This application relates to the use of certain amines of formula (I) for combatting and preventing systemic and local complement activation, and in particular to the use of meglumine and derivatives and optionally salts thereof in combatting and preventing said activation. The amines are also of use in combatting activation of the kinin/kallikrein system or blood coagulation system.
1. A method for combating or preventing complement activation and/or for combating or preventing activation of the kinin/kallikrein system comprising administering to a human or non-human subject an effective amount of a therapeutically active compound of formula (I)
wherein each R independently represents hydrogen or a C 1-6 hydrocarbyl group,
m is 0–2 and
n is 0–5,
or a physiologically tolerable salt thereof.
2. A method of claim 1 wherein at least one R of the compound of formula (I) is hydrogen.
3. A method of claim 1 where R in the compound of formula (I) represents hydrogen.
4. A method of claim 1 , wherein the compound of formula (I) is meglumine, 3-methylamino- 1,2 propandiol or 2-(methylamino)-ethanol.
5. A method for combating or preventing complement activation, for combating or preventing activation of the kinin/kallikrein system and/or for combating or preventing activation of the blood coagulation system comprising administering to a human or non-human subject an effective amount of a therapeutically active compound of formula (I),
wherein each R independently represents hydrogen or a C 1-6 hydrocarbyl group,
m is 0–2 and
n is 0–5,
together with a non-ionic pharmaceutical product.
6. A method of claim 1 wherein at least one R of the compound of formula (I) represents a C 1-6 alkyl group.
7. A method of claim 6 wherein the C 1-6 alkyl group represents a methyl and/or ethyl group.
8. A method of claim 1 , wherein the compound of formula (I) is in its salt form where the cationic portion represents a compound of formula (I) and the anionic portion is a pharmaceutical compound.
9. A method for combating or preventing complement activation, for combating or preventing activation of the kinin/kallikrein system and/or for combating or preventing activation of the blood coagulation system comprising administering to a human or non-human subject an effective amount of a therapeutically active compound of formula (I),
wherein each R independently represents hydrogen or a C 1-6 hydrocarbyl group,
m is 0–2 and
n is 0–5,
or a physiologically tolerable salt thereof,
wherein the compound of formula (I) is in its salt form where the cationic portion represents a compound of formula (I) and the anionic portion is an in vivo contrast agent.
10. A method for combating or preventing complement activation, for combating or preventing activation of the kinin/kallikrein system and/or for combating or preventing activation of the blood coagulation system comprising administering to a human or non-human subject an effective amount of a therapeutically active compound of formula (I),
wherein each R independently represents hydrogen or a C 1-6 hydrocarbyl group,
m is 0–2 and
n is 0–5,
or a physiologically tolerable salt thereof,
wherein the compound of formula (I) is in its non-salt form.
11. A method of claim 5 , wherein the non-ionic pharmaceutical product comprises a non-ionic x-ray contrast agent.
12. A method of claim 11 , wherein the non-ionic x-ray contrast agent comprises iodixanol, iohexol, ioversol, iopamidol, iopentol, iopromide, iomeprol, iosimide, metrizamide, iotasol and iotrolan.
13. A method of claim 5 wherein at least one R of the compound of formula (I) is hydrogen.
14. A method of claim 5 where R in the compound of formula (I) represents hydrogen.
15. A method of claim 5 , wherein the compound of formula (I) is meglumine, 3-methylamino-1,2 propandiol or 2-(methylamino)-ethanol.
16. A method of claim 5 wherein at least one R of the compound of formula (I) represents a C 1-6 alkyl group.
17. A method of claim 16 wherein the C 1-6 alkyl group represents a methyl andior ethyl group.