HK1003620B - Chalcones and esters thereof with antiproliferative activity in uterus, ovary and breast tumours - Google Patents

Description

The present invention relates to chalcone-compounds esters with acetic, butyric, palmitic and ximeninic acids, or chalcone-compounds complexes with phospholipids, in connection with the therapy and prevention of uterus, ovary and breast tumours, as well as to formulations containing them.

Recently, some flavonoids proved to have anticancer activity (Cancer Research 48, 5754, 1988) and chemopreventive activity in some tumours (J. Nat. Prod. 53, 23, 1990). In particular quercetin, a flavonoid almost ubiquitous in plants, has shown some inhibiting activity on the proliferation of human leukemia cells (Br. J. of Haematology 75, 489, 1990) and on other cell lines (Br. J. Cancer 62, 942, 1990 - Int. J. Cancer 46, 1112, 1990 - Cancer Chemother. Pharmacol. 28, 255, 1991 - Gynecologic Oncology 45, 13, 1991, 1992) besides a synergistic activity with the conventional chemotherapeutics. Although the mechanism of such an inhibiting action on proliferation is unknown, it is likely to be related to the interaction of this flavonoid with the estrogen receptors of type II (J. Steroid Biochem. 30, 71, 1988). These sites have first been described by Clark (J. Biol. Chem. 253, 7630, 1978) in 1978 in the rat uterus while displaying the same steroid and tissue specificity are distinct from the "true" estrogen receptors (ER) since they are present in a higher concentration than ER and have a lower apparent affinity dissociation constant (KD: 10-20 nM) for estradiol than ER (KD: 0.2-1 nM).

The chalcone-structure compounds isocordoin, 4-hydroxyderricin, 2-hydroxyderricin, 3-hydroxyderricin, 2',4'-dihydroxychalcone, 4,2',4'-trihydroxychalcone and cordoin have a remarkable affinity to estrogen receptors of type II, together with a marked antiproliferative activity on uterus, ovary and breast tumour cell lines.

The structures of the compounds cited above are as follows:

S1 Isocordoin	H	H	Prenyl	H	H
S2 4-hydroxyderricin	Me	OH	Prenyl	H	H
S3 2-hydroxyderricin	Me	H	Prenyl	OH	H
S4 3-hydroxyderricin	Me	H	Prenyl	H	OH
S5 2',4'-dihydroxychalcone	H	H	H	H	H
S6 4,2',4'-trihydroxychalcone	H	OH	H	H	H
S7 Cordoin	Prenyl	H	H	H	H

Other chalcones strictly related to the former as far as the chemical structure is concerned, such as 4-hydroxycordoin and dihydrocordoin, whose structures are reported below, show no affinity to the above mentioned receptors.

Chalcones
S8 4-hydroxycordoin	prenyl	OH	H
S9 Dihydrocordoin	prenyl	H	H

Compounds (I) can be prepared according to conventional methods reported by Il Farmaco, 30, 449-55, 1975; Il Farmaco, 32, 261-69, 1977; Il Farmaco, 30, 326-42, 1975.

The affinity of compounds I to the estrogen receptors of type II and the antiproliferative activity on ovary tumour cells is reported in the following table. Table -

Chalcones
S1	1.2	1.2
S2	17.0	10.6
S3	4.2	18.0
S4	5.0	12.1
S5	2.5	0.6
S6	5.0	3.2
S7	6.0	4.2

Table -

°° Concentration giving a 50% inhibition on cell proliferation.

°°° Concentration giving a 50% displacement* of labelled estradiol (40nM) from the receptor.

The evaluation of the estrogen receptor binding has been carried out on tumour cells of ovary and other organs. Cells were growth in a monolayer culture on the minimum essential medium added with calf serum and with 200 units/ml of penicillin to maintain the medium sterile. In order to make the tests reproducible, the cells were trypsinated every week and placed on plates at a density of 8x10^-4 and incubated at 37°C under air atmosphere containing 5% CO₂ and humidity. To evaluate the activity of the compounds, the cells were placed into wells (Falcon 3046, Becton Dickinson NY) at a concentration of 1x10^-5/ml in the minimum amount of substrate. After 24 hours the substrate was replaced with fresh substrate and the chalcones dissolved in absolute ethanol were added. Controls were treated analogously with the carrier, in the absence of the active ingredient to test. The treatment described above was repeated at 24 hours time intervals during the 72 hours time of the test. The cells after 24 hours were incubated with scalar amounts of labelled estradiol (³H-E2 40Ci/mmol Amershan UK) alone or in the presence of a 100-fold amount of diethylstilbestrol at 4°C for 2.5 hours. At the end of the incubation time, the cells were quickly washed with fresh substrate and incubated for 30 minutes with 1M NaOH. The radioactivity was measured by means of a scintiller and the binding specificity was calculated as the difference between the preparations containing or not diethylstilbestrol. The results are expressed as the number of binding sites per cell, according to conventional methods. The inhibition on the cell proliferation is evaluated by direct count of the cells comparing the growth of the controls versus that of the treated.

The esters of the compounds of formula (I) with acetic, butyric, palmitic or ximeninic acids, as well as the complexes of compounds (I) with phospholipids, have been found to possess a marked antitumor activity and are the object of the present invention.

Furthermore, the invention provides the use of the esters of compounds of formula (I), as above specified, or the complexes of compounds (I) with phospholipids, for the preparation of medicaments with anticancer activity, in particular for the treatment of tumours expressing estrogen receptors of type II. The compounds of the invention inhibited in vivo the cell proliferation, as proved by measurement of the size of the tumours implanted into the nude athymic mouse, according to the conventional conditions of literature. The treatment of the animals with doses ranging from 1 to 100 mg/kg evidenced the marked regression of the studied tumours until their disappearance in a high percentage of individuals. In the man, the compounds of the invention showed activity on ovary, breast and uterus tumours higher than that of known medicaments such as Tamoxifen.

In the above cited tests, the esters of isocordoin, cordoin and 2',4'-dihydroxychalcone showed a particularly marked activity.

According to a further aspect, the invention provides pharmaceutical compositions containing the esters or complexes of the invention as active ingredients, in admixture with suitable excipients.

The esters of the invention can be advantageously administered orally or by infusion. For the oral administration, complexes of compounds (I) with natural or synthetic phospholipids turned out to be particularly useful since they form stable liposoluble complexes with chalcones; medium chain triglycerides and the related excipients also proved to be useful. The dosages of the compounds of the invention can vary within wide ranges, for example from 10 to 300 mg/day, mainly administered by the oral route.

In the above cited tests, the esters of isocordoin, cordoin and 2',4'-dihydroxychalcone showed a particularly marked activity.

The compounds of the invention can be advantageously administered orally or by infusion; for the oral administration, natural or synthetic phospholipids turned out to be particularly useful since they form stable liposoluble complexes with chalcones; medium chain triglycerides and the related excipients also proved to be useful. The dosages of the compounds of the invention can vary within wide ranges, for example from 10 to 300 mg/day, mainly administered by the oral route.

The following examples further illustrate the invention.

Example I - Preparation of cordoin ximeninate.

7 g of 4-O-prenyl-2-hydroxyacetophenone are reacted with 7 g of benzaldehyde in 10 g of piperidine and 70 ml of ethanol at 60-70°C. After 36 hours the solvent is removed under vacuum and the residue is taken up with 100 ml of benzene which is washed thoroughly with 2N HCl. After removing benzene the residue is purified on a silica gel column to obtain 3.5 g of cordoin. The resulting cordoin is reacted in 20 ml of anhydrous pyridine with 3 g of ximeninic acid chloride. The reaction mixture is poured into water and the product is extracted with methylene chloride. After crystallization from methanol, 4.2 g of cordoin ximeninate are obtained, having m.p. 164-166°C.

Example II - Preparation of isocordoin palmitate.

10 g of 3-C-prenylresacetophenone and 10 g of p-hydroxybenzaldehyde are dissolved in 15 g of piperidine and 200 ml of absolute ethanol and maintained for 4 hours at 60°C. After removing the solvent, the residue is suspended in 50 ml of 2N HCl and the product is extracted with methylene chloride. After removing the chlorinated solvent, the residue is purified on silica gel to obtain 4.1 g of isocordoin having m.p. 160-1°C. This product is reacted with 8 g of palmitoyl chloride in 30 ml of anhydrous pyridine. After dilution of the reaction mixture with water and purification on silica gel, 6.2 g of dipalmitoylisocordoin are obtained, having m.p. 131-132°C.

Example III - Preparation of cordoin and isocordoin acetates and butyrates.

These products are prepared according to the examples I and II using respectively the chlorides or the anhydrides of the corresponding acids. (Cordoin acetate m.p. 131-3°C; cordoin butyrate m.p. 124-6°C).

Example IV - Preparation of the complex of isocordoin with dipalmitoyl phosphatidylcholine.

3.08 g of isocordoin are suspended in 30 ml of methylene chloride and added with 7.9 g of dipalmitoyl phosphatidylcholine and left to react for 1 hour with stirring. When the reagents are completely dissolved, the reaction mixture is concentrated to small volume and the concentrate is poured into in 50 ml of n-hexane. The precipitated solid material is filtered and dried at 40°C overnight under vacuum, to obtain 7.2 g of phospholipid isocordoin complex having m.p. 70°C.

Claims (5)

1. The esters of isocordoin, cordoin, 4-hydroxyderricin, 2-hydroxyderricin, 3-hydroxyderricin, 2',4'-dihydroxychalcone, 4,2',4'-trihydroxychalcone with acetic, butyric, palmitic, ximeninic acids.
2. The cordoin or isocordonine esters according to claim 1.
3. Complexes of isocordoin, cordoin, 4-hydroxyderricin, 2-hydroxyderricin, 3-hydroxyderricin, 2',4'-dihydroxychalcone, 4,2',4'-trihydroxychalcone with natural or synthetic phospholipids.
4. Pharmaceutical compositions containing as active ingredients the esters of claims 1-2 or the complexes of claim 3 in admixture with suitable excipients.
5. The use of the esters of claim 1, or of the complexes of claim 3, for the preparation of medicaments with anticancer and antagonistic activities on the estrogen receptors of type II.