Fatty amine drug conjugates

Inactive Publication Date: 2008-06-26
LUITPOLD PHARMA INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009]The invention relates to the surprising discovery that fatty amines can be conjugated to pharmaceutical agents for treatment of a variety of disorders, including but not limited to cancer, viral infections, and psychiatric diseases. The benefits of these pharmaceutical-fatty amine conjugates include one or more of the following: targeting of the drug to the tissue of interest; favorably affecting the volume of distribution of the drug in the tissue of interest; reducing toxicity of the drug; reducing side effects of the drug; reducing clearance of the drug; reducing the necessary volume and / or frequency of administration of the drug, or increasing the amount of drug that a subject can tolerate by favorably affecting volume of distribution, tissue distribution, and / or release kinetics of active drug from an inactive conjugate in certain embodiments. Another surprising aspect of the fatty amine-pharmaceutical agent conjugates is that once the fatty amines are separated from conjugation to the pharmaceutical agents in vivo, the fatty amines may be metabolized and eliminated.
[0010]Any and all of these aforementioned characteristics of the fatty amine-pharmaceutical agent conjugates may benefit subjects in need of treatment for diseases such as cancer, psychiatric disorders, and viral diseases and may allow altered dosages of drugs to be administered less frequently, with better results and fewer side effects.
[0108]The conjugated anticancer compounds described herein are less toxic and more effective than the corresponding unconjugated anticancer compounds. Therefore the fatty amine-anticancer compound conjugates can be administered in amounts which are equally toxic but more effective, or in doses which are equally effective and less toxic than the corresponding unconjugated anticancer compounds. In general, conjugation of fatty amine to anticancer compounds permits an increase in the maximum tolerated dose relative to unconjugated anticancer compounds.

Problems solved by technology

This is particularly the case for toxic agents such as anticancer agents because achieving therapeutic doses effective for treating the cancer is often limited by the toxic side effects of the anticancer agent on normal, healthy tissue.
This increase in potency, however, was not observed when the same lipid derivatives of adenosine receptor antagonists were used, and generalizations thus were not made possible by those studies.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Examples of Paclitaxel Conjugates

[0173]The length of the fatty moiety chain is governed by the synthetic procedure. For example, preparation of the fatty amine from the corresponding fatty acid (with an even number of carbons) generally results in a carbon chain with an odd number of carbons. Alternatively, preparation of the fatty amine from the corresponding fatty alcohol (with an even number of carbons) generally results in a carbon chain with an even number of carbons. The following paclitaxel-fatty amine conjugates with an even number and odd number of carbons in the fatty moiety, respectively, are prepared in accordance with the methods of the invention:

example 2

Preparation of N-Methyl Fatty Amine Conjugates

[0174]The conjugates may be prepared with N-methyl group at the amino moiety of the fatty amine as shown below:

to prevent internal self-immolative destruction. N-methylated fatty amines may be prepared from fatty acids using the procedures described in the Examples and described generally (in Yamada, F., et al. Heterocycles 1986, 24, 1223 and Somei, M., et al. Heterocycles 1987, 26, 895, both hereby incorporated by reference).

example 3

Synthesis of a Fatty Amine-Adefovir Conjugate Via a Urea Linkage

[0175]Adefovir (PMEA) was conjugated to a fatty amine using the following procedures:

wherein Y is methyl or ethyl, (PhO)2P(O)N3 is diphenylphosphoryl azide, and TMSBr is bromotrimethylsilane. One skilled in the art will appreciate that the number of carbons in the fatty amine moiety of the conjugate is governed by both the starting material and synthetic method chosen.

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Abstract

The invention provides conjugates of fatty amines and pharmaceutical agents useful in treating cancer, viruses, psychiatric disorders. Compositions, pharmaceutical preparations, and methods of preparations of the fatty amine-pharmaceutical agent conjugates are provided.

Description

RELATED APPLICATIONS[0001]This application is a divisional application of U.S. non-provisional application Ser. No. 10 / 108,255, filed Mar. 25, 2002, currently pending, which claims benefit under 35 U.S.C. § 119(e) of U.S. provisional Patent Application No. 60 / 278,552, filed Mar. 23, 2001, the entire contents of both of which are herein incorporated by reference.FIELD OF THE INVENTION[0002]The invention relates to conjugates of fatty amines and pharmaceutical agents such as anticancer, antiviral, and antipsychotic agents useful, for example, in treating cancer, viruses, and psychiatric disorders, and compositions and formulations thereof. Methods for making and using the conjugates also are provided.BACKGROUND OF THE INVENTION[0003]Improving drug selectivity for target tissue is an established goal in the medical arts. In general, it is desirable to deliver a drug selectively to its target, so that dosage and, consequently, side effects can be reduced. This is particularly the case f...

Claims

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Application Information

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IPC IPC(8): A61K31/337C07C271/06C07D493/22A61P35/00A61K31/27A61K31/131A61K31/26A61K31/351A61K31/453A61K31/475A61K31/506A61K31/52A61K31/5513A61K31/664A61K31/7048A61K31/7068A61P1/00A61P1/10A61P1/16A61P3/06A61P3/10A61P5/14A61P7/00A61P7/02A61P9/00A61P9/04A61P13/12A61P15/08A61P15/18A61P17/06A61P17/16A61P25/18A61P25/28A61P31/12A61P35/02A61P43/00C07C265/06C07C271/12C07C275/20C07D209/48C07D243/38C07D305/14C07D309/14C07D405/04C07D473/16C07D473/24C07D491/22C07D519/04C07F9/645C07F9/6524C07F9/6558C07F9/6561C07H15/252C07H17/04C07H19/06
CPCC07C265/06C07C271/12C07C275/20C07D209/48C07D243/38C07D305/14C07H19/06C07D473/24C07D519/04C07F9/65583C07F9/65616C07H15/252C07D405/04A61P1/00A61P1/10A61P1/16A61P13/12A61P15/08A61P15/18A61P17/06A61P17/16A61P25/18A61P25/28A61P31/12A61P35/00A61P35/02A61P3/06A61P43/00A61P5/14A61P7/00A61P7/02A61P9/00A61P9/04A61P3/10
Inventor SWINDELL, CHARLES S.FEGLEY, GLENN G.
Owner LUITPOLD PHARMA INC
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