Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
  • C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
  • C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
  • C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
  • C07C237/30—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to hydrogen atoms or to acyclic carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
  • C07C309/63—Esters of sulfonic acids
  • C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
  • C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
  • C07C309/66—Methanesulfonates
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
  • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
  • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
  • C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
  • C07C311/39—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
  • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
  • C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
  • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
  • C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
  • C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D317/28—Radicals substituted by nitrogen atoms

Definitions

• the present invention relates to the preparation of nitroaniline-based unsymmetrical mustards, and their use as prodrugs for GDEPT (gene-dependent enzyme-prodrug therapy) and cell ablation therapy in conjunction with nitroreductase enzymes, as hypoxia-selective cytotoxins, and as anticancer agents.
• GDEPT gene-dependent enzyme-prodrug therapy
• cell ablation therapy in conjunction with nitroreductase enzymes, as hypoxia-selective cytotoxins, and as anticancer agents.
• tumour-selective prodrugs reactively inactive compounds that can be selectively converted to more active compounds in vivo
• a prodrug may be converted into an anti-tumour agent under the influence of an enzyme that is linkable to a monoclonal antibody that will bind to a tumour associated antigen.
• an enzyme that is linkable to a monoclonal antibody that will bind to a tumour associated antigen.
• the combination of such a prodrug with such an enzyme monoclonal/antibody conjugate represents a very powerful clinical agent.
• This approach to cancer therapy often referred to as "antibody directed enzyme/prodrug therapy” (ADEPT)
• ADPT antibody directed enzyme/prodrug therapy
• NDEPT virus-directed enzyme prodrug therapy
• Tumour cells are targeted with a viral vector carrying a gene encoding an enzyme capable of activating a prodrug.
• the gene may be transcriptionally regulated by tissue specific promoter or enhancer sequences.
• the viral vector enters tumour cells and expresses the enzyme, in order that a prodrug is converted to an active drug within the tumour cells (Huber et al., Proc. Natl. Acad. Sci. USA (1991) 88, 8039).
• non- viral methods for the delivery of genes have been used.
• GDEPT gene-directed enzyme prodrug therapy
• 4-Nitroaromatic compounds are reduced by both mammalian and bacterial flavoprotein enzymes, which effect stepwise addition of up to six electrons.
• the major enzymic metabolite is usually the 4-electron species (hydroxylamine).
• the present invention relates to novel nitroaniline-based unsymmetrical mustards having cytotoxic activity, to methods of preparing the novel compounds, and to the use of these compounds as prodrugs for GDEPT and for cell ablation therapy in conjunction with nitroreductase enzymes (particularly the nitro reductases encoded by the nfsB gene of E. coli or by Clostridia species), as hypoxia-selective cytotoxins, and as anticancer agents.
• GDEPT gene-dependent enzyme-prodrug therapy
• cell ablation therapy in conjunction with nitroreductase enzymes, as hypoxia-selective cytotoxins, and as anticancer agents or to at least provide the public with a useful alternative.
• the present invention provides a nitroaniline-based unsymmetrical mustard represented by the general formula (I);
• X represents one of the groups NO 2 , CN, or SO ⁇ 1 , where R 1 represents a C ⁇ . 6 - lower alkyl optionally substituted with one or more hydroxy and/or one or more amino groups and wherein when R 1 represents a tertiary amine the N-oxide derivative of the tertiary amine is further included;
• Y represents one of the groups OR 2 , NHCOR 2 , CONR 2 CO 2 R 3 , CONR 2 morpholide,
• a and B each independently represent halogen, OSO 2 R 4 , OSO 2 NH 2 , OSO 2 NHR 4 or
• each R 4 and R 5 independently represent a C ⁇ . 6 -lower alkyl optionally substituted with one or more hydroxy and/or one or more amino groups and wherein when each R 4 and R 5 independently represents a tertiary amine the N-oxide derivative of the tertiary amine is further included; and pharmaceutically acceptable derivatives and salts thereof; with the proviso
• nitroaniline-based unsymmetrical mustard is selected from a compound represented by one of formulae (Ila-IIc)
• nitroaniline-based unsymmetrical mustard is selected f om a compound represented by one of formulae (TRa-JJlc)
• X represents one of the groups NO 2 , CN, or SO 2 R 1 , where R 1 represents a C ⁇ - 6 - lower alkyl optionally substituted with one or more hydroxy and/or one or more amino groups and wherein when R 1 represents a tertiary amine the N-oxide derivative of the tertiary amine is further included;
• Y represents one of the groups OR 2 , NHCOR 2 , CONR 2 CO 2 R 3 , CONR 2 morpholide, CONHR 2 , CONR 2 R 3 .
• the polar solvent is selected from acetonitrile, dimethylformamide, ethyl acetate, triethylamine, acetone and mixtures thereof.
• the alkah metal halide is selected from one or more of the following; LiCl, LiBr, Nal and NaBr.
• the present invention provides a method for the use as prodrugs suitable for GDEPT (gene-dependent enzyme-prodrug therapy) in conjunction with at least one nitroreductase enzyme, as hypoxia-selective cytotoxins, including the step of administering a compound ofFormula I as defined above or a compound of Formulae la-Ic, Ila - lie and Illa-c as defined above or a mixture thereof in a "therapeutically effective amount" to tumour cells in a subject.
• GDEPT gene-dependent enzyme-prodrug therapy
• the nitroreductase enzyme is encoded for by the nfsB gene of either E. Coli or by Clostridia species.
• the present invention provides a method for the use as prodrugs suitable for GD ⁇ PT (gene-dependent enzyme-prodrug therapy) in conjunction with at least one nitroreductase enzyme, as an anticancer agent including the step of administering a compound ofFormula I as defined above or a compound of Formulae la-Ic, Ila - lie and Illa-c as defined above or a mixture thereof in a "therapeutically effective amount" to target tumour cells in a subject.
• GD ⁇ PT gene-dependent enzyme-prodrug therapy
• nitroreductase enzyme is encoded for by the nfsB gene of either E. Coli or by Clostridia species.
• a method of cell ablation therapy utilising at least one nitroreductase enzyme includes the step of administering a compound of Formula I as defined above or a compound of Formulae la-Ic, Ila - He and Illa-c as defined above or a mixture thereof in a "therapeutically effective amount" to ablate tumour cells in tissue in a subject, wherein said tissue expresses the at least one nitroreductase enzyme.
• nitroreductase enzyme is encoded for by the nfsB gene of either E. Coli or by Clostridia species.
• the cell ablation therapy provides a substantially minimal bystander effect.
• a pharmaceutical " composition including a therapeutically effective amount of a compound of formula I or a compound of formulae Ia-c, Ila-c, Illa-c or a mixture thereof, and a pharmaceutically acceptable excipient, adjuvant, carrier, buffer or stabiliser.
• the pharmaceutically acceptable excipient, adjuvant, carrier, buffer or stabiliser should preferably be non-toxic and should not interfere with the efficacy of the active ingredient.
• the precise nature of the carrier or other material will depend on the route of administration, which may be oral, or by injection, such as cutaneous, subcutaneous, or intravenous. It is to be appreciated that these factors could be readily determined by someone skilled in the art without undue experimentation.
• compositions for oral administration may be in tablet, capsule, powder or liquid form.
• a tablet may comprise a solid carrier or an adjuvent.
• Liquid pharmaceutical compositions generally comprise a liquid carrier such as water, petroleum, animal or vegetable oils, mineral oil or synthetic oil. Physiological saline solution, dextrose or other saccharide solution or glycols such as ethylene glycol, propylene glycol or polyethylene glycol may be included.
• a capsule may comprise a solid carrier such as gelatin.
• the active ingredient will be in the form of a parenterally acceptable aqueous solution which is pyrogen-free and has a suitable pH, isotonicity and stability.
• a parenterally acceptable aqueous solution which is pyrogen-free and has a suitable pH, isotonicity and stability.
• isotonic vehicles such as Sodium Chloride injection, Ringer's injection, Lactated Ringer's injection.
• Preservatives, stabilisers, buffers antioxidants and/or other additives may be included as required.
• an eighth aspect of the present invention there is provided, the use in the manufacture of a medicament of an effective amount of a compound of Formula I as defined above or a compound of Formulae la-Ic, Ila - He and IIIa-c as defined above, for use in GDEPT to target cancer cells in a subject in need thereof.
• a ninth aspect of the present invention there is provided, the use in the manufacture of a medicament of an effective amount of a compound of Formula I as defined above or a compound of Formulae la-Ic, Ila- IIc and IIIa-c as defined above, for use in cell ablation therapy to target cancer cells in a subject in need thereof.
• While the compounds of the present invention will typically be used to target tumour cells or tumour tissues in human subjects, they may be used to target tumour cells or tissues in other warm blooded animal subjects such as other primates, farm animals such as cattle, and sports animals and pets such as horses, dogs, and cats.
• terapéuticaally effective amount is to be understood as an amount of a compound of Formula I as defined above or a compound of any one of compounds Ia-c, Ila-c and ffla-c as defined above or a mixture thereof that is sufficient to show benefit to a subject with cancer cells.
• the actual amount, rate and time- course of administration, will depend on the nature and severity of the disease being treated. Prescription of treatment is within the responsibility of general practitioners and other medical doctors.
• the compounds of the invention as defined above may be administered alone or in combination with other treatments, especially radiotherapy, either simultaneously or sequentially dependent upon the condition to be treated.
• the pharmaceutically acceptable derivatives and salts thereof include acid derived salts formed from are hydrochloric, sulfuric, phosphoric, acetic, citric, oxalic, malonic, salicylic, malic, fumaric, succinic, ascorbic, maleic, methanesulfonic, isethionic acids and the like and base derived salts formed from sodium and potassium carbonate, sodium and potassium hydroxide, ammonia, triethylamine, triethanolamine and the like.
• This therapy can be used to selectively ablate specified target cells or tissue through specific enzymatic expression of a nitroreductase for example, that is specifically expressed by the tissue and which can then be employed to active a prodrug into an active metabolite to ablate the specified target cells or tissue.
• a nitroreductase for example
• substantially minimal bystander effect is to be understood as meaning that the killing of adjoining non-targeted tumour cells is minimal as a result of diffusion between the targeted tumour cells and non-targeted tumour cells of an activated metabolite that arises from the enzymatic activation of a compound of Formula I as defined above or a compound of any one of compounds Ia-c, Ila-c and IIIa-c as defined above or a mixture thereof.
• the key reaction is reaction of the dimesylates 6, 9, 13a-13g and 18a-18d with strictly controlled amounts of LiBr or Nal in a polar solvent like DMF or MeCN to give the unsymmetrical bromo- and iodo-mesylate mustards.
• the method can also be adapted to reaction of the known chloromesylate (5) to give the unsymmetrical chloro/bromo mustard IIa2. While this reaction gives varying amounts of the corresponding bis(bromo) or bis(iodo) compounds as well, these can be easily separated by chromatography to give the pure unsymmetrical mustards.
• Example A Preparation of analogues of class Ila by the method outlined in Scheme 1.
• Methyl alanine hydrochloride (2.55 g, 18.3 mmol) was dissolved in water (12 mL), and the solution was diluted with Me 2 CO (20 mL) and Et 2 O (50 mL).
• Example C Preparation of analogues of class lie by the method outlined in Scheme 3.
• d IC 5 o the concentration of drug (in micromolar) required to reduce cell numbers to
• Footnotes for Table 3. a Human lung carcinoma line. b Wild-type.
• °Ratio IC 5 o(aerobic)/IC 5 o(anoxic).
• P450R human cytochrome P450 reductase
• nitroaniline derivatives of the invention include compounds which are active as cytotoxic agents, and which have the additional capability of being reductively activated by the E. coli NTR and/or by endogenous reductase enzymes under hypoxia.

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• 2002
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• 2003
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