotics—new compounds and synthetic methods. Part 4: Study of the reaction of 3-formylrifamycin SV with secondary amines and ketones;Tetrahedron;2015-01
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