321745-36-2Relevant academic research and scientific papers
Cyclohexapeptide compounds, processes for their production and their use as a pharmaceutical
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Page/Page column 16; 17, (2008/06/13)
A cyclohexapeptide compound of general formula (I), wherein R1 is C1–C20 alkyl; C9–C20 alkenyl; C9–C20 alkoxyphenyl; an aryl group selected from: phenyl, biphenyl, terphenyl and
Mannich reaction: An approach for the synthesis of water soluble mulundocandin analogues
Lal, Bansi,Gund, Vitthal Genbhau,Bhise, Nandu Baban,Gangopadhyay, Ashok Kumar
, p. 1751 - 1768 (2007/10/03)
Semisynthetic modifications at Hydroxy tyrosine (Htyr) unit of mulundocandin (1) were carried out to improve its aqueous solubility. A single step introduction of substituted aminomethyl groups at the ortho position(s) of phenolic hydroxyl of HTyr unit of
Semisynthetic modifications of hemiaminal function at ornithine unit of mulundocandin, towards chemical stability and antifungal activity
Lal, Bansi,Gund, Vitthal Genbhau,Gangopadhyay, Ashok Kumar,Nadkarni,Dikshit, Vidula,Chatterjee,Shirvaikar
, p. 5189 - 5198 (2007/10/03)
Mulundocandin (1), is an echinocandin class of lipopeptide. It has wide spectrum of antifungal activity against Candida and Aspergillus species. Semisynthetic modification at Ornithine-5-hydroxyl (hemiaminal function) of 1 was carried out to improve solut
