Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ether doai
Reexamination Certificate
2000-08-07
2004-01-13
Keys, Rosalynd (Department: 1621)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ether doai
C514S721000, C436S064000, C435S156000, C568S646000
Reexamination Certificate
active
06677383
ABSTRACT:
The present invention concerns enzymatic aromatic hydroxylation-activated prodrugs. particularly anti-tumour prodrugs and those which are specifically activated by the hydroxylation activity of the enzyme CYP1B1.
Many conventional cytotoxic drugs are known which can be used for chemotherapeutic purposes. However. they typically suffer from the problem that they are generally cytotoxic and therefore may affect cells other than those which it is wished to destroy. This can be alleviated somewhat by using targetted drug delivery systems, for example direct injection to a site of tumourous tissue, or by e.g. binding the cytotoxic agent to antibody which specifically recognises an antigen displayed by cancerous cells. Alternatively, electromagnetic radiation may be used to cause chemical changes in an agent at a desired site in the body such that it becomes cytotoxic. However, all of these techniques have, to a greater or lesser extent, certain limitations and disadvantages.
It has been reported (Murray, G. I. et al., Jul. 15, 1997. Cancer Research, 57: 3026-3031) that the enzyme CYP1B1, a member of the cytochrome P450 family of xenobiotic metabolizing enzymes, is expressed at a high frequency in a range of human cancers including cancers of the breast, colon, lung, oesophagus, skin, lymph node, brain and testis, and that it is not detectable in normal tissues. This led to the conclusion (p. 3030, final sentence) that “ . . . the expression of CYP1B1 in tumour cells provides a molecular target for the development of new anticancer drugs that could be selectively activated by the presence of CYP1B1 in tumour cells”. No specific anticancer drugs are suggested.
The present inventors have now succeeded in creating a range of prodrugs which have little or negligible cytotoxic effect when in their normal state, but which are highly cytotoxic (i,e. have a substantially increased cytotoxicity) when hydroxylated by CYP1B1. This provides for a self-targetting drug delivery system in which a non-cytotoxic (or at leat negligibly cytotoxic) compound can be administered to a patient, for example in a systemic manner, the compound then being hydroxylated at the site of tumour cells (intratumoural hydroxylation) to form a highly cytotoxic compound which acts to kill the tumour cells. The fact that CYP1B1 is not expressed by normal cells means that the hydroxylation of the compound only occurs at the site of tumour cells and therefore only tumour cells are affected, thus providing a self-targetting drug delivery system.
The prodrugs of the present invention have the distinct advantage of being useful in the treatment of tumours at any site in the body, meaning that even tumours which have undergone metastasis (which are not normally susceptible to site-specific therapies) may be treated, as well of course as primary and secondary tumours.
According to the present invention there is provided a prodrug activated by enzymatic aromatic hydroxylation and having the formula (I):
wherein:
X=H, OH or OMe;
R
1
=H, C
1-4
lower alkyl, CN or Ar;
R
2
=H, CN, CONH
2
, CSNH
2
. COAr or Ar; and
Ar=phenyl, pyridyl or substituted aryl;
and:
R
3
=H or C
1-4
lower alkyl; and
R
4
=H, OH or OMe;
or:
R
3
,R
4
=(CH
2
)
n
, n=2, 3 or 4
The prodrug may be an anti-tumour prodrug. Examples of tumours include cancers (malignant neoplasms) as well as other neoplasms e.g. “innocent” tumours. The prodrug may be activated by hydroxylation by CYP1B1.
These prodrugs are styrene- or calchone-derivatives and their specific anti-tumour use is neither suggested nor disclosed by Murray, G. I. et al. (supra), nor is the fact that they are in fact prodrugs having an “activated” hydroxylated form. Where compounds of formula (I) have been previously identified and made, they have not been identified as anti-tumour agents due to their poor (or negligible) cytotoxicity. Thus the intratumoural hydroxylation of the prodrugs of the present invention provides them with a surprising and unexpected efficacy.
The styrene sub-structure of the compounds of formula (I) is essential in providing their efficacy. The Ar group may, for example, be a substituted aryl comprising 4-methoxyphenyl, 4-nitrophenyl, 3,5-dihydroxyphenyl or 3,4,5-trimethoxyphenyl, although other substituted aryls are, of course, also possible.
X may be hydroxy or methoxy.
As specified in formula (I) R
3
an R
4
may together form an alkyl chain having 2-4 carbon atoms, and thus may form part of a cycloalkyl group having 5,6 or 7 carbon atoms.
The prodrug may have the formula of any one of formulae (II)-(V):
wherein X=OMe or OH, and Y=NO
2
or OMe.
Alternatively, the prodrug may have the formula of either one of formulae (VI) or (VII):
Alternatively the prodrug may have the formula of any one of formulae (VIII)-(XII):
Hydroxylated forms of compounds (II)-(V) are potent tyrosine kinase inhibitors, and hydroxylated forms of compounds (VI) and (VII) are potent antimitotic agents. Previously, tyrosine kinase inhibitors have been of little chemotherapeutic benefit since the tyrosine kinase enzymes are ubiquitous in both normal and tumour cells and are thus not in themselves tumour-specific. However, the targetted production of tyrosine kinase inhibitor in tumour cells means that the inhibitory action will be specific to tumour cells. Furthermore, since the inhibitory activity will only be found in tumour cells, the tyrosine kinase inhibitor itself need not be isoform specific for a particular tyrosine kinase enzyme since any inhibition of tyrosine kinase activity will contribute to tumour inhibition and cell destruction.
Similarly, the antimitotic prodrugs of formulae (VI) and (VII) and (VIII)-(XII) are particularly useful since present antimitotic agents are of limited use due to the severe side-effects resulting from the poisoning of both normal and tumour cells. The present invention however allows for the specific in situ generation of the antimitotic agent at tumour cells, resulting in their specific targetting.
Methods of synthesis of the prodrugs of the present invention will be readily apparent to one skilled in the art, for example as exemplified below. The compounds of the invention may be prepared in a variety of different ways, for example by aldol condensation (Vogels Textbook of Practical Organic Chemistry, 4th Edition, p.146), by McMurry coupling (McMurry and Fleming, 1974, J. Am. Chem. Soc., 96: 4708-4709), or by the Wittig reaction (1973, Org. Synth. Coll., 5: 751).
Also provided according to the present invention is a prodrug according to the present invention for use in a method of treatment or diagnosis of the human or animal body, particularly the treatment or diagnosis of tumours.
Also provided according to the present invention is the use of a prodrug according to the present invention in the manufacture of a medicament for the treatment of tumours.
Also provided according to the present invention is a method of manufacture of a medicament, comprising the use of a prodrug according to the present invention. The medicament may be for the treatment of a tumour.
Also provided according to the present invention is a method of treatment or diagnosis of a tumour in a patient, comprising administering to the patient a prodrug according to the present invention.
Methods of manufacture of medicaments are well known. For example a medicament may additionally comprise a pharmaceutically acceptable carrier, diluant or excipient (Reminton's Pharmaceutical Sciences and US Pharmacopeia, 1984, Mack Publishing Company, Easton, Pa., USA).
The exact dose (i.e. a pharmaceutically acceptable dose) of prodrug to be administered to a patient may be readily determined by one skilled in the art, for example by the use of simple dose-response experiments.
Since the prodrugs of the present invention are specific to tumour cells, they may not only be used to treat tumours, but may also be used to determine whether or not a patient (or a sample taken from a patient) has tumour cells. For example, cell numbers in a
Burke Michael Danny
Butler Paul Crispin
Patterson Lawrence Hylton
Potter Gerard Andrew
Baker & Botts L.L.P.
De Montfort University
Keys Rosalynd
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