Triterpene derivative and medicinal composition

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

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514460, 560 8, 560129, 562498, A61K 3153, A61K 3135, C07C 6976, C07C 6112

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active

058859926

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BRIEF SUMMARY
This is 371 of PCT/JP95/01249 filed Jun. 22, 1995.


TECHNICAL FIELD

The present invention relates to a hederagenin derivative, its pharmacologically acceptable salt, and a solvate of either of said derivative and salt, which are of value as medicines.
The compounds according to the present invention have inhibitory activity of mesangial cell proliferation and are useful for the treatment of nephritis.


BACKGROUND TECHNOLOGY

According to the site of principal lesions, nephritis is classified into glomerulonephritis, interstitial nephritis and pyelonephritis, for instance. The most representative of all is glomerulonephritis in which the glomerular tuft is the affected site. Today, nephritis is synonymous with glomerulonephritis (Medical Dictionary, 1st ed., 570, 1987).
Histopathological findings which are most frequently obtained in human glomerulonephritis and considered to be of prognostic importance are mesangial cell proliferation and hyperplasia of the matrix produced by mesangial cells (hereinafter referred to as mesangial matrix). These findings are noted in nearly all types of proliferative glomerulonephritis, inclusive of IgA nephropathy, membranous proliferative glomerulonephritis, and lupus nephritis, in common (Iida: Kindney and Dialysis, 35, 505-509, 1993). And as the mesangial cell proliferation and associated production of mesangial matrix progress, the glomeruli fall into a terminal stage, so call glomerulosclerosis. Therefore, any compound that inhibits mesangial cell proliferation and production of mesangial matrix is of great value as a therapeutic agent for glomerulonephritis.
Two processes are known for mesangial cell proliferation in glomerulonephritis. In the first process, the complement, platelets, and infiltrating cells are involved. Thus, deposition of the immune complexes produced by immunological mechanisms on the glomeruli takes place in situ and activation of the complement and platelets and infiltration of macrophages and neutrophils then occur. These cells release a variety of growth factors and cytokines to activate the mesangial cells and stimulate their proliferation. The second process is a process wish which mesangial cells themselves are associated. Thus, it is a process in which activated mesangial cells themselves release a variety of growth factors and cytokines and the cells releasing them and the adjacent mesangial cells become activated or proliferate. Thus, mesangial cells are activated and proliferate through a complex system consisting of a plurality of processes.
Therefore, when the treatment of glomerulonephritis is considered, it is inconceivable that the mesangial cell proliferation can be sufficiently inhibited even if a given stage in first process mentioned above, for example the stage mediated by the complement and platelets, is inhibited. In fact, it is reported that administration of an antiplatelet drug alone is therapeutically little effective for human nephritis in active stage (Dohi et al., Clinics All-round, 38, 865-870, 1989).
It is known that, among natural substances of the plant origin, there exist compounds having antinephritic activity. For example, the usefulness of pentacyclic triterpene derivatives in the treatment of nephritis and other diseases is indicated in Japanese Laid-Open S61-37749 (an oleanene derivative), Japanese Laid-Open S61-85344 (an oleanene derivative), Japanese Laid-Open H2-73012 (a bryonolic acid derivative), Japanese Laid-Open H4-290846 (a bryonolic acid derivative), and Japanese Laid-Open S61-43141 (a lupane derivative). However, there is no disclosure of an experimental example demonstrating the utility of such compounds in the treatment of nephritis, nor is there a suggestion that they ever have mesangial cell proliferation inhibitory activity.
Hederagenin (3.beta.,23-dihydroxyolean-12-en-28-oic acid) according to the present invention is a pentacyclic triterpene derivative available from natural sources such as Sapindus mukorossi, Hedera rhombea, Hedera helix, Fatsia japonica, etc. Hederagenin is known to hav

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