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char = o;code = 111
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result sql = Synthesis and in vitro antiprotozoal activities of water-soluble, inexpensive 3,7-bis(dialkylamino)phenoxazin-5-ium derivatives.
Synthesis and in vitro antiprotozoal activities of water-soluble, inexpensive 3,7-bis(dialkylamino)phenoxazin-5-ium derivatives.
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char = i;code = 105
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char = m;code = 109
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char = m;code = 109
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char = l;code = 108
char = c;code = 99
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char = p;code = 112
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char = r;code = 114
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char = a;code = 97
char = n;code = 110
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char = o;code = 111
char = m;code = 109
char = a;code = 97
char = ;code = 32
char = c;code = 99
char = r;code = 114
char = u;code = 117
char = z;code = 122
char = i;code = 105
char = ,;code = 44
char = ;code = 32
char = T;code = 84
char = .;code = 46
char = ;code = 32
char = b;code = 98
char = r;code = 114
char = u;code = 117
char = c;code = 99
char = e;code = 101
char = i;code = 105
char = ;code = 32
char = r;code = 114
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char = o;code = 111
char = d;code = 100
char = e;code = 101
char = s;code = 115
char = i;code = 105
char = e;code = 101
char = n;code = 110
char = s;code = 115
char = e;code = 101
char = ,;code = 44
char = ;code = 32
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char = d;code = 100
char = ;code = 32
char = L;code = 76
char = e;code = 101
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char = s;code = 115
char = h;code = 104
char = m;code = 109
char = a;code = 97
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char = i;code = 105
char = a;code = 97
char = ;code = 32
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char = o;code = 111
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char = a;code = 97
char = n;code = 110
char = i;code = 105
char = .;code = 46
char = ;code = 32
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char = o;code = 111
char = t;code = 116
char = a;code = 97
char = b;code = 98
char = l;code = 108
char = y;code = 121
char = ,;code = 44
char = ;code = 32
char = t;code = 116
char = h;code = 104
char = e;code = 101
char = ;code = 32
char = c;code = 99
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char = m;code = 109
char = p;code = 112
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char = ;code = 32
char = s;code = 115
char = h;code = 104
char = o;code = 111
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char = e;code = 101
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char = ;code = 32
char = p;code = 112
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char = l;code = 108
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char = i;code = 105
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char = t;code = 116
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char = ;code = 32
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char = e;code = 101
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char = h;code = 104
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char = s;code = 115
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char = h;code = 104
char = a;code = 97
char = n;code = 110
char = ;code = 32
char = t;code = 116
char = h;code = 104
char = r;code = 114
char = e;code = 101
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char = ;code = 32
char = c;code = 99
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char = n;code = 110
char = ;code = 32
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char = o;code = 111
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char = s;code = 115
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char = s;code = 115
char = s;code = 115
char = e;code = 101
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char = ;code = 32
char = g;code = 103
char = o;code = 111
char = o;code = 111
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char = ;code = 32
char = a;code = 97
char = c;code = 99
char = t;code = 116
char = i;code = 105
char = v;code = 118
char = i;code = 105
char = t;code = 116
char = i;code = 105
char = e;code = 101
char = s;code = 115
char = ;code = 32
char = w;code = 119
char = i;code = 105
char = t;code = 116
char = h;code = 104
char = ;code = 32
char = h;code = 104
char = i;code = 105
char = g;code = 103
char = h;code = 104
char = ;code = 32
char = s;code = 115
char = e;code = 101
char = l;code = 108
char = e;code = 101
char = c;code = 99
char = t;code = 116
char = i;code = 105
char = v;code = 118
char = e;code = 101
char = ;code = 32
char = i;code = 105
char = n;code = 110
char = d;code = 100
char = i;code = 105
char = c;code = 99
char = e;code = 101
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char = <;code = 60
char = b;code = 98
char = r;code = 114
char = /;code = 47
char = >;code = 62
result sql = 3,7-Bis(dialkylamino)phenoxazinium salts were synthesized and evaluated for in vitro activities against Plasmodium falciparum, Trypanosoma cruzi, T. brucei rhodesiense, and Leishmania donovani. Notably, the compounds showed potent antiprotozoal activities, especially against P. falciparum and T. cruzi. The compounds with alkyl side chains less than three carbons in length possessed good activities with high selective indices.

Publication: J. Med. Chem. 2008 Jun 26 ;51(12)::3654-8. :doi: 10.1021/jm8003619.
Publication Date: 2008 Jun 26
Study Author(s): Ge, Jian-Feng;Arai, Chika;Kaiser, Marcel;Wittlin, Sergio;Brun, Reto;Ihara, Masataka;
Institution: Institute of Medicinal Chemistry, Hoshi University, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan.
Shortcut link to this study:
3,7-Bis(dialkylamino)phenoxazinium salts were synthesized and evaluated for in vitro activities against Plasmodium falciparum, Trypanosoma cruzi, T. brucei rhodesiense, and Leishmania donovani. Notably, the compounds showed potent antiprotozoal activities, especially against P. falciparum and T. cruzi. The compounds with alkyl side chains less than three carbons in length possessed good activities with high selective indices.
PMID: 18476684

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