Tovmasyan et al., 2013 - Google Patents
Design, mechanism of action, bioavailability and therapeutic effects of mn porphyrin-based redox modulatorsTovmasyan et al., 2013
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- 4423052806939591403
- Author
- Tovmasyan A
- Sheng H
- Weitner T
- Arulpragasam A
- Lu M
- Warner D
- Vujaskovic Z
- Spasojevic I
- Batinic-Haberle I
- Publication year
- Publication venue
- Medical Principles and Practice
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Based on aqueous redox chemistry and simple in vivo models of oxidative stress, Escherichia coli and Saccharomyces cerevisiae, the cationic Mn (III) N-substituted pyridylporphyrins (MnPs) have been identified as the most potent cellular redox modulators …
- 230000001225 therapeutic 0 title abstract description 29
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- A61K31/47—Quinolines; Isoquinolines
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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