(19)
(11)EP 2 180 893 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
12.11.2014 Bulletin 2014/46

(21)Application number: 08808006.4

(22)Date of filing:  10.08.2008
(51)International Patent Classification (IPC): 
A61K 31/496(2006.01)
A61P 35/00(2006.01)
C07D 513/02(2006.01)
(86)International application number:
PCT/IL2008/001099
(87)International publication number:
WO 2009/019708 (12.02.2009 Gazette  2009/07)

(54)

Pharmaceutical compositions and methods for the treatment of cancer

Pharmazeutische Zusammensetzungen und Verfahren zur Behandlung von Krebs

Compositions pharmaceutiques et procédés pour le traitement du cancer


(84)Designated Contracting States:
AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR

(30)Priority: 09.08.2007 US 935364 P
15.01.2008 US 6455

(43)Date of publication of application:
05.05.2010 Bulletin 2010/18

(73)Proprietor: Urifer Ltd
Raanana 43613 (IL)

(72)Inventors:
  • NIR, Uri
    D.N Merkaz 73130 (IL)
  • SHPUNGIN, Sally
    Ramat-Gan 52275 (IL)
  • YAFFE, Etai
    Oranit 44813 (IL)
  • COHEN, Moshe
    Raanana 43613 (IL)

(74)Representative: Becker, Philippe et al
Cabinet Becker & Associés 25, rue Louis Le Grand
75002 Paris
75002 Paris (FR)


(56)References cited: : 
EP-A- 1 547 996
WO-A-02/092086
WO-A-2004/111061
WO-A-2007/072093
WO-A-02/066478
WO-A-03/017817
WO-A-2006/101455
  
  • DATABASE WPI Week 199927 Thomson Scientific, London, GB; AN 1999-323456 XP002519065 -& JP 11 116481 A (SUMITOMO SEIYAKU KK) 27 April 1999 (1999-04-27)
  • KHAZI I M ET AL: "Synthesis and biological activity of some 3-methyl/ethoxycarbonyl-6-arylimidazo[2,1- b]-thiazoles and their 5-bromo/5-formyl derivatives" INDIAN JOURNAL OF CHEMISTRY, vol. 43b, no. 2, February 2004 (2004-02), pages 393-398, XP009113585 ISSN: 0376-4699
  • ANDREANI A ET AL: "6-Thienyl and 6-phenylimidazo[2,1-b]thiazoles as inhibitors of mitochondrial NADH dehydrogenase" EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, EDITIONS SCIENTIFIQUE ELSEVIER, PARIS, FR, vol. 34, no. 10, 1 October 1999 (1999-10-01), pages 883-889, XP004202943 ISSN: 0223-5234
  • BUU-HOI NG PH ET AL: "2-Arylpyrrocolines and 2-Arylpyrimidazoles" JOURNAL OF ORGANIC CHEMISTRY, 1 January 1954 (1954-01-01), pages 1370-1375, XP002422941 ISSN: 0022-3263
  • BARLIN G B ET AL: "Imidazo[1,2-b]pyridazines. XXI. Syntheses of some 3-Acylaminomethyl-6-(chloro and iodo)- 2-(substituted phenyl)-imidazo[1,2-b]pyridazines and -imidazo[1,2-a]pyridines and their Interaction with Central and Mitochondrial Benzodiazepine" AUSTRALIAN JOURNAL OF CHEMISTRY, vol. 50, 1 January 1997 (1997-01-01), pages 61-67, XP001007026 ISSN: 0004-9425
  • PRÉVOST G P ET AL: "Anticancer activity of BIM-46174, a new inhibitor of the heterotrimeric Galpha/Gbetagamma protein complex." CANCER RESEARCH 15 SEP 2006, vol. 66, no. 18, 15 September 2006 (2006-09-15), pages 9227-9234, XP009113736 ISSN: 0008-5472
  • HAYUN RAMI ET AL: "Novel involvement of the immunomodulator AS101 in IL-10 signaling, via the tyrosine kinase Fer.", ANNALS OF THE NEW YORK ACADEMY OF SCIENCES JAN 2007 LNKD- PUBMED:17404037, vol. 1095, January 2007 (2007-01), pages 240-250, XP009138110, ISSN: 0077-8923
  
Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


Description

FIELD OF THE INVENTION



[0001] This invention relates to pharmaceutical compositions and and their use in methods for the treatment of cancer.

BACKGROUND OF THE INVENTION



[0002] The following references are considered to be relevant for an understanding of the invention.

References



[0003] 

Allard P, Zoubeidi A, Nguyen LT, Tessier S, Tanguay S, Chevrette M, Aprikian A and Chevalier S. (2000). Mol. Cell. Endocrinol., 159, 63-77.

Berridge,M.V., Herst,P.M., and Tan,A.S. (2005). Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction. Biotechnol. Annu. Rev. 11, 127-152]

Craig AW and Greer PA. (2002). Mol. Cell. Biol., 22, 6363-6374.

Craig AW, Zirngibl R, Williams K, Cole LA and Greer PA. (2001). Mol. Cell. Biol., 21, 603-613.

Greer P. (2002). Nat. Rev. Mol. Cell Biol., 3, 278-289.

Hao Q-L, Heisterkamp N and Groffen J. (1989). Mol. Cell. Biol., 9, 1587-1593.

Kim L and Wong TW. (1998). J. Biol. Chem., 273, 23542-23548.

Orlovsky K, Ben-Dor I, Priel-Halachmi S, Malovany H and Nir U. (2000). Biochemistry, 39, 1084-11091.

Penhallow RC, Class K, Sonoda H, Bolen JB and Rowley RB. (1995). J. Biol. Chem., 270, 23362-23365.

Pasder, O., Shpungin, S., Salem, Y., Makovsky, A., Vilchick, S., Michaeli, S., Malovani, H. and Nir, U. (2006) Oncogene, 25, 4194-4206.

Pasder, O., Salem, Y., Yaffe, E., Shpungin, S. and Nir, U. (2007) Drugs of the Future, 32, 61-70.



[0004] Fer is an intracellular tyrosine kinase that resides in both the cytoplasm and nucleus of mammalian cells and is activated by growth factors such as EGF and PDGF in fibroblastic cells (Kim and Wong, 1998), and by occupation of the Fcγ receptor in mast cells (Penhallow et al., 1995). Although present in a wide variety of tissues and cells, the functional role of Fer has been elucidated mainly in cells which carry out innate immune responses (Craig and Greer, 2002; Greer, 2002). Mice devoid of an active Fer develop normally and the proliferation of fibroblasts derived from these mice is not impaired in vitro (Craig et al., 2001).

[0005] Fer has been detected in all human malignant cell lines analyzed (Hao et al., 1989; Orlovsky et al., 2000) and its levels in malignant prostate tumors are significantly higher then those detected in benign prostate tumors (Allard et al., 2000). Furthermore, down-regulation of Fer impaired the proliferation of prostate and breast carcinoma cells (Pasder et al.,2006) and abolished the ability of prostate carcinoma PC3 cells to form colonies in soft agar (Allard et al., 2000). US Patent application 10/486,101 having Publication Number 20050063973 discloses short interfering RNA (siRNA) molecules directed to sequences of the fer gene. These siRNA molecules were found to inhibit the growth of PC3 cells and to arrest tumor growth in an animal model (Pasder et al., 2007); WO02/092086; JP11116481; EP1547996; WO2007/072093; WO2006/101455; WO02/066478; WO2004/111061; Ind. J. Chem. 2004, 43b p393 and Canc. Res. 2006, 66, p9227 relate to compositions comprising different heterocyclic molecules for use in the treatment of certain disorders.

SUMMARY OF THE INVENTION



[0006] In its first aspect, the present invention provides a pharmaceutical composition as defined in the claims. A pharmaceutical composition as also disclosed herein comprises as an active component a compound of formula (I):

X is selected from the following:



wherein R1 is independently selected from H, F, Cl, Br, I or a C1-5 linear or branched alkyl; n is 1, 2, 3, 4 or 5; R2 is N(R)2, R being independently hydrogen or linear or branched C1-5alkyl group; R3 is a linear or branched C1-5alkyl group; R4 is a group of formula

R5 being a 5- or 6-membered aromatic or non-aromatic ring optionally having one, two or three heteroatoms selected from O, N or S; R6 being a 5- or 6-membered aromatic or non-aromatic ring optionally having one, two or three heteroatoms selected from O, N or S optionally having one or two substituents independently selected from halogen and a linear or branched C1-5alkyl group; Z is selected from O or S; Y is C-H or N; and A is a 5- or 6-membered fused aromatic or non aromatic ring optionally being a heterocyclic ring comprising 1 to 3 heteroatoms selected from O, N or S;
physiological acceptable carrier.

[0007] C1-5 Linear or branched alkyl means a methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, n-pentane, iso-pentane, sec.-pentane or tert.-pentane that may optionally be partially substituted by halogen selected from F, Cl, Br, or I.

[0008] Also disclosed herein is a pharmaceutical composition comprising as an active ingredient a compound of formula (I) as defined above, where R1 is H, F, Cl, CH3, C2H5 or C3H7; n is 1, 2 or 3; X is a compound selected from formulae (II) to (VI); R2 is N(R)2, R being independently hydrogen or CH3, C2H5 or C3H7; R3 is a linear or branched C1-5alkyl group; R4 is a group of formula:

R5 being a 5- or 6-membered aromatic or non-aromatic ring optionally having one, two or three heteroatoms selected from O, N or S; R6 being a 5- or 6-membered aromatic or non-aromatic ring optionally having one, two or three heteroatoms selected from O, N or S optionally having one or two substituents independently selected from halogen and a linear or branched C1-5alkyl group; Z is selected from O or S; Y is C-H or N; and A is a 5- or 6-membered fused aromatic or non aromatic ring optionally being a heterocyclic ring comprising 1 to 3 heteroatoms selected from O, N or S.

[0009] In particular, the pharmaceutical compositions disclosed in the invention have been found to inhibit the growth of cancer cells. Without wishing to be bound by a particular theory, it is believed that the pharmaceutical compositions of the invention inhibit the expression or the activity of Fer in the treated cells.

[0010] The pharmaceutical composition of the invention comprises a compound, referred to herein as "compound E626-0342", having the chemical formula C22H28N6OS (X):



[0011] In its second aspect, the invention provides a compound E626-0342 for use in a method for treating cancer. In accordance with this aspect of the invention, an individual in need of such treatment is administered an effective amount of a pharmaceutical composition of the invention.

[0012] The invention further discloses the use of a compound of formula (I):

X is selected from the following:



wherein R1 is independently selected from H, F, Cl, Br, I or a C1-5 linear or branched alkyl; n is 1, 2, 3, 4 or 5; R2 is N(R)2, R being independently hydrogen or linear or branched C1-5alkyl group; R3 is a linear or branched C1-5alkyl group; R4 is a group of formula

R5 being a 5- or 6-membered aromatic or non-aromatic ring optionally having one, two or three heteroatoms selected from O, N or S; R6 being a 5- or 6-membered aromatic or non-aromatic ring optionally having one, two or three heteroatoms selected from O, N or S optionally having one or two substituents independently selected from halogen and a linear or branched C1-5alkyl group; Z is selected from O or S; Y is C-H or N; and A is a 5- or 6-membered fused aromatic or non aromatic ring optionally being a heterocyclic ring comprising 1 to 3 heteroatoms selected from O, N or S;
for the preparation of a medicament for the treatment of cancer.

BRIEF DESCRIPTION OF THE DRAWINGS



[0013] In order to understand the invention and to see how it may be carried out in practice, embodiments will now be described, by way of non-limiting example only, with reference to the accompanying drawings, in which:

Fig. 1 shows the effect of compound 497 on HT29 human colorectal carcinoma cells;

Fig. 2 shows the effect of compound 497 on HCT116 human colorectal carcinoma cells;

Fig. 3 shows the effect of compound 497 on FS 11 human fibroblastic cells;

Fig. 4 shows the effect of compound 631 on HT29 colorectal carcinoma cells;

Fig. 5 shows the effect of compound 631 on HcT116 colorectal carcinoma cells;

Fig. 6 shows the effect of compound 631 on FS 11 human fibroblastic cells;

Fig. 7 shows the effect of the compound E626-0342 on HT29 human colon carcinoma cells;

Fig. 8 shows the effect of compound E626-0342 on HCT116 human colon carcinoma cells;

Fig. 9 shows the effect of compound E626-0342 on FS 11 normal human fibroblasts;

Fig. 10 shows inhibition of tyrosine kinase Fer activity by E626-0342;

Fig. 11 shows the effect of E626-0342 on the progression of Ht29 xenografts in "nude" mice; and

Fig. 12 shows inhibition of the kinase activity of Fer in yeast cells by compounds 497 and 631.


EXAMPLES


Illustrative Compounds 497,631,115 and 540



[0014] The effect of the four compounds 497, 631,115 and 540 on the growth profile of cancer cells which express Fer was tested. The cells that were tested were: the colon cancer cell lines HT29 and HCT 116, the breast cancer cell lines MDA-MB-231 and MCF-7, and the prostate cancer cell lines PC3 and DU145. The effect of each of the four compounds on FS11 cells, a non malingnant fibroblastic cell line, was also studied.

[0015] The cells were seeded in 96 wells microplates and were left to grow untreated overnight. Each of the three compounds was dissolved in DMSO and was then added to each well in a dose dependent manner from 0.4 to 80µM. The concentration of DMSO in each well was 0.4% v/v. Untreated cells and cells subjected to 0.4% DMSO alone, served as controls. The number of viable cells in each well was determined 48, 72, 96 hours after compounds addition, using the XTT test (Berridge,M.V. et al, 2005). In cases where complete inhibition of cell growth was observed in the presence of one of the three compounds tested at one of the concentrations tested, the IC50 of the compound on that cell line was determined.

[0016] Figs. 1 and 2 show the effect of compound 497 on the growth of the colorectal cancer cell lines HT29 and HCT116, respectively. In Figs 1 and 2, it can be seen that compound 497 caused a profound reduction in the number of viable cells in both cell lines of treated cultures with an IC50 of 2µM for HT29 and HCT116 after 96h. Fig. 3 shows the effect of compound 497 on the non-malignant FS 11 cell line.

[0017] Figs. 4 and 5 show the effect of compound 631 on on the growth of the colorectal cancer cell lines HT29 and HCT116, respectively. Fig. 6 shows the effect of compound 631 on the non-malignant FS 11 cell line. Compound 631 also caused a decrease in cell viability with an EC50 of 40µM for HT29 and 24µM for HCT116 (Figs. 7, 8). Compound 631 did not affect FS11 cells up to a concentration of 80µM (Fig. 6).

[0018] Table 1 shows the EC50 in µM of the four compounds on the various cell lines examined for those cases where an EC50 could be determined from the concentrations of the compounds that were tested (up to 80µM).
Table 1
 Compound
Cell LineCompound 497Compound 631Compound 115Compound 540
HT29 2 30 32 40
HCT116 2 24 32 40
MDA-MB-231 2 32 40 25
MCF-7 8   8 25
PC3 4 32   15
DU145 8     20
FS11 4   >80 40


[0019] To examine whether the above listed compounds affect the enzymatic activity of Fer, the protein tyrosine phosphorylation profile in yeast cells which ectopically express the murine Fer, was analyzed using the yeast system disclosed in WO2007/107991. Since the S. cerevisae yeast cells lack almost completely detectable, endogenous, tyrosine phosphorylation activity, the detected tyrosine phosphrylation signals result essentially from the kinase activity of the ectopic Fer. Furthermore, considering the neglegible tyrosine-phosphrylation background in the cells, it is possible to specifically track the tyrosine phosphorylation level of Fer in the treated yeast cells.

[0020] Yeast cells expressing an ectopic Fer were treated with 40 µM of one of the compounds 497, 631, 115 and 540 for 48 h. Whole cell lysates were then prepared and resolved in SDS-poly acrylamide gel. The expression levels of Fer and the tyrosine phosphorylation profiles of the proteins before and after treatment with the compounds were determined using a western-blot analysis. Fig. 12 shows a Western Blot in which lane 4 of shows yeast cells containing the empty expression vector- pAES, lane 3 shows yeast cells harboring the plasmid pAES-Fer and expressing an ectopic Fer, lane 2 shows cells harboring pAES-Fer, expressing Fer and treated with compound 631 and lane 1 shows cells harboring pAES-Fer, expressing Fer and treated with compound 497. The lower panel shows- membrane reacted with anti-phosphotyrosine antibody. The arrow indicates the tyrosine phosphorylated Fer (pFer). The upper panel shows membrane reacted with an anti-Fer antibody, thus representing the level of the Fer protein. The middle panel shows the level of the house-keeping protein actin, which served as a control for protein loading quantities. This revealed a significant reduction in the tyrosine phosphorylation level of the 94 kD band which represents the Fer protein, in cells treated with compounds 631 and 497 (Fig. 12). Thus, the compounds 631 and 497 significantly inhibit the Fer kinase autophosphorylation enzymatic activity.

Compound E626-0342



[0021] The effect of compound E626-0342 on the growth profile of cancer cells which express Fer was tested. The compound was added to the growth media of FS11-normal primary human fibroblasts and to two colon cancer cell lines, HCT116 and HT29, which express Fer.

[0022] Various cell lines were seeded in 96 wells microplates and were left to grow untreated overnight. Compound E626-0342, dissolved in DMSO at a stock concentration of 10mM was then added to each well in a dose dependent manner, resulting in final concentrations extending from 0.5 to 15µM. The final concentration of DMSO in each well was 1% v/v. Untreated cells and cells subjected to 1% DMSO alone, served as controls. The number of viable cells in each well was determined 96 hours after addition of the compound, using the XTT test (Berridge,M.V. et al, 2005).

[0023] In Figures 7 and 8, it can be seen that compound E626-0342 caused a profound reduction in the number of viable cells in the two colon cancer cell lines, to which it was added. The compound exhibited an EC50 of 1µM for both HT29 and HCT116, after 96h of treatment. At a concentration of 10 µM, less then 10 % of viable cells were left in each of the two treated colon cell lines.

[0024] Notably, E626-0342 did not affect normal human FS11 fibroblasts, up to a concentration of 10µM (Fig. 9).

[0025] To examine whether E626-0342 affects the enzymatic activity of Fer, the protein tyrosine phosphorylation profile in yeast cells which ectopically express the murine Fer, was analyzed. Since the S. cerevisae yeast cells lack almost completely detectable, endogenous, tyrosine phosphorylation activity, the detected tyrosine phosphrylation signals result essentially from the kinase activity of the ectopic Fer. Furthermore, considering the neglegible tyrosine-phosphrylation background in the cells, it is possible to specifically track the tyrosine phosphorylation level of Fer in the treated yeast cells.

[0026] Yeast cells expressing an ectopic Fer were treated with 40 µM E626-0342 compound for 48 h. Whole cell lysates were then prepared and resolved in SDS-poly acrylamide gel. The expression levels of Fer and the tyrosine phosphorylation profile of the proteins before and after treatment with the compound were determined using a western-blot analysis. This revealed a significant reduction in the tyrosine phosphorylation level of a 94 kD band which represents the Fer protein (Fig. 10). Thus, the E626-0342 compound significantly inhibits the Fer kinase autophosphorylation enzymatic activity.

[0027] Referring now to Fig. 10 a Western Blot is shown. Lane 1 shows yeast cells containing the empty expression vector- pAES, lane 2 shows yeast cells harboring the plasmid pAES-Fer and expressing an ectopic Fer, and lane 3 shows cells harboring pAES-Fer, expressing Fer and treated with E626-0342. The upper panel shows-membrane reacted with anti-phosphotyrosine antibody. Arrow indicates the tyrosine phosphorylated Fer (pFer). The lower panel shows membrane reacted with an anti-Fer antibody and anti-actin antibody, which served as a control for protein loading quantities. The upper arrow indicates the Fer protein, the lower arrow indicates actin.

[0028] As seen in Fig. 10, compound E626-0342 exhibited a significant dose dependent growth restoring effect on the HA-Fer expressing yeasts cells. This indicated an effect of this compound on the functioning of the tyrosine kinase Fer. This compound was not toxic to yeast cells in concetrations up to 40µM.

[0029] To test the effect of the E626-0342 compound on tumor progression in-vivo, 1x106 HT29 colon carcinoma cells were injected subcutaneously to immuno-compromised "nude" mice. Xenografts were allowed to develop for 7 days in each mouse, and then 50 µl of 10 µm E626-0342 dissolved in 2 % DMSO in Hank's Balanced Salt Solution (HBSS) buffer (CaCl2 - 0.14 g/l, KCl - 0.4 g/l, KH2PO4 - 0.06 g/l, MgCl2*6H2O - 0.1 g/l, MgSO4*7H2O - 0.1 g/l, NaCl - 8 g/l, NaHCO3 - 0.35 g/l, Na2HPO4*7H2O - 0.09 g/l and D-Glucose - 1 g/l) were injected every other day into the tumor of each of 12 mice. A 2 % DMSO solution in HBSS was injected to the tumor of each of 15 mice that served as a control group. Tumor sizes were measured twice a week and the differences in the size of each tumor were determined. The average difference in tumor size in each of the two groups was plotted after determining standard error. In Figure 11 it can be seen that E626-0342 significantly attenuated the progression of the HT29 xenografts.


Claims

1. A pharmaceutical composition comprising as an active component a compound of formula :

and a physiological acceptable carrier.
 
2. Use of a compound of formula:

for the preparation of a medicament for the treatment of cancer.
 
3. Compound of formula:

for use in the treatment of cancer.
 


Ansprüche

1. Eine pharmazeutische Zusammensetzung, umfassend als eine aktive Komponente eine Verbindung der Formel:

und einen physiologisch annehmbaren Träger.
 
2. Verwendung einer Verbindung der Formel:

zur Herstellung eines Medikaments zur Behandlung von Krebs.
 
3. Verbindung der Formel:

zur Verwendung in der Behandlung von Krebs.
 


Revendications

1. Composition pharmaceutique comprenant en tant que composant actif un composé de formule :

et un véhicule physiologiquement acceptable.
 
2. Utilisation d'un composé de formule :

pour la préparation d'un médicament pour le traitement du cancer.
 
3. Composé de formule:

pour son utilisation pour le traitement du cancer.
 




Drawing





























Cited references

REFERENCES CITED IN THE DESCRIPTION



This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

Patent documents cited in the description




Non-patent literature cited in the description