Seco-baccatin III derivatives of formula:
##STR00001##
wherein R, R1-R4, R1 R′, R11 R″, and R111 R′″ are disclosed herein; pharmaceutical compositions comprising seco-baccatin III derivative; and methods for treating cancer, arthritis, and inhibiting angiogenesis in an animal comprising administrating to a patient in need thereof a therapeutically effective amount of a seco-baccatin III derivative are disclosed.
|
1. A compound of formula:
##STR00003##
wherein R and R1 are each independently hydrogen, a C1-C18 acyl group, an aroyl group which may be substituted or unsubstituted, or —CONR6R7;
R2 is hydrogen or R2 forms a carbonate or thiocarbonate with R3;
R3 is hydrogen, hydrogen or —OH, or R3 forms a carbonate or thiocarbonate with R2;
R4 is a benzoyl group which is unsubstituted or substituted at the meta position or a hetaroyl group;
R6 and R7 are a C1-C4 alkyl group, a benzyl group, or a phenyl group;
R1 R′ is hydrogen or a C1-C4 alkyl group;
R11 R″ is a C1-C4 alkyl group, a C2-C6 alkenyl group, an aryl group, or a hetaryl group; and
R111 R′″ is a C1-C4 alkyl group, a C1-C18 acyl group, an aryl group, or a tert-butoxy group, with the proviso that both R and R1 cannot be hydrogen.
2. The compound of
R2 is hydrogen;
R3 is hydrogen;
R4 is benzoyl;
R1 R′ is hydrogen or methyl;
R11 R″ is a C1-C4 alkyl group or a C2-C6 alkenyl group; and
R111 R′″ is a tert-butoxy group.
5. The compound of
6. The compound of
R1 is a C1-C18 acyl group, an aroyl group which may be substituted or unsubstituted, or —CONR6R7;
R2 and R3 are hydrogen;
R4 is benzoyl;
R1 R′ is hydrogen or methyl;
R11 R″ is a C1-C4 alkyl group, a C2-C6 alkenyl group; and
R111 R′″ is a tert-butoxy group.
7. The compound of
13-[(2R, 3S)-3-iso-butyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehyrdo-10-deacetyl-7,9-bis-acetyl-baccatine III
13-[(2R, 3S)-3-iso-butyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III;
13-[(2R, 3S)-3-phenyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehyrdo-10-deacetyl-7,9-bis-acetyl-baccatine III
13-[(2R, 3S)-3-phenyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III;
13-[(2R, 3S)-3-phenyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehyrdo-10-deacetyl-7,9-bis-trimethoxybenzoyl-baccatine III
13-[(2R, 3S)-3-phenyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehydro-10-deacetyl-7,9-bis-trimethoxybenzoyl-baccatine III;
13-[(2R, 3S)-3-phenyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehyrdo-10-deacetyl-7,9-bis-acetyl-baccatine III 1,14-carbonate
13-[(2R, 3S)-3-phenyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III 1,14-carbonate.
8. A pharmaceutical composition comprising the compound of
9. A pharmaceutical composition comprising the compound of
10. A pharmaceutical composition comprising the compound of
11. A pharmaceutical composition comprising the compound of
12. A pharmaceutical composition comprising the compound of
13. A pharmaceutical composition comprising the compound of
14. A pharmaceutical composition comprising the compound of
15. A method of treating cancer comprising administering to a patient in need thereof a therapeutically effective amount of the compound of
16. The method of
17. The method of
18. A method of treating rheumatoid arthritis comprising administering to a patient in need thereof a therapeutically effective amount of the compound of
19. The method of
20. A method of inhibiting angiogenesis comprising administering to a patient in need there of a therapeutically effective amount of the compound of
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
This application is a continuation of PCT/EP01/00386 dated Jan. 15, 2001.
The present invention relates to seco-baccatin III derivatives.
Taxane-skeleton diterpenes, in particular Pacliataxel and Docetaxel, are at present used in medicine for the treatment of tumors of different origin.
However, the presently available taxane derivatives have remarkable side effects and also quickly induce resistance, analogously to other antitumor drugs.
The present invention relates to derivatives of seco-baccatine III, which is disclosed in U.S. Pat. No. 5,756,776, characterized by bioavailability through the oral route, reduced toxicity and extremely high antiangiogentic activity.
The compounds of the present invention have the following general formula (I)
##STR00002##
wherein
R3 is hydrogen, —OR5 group, wherein R5 is hydrogen, or it forms with R2 a carbonate or thiocarbonate residue;
R4 is a benzoyl group optionally substituted at the meta-position, or hetaroyl group;
R1 R′ is hydrogen or a C1-C4 alkyl group;
R11 R″ is a C1-C4 alkyl, a C2-C6 alkenyl, aryl or hetaryl;
R111 R′″ is a C1-C4 alkyl, C1-C18 acyl, aryl group or tert-butoxy group, with the proviso that R and R1 cannot be both hydrogen.
A C1-C18 acyl group is preferably a formyl, acetyl, n-propanoyl, n-hexanoyl group.
An optionally substituted aroyl group is preferably benzoyl, optionally substituted with one or three substituents selected from halogen atoms or C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano, nitro groups.
A meta-substituted benzoyl group is preferably a 3-halo-benzyl or 3-methoxybenzoyl group.
A hetaroyl group is preferably a 5- or 6-membered heteroaryl having one or two oxygen, nitrogen or sulfur atoms in the ring and substituted with a carbonyl group, for example 2- or 3-thenoyl, nicotinoyl, 2- or 3-furoyl.
Aryl is preferably phenyl and hetaryl is preferably 2- or 3-furyl, 2- or 3-thienyl, 2- 3- or 4-pyridyl.
A preferred group of compounds of formula (I) is that in which:
R2 is hydrogen;
R3 is hydrogen;
R4 is benzoyl;
R′ is hydrogen or methyl;
R′″ is a tert-butoxy group.
A further group of preferred compounds is the one in which R is hydrogen and R1 is an acyl, aroyl or CONR6R7 group as defined above, R2 and R3 are hydrogen, R4 is benzoyl, R1 is hydrogen or methyl, R″ is C1-C4 alkyl or C2-C6 alkenyl and R′″ is tert-butoxy.
The esterification of the hydroxyls at C-7 and C-9 induces, compared with known compounds, an increase in the cytotoxic activity on the resistant cell lines as well as improved absorption through the oral route. The compounds of the invention are less potent than Paclitaxel, taken as the reference drug, in binding with tubulin, while keeping comparable cytotoxicity on the sensitive cancer lines. These compounds mainly differ from those of prior art in the antiangiogenetic activity. Table shows the in vivo activity of some C-seco-10-dehydro-10-deacetyl-7,9-bisacetyl-baccatine III and C-seco-10-dehydro-10-deacetyl-7,9-bisacetyl-1,14-carbonate-baccatine III derivatives having the same isoserine chain.
The antiangiogenic activity was evaluated by means of the Matrigel test, in which angiogenesis is induced by FGF-2 (150 mg/pellet) adsorbed on a Matrigel pellet (12.5 mg/ml, 0.5 mL) injected subcutaneously in C57BL6N mice.
The tested compound was administered through the oral route daily or through the intraperitoneal route on alternate days, at the shown concentration. After 7 days, the angiogenic response was evaluated by measuring the hemoglobin content in the pellets, according to the procedure by Drabkin.
TABLE
In vivo antiangiogenetic activity of the compound of example II.
Compound
Hemoglobin g/dl
%
Control
0.01 ± 0.001
—
FGF-2
0.03 ± 0.001
+300
Example II
90 mg/kg i.p.
0.015 ± 0.001
−50
150 mg/kg p.o.
0.009 ± 0.001
−70
Example VII
50 mg/kg i.p.
0.014
−40
100 mg/kg p.o.
0.009
−70
The compounds of the invention are prepared by reacting C-seco-10-dehydro-10-deacetyl-7,9-hydroxy baccatine III described in U.S. Pat. No. 5,756,776 with a carboxylic acid reactive derivative (chloride or anhydride), according to known acylation methods.
The C7 and C9 diesters can be prepared by using at least two equivalents of the reactive derivative. The carbamate groups can be introduced with conventional methods, for example by reaction with phosgene and an amine of formula R6R7NH.
The resulting compounds are then reacted, according to known procedures, with an isoserine derivative, usually an oxazolidine derivative, which, by acid treatment under mild conditions gives compounds (I).
The compounds of the invention are characterized by low systemic toxicity: at doses effective in inhibiting the tumor growth they induce neither weight loss nor evident neuro-toxicity; in the nude mouse transplanted with human tumor cells, a dose of Paclitaxel, used as the reference drug, exerting the same antitumor activity, also induces tremors and weight loss up to 20%.
The compounds of the present invention, thanks to their high water solubility, can be easily formulated in injectable preparations.
Compounds (I) can also be formulated in the form of conventional oral compositions (capsules or tablets).
Thanks to their low toxicity, compounds (I) can be administered intravenously at dosages up to 600 mg/m2 and orally at dosages up to 1000 mg/m2. Dosages can be decreased to 50 mg/m2 in the treatment of rheumatoid arthritis.
The following examples further illustrate the invention without limiting its scope.
A solution of 300 mg of 10-dehydro-10-deacetylbaccatine III in 5 ml of methanol is added with 1 equiv. of CeCl3.3H2O and the reaction mixture is stirred for 10 min. After complete dissolution, 80 mg of NaBH4 are added in small portions. After 10 min the solution is treated with an equal volume of a NH4Cl aqueous solution and extracted with CH2Cl2. The chlorinated solvent is removed, the residue is taken up in 1 ml of pyridine, cooled to 0° C. in 1 h, then added with 150 mg of acetic anhydride. The solution is left to stand for 2 h at 0° C., then diluted with 10 ml of water and back-extracted with CH2Cl2. The chlorinated solvent is distilled off under vacuum and the residue is chromatographed on silica gel eluting with a mixture of n-hexane/ethyl acetate to obtain 260 mg of C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III (m/z 630).
630 mg of C-sero-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III are dissolved in 5 ml of toluene and added with 335 mg of dicyclohexylcarbodiimide (DCC), 500 mg of (4S,5R)-N-Boc-2-(2,4-dimethoxyphenyl)-4isobutyl-5-oxazolidine-carboxylic acid and 20 mg of 4-dimethylaminopyridine. The solution is heated at 60° C. for 24 h, then treated with ethyl acetate and a NaHCO3 saturated solution. The organic phase is dried and filtered through silica gel to remove urea. The solvent is evaporated to dryness under vacuum and the residue is taken up in methanol/hydrochloric acid, keeping a temperature of 0° C. for 1 h. The solution is neutralized to pH 5, then diluted with water and the desired compound is back-extracted with CH2Cl2. The solvent is evaporated off to obtain 700 mg of 13-[(2R, 3S)-3-iso-butyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco 10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III.
630 mg of C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III are dissolved in 5 ml of toluene and added with 335 mg of DCC, 525 mg of (4S,5R)-N-Boc-2-(2,4-dimethoxyphenyl)4-isobutyl-5-oxazolidine-carboxylic acid and 20 mg of 4dimethylaminopyridine. The solution is heated at 60° C. for 24 h, then treated with ethyl acetate and a NaHCO3 saturated solution. The organic phase is dried and filtered through silica gel to remove urea. The solvent is evaporated to dryness under vacuum and the residue is taken up in methanol/hydrochloric acid, keeping a temperature of 0° C. for 1 h. The solution is neutralized to pH 5, then diluted with water and the desired compound is back-extracted with CH2Cl2. The solvent is evaporated off to obtain 700 mg of 13-[(2R, 3S)-3-iso-butyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III, which is crystallized from ethyl acetate to yield 645 mg of pure compound.
A solution of 546 mg of C-seco-10-dehydro-10-deacetyl-baccatine III in 3 ml of pyridine is added with 575 mg of trimethoxybenzoyl chloride in small portions. After 3 h the solution is poured into 30 ml of water and extracted with CH2Cl2; the organic phase is washed with acids until pyridine is completely removed. The solvent is evaporated off to obtain 905 mg of C-seco-10-dehydro-10-deacetyl-7,9-bis-trimethoxybenzoyl-baccatine III. (m/z 936).
930 mg of 13-[(2R, 3S)]-C-seco-10-dehydro-10-deacetyl-7,9-bis-trimethoxy-benzoyl-baccatine III are dissolved in 15 ml of toluene and added with 335 mg of DCC, 525 mg of (4S, 5R)-N-boc-2-(2,4-dimethoxyphenyl)4isobutyl-5-oxazolidinecarboxylic acid and 20 mg of 4-dimethylaminopyridine. The solution is heated at 60° C. for 24 h, then treated with ethyl acetate and a NaHCO3 saturated solution. The organic phase is dried and filtered through silica gel to remove urea. The solvent is evaporated to dryness under vacuum and the residue is taken up in methanol/hydrochloric acid, keeping a temperature of 0° C. for 1 h. The solution is neutralized to pH 5, then diluted with water and the desired compound is back-extracted with CH2Cl2. The solvent is evaporated off to obtain 940 mg of 13-(2R, 3S)-3-isobutyl-2-hydroxy-3-tert-butoxycarbonylamino-propanoyl]-C-seco-10-dehydro-10-deacetyl-7,9-bis-trimethoxybenzoyl-baccatine III, which is crystallized from ethyl acetate to yield 878 mg of pure compound.
1 g of 10-deacetyl-14β-hydroxybaccatine III 1,14 carbonate, prepared as disclosed in U.S. Pat. No. 5,698,712, are dissolved in methanol and treated with 6 g of Cu(OAc)2 and the reaction mixture is stirred for 120 hrs. The salt is filtered off, the solvent is removed and the residue is chromatographed on silica gel column, eluting with a 6:4 mixture of hexane/ethyl acetate, to obtain 0.9 g of 10-dehydro-10-deactyl-14,β-hydroxy-baccatine III 1,14carbonate (M+568). 300 mg of this compound are dissolved in methanol and treated with 1 equiv. of CeCl3.3H2O and the reaction mixture is stirred for 10 min. After complete dissolution, 80 mg of NaBH4 are added in small portions. After 10 min the solution is treated with an equal volume of a NH4Cl aqueous solution and extracted with CH2Cl2. The chlorinated solvent is removed, the residue is taken up in 1 ml of pyridine, cooled to 0° C. in 1 h, then added with 150 mg of acetic anhydride under stirring. The solution is left to stand for 2 h at 0° C., then diluted with 10 ml of water and back-extracted with CH2Cl2. The chlorinated solvent is distilled off under vacuum and the residue is chromatographed on silica gel eluting with a mixture of n-hexane/ethyl acetate to obtain 250 mg of C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III 1,14-carbonate (m/z 658).
600 mg of C-seco-10-dehydro-10-deacetyl-7,9-bis-acetyl-baccatine III 1,14-carbonate are treated as described in Example II, to obtain 680 mg of the title compound.
Bombardelli, Ezio, Pontiroli, Alessandro
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 5756776, | Jul 26 1994 | Indena S.p.A. | Semi-synthetic taxanes with anti-tumoural activity |
| WO9603394, |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Jun 20 2005 | Indena S.p.A. | (assignment on the face of the patent) | / |
| Date | Maintenance Fee Events |
| Dec 28 2010 | M1552: Payment of Maintenance Fee, 8th Year, Large Entity. |
| Jan 03 2015 | M1553: Payment of Maintenance Fee, 12th Year, Large Entity. |
| Date | Maintenance Schedule |
| Jul 10 2010 | 4 years fee payment window open |
| Jan 10 2011 | 6 months grace period start (w surcharge) |
| Jul 10 2011 | patent expiry (for year 4) |
| Jul 10 2013 | 2 years to revive unintentionally abandoned end. (for year 4) |
| Jul 10 2014 | 8 years fee payment window open |
| Jan 10 2015 | 6 months grace period start (w surcharge) |
| Jul 10 2015 | patent expiry (for year 8) |
| Jul 10 2017 | 2 years to revive unintentionally abandoned end. (for year 8) |
| Jul 10 2018 | 12 years fee payment window open |
| Jan 10 2019 | 6 months grace period start (w surcharge) |
| Jul 10 2019 | patent expiry (for year 12) |
| Jul 10 2021 | 2 years to revive unintentionally abandoned end. (for year 12) |