HYDROXYLAMINES AND DERIVATIVES FOR TREATMENT OF INFLAMMATORY CONDITIONS OF THE LIVER
Methods for the treatment and inhibition of hepatitis are disclosed. The methods utilize hydroxylamine compounds or ester derivatives thereof, administered to patients in an amount effective to treat or inhibit hepatitis.
1 . A method for treating or inhibiting hepatitis in a subject in need of such treatment, comprising administering to the subject a composition comprising a pharmaceutically acceptable carrier and at least one hydroxylamine compound or ester derivative thereof in a therapeutically sufficient amount to treat hepatitis in the subject, wherein the ester derivative has the formula I:
wherein:
R 1 and R 2 are, independently, H or C 1 to C 3 alkyl;
R 3 and R 4 are, independently C 1 to C 3 alkyl, or wherein R 1 and R 2 , taken together, or
R 3 and R 4 , taken together, or R 1 and R 2 , taken together and R 3 and R 4 taken together, are each cycloalkyl;
R 5 is H, OH, or C 1 to C 6 alkyl;
R 6 is or C 1 to C 6 alkyl, alkenyl, alkynyl, or substituted alkyl or alkenyl;
R 7 is C 1 to C 6 alkyl, alkenyl, alkynyl, or substituted alkyl or alkenyl; or R 6 and R 7 taken together, or R 5 , R 6 , and R 7 taken together, form a carbocycle having from 3 to 7 atoms in the ring or form a heterocycle having from 3 to 7 atoms in the ring.
2 . The method of claim 1 , wherein the hydroxylamine compound is:
3 . The method of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 are each independently C 1 -C 3 alkyl.
4 . The method of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 are ethyl.
5 . The method of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 are methyl.
6 . The method of claim 1 , wherein R 5 is H or methyl, R 6 is methyl substituted with benzyloxy or C 1 -C 6 alkoxy, and R 7 is methyl.
7 . The method of claim 6 , wherein R 5 is H or methyl, and R 6 and R 7 , taken together, form a cyclopropyl group.
8 . The method of claim 6 wherein: R 5 , R 6 and R 7 , taken together, form a furanyl group.
9 . The method of claim 6 wherein: R 5 is H; and R 6 and R 7 , taken together, form a tetrahydrofuranyl group.
10 . The method of claim 6 wherein: R 5 is H; and R 6 and R 7 , taken together, form a cyclopropyl group.
11 . The method of claim 1 , wherein the subject is a mammal.
12 . The method of claim 11 , wherein the mammal is a human.
13 . The method of claim 1 , further comprising administering an antioxidant to the subject.
14 . The method of claim 1 , further comprising administering a reducing agent to the subject.
15 . The method of claim 1 , wherein the hepatitis is infectious hepatitis.
16 . The method of claim 15 , wherein the infectious hepatitis is caused by HAV, HBV, HCV, HDV, or HEV.
17 . The method of claim 1 , wherein the hepatitis is noninfectious hepatitis.
18 . The method of claim 17 , wherein the noninfectious hepatitis is alcoholic hepatitis, toxic/drug-induced hepatitis, autoimmune hepatitis, or granulomatus hepatitis.
19 . The method of claim 1 , wherein the subject has cirrhosis of the liver.
20 . The method of claim 1 , wherein the composition is administered to achieve in the liver of the subject a hydroxylamine concentration of about 0.1 μM to about 10 mM.
21 . The method of claim 1 , wherein the composition is administered to achieve in the liver of the subject a hydroxylamine concentration of about 1 μM to about 5 mM.
22 . The method of claim 1 , wherein the composition is administered to achieve in the liver of the subject a hydroxylamine concentration of about 10 μM to about 2.5 mM.
23 . The method of claim 1 , wherein the composition is administered to achieve in the liver of the subject a hydroxylamine concentration of about 50 μM to about 1 mM.
24 . The method of claim 1 , wherein the composition is administered to achieve in the liver of the subject a hydroxylamine concentration of about 1 μM to about 100 μM.
25 . The method of claim 1 , further comprising administering an additional anti-inflammatory agent.
26 . The method of claim 25 , wherein the additional anti-inflammatory agent is a non-steroidal anti-inflammatory drug, corticosteroid, lactoferrin, or extract from Silybum marianum , Phyllanthus, glycyrrhizin, Picrorhiza kurroa, Cudrania cochinchinensis var. gerontogea, Bidens pilosa , Glossogyne tenuifolia, Artemisia capillaries , or Sargassum polycystum.