- Clorobiocin
-
Clorobiocin Systematic (IUPAC) name [(3R,4S,5R,6S)-6-[8-Chloro-2-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-4-oxochromen-7-yl]oxy-5-hydroxy-3-methoxy-2,2-dimethyloxan-4-yl] 5-methyl-1H-pyrrole-2-carboxylate Clinical data Pregnancy cat. ? Legal status ? Identifiers CAS number 39868-96-7 ATC code None PubChem CID 73622 ChEMBL CHEMBL303984 Synonyms Chlorobiocin Chemical data Formula C35H37ClN2O11 Mol. mass 697.13 g/mol SMILES eMolecules & PubChem (what is this?) (verify) Clorobiocin is an aminocoumarin.[1][2]
References
- ^ Pojer, F.; Wemakor, E.; Kammerer, B.; Chen, H.; Walsh, C.; Li, S.; Heide, L. (2003). "CloQ, a prenyltransferase involved in clorobiocin biosynthesis". Proceedings of the National Academy of Sciences of the United States of America 100 (5): 2316–2321. Bibcode 2003PNAS..100.2316P. doi:10.1073/pnas.0337708100. PMC 151338. PMID 12618544. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=151338.
- ^ Heide, L. (2009). "Genetic engineering of antibiotic biosynthesis for the generation of new aminocoumarins". Biotechnology advances 27 (6): 1006–1014. doi:10.1016/j.biotechadv.2009.05.017. PMID 19463934.
Other/ungroupedCombinationsTopoisomerase
inhibitors/
quinolones/
(inhibits
DNA replication)1st g.2nd g.Ciprofloxacin# • Enoxacin‡ • Fleroxacin‡ • Lomefloxacin • Nadifloxacin • Ofloxacin • Norfloxacin • Pefloxacin • Rufloxacin3rd g.4th g.Besifloxacin • Clinafloxacin† • Garenoxacin • Gemifloxacin • Moxifloxacin • Gatifloxacin‡ • Sitafloxacin • Trovafloxacin‡/Alatrofloxacin‡ • PrulifloxacinVet.Related (DG)Anaerobic DNA
inhibitorsNitrofuran derivativesRNA synthesis Categories:- Antibiotic stubs
- Antibiotics
- Imidazoles
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