HK1033651B - Semi-synthetic ecteinascidins - Google Patents

Description

BACKGROUND OF THE INVENTION

The ecteinascidins (herein abbreviated Et or Et's) are exceedingly potent antitumor agents isolated from the marine tunicate Ecteinascidia turbinara. In particular, Et's 729.743 and 722 have demonstrated promising: efficacy in vivo, including activity against P388 murine leukemia, B16 melanoma, Lewis lung carcinoma, and several human tumor xenograft models in mice. The antitumor activities of Et 729 and Et 743 have been evaluated by the NCl and recent experiments have shown that Et 729 gave 8 of 10 survivors 60 days following infection with B16 melanoma. In view of these impressive results, the search for additional ecteinascidin compounds continues.

SUMMARY OF THE INVENTION

The present invention is directed to two new ecteinascidin compounds, prepared semi-synthetically, i.e., using previously discovered ecteinascidin compounds as the starting materials therefor. The structures of the new Et's of the present invention are as shown below:

The new ecteinascidin compounds shown above have been found to possess similar antitumor activity profiles as the known ecteinascidin compounds, and as such they will be useful as therapeutic compounds, e.g.. for the treatment of mammalian tumors including melanoma, and lung carcinoma. The dosages and routes of administration will vary according to the needs of the patient and the specific activity of the active ingredient. The determination of these parameters is within the ordinary skill of the practicing physician.

BRIEF DESCRIPTION OF THE DRAWINGS

• Figures 1A and I B show the LRFAB Mass Spectrum of Et 757 in Magic Bullet (MB). See. Rinehart et al., Biochem. Biophys. Res. Commun, 1984. 124,350.
• Figures 2A and 2B show the tandem FABMS/MS spectrum of Et 757 in MB.
• Figure 3 shows the 'H NMR (500 MHz) spectrum of Et 737 in CD3OD.
• Figures 4A and 4B show the LRFAB Mass Spectrum of Boc-Ec 729 in MB.
• Figures 5A and 5B show the tandem FABMS/MS spectrum of Boc-Et 729 in MB.
• Figure 6 shows the LRFAB Mass Spectrum of Iso-Et 743 in MB.
• Figures 7A and 7B show the tandem FABMS/MS spectrum of Iso-Et 743 in MB.
• Figure 8 shows the 1H NMR (500 MHz) spectrum of lso-Et 743 in CD3OD.
• Figure 9 shows expansion of the HMBC (750 MHz) spectrum of Iso-Et 743 in CD3OD.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As described above, a number of bioactive ecteinascidin compounds have been isolated from specimens of Ecteinascidia turbinata. See for example Ecteinascidins 729, 743, 745, 759A, 759B and 770, disclosed in U.S.Patent Nos. 5,089,273 and 5,256,663 , the disclosures of which are hereby incorporated herein by reference. See also, Ecteinascidins 736 and 722, disclosed in U.S. Patent No. 5,149,804 , which is hereby incorporated herein by reference. See also, U.S. Patent Nos. 5,478,932 and 5,654,426 , which are hereby incorporated herein by reference.

The present invention will be further illustrated with reference to the following examples which aid in the understanding of the present invention, but which are not to be construed as limitations thereof. All percentages reported herein, unless otherwise specified, are percent by weight. All temperatures are expressed in degrees Celsius.

Example 1- Semi-synthesis of Et 757

To a solution of Et 729 (9.2 mg. 0.012 mmol, 1 eq), diisopropylamine (12.9 µL, 0.074 mmol, 6 eq) and CH₃CN (300 µL) was added CH₃l (1.5 µL, 0.024 mmol, 2 eq) and the resulting solution was stirred at 60°C for 24 hours. The reaction mixture was concentrated to dryness under a nitrogen stream. The residue was purified by reversed phase HPLC (Phenomenex/Ultracarb-ODS, 2 mL/min) using 75% MeOH/H₂O containing 0.02 M NaCl as mobile phase to yield Et 757 (2.2 mg, 24%) and Et 743 (2.3 mg, 25%) and a complex mixture of permethylated products. Et 757 was further purified by HPLC (Ultracarb-ODS) using 60% MeOH/H₂O with 0.02 M NaCl as mobile phase to afford pure Et 757 (1.4 mg, 15%). HRFABMS, Calcd for C₄₀H₄₄N₃O₁₀S [M + H - H₂O]⁺ m/z 758.2747, Found 758.2765, see Figs. 1 and 2; ¹H NMR, see Fig. 3.

Example 2 - Semi-synthesis of Iso-Et 743

Step A - Boc-Et 729

To a solution of Et 729 (12.5 mg, 0.017 mmol, 1 eq), diisopropylethylamine (1.5 µL, 0.07 mmol, 4 eq) and CH₃CN (300 µL) was added di-tert-butyl dicarbonate (3.6 mg, 0.017 mmol, 1.0 eq) and the resulting solution was stirrred at room temperature for 9 hours. The reaction mixture was concentrated to dryness under a nitrogen stream. The residue was purified by flash chromatography (gradient elution: 100% CHCl₃ ----> 90% CHCl₃/MeOH) to aford Boc-Et 729 (11.6 mg, 91%, R_f 0.53 in 90% CHCl₃/MeOH); HRFABMS, Calcd for C₄₃H₄₈N₃O₁₂S [M + H]^- m/z 830.2958. Found 830.2942, see Figs. 4 and 5.

Step B - Iso-Et 743

To a reaction flask containing Boc-Et 729 (11.6 mg, 0.014 mmol, 1 eq), diisopropylethyl amine (7.1 µL, 0.041 mmol, 3 eq), 500 µL of CH₃CN and a magnetic stirrer was added CH₃l (2.1 mg, 0.015 mmol, 1.1 eq), and the resulting solution was stirred at 60°C for 24 hours. The reaction mixture was concentrated to dryness under a nitrogen stream, then 700 µL of TFA/CH₂CI/H2O (4:1:1) was added. After the mixture was stirred at room temperature for 30 minutes, it was concentrated to dryness under a nitrogen stream. The residue was purified by reversed phase HPLC (Alltech-C18, 2 mL/min) using 60% MeOH/H₂O containing 0.02 M NaCl as mobile phase to yield Iso-Et 743 (1.9 mg, 28%.based upon recovered Et 729) and unreacted Et 729 (3.6 mg). HRFABMS, Calcd for C₁₉H₁₂N₃O₁₀S [M+H- H₂O]^- m/z 744.2591, Found 744,2619. see Figs. 6 and 7; ¹H NMR and HMBC, see Figs. 8 and 9 respectively.

BIOLOGICAL ACTIVITIES

As described above, the ecteinascidins are highly functionalized bis- or tris-(tetrahydroisoquinoline) alkaloids that exhibit potent in vivo antitumor activity. These compounds have chiefly been isolated as natural products from the mangrove tunicate Ecreinascidia turbinata, which grows throughout the Caribbean and the Gulf of Mexico. The major product of most extractions. Et 743. is currently undergoing Phase I clinical trials for treatment of human solid tumors. See for example, Kuffel et al., Proceedings of the American Association for Cancer Research, 38: 596 (1997); Moore et al., Proceedings of the American Association for Cancer Research. 38; 314 (1997); Mirsalis et al., Proceedings of the American Association for Cancer Research. 38: 309 (1997), Reid et al.. Cancer Chemotherapy and Pharmacology, 38: 329-334 (1996); Faircloth et al.. European Journal of Cancer. 32A. Supp. 1, pp. S5 (1996); Garcia-Rocha et aL British Journal of Cancer, 73: 875-883 (1996) ; Eckhardt et al., Proceedings of the American Association for Cancer Research. 37: 409 (1996): and Hendriks et al., Proceedings of the American Association for Cancer Research, 37: 389 (1996).

In view of the exceptional antitumor properties of the natural ecteinascidins, the present invention has studied the antitumor activities of the semi-synthetic analogs prepared herein. Table I shows the in vitro cytotoxic activities of the new Et compounds compared to the activity of two natural products. Et 743 and Et 729:

Compound Name	Cytotoxicity to L1210 murine leukemia
Et 729	0.05	10
Et 743	0.5	1
Et 757	0.01	50
Iso-Et 743	0.03	17

As shown by the in vitro data presented in Table 1, the new compounds of the present invention possess cytotoxic activities levels up to 10 times better than those of two natural ecteinascidin compounds. Accordingly, it is expected that these compounds will also prove useful as pharmaceutical compositions for the treatment of mammalian, and particularly, human tumors in vivo.

REFERENCES

The following publications are cited as additional background information:

1. 1. Rinehart. K.L. et al. J. Not. Prod., 53: 771-791 (1990).
2. 2. Wright, A.E. et al.. J. Org. Chem. 55: 4508-4512 (1990).
3. 3. Sakai et al., Proc. Nat. Acad. Sci U.S.A., 89: 11456-11460 (1992).
4. 4. Rinehart et al, J. Org. Chem., 55: 4512-4515 (1990).

The present invention has been described in detail, including the preferred embodiments thereof.

Claims (6)

1. The compound Et 757, which has the following structure:
2. The compound Iso-Et 743, which has the following structure:
3. A pharmaceutical composition comprising the compound Et 757 and a pharmaceutically acceptable diluent, carrier or excipient.
4. A pharmaceutical composition comprising the compound Iso-Et 743 and a pharmaceutically acceptable diluent carrier, or excipient.
5. The use of Et 757 in the preparation of a medicament for a method of treating patient suffering from a mammalian tumor selected from the group consisting of mammalian leukemia, mammalian melanoma and mammalian lung carcinoma, comprising administering to said patient, an effective antitumor amount of carcinoma, comprising administering to said patient an effective antitumor amount of the substantially pure compound designated herein as Et 757 and a pharmaceutically acceptable carrier, diluent or excipient.
6. The use of Iso-Et 743 in the preparation of a medicament for a method of treating a patient suffering from a mammalian tumor selected from the goup consisting of mammalian leukemia, mammalian melanoma and mammalian lung carcinoma, comprising administering to said patient, an effective antitumor amount of the substantially pure compound designated herein as Iso-Et 743 and a pharmaceutically acceptable carrier, diluent or excipient.