WO2000071532A1 - Heterocyclic derivatives useful as anticancer agents - Google Patents

Heterocyclic derivatives useful as anticancer agents Download PDF

Info

Publication number
WO2000071532A1
WO2000071532A1 PCT/IB2000/000570 IB0000570W WO0071532A1 WO 2000071532 A1 WO2000071532 A1 WO 2000071532A1 IB 0000570 W IB0000570 W IB 0000570W WO 0071532 A1 WO0071532 A1 WO 0071532A1
Authority
WO
WIPO (PCT)
Prior art keywords
aryl
group
ureιdo
dιmethyl
groups
Prior art date
Application number
PCT/IB2000/000570
Other languages
French (fr)
Inventor
Thomas George Gant
Mark Carl Noe
Original Assignee
Pfizer Products Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Products Inc. filed Critical Pfizer Products Inc.
Priority to MXPA01011920A priority Critical patent/MXPA01011920A/en
Priority to CA002374247A priority patent/CA2374247C/en
Priority to EP00920969A priority patent/EP1187826B1/en
Priority to BR0010746-8A priority patent/BR0010746A/en
Priority to AU41374/00A priority patent/AU4137400A/en
Priority to DE60032601T priority patent/DE60032601T2/en
Priority to JP2000619789A priority patent/JP3692041B2/en
Publication of WO2000071532A1 publication Critical patent/WO2000071532A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Definitions

  • This invention relates to novel isothiazole derivatives that are useful in the treatment of hyperproliferative diseases, such as cancers, in mammals
  • This invention also relates to a method of using such compounds in the treatment of hyperproliferative diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds
  • a cell may become cancerous by virtue of the transformation of a portion of its DNA into an oncogene (i e a gene that upon activation leads to the formation of malignant tumor cells)
  • oncogenes encode proteins which are aberrant tyrosine kinases capable of causing cell transformation
  • the overexpression of a normal proto-oncogenic tyrosine kinase may also result in proliferative disorders, sometimes resulting in a malignant phenotype
  • certain tyrosine kinases may be mutated or overexpressed in many human cancers such as brain, lung, squamous cell, bladder, gastric, breast, head and neck, oesophageal, gynecological and thyroid cancers
  • the overexpression of a ligand for a tyrosine kinase receptor may result in an increase in the activation state of the receptor, resulting in proliferation of the tumor cells or endothelial cells
  • polypeptide growth factors such as vascular endothelial growth factor (VEGF) having a high affinity to the human kinase insert-domain-containing receptor (KDR) or the murine fetal liver kinase 1 (FLK-1 ) receptor
  • KDR human kinase insert-domain-containing receptor
  • FLK-1 murine fetal liver kinase 1
  • Z is S, O, or NR 6 ;
  • X is N or CR 4 ;
  • X I is O, S, SO, S0 2 , NR 6 , or CR 5 R 6 ;
  • R is -CONR 5 R 6 , -C0 2 R 5 , -NR 5 R 6 , -NR 5 S0 2 R 6 , -S0 2 NR 5 R 6 , -NR 6 C(0)R 5 or an C 6 -C 10 aryl or 4-10 membered heterocyclic group containing 1-4 heteroatoms from the group N, O, S, or S0 2 ;
  • R 2 is H, C,-C 10 alkyl, C 2 -C 10 alkenyl, C 2 -C 10 alkynyl, -C(O)(C r C 10 alkyl), -(CH 2 ) t (C 6 -C 10 aryl), -(CH 2 ),(4-10 membered heterocyclic), -C(O)(CH 2 ),(C 6 -C 10 aryl), or -C(O)(CH 2 ) t (4-10 membered heterocyclic), wherein t is an integer from 0 to 5; said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R 6 )- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other; said aryl and heterocyclic R 1 groups are optionally fused to a C 6 -C 10 aryl group, a C 5 -C 8 saturated cyclic group
  • R 3 is -CR 5 R 6 R 7 , S0 2 R 5 , or -CONR 5 R 6 ,
  • R 3 is CONR 5 R 6 where R 5 is H and R 6 is -(CH 2 ),(4-10 membered heterocyclic), wherein t is an integer from 0 to 6, said heterocyclic group is optionally fused to a C 6 -C 10 aryl group, a C 3 -C 8 saturated cyclic group, or a 4-10 membered heterocyclic group, and said R 6 group, including the optionally fused portions of said R 6 group, is optionally substituted by 1 or 2 substituents independently selected from C r C 4 alkyl, hydroxy and hydroxymethyl
  • Specific preferred heterocyclic groups of said R 6 group are morpho no, pyrrolidmyl, imidazolyl, piperazmyl, pipe dinyl, and 2,5-d ⁇ aza- b ⁇ cyclo[2 2 1]hept-2-yl, the t variable of said R 6 group ranges from 2 to 6, and said heterocyclic groups are optionally substituted by hydroxy, hydroxy
  • Specific embodiments of the present invention include the following compounds 2-(3,3-D ⁇ methyl-ure ⁇ do)-4-propoxy-th ⁇ ophene-3-carboxyl ⁇ c acid amide, 4-Butoxy-2-(3,3-d ⁇ methyl-ure ⁇ do)-th ⁇ ophene-3-carboxyl ⁇ c acid amide,
  • the invention also relates to a pharmaceutical composition for the treatment of a hyperproliferative disorder in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier
  • said pharmaceutical composition is for the treatment of cancer such as brain, lung, squamous cell, bladder, gastric, pancreatic, breast, head, neck, renal, prostate, colorectal, oesophageal
  • the invention also relates to a pharmaceutical composition for the treatment of pancreatitis or kidney disease (including proliferative glomeruloneph ⁇ tis and diabetes-induced renal disease) in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier
  • the invention also relates to a pharmaceutical composition for the prevention of blastocyte implantation in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier
  • the invention also relates to a pharmaceutical composition for treating a disease related to vasculogenesis or angiogenesis in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier
  • said pharmaceutical composition is for treating a disease selected from the group consisting of tumor angiogenesis, chronic inflammatory disease such as rheumatoid arthritis, atherosclerosis, skin diseases such as psoriasis, excema, and scleroderma, diabetes, diabetic retinopathy, retinopathy of prematurity, age-related macular degeneration, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer
  • the invention also relates to a method of treating a hyperproliferative disorder in a mammal which comprises administering to said mammal a therapeutically effective amount of the compound of formula 1_. or a pharmaceutically acceptable salt or hydrate thereof
  • said method relates to the treatment of cancer such as brain, squamous cell, bladder, gastric, pancreatic, breast, head, neck, oesophageal, prostate, colorectal, lung, renal, gynecological (such as ovarian) or thyroid cancer
  • said method relates to the treatment of a non-cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e g , psoriasis) or prostate (e g , benign prostatic hypertropy (BPH))
  • the invention also relates to a method for the treatment of a hyperproliferative disorder in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, in combination with an anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylatmg agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, anti-hormones, and anti-androgens
  • an anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylatmg agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, anti-hormones, and anti-androgens
  • the invention also relates to a method of treating pancreatitis or kidney disease in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof
  • the invention also relates to a method of preventing blastocyte implantation in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof
  • the invention also relates to a method of treating diseases related to vasculogenesis or angiogenesis in a mammal which comprises administering to said mammal an effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof
  • said method is for treating a disease selected from the group consisting of tumor angiogenesis, chronic inflammatory disease such as rheumatoid arthritis, atherosclerosis, skin diseases such as psoriasis, excema, and scleroderma, diabetes, diabetic retinopathy, retinopathy of prematurity, age-related macular degeneration, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer
  • Patients that can be treated with the compounds of formulas 1_, and the pharmaceutically acceptable salts and hydrates of said compounds, according to the methods of this invention include, for example, patients that have been diagnosed
  • halo as used herein unless otherwise indicated, includes fluoro, chloro, bromo or lodo Preferred halo groups are fluoro, chloro and bromo
  • alkyl as used herein, unless otherwise indicated, includes saturated monovalent hydrocarbon radicals having straight, cyclic or branched moieties It is understood that for cyclic moieties at least three carbon atoms are required in said alkyl group
  • alkenyl as used herein, unless otherwise indicated, includes monovalent hydrocarbon radicals having at least one carbon-carbon double bond and also having straight, cyclic or branched moieties as provided above in the definition of "alkyl”
  • alkynyl as used herein, unless otherwise indicated, includes monovalent hydrocarbon radicals having at least one carbon-carbon triple bond and also having straight, cyclic or branched moieties as provided above in the definition of “alkyl”
  • alkoxy as used herein, unless otherwise indicated, includes O-alkyl groups wherein “alkyl” is as defined above
  • aryl as used herein, unless otherwise indicated, includes an organic radical derived from an aromatic hydrocarbon by removal of one hydrogen, such as phenyl or naphthyl
  • 4-10 membered heterocyclic includes aromatic and non-aromatic heterocyclic groups containing one or more heteroatoms each selected from O, S and N, wherein each heterocyclic group has from 4-10 atoms in its ring system
  • Non-aromatic heterocyclic groups include groups having only 4 atoms in their ring system, but aromatic heterocyclic groups must have at least 5 atoms in their ring system
  • An example of a 4 membered heterocyclic group is azetidinyl (derived from azetidine)
  • An example of a 5 membered heterocyclic group is thiazolyl and an example of a 10 membered heterocyclic group is qumolinyl
  • non-aromatic heterocyclic groups are pyrrolidmyl, tetrahydrofurany
  • phrases "pharmaceutically acceptable salt(s)", as used herein, unless otherwise indicated, includes salts of acidic or basic groups which may be present in the compounds of formula 1_
  • the compounds of formula 1_ that are basic in nature are capable of forming a wide variety of salts with various inorganic and organic acids
  • the acids that may be used to prepare pharmaceutically acceptable acid addition salts of such basic compounds of formula 1_ are those that form non-toxic acid addition salts, ⁇ _e_, salts containing pharmacologically acceptable anions, such as the hydrochlo ⁇ de, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, sa cylate, citrate, acid citrate, tartrate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, format
  • Those compounds of the formula X_ that are acidic in nature are capable of forming base salts with various pharmacologically acceptable cations
  • Examples of such salts include the alkali metal or alkaline earth metal salts and particularly, the sodium and potassium salts
  • the subject invention also includes isotopically-labelled compounds, and the pharmaceutically acceptable salts thereof, which are identical to those recited in formula 1 ⁇ . but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature
  • isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine and chlorine, such as 2 H, 3 H, 13 C, 14 C, 15 N, 18 0, 17 0, 35 S, 18 F, and 36 CI, respectively
  • Compounds of the present invention, prodrugs thereof, and pharmaceutically acceptable salts of said compounds or of said prodrugs which contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of this invention
  • Certain isotopically-labelled compounds of the present invention for example those into which radioactive isotopes such as 3 H and 14 C are incorporated, are useful in drug and
  • free carboxyl groups can be de ⁇ vatized as amides or alkyl esters
  • the amide and ester moieties may incorporate groups including but not limited to ether, amine and carboxylic acid functionalities
  • Free hydroxy groups may be de vatized using groups including but not limited to hemisuccmates, phosphate esters, dimethylammoacetates, and phosphoryloxymethyloxycarbonyls, as outlined in D Fleisher, R Bong, B H Stewart, Advanced Drug Delivery Reviews (1996) 19, 115 Carbamate prodrugs of hydroxy and ammo groups are also included, as are carbonate prodrugs and sulfate esters of hydroxy groups De ⁇ vatization of hydroxy groups as (acyloxy)methyl and (acyloxy)ethyl ethers wherein the acyl group may be an alkyl ester, optionally substituted with groups including but not limited to ether, amine and carboxylic acid functionalities, or where the acyl group
  • Certain compounds of formula 1_ may have asymmetric centers and therefore exist in different enantiome ⁇ c forms This invention relates to the use of all optical isomers and stereoisomers of the compounds of formula 1_ and mixtures thereof.
  • the compounds of formula 1_ may also exist as tautomers This invention relates to the use of all such tautomers and mixtures thereof
  • Scheme 1 illustrates the condensation of a potassium salt of 2-cyano-3,3-d ⁇ mercapto- acrylamide with an R 1 containing electrophile, cyc zation with an R 6 containing hydrazine, acylation with phenyl chloroformate and reaction with an R 5 R 6 containing amine to give the final compound
  • the compound of formula 3 may be prepared by treating an ammonium salt of the compound of formula 2 with an R 1 -conta ⁇ n ⁇ ng alkyl bromide, iodide, mesylate or t ⁇ flate in a polar aprotic solvent such as dimethylformamide at a temperature between 0 °C and 100, preferably at 70 °C for a period of time between 30 mm and 24 h, preferably 1 h
  • the compound of formula 4 may be prepared by treating the compound of formula 3 with between 1 and 2 equivalents, preferably 1 2 equivalents, of an R 6 containing hydrazin
  • the compound of formula 6 may be prepared by treating the compound of formula 3 with between 1 and 5 equivalents, preferably 2 equivalents, of a salt of hydroxylamine, preferably hydroxylamine hydrochlo ⁇ de and between 1 and 5 equivalents, preferably 2 equivalents, of a suitably strong base, such as a hydroxide base, preferably potassium hydroxide, in a polar solvent, such as water or an alcoholic solvent, prerferably water, at a temparature between 23 °C and 80 °C, preferably 23 °C for 12 to 72 hours, preferably 48 hours
  • the compound of formula 7 may be prepared by treating a compound of formula 6 with between 1 and 5 equivalents, preferably 3 equivalents, of an arylchloroformate, preferably phenylchloroformate, in the presence of a suitably strong base, such as an aromatic amine, preferably pyndine in a polar aprotic solvent, such as an ethereal solvent,
  • a suitably strong base such as
  • a condensation partner such as the ketoester 8 may be reacted with a suitable base such as sodium hydride in a suitable solvent such as tetrahydrofuran (THF) followed by reaction with an aminoacylisothiocyanate such as compound 9 at a temperature range between -20°C and reflux, preferably 0°C, until reaction is complete to afford thiophenone 10.
  • a suitable base such as sodium hydride
  • a suitable solvent such as tetrahydrofuran (THF)
  • an aminoacylisothiocyanate such as compound 9 at a temperature range between -20°C and reflux, preferably 0°C, until reaction is complete to afford thiophenone 10.
  • the thiophenone may then be reacted with an appropriate alcohol in a suitable solvent, such as the alcohol itself, with an appropriate amount of an appropriate catalyst, such as H 2 S0 4 at an appropnate temperature, such as reflux, until such time as the reaction is complete to afford the thiophene 1_1_
  • a suitable solvent such as the alcohol itself
  • an appropriate catalyst such as H 2 S0 4
  • an appropnate temperature such as reflux
  • the thiophene 1_1_ may be prepared by treatment of the thiophene 10 with a mixture of ammonium chloride and ammonium hydroxide (concentrated aqueous solution) in a sealed tube at 23 to 70 °C for a period of time sufficient to effect complete conversion of 10 to 11.
  • the compound V is then treated with a suitable sulfur transfer reagent, preferably Lawesson's reagent in a nonpolar solvent, such as toluene at a temperature between 23 °C and 140 °C for a period of time sufficient to effect complete consumption of compound 10
  • a suitable sulfur transfer reagent preferably Lawesson's reagent in a nonpolar solvent, such as toluene at a temperature between 23 °C and 140 °C for a period of time sufficient to effect complete consumption of compound 10
  • the thiophene 11 is then treated with a suitable alkyl halide, such as an alkyl chloride, bromide or iodide, and a suitably strong base, such as a tertiary amine base, in a polar solvent, such as THF or DMF, preferably a 6 1 mixture of THF DMF (NN-dimethylforamide) for at a temperature of 0 °C to 100 °C for a period of time sufficient
  • the compounds of the present invention may have asymmetric carbon atoms
  • Such diasterome ⁇ c mixtures can be separated into their individual diastereomers on the basis of their physical chemical differences by methods known to those skilled in the art, for example, by chromatography or fractional crystallization
  • Enantiomers can be separated by converting the enantiome ⁇ c mixtures into a diastereome ⁇ c mixture by reaction with an appropriate optically active compound (e g , alcohol), separating the diastereomers and converting (e g , hydrolyzmg) the individual diastereomers to the corresponding pure enantiomers All such isomers, including diastereomer mixtures and pure enantiomers are considered as part of the invention
  • the compounds of formula _ that are basic in nature are capable of forming a wide variety of different salts with various inorganic and organic acids Although such salts must be pharmaceutically acceptable for administration to animals, it is often desirable in practice to initially isolate the compound of formula 1_ from the reaction mixture as a pharmaceutical
  • Those compounds of formula 1_ that are acidic in nature are capable of forming base salts with various pharmacologically acceptable cations
  • Examples of such salts include the alkali metal or alkaline-earth metal salts and particularly, the sodium and potassium salts.
  • the chemical bases which are used as reagents to prepare the pharmaceutically acceptable base salts of this invention are those which form non-toxic base salts with the acidic compounds of formulas X_
  • Such non-toxic base salts include those derived from such pharmacologically acceptable cations as sodium, potassium, calcium and magnesium, etc
  • These salts can easily be prepared by treating the corresponding acidic compounds with an aqueous solution containing the desired pharmacologically acceptable cations, and then evaporating the resulting solution to dryness, preferably under reduced pressure
  • they may also be prepared by mixing lower alkanolic solutions of the acidic compounds and the desired alkali metal alkoxide together, and then evaporating the resulting solution to dryness in the same manner as before
  • stoichiometnc quantities of reagents are preferably employed in order to ensure completeness of reaction and maximum yields of the desired final product
  • Included in the present invention are compounds identical to the compounds of formula ⁇ _ but for the fact that one or more hydrogen or carbon atoms are replaced by isotopes thereof Such compounds are useful as research and diagnostic tools in metabolism pharmokinetic studies and in binding assays Specific applications in research include radio gand binding assays, autoradiography studies and in vivo binding studies Included among the radiolabelled forms of the compounds of formula 1_ are the tritium and C 14 isotopes thereof
  • the in vitro activity of the compounds of formula 1_ in inhibiting the KDR ⁇ /EGF receptor may be determined by the following procedure
  • the ability of the compounds of the present invention to inhibit tyrosine kinase activity may be measured using a recombinant enzyme in an assay that measures the ability of compounds to inhibit the phosphorylation of the exogenous substrate, polyGluTyr (PGT, SigmaTM, 4 1 )
  • PGT polyGluTyr
  • the kinase domain of the human KDR/VEGF receptor (ammo acids 805-1350) is expressed in Sf9 insect cells as a glutathione S-transferase (GST)-fus ⁇ on protein using the baculovirus expression system
  • the protein is purified from the lysates of these cells using glutathione agarose affinity columns
  • the enzyme assay is performed in 96-well plates that are coated with the PGT substrate (0 625 ⁇ g PGT per well) Test compounds are diluted in dimethylsulfoxide (DMSO), and then added to the PGT plates so that the final concentration of DMSO in the assay is 1 6% (v
  • Biol. Chem. 269:26988, 1994 may be used.
  • Cells are plated and allowed to attach to 96-well dishes in the same media (Ham's F12) with 10% FBS (fetal bovine serum).
  • FBS fetal bovine serum
  • the cells are then washed, re-fed with serum depleted media that contains 0.1 % (v/v) bovine serum albumin (BSA), and allowed to incubate for 24 hours.
  • BSA bovine serum albumin
  • Test compounds, dissolved in DMSO are diluted into the media (final DMSO concentration 0.5% (v/v)).
  • VEGF 165 (50 ng/ml final) is added to the media for an 8 minute incubation.
  • the cells are washed and lysed in HNTG buffer (20 mM Hepes, pH 7.5, 150 mM NaCl, 0.2% TritonTM X-100, 10% glycerol, 0.2 mM PMSF (phenymethylsulfonyl fluoride), 1 ⁇ g/ml pepstatin, 1 ⁇ g/ml leupeptin, 1 ⁇ g/ml aprotonin, 2 mM sodium pyrophosphate, 2 mM sodium orthovanadate).
  • HNTG buffer 20 mM Hepes, pH 7.5, 150 mM NaCl, 0.2% TritonTM X-100, 10% glycerol, 0.2 mM PMSF (phenymethylsulfonyl fluoride), 1 ⁇ g/ml pepstatin, 1 ⁇ g/ml leupeptin, 1 ⁇
  • the 96-well plates are coated with 1 ⁇ g per well of goat anti-rabbit antibody. Unbound antibody is washed off the plate and remaining sites are blocked with Superblock buffer (Pierce) prior to addition of the anti-flk-1 C- 20 antibody (0.5 ⁇ g per plate, Santa Cruz). Any unbound antibody is washed off the plates prior to addition of the cell lysate. After a 2 hour incubation of the lysates with the flk-1 antibody, the KDR associated phosphotyrosine is quantitated by development with the HRP- conjugated PY-54 antibody and TMB, as described above. The ability of the compounds to inhibit the VEGF-stimulated autophosphorylation reaction by 50%, relative to VEGF- stimulated controls is reported as the IC 50 value for the test compound.
  • HUVE cells human umbilical vein endothelial cells, CloneticsTM.
  • This assay has been well described in the literature (Waltenberger J et al. J. Biol. Chem. 269: 26988, 1994; Cao Y et al. J. Biol. Chem. 271 : 3154, 1996). Briefly, 10" cells are plated in collagen-coated 24-well plates and allowed to attach.
  • Cells are re-fed in serum-free media, and 24 hours later are treated with various concentrations of compound (prepared in DMSO, final concentration of DMSO in the assay is 0.2% v/v), and 2-30 ng/ml VEGF 165 .
  • the cells are pulsed with 3 H thymidine (NEN, 1 ⁇ Ci per well).
  • the media are then removed, and the cells washed extensively with ice-cold Hank's balanced salt solution, and then 2 times with ice cold trichloroacetic acid (10% v/v).
  • the cells are lysed by the addition of 0.2 ml of 0.1 N NaOH, and the lysates transferred into scintillation vials.
  • the activity of the compounds of formula 1_. m vivo can be determined by the amount of inhibition of tumor growth by a test compound relative to a control
  • the tumor growth inhibitory effects of various compounds are measured according to the methods of Corbett T H , et al "Tumor Induction Relationships in Development of Transplantable Cancers of the Colon in Mice for Chemotherapy Assays, with a Note on Carcinogen Structure", Cancer Res , 35, 2434-2439 (1975) and Corbett, T H , et al , "A Mouse Colon-tumor Model for Experimental Therapy", Cancer Chemother Rep (Part 2)", 5, 169-186 (1975), with slight modifications Tumors are induced in the flank by s c injection of 1 X 10 6 log phase cultured tumor cells suspended in 0 1- 0 2 ml PBS After sufficient time has elapsed for the tumors to become palpable (5-6 mm in diameter), the test animals (athymic mice) are treated with active compound (formulated by dissolution in appropriate
  • Administration of the compounds of the present invention can be effected by any method that enables delivery of the compounds to the site of action These methods include oral routes, intraduodenal routes, parenteral injection (including intravenous, subcutaneous, intramuscular, intravascular or infusion), topical, and rectal administration
  • an effective dosage is in the range of about 0 001 to about 100 mg per kg body weight per day, preferably about 1 to about 35 mg/kg/day, in single or divided doses For a 70 kg human, this would amount to about 0.05 to about 7 g/day, preferably about 0 2 to about 2 5 g/day
  • dosage levels below the lower limit of the aforesaid range may be more than adequate, while in other cases still larger doses may be employed without causing any harmful side effect, provided that such larger doses are first divided into several small doses for administration throughout the day
  • the active compound may be applied as a sole therapy or may involve one or more other anti-tumour substances for example those selected from, for example, mitotic inhibitors, for example vinblastine, alkylating agents, for example ⁇ s-platin, carboplatm and cyclophosphamide, anti-metabolites, for example 5-fluorourac ⁇ l, cytosme arabinoside and hydroxyurea, or, for example, one of the preferred anti-metabolites disclosed in European Patent Application No 239362 such as N-(5-[N-(3,4-d ⁇ hydro-2-methyl-4-oxoqu ⁇ nazol ⁇ n-6-ylmethyl)-N- methylam ⁇ no]-2-thenoyl)-L-glutam ⁇ c acid, growth factor inhibitors, cell cycle inhibitors, intercalating antibiotics, for example adriamycm and bleomycin, enzymes, for example interferon, and anti-hormones, for example anti-estrogens such as Nolva
  • the pharmaceutical composition may, for example, be in a form suitable for oral administration as a tablet, capsule, pill, powder, sustained release formulations, solution, suspension, for parenteral injection as a sterile solution, suspension or emulsion, for topical administration as an ointment or cream or for rectal administration as a suppository
  • the pharmaceutical composition may be in unit dosage forms suitable for single administration of precise dosages
  • the pharmaceutical composition will include a conventional pharmaceutical carrier or excipient and a compound according to the invention as an active ingredient In addition, it may include other medicinal or pharmaceutical agents, carriers, adjuvants, etc
  • Exemplary parenteral administration forms include solutions or suspensions of active compounds in sterile aqueous solutions, for example, aqueous propylene glycol or dextrose solutions
  • Suitable pharmaceutical carriers include inert diluents or fillers, water and various organic solvents
  • the pharmaceutical compositions may, if desired, contain additional ingredients such as flavorings, binders, excipients and the like
  • tablets containing various excipients, such as citric acid may be employed together with various dismtegrants such as starch, alginic acid and certain complex silicates and with binding agents such as sucrose, gelatin and acacia
  • lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often useful for tabletmg purposes
  • Solid compositions of a similar type may also be employed in soft and hard filled gelatin capsules Preferred materials, therefore, include lactose or milk sugar and high molecular weight polyethylene glyco
  • Example 1 2-(3,3-D ⁇ methyl-ure ⁇ do)-4-propoxy-th ⁇ ophene-3-carboxyl ⁇ c acid amide
  • a solution of 2-(3,3-D ⁇ methyl-ure ⁇ do)-4-propoxy-th ⁇ ophene-3-carboxyl ⁇ c acid methyl ester () in ethanol (6 mL) was treated with concentrated ammonium hydroxide (6 mL) in a sealed tube and heated to 40°C for 5 hours.

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)

Abstract

The present invention relates to compounds of formula (1) and to pharmaceutically acceptable salts, prodrugs and solvates thereof, wherein Z, X, X?1, R1, R2 and R3¿ are as defined herein as it relates to pharmaceutical compositions containing the above compounds for the treatment of disorders mediated by angiogenesis in mammals by administration of the above compounds.

Description

HETEROCYCLIC DERIVATIVES USEFUL AS ANTICANCER AGENTS
Background Of The Invention This invention relates to novel isothiazole derivatives that are useful in the treatment of hyperproliferative diseases, such as cancers, in mammals This invention also relates to a method of using such compounds in the treatment of hyperproliferative diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds
It is known that a cell may become cancerous by virtue of the transformation of a portion of its DNA into an oncogene (i e a gene that upon activation leads to the formation of malignant tumor cells) Many oncogenes encode proteins which are aberrant tyrosine kinases capable of causing cell transformation Alternatively, the overexpression of a normal proto-oncogenic tyrosine kinase may also result in proliferative disorders, sometimes resulting in a malignant phenotype It has been shown that certain tyrosine kinases may be mutated or overexpressed in many human cancers such as brain, lung, squamous cell, bladder, gastric, breast, head and neck, oesophageal, gynecological and thyroid cancers Furthermore, the overexpression of a ligand for a tyrosine kinase receptor may result in an increase in the activation state of the receptor, resulting in proliferation of the tumor cells or endothelial cells Thus, it is believed that inhibitors of receptor tyrosine kinases, such as the compounds of the present invention, are useful as selective inhibitors of the growth of mammalian cancer cells
It is known that polypeptide growth factors, such as vascular endothelial growth factor (VEGF) having a high affinity to the human kinase insert-domain-containing receptor (KDR) or the murine fetal liver kinase 1 (FLK-1 ) receptor, have been associated with the proliferation of endothelial cells and more particularly vasculogenesis and angiogenesis See PCT international application publication number WO 95/21613 (published August 17, 1995) Agents, such as the compounds of the present invention, that are capable of binding to or modulating the KDR/FLK-1 receptor may be used to treat disorders related to vasculogenesis or angiogenesis such as diabetes, diabetic retinopathy, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer Isothiazole derivatives useful in the treatment of hyperproliferative disorders are referred to in United States provisional application no 60/087,973, filed June 4, 1998, which is incorporated herein by reference in its entirety Summary Of The Invention The present invention relates to compounds of the formula _
Figure imgf000003_0001
1 and to pharmaceutically acceptable salts, prodrugs and solvates thereof, wherein:
Z is S, O, or NR6;
X is N or CR4;
XI is O, S, SO, S02, NR6, or CR5R6;
R is -CONR5R6, -C02R5, -NR5R6, -NR5S02R6, -S02NR5R6, -NR6C(0)R5 or an C6-C10 aryl or 4-10 membered heterocyclic group containing 1-4 heteroatoms from the group N, O, S, or S02;
R1 is H, CrC10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -(CH2),(C6-C10 aryl), or -(CH2)t(4-10 membered heterocyclic), wherein t is an integer from 0 to 5; said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R5)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other; said aryl and heterocyclic R1 groups are optionally fused to a C6-C10 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group; 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety; the -(CH2)t- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R1 groups other than H are optionally substituted by 1 to 5 R8 groups;
R2 is H, C,-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -C(O)(CrC10 alkyl), -(CH2)t(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), -C(O)(CH2),(C6-C10 aryl), or -C(O)(CH2)t(4-10 membered heterocyclic), wherein t is an integer from 0 to 5; said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other; said aryl and heterocyclic R1 groups are optionally fused to a C6-C10 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group; 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety; the -(CH2)t- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R1 groups, except H, are optionally substituted by 1 to 5 R8 groups,
R3 is -CR5R6R7, S02R5, or -CONR5R6,
R4 is H or CrC6 alkyl and may be taken together with X1 or R1 to form a 5 to 6 membered saturated ring or a 5 to 6 membered heteroaryl ring, wherein said saturated and heteroaryl rings optionally include 1 to 3 heteroatoms in addition to X1, selected from O, S and -N(R6), where said -N(R6)- is optionally =N- or -N=, said saturated ring optionally may be partially unsaturated by including 1 or 2 carbon-carbon double bonds, and said saturated and heteroaryl rings, including the R6 group of said -N(R6)-, are optionally substituted by 1 to 5 R8 groups, each R5 is independently H, CrC10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -C(O)(C1-C10 alkyl), -(CH2),(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), -C(O)(CH2),(C6-C10 aryl), or -C(O)(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 5, said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R1 groups are optionally fused to a C6-C10 aryl group, a C5-C8 saturated cyclic group, or a 5-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, the -(CH2)t- moieties of the foregoing R groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R5 groups, except H, are optionally substituted by 1 to 5 R8 groups, each R6 is independently selected from the list of substituents provided in the definition of R5, -SO2(CH2),(C6-C10 aryl), -SO2(CH2),(4-10 membered heterocyclic), and -OR5, t is an integer from 0 to 5, the -(CH2)t- moieties of the foregoing R2 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R6 groups are optionally substituted by 1 to 5 R8 groups, each R7 is independently H, C.-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -C(O)(C.,-C10 alkyl), -(CH2)t(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), -C(O)(CH2)t(C6-C10 aryl), or -C(O)(CH2)t(4-10 membered heterocyclic), wherein t is an integer from 0 to 5, said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R1 groups are optionally fused to a C6-C10 aryl group, a C5-Cβ saturated cyclic group, or a 4-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, the -(CH2)t- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R7 groups, except H, are optionally substituted by 1 to 5 R8 groups, or R5 and R6 may be taken together with the nitrogen to which each is attached to form a 4-10 membered saturated monocyclic or polycyclic ring or a 5-10 membered heteroaryl ring, wherein said saturated and heteroaryl rings optionally include 1 or 2 heteroatoms selected from O, S and -N(R6)- in addition to the nitrogen to which R5 and R6 are attached, said -N(R6)- is optionally =N- or -N= where R5 and R6 are taken together as said heteroaryl group, said saturated ring optionally may be partially unsaturated by including 1 or 2 carbon- carbon double bonds, and said saturated and heteroaryl rings, including the R6 group of said -N(R6)- are optionally substituted by 1 to 5 R8 groups, each R8 is independently selected from H, 0,-0,0 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, halo, cyano nitro, tπfluoromethyl, tnfluoromethoxy, azido, -OR5, -C(0)R5, -C(OJOR5, -NR6C(0)OR5, -OC(0)R5, -NR5S02R5, -S02NR5R6, -NR6C(0)R5, -C(0)NR5R6, -NR5R6, -S(0),R7 wherein j is an integer from 0 to 2, -S03H, -NR5(CR6R7),OR6, -(CH2)t(C6-C10 aryl), -SO2(CH2),(C6-C10 aryl), -S(CH2),(C6-C10 aryl), -O(CH2),(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), and -(CR6R7)mOR6, wherein m is an integer from 1 to 5 and t is an integer from 0 to 5, said alkyl group optionally contains 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R4 groups are optionally fused to a C6-C10 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, and the alkyl, aryl and heterocyclic moieties of the foregoing R8 groups are optionally substituted by 1 to 5 substituents independently selected from halo, cyano, nitro, tπfluoromethyl, tnfluoromethoxy, azido, -NR10SO2R9, -S02NR9R10, -C(0)R9, -C(0)OR9, -O0(O)R9, -NR10C(O)R9, -C(0)NR9R10, -NR9R10, -(CR10R7)mOR10 wherein m is an integer from 1 to 5, and R9 and R10 are each defined as H, CrC6 alkyl, -(CH2)t(C6-C10 aryl) or -(CH2)t(4-10 membered heterocyclic) and t is an integer from 0 to 5
Compounds excluded from the present invention include those wherein all of the following conditions are met simultaneously Z is S, and X1 is O or S, and X is N, and R is CONH2, and R2 is H, and R3 is CONR5R6 Preferred compounds include those of formula 1_ wherein Z = S and wherein R1 is C
C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -(CH2),(C6-C10 aryl), or -(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 5 and R2 is H
Other preferred compounds include those of formula _ wherein R3 is CONR5R6 where R5 is H and R6 is -(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 6, said heterocyclic group is optionally fused to a C6-C10 aryl group, a C3-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, and said R6 group, including the optionally fused portions of said R6 group, is optionally substituted by 1 or 2 substituents independently selected from CrC4 alkyl, hydroxy and hydroxymethyl Specific preferred heterocyclic groups of said R6 group are morpho no, pyrrolidmyl, imidazolyl, piperazmyl, pipe dinyl, and 2,5-dιaza- bιcyclo[2 2 1]hept-2-yl, the t variable of said R6 group ranges from 2 to 6, and said heterocyclic groups are optionally substituted by hydroxy, hydroxymethyl and methyl
Specific embodiments of the present invention include the following compounds 2-(3,3-Dιmethyl-ureιdo)-4-propoxy-thιophene-3-carboxylιc acid amide, 4-Butoxy-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acid amide,
2- 3,3-Dιmethyl-ureιdo)-4-pentyloxy-thιophene-3-carboxylιc acid amide, 2- 3,3-Dιmethyl-ureιdo)-4-hexyloxy-thιophene-3-carboxylιc acid amide, 2- 3,3-Dιmethyl-ureιdo)-4-heptyloxy-thιophene-3-carboxylιc acid amide,
4-Benzylsulfanyl-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acιd amide,
2- 3,3-Dιmethyl-ureιdo)-4-hexylsulfanyl-thιophene-3-carboxylιc acid amide, 2- 3,3-Dιmethyl-ureιdo)-4-pentylsulfanyl-thιophene-3-carboxylιc acid amide, 2- 3,3-Dιmethyl-ureιdo)-4-phenethylsulfanyl-thιophene-3-carboxylιc acid amide, 2- 3,3-Dιmethyl-ureιdo)-4-(pyrιdιn-2-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
3,3-Dιmethyl-ureιdo)-4-(naphthalen-1 -ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
3,3-Dιmethyl-ureιdo)-4-(naphthalen-2-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
3,3-Dιmethyl-ureιdo)-4-(quιnolιn-2-ylmethylsulfanyl)-thιophene-3-carboxyIιc acid amide
4-Chloro-benzylsulfanyl)-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acid amide,
3,3-Dιmethyl-ureιdo)-4-(1 -phenyl-ethylsulfanyl)-thιophene-3-carboxylιc acid amide 2-Chloro-benzylsulfanyl)-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acid amide 3-Chloro-benzylsulfanyl)-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acιd amide 3,3-Dιmethyl-ureιdo)-4-(4-methyl-benzylsulfanyl)-thιophene-3-carboxylιc acid amide,
3,3-Dιmethyl-ureιdo)-4-(4-methoxy-benzylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-ι 3,3-Dιmethyl-ureιdo)-4-(4-vιnyl-benzylsulfanyl)-thιophene-3-carboxylιc acid amide; 2 3,3-Dιmethyl-ureιdo)-4-(4-trιfluoromethyl-benzylsulfanyl)-thιophene-3-carboxylιc acid amide, 2-(3,3-Dιmethyl-ureιdo)-4-(pyπdιn-4-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(pyrιdιn-3-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
5-Acetylamιno-3-pentylsulfanyl-ιsothιazole-4-carboxylιc acid amide, 5-Benzoylamιno-3-pentylsulfanyl-ιsothιazole-4-carboxylιc acid amide,
1 -Methyl-3-[3-pentylsulfanyl-4-( 1 H-tetrazol-5-yl)-ιsothιazol-5-yl]-urea, 5-(3-Methyl-ureιdo)-3-pentylsulfanyl-ιsothιazole-4-carboxylιc acid, 5-Amιno-3-pentylsulfanyl-pyrazole-1 ,4-dιcarboxylιc acid 4-amιde 1-methylamιde, 5-Amιno-3-pentylsulfanyl-pyrazole-1 ,4-dιcarboxylιc acid 4-amιde 1-dιmethylamιde, 5-(3,3-Dιmethyl-ureιdo)-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide,
5-Acetylamιno-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide, 5-Benzoylamιno-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide, 5-Amιno-1 -benzoyl-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide, and the pharmaceutically acceptable salts and hydrates of the foregoing compounds The invention also relates to a pharmaceutical composition for the treatment of a hyperproliferative disorder in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier In one embodiment, said pharmaceutical composition is for the treatment of cancer such as brain, lung, squamous cell, bladder, gastric, pancreatic, breast, head, neck, renal, prostate, colorectal, oesophageal, gynecological (such as ovarian) or thyroid cancer In another embodiment, said pharmaceutical composition is for the treatment of a non- cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e g , psoriasis) or prostate (e g , benign prostatic hypertropy (BPH))
The invention also relates to a pharmaceutical composition for the treatment of pancreatitis or kidney disease (including proliferative glomerulonephπtis and diabetes-induced renal disease) in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier
The invention also relates to a pharmaceutical composition for the prevention of blastocyte implantation in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier
The invention also relates to a pharmaceutical composition for treating a disease related to vasculogenesis or angiogenesis in a mammal which comprises a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier In one embodiment, said pharmaceutical composition is for treating a disease selected from the group consisting of tumor angiogenesis, chronic inflammatory disease such as rheumatoid arthritis, atherosclerosis, skin diseases such as psoriasis, excema, and scleroderma, diabetes, diabetic retinopathy, retinopathy of prematurity, age-related macular degeneration, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer
The invention also relates to a method of treating a hyperproliferative disorder in a mammal which comprises administering to said mammal a therapeutically effective amount of the compound of formula 1_. or a pharmaceutically acceptable salt or hydrate thereof In one embodiment said method relates to the treatment of cancer such as brain, squamous cell, bladder, gastric, pancreatic, breast, head, neck, oesophageal, prostate, colorectal, lung, renal, gynecological (such as ovarian) or thyroid cancer In another embodiment, said method relates to the treatment of a non-cancerous hyperproliferative disorder such as benign hyperplasia of the skin (e g , psoriasis) or prostate (e g , benign prostatic hypertropy (BPH))
The invention also relates to a method for the treatment of a hyperproliferative disorder in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof, in combination with an anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylatmg agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, anti-hormones, and anti-androgens
The invention also relates to a method of treating pancreatitis or kidney disease in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof
The invention also relates to a method of preventing blastocyte implantation in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof
The invention also relates to a method of treating diseases related to vasculogenesis or angiogenesis in a mammal which comprises administering to said mammal an effective amount of a compound of formula 1_, or a pharmaceutically acceptable salt or hydrate thereof In one embodiment, said method is for treating a disease selected from the group consisting of tumor angiogenesis, chronic inflammatory disease such as rheumatoid arthritis, atherosclerosis, skin diseases such as psoriasis, excema, and scleroderma, diabetes, diabetic retinopathy, retinopathy of prematurity, age-related macular degeneration, hemangioma, glioma, melanoma, Kaposi's sarcoma and ovarian, breast, lung, pancreatic, prostate, colon and epidermoid cancer Patients that can be treated with the compounds of formulas 1_, and the pharmaceutically acceptable salts and hydrates of said compounds, according to the methods of this invention include, for example, patients that have been diagnosed as having psoriasis, BPH, lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head and neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer or cancer of the anal region stomach cancer, colon cancer, breast cancer, gynecologic tumors (e g , uterine sarcomas, carcinoma of the fallopian tubes, carcinoma of the endometπum, carcinoma of the cervix carcinoma of the vagina or carcinoma of the vulva), Hodgkin's disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system (e g , cancer of the thyroid, parathyroid or adrenal glands), sarcomas of soft tissues, cancer of the urethra, cancer of the penis, prostate cancer, chronic or acute leukemia, solid tumors of childhood, lymphocytic lymphonas, cancer of the bladder, cancer of the kidney or ureter (e g , renal cell carcinoma, carcinoma of the renal pelvis), or neoplasms of the central nervous system (e g , primary CNS lymphoma, spinal axis tumors, brain stem g omas or pituitary adenomas)
The term "halo", as used herein unless otherwise indicated, includes fluoro, chloro, bromo or lodo Preferred halo groups are fluoro, chloro and bromo
The term "alkyl", as used herein, unless otherwise indicated, includes saturated monovalent hydrocarbon radicals having straight, cyclic or branched moieties It is understood that for cyclic moieties at least three carbon atoms are required in said alkyl group
The term "alkenyl", as used herein, unless otherwise indicated, includes monovalent hydrocarbon radicals having at least one carbon-carbon double bond and also having straight, cyclic or branched moieties as provided above in the definition of "alkyl"
The term "alkynyl", as used herein, unless otherwise indicated, includes monovalent hydrocarbon radicals having at least one carbon-carbon triple bond and also having straight, cyclic or branched moieties as provided above in the definition of "alkyl" The term "alkoxy", as used herein, unless otherwise indicated, includes O-alkyl groups wherein "alkyl" is as defined above
The term "aryl", as used herein, unless otherwise indicated, includes an organic radical derived from an aromatic hydrocarbon by removal of one hydrogen, such as phenyl or naphthyl The term "4-10 membered heterocyclic", as used herein, unless otherwise indicated, includes aromatic and non-aromatic heterocyclic groups containing one or more heteroatoms each selected from O, S and N, wherein each heterocyclic group has from 4-10 atoms in its ring system Non-aromatic heterocyclic groups include groups having only 4 atoms in their ring system, but aromatic heterocyclic groups must have at least 5 atoms in their ring system An example of a 4 membered heterocyclic group is azetidinyl (derived from azetidine) An example of a 5 membered heterocyclic group is thiazolyl and an example of a 10 membered heterocyclic group is qumolinyl Examples of non-aromatic heterocyclic groups are pyrrolidmyl, tetrahydrofuranyl, tetrahydrothienyl, tetrahydropyranyl, tetrahydrothiopyranyl, pipeπdino, morpholino, thiomorpholino, thioxanyl, piperazinyl, azetidinyl, oxetanyl, thietanyl, homopipeπdinyl, oxepanyl thiepanyl, oxazepinyl, diazepinyl, thiazepinyl, 1,2,3,6- tetrahydropyπdinyl, 2-pyrrolιnyl, 3-pyrrolιnyl, indolmyl, 2H-pyranyl, 4H-pyranyl, dioxanyl, 1 ,3- dioxolanyl, pyrazolinyl, dithianyl, dithiolanyl, dihydropyranyl, dihydrothienyl, dihydrofuranyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, 3-azabιcyclo[3 1 0]hexanyl, 3- azabιcyclo[4 1 0]heptanyl 3H-ιndolyl and quinolizinyl Examples of aromatic heterocyclic groups are pyπdinyl, imidazolyl, pyπmidinyl, pyrazolyl, tπazolyl, pyrazmyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, qumolinyl, isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl, cmnolinyl, mdazolyl, mdolizinyl, phthalazinyl, pyπdazinyl, tπazinyl, isomdolyl, pteπdinyl, puπnyl, oxadiazolyl, thiadiazolyl, furazanyl, benzofurazanyl, benzothiophenyl, benzothiazolyl, benzoxazolyl, quinazo nyl, quinoxalmyl, naphthyπdinyl, and furopyπdinyl The foregoing groups, as derived from the compounds listed above, may be C- attached or N-attached where such is possible For instance, a group derived from pyrrole may be pyrrol-1-yl (N-attached) or pyrrol-3-yl (C-attached)
The phrase "pharmaceutically acceptable salt(s)", as used herein, unless otherwise indicated, includes salts of acidic or basic groups which may be present in the compounds of formula 1_ The compounds of formula 1_ that are basic in nature are capable of forming a wide variety of salts with various inorganic and organic acids The acids that may be used to prepare pharmaceutically acceptable acid addition salts of such basic compounds of formula 1_ are those that form non-toxic acid addition salts, ι_e_, salts containing pharmacologically acceptable anions, such as the hydrochloπde, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, sa cylate, citrate, acid citrate, tartrate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate and pamoate [ι_e_, 1 ,1'-methylene-bιs-(2-hydroxy-3- naphthoate)] salts
Those compounds of the formula X_ that are acidic in nature, are capable of forming base salts with various pharmacologically acceptable cations Examples of such salts include the alkali metal or alkaline earth metal salts and particularly, the sodium and potassium salts
The subject invention also includes isotopically-labelled compounds, and the pharmaceutically acceptable salts thereof, which are identical to those recited in formula 1^. but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine and chlorine, such as 2H, 3H, 13C, 14C, 15N, 180, 170, 35S, 18F, and 36CI, respectively Compounds of the present invention, prodrugs thereof, and pharmaceutically acceptable salts of said compounds or of said prodrugs which contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of this invention Certain isotopically-labelled compounds of the present invention, for example those into which radioactive isotopes such as 3H and 14C are incorporated, are useful in drug and/or substrate tissue distribution assays Tπtiated, i e , 3H, and carbon-14, i e , 1 C, isotopes are particularly preferred for their ease of preparation and detectability Further, substitution with heavier isotopes such as deuterium, i e , 2H, can afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements and, hence, may be preferred in some circumstances Isotopically labelled compounds of formula 1_ of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the Schemes and/or in the Examples and Preparations below, by substituting a readily available isotopically labelled reagent for a non-isotopically labelled reagent This invention also encompasses pharmaceutical compositions containing and methods of treating bacterial infections through administering prodrugs of compounds of the formula 1 Compounds of formula 1 having free ammo, amido, hydroxy or carboxylic groups can be converted into prodrugs Prodrugs include compounds wherein an ammo acid residue, or a polypeptide chain of two or more (e g , two, three or four) ammo acid residues is covalently joined through an amide or ester bond to a free ammo, hydroxy or carboxylic acid group of compounds of formula 1_ The ammo acid residues include but are not limited to the 20 naturally occurring ammo acids commonly designated by three letter symbols and also includes 4- hydroxyprolme, hydroxylysine, demosme, isodemosme, 3-methylhιstιdιne, norva n, beta-alanine, gamma-aminobutyπc acid, citrulline homocysteine, homosenne, ornithine and methionine sulfone
Additional types of prodrugs are also encompassed For instance, free carboxyl groups can be deπvatized as amides or alkyl esters The amide and ester moieties may incorporate groups including but not limited to ether, amine and carboxylic acid functionalities Free hydroxy groups may be de vatized using groups including but not limited to hemisuccmates, phosphate esters, dimethylammoacetates, and phosphoryloxymethyloxycarbonyls, as outlined in D Fleisher, R Bong, B H Stewart, Advanced Drug Delivery Reviews (1996) 19, 115 Carbamate prodrugs of hydroxy and ammo groups are also included, as are carbonate prodrugs and sulfate esters of hydroxy groups Deπvatization of hydroxy groups as (acyloxy)methyl and (acyloxy)ethyl ethers wherein the acyl group may be an alkyl ester, optionally substituted with groups including but not limited to ether, amine and carboxylic acid functionalities, or where the acyl group is an ammo acid ester as described above, are also encompassed Prodrugs of this type are described in R P Robinson et al , J Medicinal Chemistry (1996) 39, 10.
Certain compounds of formula 1_ may have asymmetric centers and therefore exist in different enantiomeπc forms This invention relates to the use of all optical isomers and stereoisomers of the compounds of formula 1_ and mixtures thereof. The compounds of formula 1_ may also exist as tautomers This invention relates to the use of all such tautomers and mixtures thereof
Detailed Description of the Invention Compounds of the formula _ and their pharmaceutically acceptable salts and solvates may be prepared as referenced
Scheme 1.
Figure imgf000013_0001
Figure imgf000013_0002
Figure imgf000013_0003
Scheme 1 cont'd
Figure imgf000014_0001
Scheme 1 illustrates the condensation of a potassium salt of 2-cyano-3,3-dιmercapto- acrylamide with an R1 containing electrophile, cyc zation with an R6 containing hydrazine, acylation with phenyl chloroformate and reaction with an R5R6 containing amine to give the final compound In Step 1 of Scheme 1 , the compound of formula 3 may be prepared by treating an ammonium salt of the compound of formula 2 with an R1-contaιnιng alkyl bromide, iodide, mesylate or tπflate in a polar aprotic solvent such as dimethylformamide at a temperature between 0 °C and 100, preferably at 70 °C for a period of time between 30 mm and 24 h, preferably 1 h In step 2 of Scheme 1 , the compound of formula 4 may be prepared by treating the compound of formula 3 with between 1 and 2 equivalents, preferably 1 2 equivalents, of an R6 containing hydrazine (where R6 is an alkyl or aryl group) salt and between 1 and 2 equivalents, preferably 1 2 equivalents, of a suitably strong base, such as a hydroxide base, preferably potassium hydroxide, in a polar solvent, preferably and alcoholic solvent, such as methanol, at a temparature between 23 °C and 120 °C, preferably 80 °C for 12 to 48 hours, preferably 24 hours In Step 3 of Scheme 1 , the compound of formula 5 may be prepared by treating a compound of formula 4 with between 1 and 10 equivalents, preferably 1 to 4 equivalents, of an arylchloroformate, preferably phenylchloroformate, in the presence of a suitably strong base, such as an aromatic amine, preferably pyπdine in a polar aprotic solvent, such as an ethereal solvent, preferably THF (tetrahydrofuran) at a temperature between -10 and 80 °C, for 1 to 12 hours, preferably 6 hours In Step 4 of Scheme 1 , the compound of formula 1_ may be prepared by treating the compound of formula 5 with a desired amine of the formula R5R6NH at a temperature sufficient to effect reaction, typically 0 °C to 100 °C, preferably 50 °C to 70 °C , for a period ranging from 1 hour to 48 hours, preferably overnight The compound of formula 1_ is then isolated
Scheme 2.
Figure imgf000016_0001
Figure imgf000016_0002
Figure imgf000016_0003
In step 1 of Scheme 2, the compound of formula 6 may be prepared by treating the compound of formula 3 with between 1 and 5 equivalents, preferably 2 equivalents, of a salt of hydroxylamine, preferably hydroxylamine hydrochloπde and between 1 and 5 equivalents, preferably 2 equivalents, of a suitably strong base, such as a hydroxide base, preferably potassium hydroxide, in a polar solvent, such as water or an alcoholic solvent, prerferably water, at a temparature between 23 °C and 80 °C, preferably 23 °C for 12 to 72 hours, preferably 48 hours In Step 2 of Scheme 2, the compound of formula 7 may be prepared by treating a compound of formula 6 with between 1 and 5 equivalents, preferably 3 equivalents, of an arylchloroformate, preferably phenylchloroformate, in the presence of a suitably strong base, such as an aromatic amine, preferably pyndine in a polar aprotic solvent, such as an ethereal solvent, preferably THF at a temperature between -10 and 80 °C for 1 to 72 hours, preferably 48 hours In Step 3 of Scheme 2, the compound of formula 1^ may be prepared by treating the compound of formula 5 with a desired amine of the formula R5R6NH at a temperature sufficient to effect reaction, typically 0 °C to 100 °C, preferably 50 °C to 70 °C , for a period ranging from 1 hour to 48 hours, preferably overnight The compound of formula 1_ is then isolated.
Scheme 3.
Figure imgf000018_0001
Figure imgf000018_0002
In Scheme 3, a condensation partner such as the ketoester 8 may be reacted with a suitable base such as sodium hydride in a suitable solvent such as tetrahydrofuran (THF) followed by reaction with an aminoacylisothiocyanate such as compound 9 at a temperature range between -20°C and reflux, preferably 0°C, until reaction is complete to afford thiophenone 10. The thiophenone may then be reacted with an appropriate alcohol in a suitable solvent, such as the alcohol itself, with an appropriate amount of an appropriate catalyst, such as H2S04 at an appropnate temperature, such as reflux, until such time as the reaction is complete to afford the thiophene 1_1_ The amide functionality may then be installed by reaction of 1_1_ with an ammonia source such as ammonium hydroxide in ethanol at an appropriate temperature, such as 40 C in a sealed tube to afford the compound of formula 1_.
Scheme 4
Figure imgf000019_0001
Figure imgf000019_0002
In Scheme 4, the thiophene 1_1_ may be prepared by treatment of the thiophene 10 with a mixture of ammonium chloride and ammonium hydroxide (concentrated aqueous solution) in a sealed tube at 23 to 70 °C for a period of time sufficient to effect complete conversion of 10 to 11. The compound V is then treated with a suitable sulfur transfer reagent, preferably Lawesson's reagent in a nonpolar solvent, such as toluene at a temperature between 23 °C and 140 °C for a period of time sufficient to effect complete consumption of compound 10 The thiophene 11 is then treated with a suitable alkyl halide, such as an alkyl chloride, bromide or iodide, and a suitably strong base, such as a tertiary amine base, in a polar solvent, such as THF or DMF, preferably a 6 1 mixture of THF DMF (NN-dimethylforamide) for at a temperature of 0 °C to 100 °C for a period of time sufficient to effect complete consumption of 1_1 The compound of formula _ is then isolated
The compounds of the present invention may have asymmetric carbon atoms Such diasteromeπc mixtures can be separated into their individual diastereomers on the basis of their physical chemical differences by methods known to those skilled in the art, for example, by chromatography or fractional crystallization Enantiomers can be separated by converting the enantiomeπc mixtures into a diastereomeπc mixture by reaction with an appropriate optically active compound (e g , alcohol), separating the diastereomers and converting (e g , hydrolyzmg) the individual diastereomers to the corresponding pure enantiomers All such isomers, including diastereomer mixtures and pure enantiomers are considered as part of the invention The compounds of formula _ that are basic in nature are capable of forming a wide variety of different salts with various inorganic and organic acids Although such salts must be pharmaceutically acceptable for administration to animals, it is often desirable in practice to initially isolate the compound of formula 1_ from the reaction mixture as a pharmaceutically unacceptable salt and then simply convert the latter back to the free base compound by treatment with an alkaline reagent and subsequently convert the latter free base to a pharmaceutically acceptable acid addition salt The acid addition salts of the base compounds of this invention are readily prepared by treating the base compound with a substantially equivalent amount of the chosen mineral or organic acid in an aqueous solvent medium or in a suitable organic solvent, such as methanol or ethanol Upon careful evaporation of the solvent, the desired solid salt is readily obtained The desired acid salt can also be precipitated from a solution of the free base in an organic solvent by adding to the solution an appropriate mineral or organic acid
Those compounds of formula 1_ that are acidic in nature, are capable of forming base salts with various pharmacologically acceptable cations Examples of such salts include the alkali metal or alkaline-earth metal salts and particularly, the sodium and potassium salts. These salts are all prepared by conventional techniques The chemical bases which are used as reagents to prepare the pharmaceutically acceptable base salts of this invention are those which form non-toxic base salts with the acidic compounds of formulas X_ Such non-toxic base salts include those derived from such pharmacologically acceptable cations as sodium, potassium, calcium and magnesium, etc These salts can easily be prepared by treating the corresponding acidic compounds with an aqueous solution containing the desired pharmacologically acceptable cations, and then evaporating the resulting solution to dryness, preferably under reduced pressure Alternatively, they may also be prepared by mixing lower alkanolic solutions of the acidic compounds and the desired alkali metal alkoxide together, and then evaporating the resulting solution to dryness in the same manner as before In either case, stoichiometnc quantities of reagents are preferably employed in order to ensure completeness of reaction and maximum yields of the desired final product
Included in the present invention are compounds identical to the compounds of formula λ_ but for the fact that one or more hydrogen or carbon atoms are replaced by isotopes thereof Such compounds are useful as research and diagnostic tools in metabolism pharmokinetic studies and in binding assays Specific applications in research include radio gand binding assays, autoradiography studies and in vivo binding studies Included among the radiolabelled forms of the compounds of formula 1_ are the tritium and C14 isotopes thereof
The in vitro activity of the compounds of formula 1_ in inhibiting the KDRΛ/EGF receptor may be determined by the following procedure
The ability of the compounds of the present invention to inhibit tyrosine kinase activity may be measured using a recombinant enzyme in an assay that measures the ability of compounds to inhibit the phosphorylation of the exogenous substrate, polyGluTyr (PGT, Sigma™, 4 1 ) The kinase domain of the human KDR/VEGF receptor (ammo acids 805-1350) is expressed in Sf9 insect cells as a glutathione S-transferase (GST)-fusιon protein using the baculovirus expression system The protein is purified from the lysates of these cells using glutathione agarose affinity columns The enzyme assay is performed in 96-well plates that are coated with the PGT substrate (0 625 μg PGT per well) Test compounds are diluted in dimethylsulfoxide (DMSO), and then added to the PGT plates so that the final concentration of DMSO in the assay is 1 6% (v/v) The recombinant enzyme is diluted in phosphorylation buffer (50 mM Hepes, pH 7 3, 125 mM NaCI, 24 mM MgCI2) The reaction is initiated by the addition of ATP to a final concentration of 10 μM After a 30 minute incubation at room temperature with shaking, the reaction is aspirated, and the plates are washed with wash buffer (PBS-contaming 0 1% Tween-20) The amount of phosphorylated PGT is quantitated by incubation with a HRP-conjugated (HRP is horseradish peroxidase) PY-54 antibody (Transduction Labs), developed with TMB peroxidase (TMB is 3,3',5,5'-tetramethylbenzιdιne), and the reaction is quantitated on a BioRad™ Microplate reader at 450 nM Inhibition of the kinase enzymatic activity by the test compound is detected as a reduced absorbance, and the concentration of the compound that is required to inhibit the signal by 50% is reported as the IC50 value for the test compound To measure the ability of the compounds to inhibit KDR tyrosine kinase activity for the full length protein that exists in a cellular context, the porcine aortic endothelial (PAE) cells transfected with the human KDR (Waltenberger et al., J. Biol. Chem. 269:26988, 1994) may be used. Cells are plated and allowed to attach to 96-well dishes in the same media (Ham's F12) with 10% FBS (fetal bovine serum). The cells are then washed, re-fed with serum depleted media that contains 0.1 % (v/v) bovine serum albumin (BSA), and allowed to incubate for 24 hours. Immediately prior to dosing with compound, the cells are re-fed with the serum depleted media (without BSA). Test compounds, dissolved in DMSO, are diluted into the media (final DMSO concentration 0.5% (v/v)). At the end of a 2 hour incubation, VEGF165 (50 ng/ml final) is added to the media for an 8 minute incubation. The cells are washed and lysed in HNTG buffer (20 mM Hepes, pH 7.5, 150 mM NaCl, 0.2% Triton™ X-100, 10% glycerol, 0.2 mM PMSF (phenymethylsulfonyl fluoride), 1 μg/ml pepstatin, 1 μg/ml leupeptin, 1 μg/ml aprotonin, 2 mM sodium pyrophosphate, 2 mM sodium orthovanadate). The extent of phosphorylation of KDR is measured using an ELISA assay. The 96-well plates are coated with 1 μg per well of goat anti-rabbit antibody. Unbound antibody is washed off the plate and remaining sites are blocked with Superblock buffer (Pierce) prior to addition of the anti-flk-1 C- 20 antibody (0.5 μg per plate, Santa Cruz). Any unbound antibody is washed off the plates prior to addition of the cell lysate. After a 2 hour incubation of the lysates with the flk-1 antibody, the KDR associated phosphotyrosine is quantitated by development with the HRP- conjugated PY-54 antibody and TMB, as described above. The ability of the compounds to inhibit the VEGF-stimulated autophosphorylation reaction by 50%, relative to VEGF- stimulated controls is reported as the IC50 value for the test compound.
The ability of the compounds to inhibit mitogenesis in human endothelial cells is measured by their ability to inhibit 3H-thymidine incorporation into HUVE cells (human umbilical vein endothelial cells, Clonetics™). This assay has been well described in the literature (Waltenberger J et al. J. Biol. Chem. 269: 26988, 1994; Cao Y et al. J. Biol. Chem. 271 : 3154, 1996). Briefly, 10" cells are plated in collagen-coated 24-well plates and allowed to attach. Cells are re-fed in serum-free media, and 24 hours later are treated with various concentrations of compound (prepared in DMSO, final concentration of DMSO in the assay is 0.2% v/v), and 2-30 ng/ml VEGF165. During the last 3 hours of the 24 hour compound treatment, the cells are pulsed with 3H thymidine (NEN, 1 μCi per well). The media are then removed, and the cells washed extensively with ice-cold Hank's balanced salt solution, and then 2 times with ice cold trichloroacetic acid (10% v/v). The cells are lysed by the addition of 0.2 ml of 0.1 N NaOH, and the lysates transferred into scintillation vials. The wells are then washed with 0.2 ml of 0.1 N HCI, and this wash is then transferred to the vials. The extent of 3H thymidine incorporation is measured by scintillation counting The ability of the compounds to inhibit incorporation by 50%, relative to control (VEGF treatment with DMSO vehicle only) is reported as the IC50 value for the test compound
The activity of the compounds of formula 1_. m vivo, can be determined by the amount of inhibition of tumor growth by a test compound relative to a control The tumor growth inhibitory effects of various compounds are measured according to the methods of Corbett T H , et al "Tumor Induction Relationships in Development of Transplantable Cancers of the Colon in Mice for Chemotherapy Assays, with a Note on Carcinogen Structure", Cancer Res , 35, 2434-2439 (1975) and Corbett, T H , et al , "A Mouse Colon-tumor Model for Experimental Therapy", Cancer Chemother Rep (Part 2)", 5, 169-186 (1975), with slight modifications Tumors are induced in the flank by s c injection of 1 X 106 log phase cultured tumor cells suspended in 0 1- 0 2 ml PBS After sufficient time has elapsed for the tumors to become palpable (5-6 mm in diameter), the test animals (athymic mice) are treated with active compound (formulated by dissolution in appropriate diluent, for example water or 5% Gelucire™ 44/14 m PBS by the intrapeπtoneal (ip) or oral (po) routes of administration once or twice daily for 5-10 consecutive days In order to determine an anti-tumor effect, the tumor is measured in millimeters with Vernier calipers across two diameters and the tumor volume (mm3) is calculated using the formula Tumor weight = (length x [wιdth]2)/2, according to the methods of Geran, R I , et al "Protocols for Screening Chemical Agents and Natural Products Against Animal Tumors and Other Biological Systems", Third Edition, Cancer Chemother Rep , 3, 1-104 (1972) The flank site of tumor implantation provides reproducible dose/response effects for a variety of chemotherapeutic agents, and the method of measurement (tumor diameter) is a reliable method for assessing tumor growth rates
Administration of the compounds of the present invention (hereinafter the "active compound(s)") can be effected by any method that enables delivery of the compounds to the site of action These methods include oral routes, intraduodenal routes, parenteral injection (including intravenous, subcutaneous, intramuscular, intravascular or infusion), topical, and rectal administration
The amount of the active compound administered will be dependent on the subject being treated, the severity of the disorder or condition, the rate of administration and the judgement of the prescribing physician However, an effective dosage is in the range of about 0 001 to about 100 mg per kg body weight per day, preferably about 1 to about 35 mg/kg/day, in single or divided doses For a 70 kg human, this would amount to about 0.05 to about 7 g/day, preferably about 0 2 to about 2 5 g/day In some instances, dosage levels below the lower limit of the aforesaid range may be more than adequate, while in other cases still larger doses may be employed without causing any harmful side effect, provided that such larger doses are first divided into several small doses for administration throughout the day
The active compound may be applied as a sole therapy or may involve one or more other anti-tumour substances for example those selected from, for example, mitotic inhibitors, for example vinblastine, alkylating agents, for example αs-platin, carboplatm and cyclophosphamide, anti-metabolites, for example 5-fluorouracιl, cytosme arabinoside and hydroxyurea, or, for example, one of the preferred anti-metabolites disclosed in European Patent Application No 239362 such as N-(5-[N-(3,4-dιhydro-2-methyl-4-oxoquιnazolιn-6-ylmethyl)-N- methylamιno]-2-thenoyl)-L-glutamιc acid, growth factor inhibitors, cell cycle inhibitors, intercalating antibiotics, for example adriamycm and bleomycin, enzymes, for example interferon, and anti-hormones, for example anti-estrogens such as Nolvadex™ (tamoxifen) or, for example anti-androgens such as Casodex™ (4'-cyano-3-(4-fluorophenylsulphonyl)-2-hydroxy-2- methyl-3'-(tπfluoromethyl)propιonanιlιde) Such conjoint treatment may be achieved by way of the simultaneous, sequential or separate dosing of the individual components of the treatment
The pharmaceutical composition may, for example, be in a form suitable for oral administration as a tablet, capsule, pill, powder, sustained release formulations, solution, suspension, for parenteral injection as a sterile solution, suspension or emulsion, for topical administration as an ointment or cream or for rectal administration as a suppository The pharmaceutical composition may be in unit dosage forms suitable for single administration of precise dosages The pharmaceutical composition will include a conventional pharmaceutical carrier or excipient and a compound according to the invention as an active ingredient In addition, it may include other medicinal or pharmaceutical agents, carriers, adjuvants, etc
Exemplary parenteral administration forms include solutions or suspensions of active compounds in sterile aqueous solutions, for example, aqueous propylene glycol or dextrose solutions Such dosage forms can be suitably buffered, if desired Suitable pharmaceutical carriers include inert diluents or fillers, water and various organic solvents The pharmaceutical compositions may, if desired, contain additional ingredients such as flavorings, binders, excipients and the like Thus for oral administration, tablets containing various excipients, such as citric acid may be employed together with various dismtegrants such as starch, alginic acid and certain complex silicates and with binding agents such as sucrose, gelatin and acacia Additionally, lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often useful for tabletmg purposes Solid compositions of a similar type may also be employed in soft and hard filled gelatin capsules Preferred materials, therefore, include lactose or milk sugar and high molecular weight polyethylene glycols When aqueous suspensions or elixirs are desired for oral administration the active compound therein may be combined with various sweetening or flavoring agents, coloring matters or dyes and, if desired, emulsifying agents or suspending agents, together with diluents such as water, ethanol, propylene glycol, glycerin, or combinations thereof
Methods of preparing various pharmaceutical compositions with a specific amount of active compound are known, or will be apparent, to those skilled in this art For examples, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easter, Pa , 15th Edition (1975)
The examples and preparations provided below further illustrate and exemplify the compounds of the present invention and methods of preparing such compounds It is to be understood that the scope of the present invention is not limited in any way by the scope of the following examples and preparations PREPARATION 1
2-(3,3-Dιmethyl-ureιdo)-4-oxo-4,5-dιhydro-thιophene-3-carboxylιc acid methyl ester
A solution of methyl 4-chloroacetoacetate (1 77 mL, 15 3 mmol) in THF (10 mL) was added to a 0 C suspension of sodium hydride (386 mg) in THF (40 mL) Stirring was continued until bubbling ceased to afford a light-yellow solution Next was added a solution of N,N-dιmethylamιnoacylιsothιocyanate (2 00 g, 15 4 mmol) in THF (10 mL) A light-yellow suspension formed after approximately one minute The reaction was stirred overnight at ambient temperature The mixture was next partitioned between water and an ethyl acetate/methylene chloride mixture The organic layer was dried (Na2S04), concentrated, and recrystal zed from methanol to afford the title compound as a light-yellow solid (2 09 g, 8 56 mmol, 56%) 1H NMR (CDCL3, 400 MHz) 3 10 (br s, 6H), 3 56 (s, 2H), 3 86 (s, 3H), 12 41 (s,
1 H)
2-(3,3-Dιmethyl-ureιdo)-4-propoxy-thιophene-3-carboxylιc acid methyl ester
A solution of 2-(3,3-Dιmethyl-ureιdo)-4-oxo-4,5-dihydro-thiophene-3-carboxylιc acid methyl ester (50 mg, 0.205 mmol) in n-propanol (5 mL) was treated with H2S04 (5 microliters) and stirred at ambient temperature for 12 hours. Little reaction was observed so the temperature was increased to 100°C Little reaction was observed after 2 hours so four angstrom seives were added and the reaction continued at 100°C for two additional hours at which point sufficient product was observed The mixture was then concentrated and the residue purified via radial chromatography on a 4 mm plate using hexanes/ethyl acetate (1/1 ) to afford the title compound as a white solid (31 mg, 0 108 mmol, 53%) 1H NMR (CDCL3, 400 MHz) 1.03 (t, 3H, J = 7.3 Hz), 1 78-1.84 (m, 2H), 3.06 (s, 6H), 3.84-3.89 (m, 5H), 5.51 (s, 1 H), 1 1.08 (s, 1 H).
Example 1 2-(3,3-Dιmethyl-ureιdo)-4-propoxy-thιophene-3-carboxylιc acid amide A solution of 2-(3,3-Dιmethyl-ureιdo)-4-propoxy-thιophene-3-carboxylιc acid methyl ester () in ethanol (6 mL) was treated with concentrated ammonium hydroxide (6 mL) in a sealed tube and heated to 40°C for 5 hours. The mixture was then cooled, evaporated, acidified with a small amount of acetic acid and purified via radial chromatography on a 2 mm plate using hexanes/ethyl acetate (3/1 ) plus 2% methanol as eluent to afford a white solid (15 mg, 55 3 micromol, 51 %) 1H NMR (CDCL3, 400 MHz) 1.03 (t, 3H, J = 7.3 Hz), 1.81-1.88 (m, 2H), 3 04 (s, 6H), 3.97 (t, 2H, J = 6.6 Hz), 5.33 (broad s, 1 H), 5.55 (s, 1 H), 7.50 (broad s, 1 H), 12.00 (s, 1 H).

Claims

A compound of the formula
Figure imgf000027_0001
1 or a pharmaceutically acceptable salt, prodrugs or solvate thereof, wherein
Figure imgf000027_0002
X1 is O, S, SO, S02, NR6, or CR5R6,
R is -CONR5R6, -C02R5, -NR5R6, -NR5S02R6, -S02NR5R6, -NR6C(0)R5 or an C6-C10 aryl or 4-10 membered heterocyclic group containing 1-4 heteroatoms from the group N, O, S, or S02,
R1 is H, C,-C,0 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -(CH2),(C6-C10 aryl), or -(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 5, said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R5)- with the proviso that two O atoms, two S atoms, or an 0 and S atom are not attached directly to each other, said aryl and heterocyclic R1 groups are optionally fused to a C6-C10 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, the -(CH2)t- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R1 groups other than H are optionally substituted by 1 to 5 R8 groups,
R2 is H, CrC10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, -0(0X0,-0,0 alkyl), -(CH2)t(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), -C(O)(CH2)t(C6-C10 aryl), or -C(O)(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 5, said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R1 groups are optionally fused to a C6-C,0 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, the -(CH2),- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R1 groups, except H, are optionally substituted by 1 to 5 R8 groups,
R3 is -CR5R6R7, S02R5, or -CONR5R6,
R4 is H or C,-C6 alkyl and may be taken together with X1 or R1 to form a 5 to 6 membered saturated ring or a 5 to 6 membered heteroaryl ring, wherein said saturated and heteroaryl rings optionally include 1 to 3 heteroatoms in addition to X1, selected from O, S and -N(R6) where said -N(R6)- is optionally =N- or -N=, said saturated ring optionally may be partially unsaturated by including 1 or 2 carbon-carbon double bonds and said saturated and heteroaryl rings, including the R6 group of said -N(R6)-, are optionally substituted by 1 to 5 R8 groups, each R5 is independently H C,-C,0 alkyl, C2-C,0 alkenyl, C2-C,0 alkynyl, -C(0)(C,-C,o alkyl) -(CH2)t(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), -C(O)(CH2)t(C6-C,0 aryl), or -C(O)(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 5, said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R1 groups are optionally fused to a C6-C,0 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, the -(CH2)t- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R5 groups, except H, are optionally substituted by 1 to 5 R8 groups, each R6 is independently selected from the list of substituents provided in the definition of R5, -SO2(CH2),(C6-C10 aryl), -SO2(CH2),(4-10 membered heterocyclic), and -OR5, t is an integer from 0 to 5, the -(CH2),- moieties of the foregoing R2 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R6 groups are optionally substituted by 1 to 5 R8 groups, each R7 is independently H, C,-C10 alkyl, C2-C10 alkenyl, C2-C,0 alkynyl, -C(O)(C,-C10 alkyl), -(CH2),(C6-C10 aryl), -(CH2),(4-10 membered heterocyclic), -C(O)(CH2)t(C6-C10 aryl), or -C(O)(CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 5, said alkyl group optionally includes 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R1 groups are optionally fused to a C6-C,0 aryl group, a C5-C8 saturated cyclic group, or a 5-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, the -(CH2)t- moieties of the foregoing R1 groups optionally include a carbon-carbon double or triple bond where t is an integer from 2 to 5, and the foregoing R7 groups, except H, are optionally substituted by 1 to 5 R8 groups, or R5 and R6 may be taken together with the nitrogen to which each is attached to form a 4-10 membered saturated monocyclic or polycyclic ring or a 5-10 membered heteroaryl ring, wherein said saturated and heteroaryl rings optionally include 1 or 2 heteroatoms selected from O S and -N(R6)- in addition to the nitrogen to which R5 and R6 are attached, said -N(R6)- is optionally =N- or -N= where R5 and R6 are taken together as said heteroaryl group, said saturated ring optionally may be partially unsaturated by including 1 or 2 carbon- carbon double bonds, and said saturated and heteroaryl rings, including the R6 group of said -N(R6)- are optionally substituted by 1 to 5 R8 groups, each R8 is independently selected from H, C,-C,0 alkyl, C2-C,0 alkenyl, C2-C10 alkynyl, halo, cyano, nitro, tπfluoromethyl, tnfluoromethoxy, azido, -OR5, -C(0)R5, -C(0)OR5, -NR6C(0)OR5, -OC(0)R5, -NR6S02R5, -S02NR5R6, -NR6C(0)R5, -C(0)NR5R6, -NR5R6, -S(0)JR7 wherein j is an integer from 0 to 2, -S03H, -NR5(CR6R7),OR6, -(CH2),(C6-C10 aryl), -SO2(CH2)t(C6-Cι0 aryl), -S(CH2),(C6-C10 aryl), -O(CH2),(C6-C,0 aryl), -(CH2)t(4-10 membered heterocyclic), and -(CR6R7)mOR6, wherein m is an integer from 1 to 5 and t is an integer from 0 to 5, said alkyl group optionally contains 1 or 2 hetero moieties selected from O, S and -N(R6)- with the proviso that two O atoms, two S atoms, or an O and S atom are not attached directly to each other, said aryl and heterocyclic R4 groups are optionally fused to a C6-C10 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, 1 or 2 carbon atoms in the foregoing heterocyclic moieties are optionally substituted by an oxo (=0) moiety, and the alkyl, aryl and heterocyclic moieties of the foregoing R8 groups are optionally substituted by 1 to 5 substituents independently selected from halo, cyano, nitro, tπfluoromethyl, tnfluoromethoxy, azido, -NR10SO2R9, -S02NR9R10, -C(0)R9, -C(0)OR9, -OC(0)R9, -NR10C(O)R9, -C(0)NR9R10, -NR9R10, -(CR10R7)mOR10 wherein m is an integer from 1 to 5, and R9 and R10 are each defined as H, C,-C6 alkyl, -(CH2)t(C6-C,0aryl) or -(CH2)t(4-10 membered heterocyclic) and t is an integer from 0 to 5 with the proviso that when X1 is O then simultaneously Z is not S, X is not N, R is not CONH2, R2 is not H, and R3 is not CONR5R6 and when X1 is S then simultaneously Z is not S, X is not N, R is not CONH2, R2 is not H and R3 is not CONR5R6 2 A compound according to claim 1 wherein Z is Sulfur, R1 is C,-C10 alkyl, C2-
C,0 alkenyl, C2 - C10 alkynyl,-(CH2)t(C6-C10 aryl), or -(CH2),(4-10 membered heterocyclic) wherein t is an integer from 0 to 5, and R2 is Hydrogen
3 A compound according to claim 2 wherein R1 is benzyl optionally substituted by 1 to 4 substitutents independently selected from halo and C,-C4 alkyl. 4 A compound according to claim 3 wherein R3 is benzyl substituted by 1 to 4 substituents independently selected from methyl, fluoro, chloro or bromo
5 A compound according to claim 1 wherein R3 is CONR5R6, wherein R5 is H and R6 is - (CH2),(4-10 membered heterocyclic), wherein t is an integer from 0 to 6, said heterocyclic group is optionally fused to a C6-C,0 aryl group, a C5-C8 saturated cyclic group, or a 4-10 membered heterocyclic group, and said R6 group, including the optionally fused portions of said R6 group, is optionally substituted by 1 or 2 substituents independently selected from C,-C4 alkyl, hydroxy and hydroxy methyl
6 A compound according to claim 5 wherein the heterocyclic moiety of said R6 group is selected from morpholino, pyrrolidinyl, imidazoly, piperazinyl, piperidinyl and 2, 5 diazabicyclo [2 21] hepta-2-yl, the t variable of said R6 group ranges from 2 to 6 and said heteracyclic groups are optionally substituted by hydroxy, hydroxy methyl and methyl
7 A compound according to claim 1 selected from the group consisting of 2-(3,3-Dιmethyl-ureιdo)-4-propoxy-thιophene-3-carboxylιc acid amide, 4-Butoxy-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acιd amide, 2-(3,3-Dιmethyl-ureιdo)-4-pentyloxy-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-hexyloxy-thιophene-3-carboxylιc acid amide, 2-(3,3-Dιmethyl-ureιdo)-4-heptyloxy-thιophene-3-carboxylιc acid amide, 4-Benzylsulfanyl-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acid amide, 2-(3,3-Dιmethyl-ureιdo)-4-hexylsulfanyl-thιophene-3-carboxylιc acid amide, 2-(3,3-Dιmethyl-ureιdo)-4-pentylsulfanyl-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-phenethylsulfanyl-thιophene-3-carboxylιc acid amide, 2-(3,3-Dιmethyl-ureιdo)-4-(pyrιdιn-2-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(naphthalen-1-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(naphthalen-2-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(quιnolιn-2-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide 4-(4-Chloro-benzylsulfanyl)-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(1 -phenyl-ethylsulfanyl)-thιophene-3-carboxylιc acid amide 4-(2-Chloro-benzylsulfanyl)-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acιd amide 4-(3-Chloro-benzylsulfanyl)-2-(3,3-dιmethyl-ureιdo)-thιophene-3-carboxylιc acιd amide 2-(3,3-Dιmethyl-ureιdo)-4-(4-methyl-benzylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(4-methoxy-benzylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(4-vιnyl-benzylsulfanyl)-thιophene-3-carboxylιc acid amide, 2-(3,3-Dιmethyl-ureιdo)-4-(4-trιfluoromethyl-benzylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(pyrιdιn-4-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
2-(3,3-Dιmethyl-ureιdo)-4-(pyπdιn-3-ylmethylsulfanyl)-thιophene-3-carboxylιc acid amide,
5-Acetylamιno-3-pentyisulfanyl-ιsothιazole-4-carboxylιc acid amide, 5-Benzoylamιno-3-pentylsulfanyl-ιsothιazole-4-carboxylιc acid amide, 1-Methyl-3-[3-pentylsulfanyl-4-(1 H-tetrazol-5-yl)-ιsothιazol-5-yl]-urea, 5-(3-Methyl-ureιdo)-3-pentylsulfanyl-ιsothιazole-4-carboxylιc acid, 5-Amιno-3-pentylsulfanyl-pyrazole-1 ,4-dιcarboxylιc acid 4-amιde 1-methylamιde,
5-Amιno-3-pentylsulfanyl-pyrazole-1 ,4-dιcarboxylιc acid 4-amιde 1-dιmethylamιde, 5-(3,3-Dιmethyl-ureιdo)-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide, 5-Acetylamιno-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide, 5-Benzoylamιno-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide, 5-Amιno-1 -benzoyl-3-pentylsulfanyl-1 H-pyrazole-4-carboxylιc acid amide
8 A pharmaceutical composition for treatment of a disorder mediated by angiogenesis in a mammal which comprises a therapeutically effective amount of a compound of formula 1 , or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable carrier 9 The pharmaceutical composition of claim 8 wherein said disorder mediated by angiogenesis is a cancer selected from brain, lung, squamous cell, bladder, gastric, pancreatic, breast, head, neck, renal, kidney, ovarian, prostate, colorectal, oesophageal, gynecological and thyroid cancer
10 The method of treating a disorder mediated by angiogenesis in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound according to claim 1
11 The method of claim 10 wherein said method is for the treatment of a cancer selected from brain, squamous all, bladder, gastric, pancreatic breast, head, neck oesophageal, prostate, colorectal, lung, renal, ovarian, gynecological and thyroid cancer 12 A pharmaceutical composition for the treatment of a hyperproliferative disorder in a mammal which comprises a therapeutically effective amount of a compound according to claim 1 and a pharmaceutically acceptable carrier
13 The pharmaceutical composition of claim 12 wherein said hyperproliferative disorder is a cancer selected from brain, lung, squamous cell, bladder, gastric, pancreatic, breast, head, neck, renal, kidney, ovarian, prostate, colorectal, oesophageal, gynecological and thyroid cancer
14 The pharmaceutical composition of claim 12 wherein said disorder is a non- cancerous hyperproliferative disorder
15 The pharmaceutical composition of claim 14 wherein said disorder is a benign hyperplasia of the skin or prostate
16 A method of treating a hyperproliferative disorder in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound according to claim 1
17 The method of claim 16 wherein said method is for the treatment of a cancer selected from brain, squamous cell, bladder, gastric, pancreatic, breast, head, neck, oesophageal, prostate, colorectal, lung, renal, kidney, ovarian, gynecological and thyroid cancer
18 The method of claim 16 wherein said method is for the treatment of a non- cancerous hyperproliferative disorder 19 The method of claim 16 wherein said method is for the treatment of a benign hyperplasia of the skin or prostate
20 A method for the treatment of a hyperproliferative disorder in a mammal which comprises administering to said mammal a therapeutically effective amount of a compound according to claim 1 in combination with an anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylating agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, anti-hormones, and anti-androgens
PCT/IB2000/000570 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents WO2000071532A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
MXPA01011920A MXPA01011920A (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents.
CA002374247A CA2374247C (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents
EP00920969A EP1187826B1 (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents
BR0010746-8A BR0010746A (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful with anticancer agents
AU41374/00A AU4137400A (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents
DE60032601T DE60032601T2 (en) 1999-05-19 2000-05-03 HETEROCYCLIC DERIVATIVES USED AS ANTICROGEN AGENTS
JP2000619789A JP3692041B2 (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13493399P 1999-05-19 1999-05-19
US60/134,933 1999-05-19

Publications (1)

Publication Number Publication Date
WO2000071532A1 true WO2000071532A1 (en) 2000-11-30

Family

ID=22465672

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2000/000570 WO2000071532A1 (en) 1999-05-19 2000-05-03 Heterocyclic derivatives useful as anticancer agents

Country Status (21)

Country Link
US (1) US6380214B1 (en)
EP (1) EP1187826B1 (en)
JP (2) JP3692041B2 (en)
AR (1) AR029634A1 (en)
AT (1) ATE349440T1 (en)
AU (1) AU4137400A (en)
BR (1) BR0010746A (en)
CA (1) CA2374247C (en)
CO (1) CO5170417A1 (en)
DE (1) DE60032601T2 (en)
DZ (1) DZ3042A1 (en)
ES (1) ES2276681T3 (en)
GT (1) GT200000069A (en)
HN (1) HN2000000051A (en)
MA (1) MA26733A1 (en)
MX (1) MXPA01011920A (en)
PA (1) PA8494101A1 (en)
PE (1) PE20010152A1 (en)
TN (1) TNSN00104A1 (en)
UY (1) UY26143A1 (en)
WO (1) WO2000071532A1 (en)

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6482842B2 (en) 2000-02-07 2002-11-19 Bristol-Myers Squibb Company 3-aminopyrazole inhibitors of cyclin dependent kinases
WO2003010163A1 (en) * 2001-07-25 2003-02-06 Astrazeneca Ab Novel compounds
WO2003010158A1 (en) * 2001-07-25 2003-02-06 Astrazeneca Ab Novel compounds
WO2002068406A3 (en) * 2001-01-12 2003-04-24 Amgen Inc Substituted amine derivatives and their use for the treatment of angiogenesis
WO2003105843A1 (en) * 2002-06-13 2003-12-24 Kinetek Pharmaceuticals, Inc. Methods of using isothiazole derivatives to treat cancer or inflammation
WO2004011461A1 (en) * 2002-07-25 2004-02-05 Pfizer Products Inc. Isothiazole derivatives useful as anticancer agents
EP1581309A2 (en) * 2002-11-15 2005-10-05 Exelixis, Inc. Kinase modulators
US7102009B2 (en) 2001-01-12 2006-09-05 Amgen Inc. Substituted amine derivatives and methods of use
CN1315820C (en) * 2003-01-15 2007-05-16 阿斯利康(瑞典)有限公司 Thiophene carboxamides as inhibitors of the enzyme IKK-2
US7358376B2 (en) 2000-02-12 2008-04-15 Astrazeneca Ab Substituted Thiophene compounds
US7572826B2 (en) 2003-01-15 2009-08-11 Astrazeneca Ab Thiophene-carboxamide derivatives and their use as inhibitors of the enzyme IKK-2
EP2116530A1 (en) * 2007-02-26 2009-11-11 Santen Pharmaceutical Co., Ltd Novel pyrrole derivative having ureide group and aminocarbonyl group as substituents
US7678811B2 (en) 2002-02-11 2010-03-16 Bayer Healthcare Llc Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
US7687533B2 (en) 2004-03-18 2010-03-30 Pfizer Inc. N-(1-arylpyrazol-4l) sulfonamides and their use as parasiticides
US7838541B2 (en) 2002-02-11 2010-11-23 Bayer Healthcare, Llc Aryl ureas with angiogenesis inhibiting activity
US7897623B2 (en) 1999-01-13 2011-03-01 Bayer Healthcare Llc ω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
US7932390B2 (en) 2006-06-29 2011-04-26 Hoffman-La Roche Inc. Substituted thieno[3,2-C]pyridine carboxylic acid derivatives
US7968554B2 (en) 2007-08-14 2011-06-28 Hoffman-La Roche Inc. Pyrazolo[3,4-d]pyrimidine derivatives
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US8207166B2 (en) 2004-04-30 2012-06-26 Bayer Healthcare Llc Substituted pyrazolyl urea derivatives useful in the treatment of cancer
US8637553B2 (en) 2003-07-23 2014-01-28 Bayer Healthcare Llc Fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
US8796250B2 (en) 2003-05-20 2014-08-05 Bayer Healthcare Llc Diaryl ureas for diseases mediated by PDGFR
EP2527326B1 (en) * 2003-03-07 2014-10-08 Santen Pharmaceutical Co., Ltd Novel compounds having 4-pyridylalkylthio group as substituent
US8916555B2 (en) 2012-03-16 2014-12-23 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
US9540351B2 (en) 2013-09-18 2017-01-10 Axikin Pharmaceuticals, Inc. Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors
US9546163B2 (en) 2014-12-23 2017-01-17 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK288015B6 (en) * 2001-06-11 2012-11-05 Virochem Pharma Inc. Thiophene derivatives as antiviral agents for flavivirus infection
US8329924B2 (en) * 2001-06-11 2012-12-11 Vertex Pharmaceuticals (Canada) Incorporated Compounds and methods for the treatment or prevention of Flavivirus infections
US6924276B2 (en) 2001-09-10 2005-08-02 Warner-Lambert Company Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors
US6989451B2 (en) * 2002-06-04 2006-01-24 Valeant Research & Development Heterocyclic compounds and uses thereof
CN101721412A (en) * 2002-07-09 2010-06-09 法斯根有限责任公司 Methods of treating microbial infections in humans and animals
EA013371B1 (en) * 2002-07-09 2010-04-30 Фасджен, Ллс. Novel compounds, pharmaceutical compositions containing same and methods of use for same
CN100413861C (en) * 2002-12-10 2008-08-27 维勒凯姆制药股份有限公司 Compounds and methods for the treatment or prevention of flavivirus infections
NZ548949A (en) * 2004-02-17 2009-09-25 Santen Pharmaceutical Co Ltd Novel cyclic compound having 4-pyridylalkylthio group having substituted or unsubstituted amino group introduced therein
ES2368153T3 (en) * 2004-02-17 2011-11-14 Santen Pharmaceutical Co., Ltd. NEW CYCLIC COMPOUND PRESENTING A 4-PIRIDILALQUILTIO GROUP THAT PRESENTS AMINO (NOT) REPLACED INTRODUCED IN THE SAME.
JP4626353B2 (en) * 2004-02-17 2011-02-09 参天製薬株式会社 Novel cyclic compound having a 4-pyridylalkylthio group having a substituted or unsubstituted amino group introduced
RU2349588C2 (en) * 2004-08-26 2009-03-20 Пфайзер Продактс Инк. Method of producing isothiazole derivatives
JP4585978B2 (en) * 2005-03-03 2010-11-24 参天製薬株式会社 Novel cyclic compounds having a quinolylalkylthio group
AP2007004245A0 (en) 2005-05-13 2007-12-31 Virochem Pharma Inc Compounds and methods for the treatment or prevention of flavivirus infections
NZ576780A (en) 2006-11-15 2011-12-22 Virochem Pharma Inc Thiophene analogues for the treatment or prevention of flavivirus infections
TW200911240A (en) * 2007-06-11 2009-03-16 Kyowa Hakko Kogyo Kk Anti-tumor agent
JP2012531433A (en) * 2009-06-25 2012-12-10 メドリューション リミテッド Substituted heterocyclic compounds as kinase inhibitors and their uses

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4057416A (en) * 1976-06-18 1977-11-08 Fmc Corporation 3-Alkylthio-, 3-alkylsulfinyl-, and 3-alkylsulfonylisothiazole derivatives as herbicides
US4059433A (en) * 1976-06-18 1977-11-22 Fmc Corporation 3-Alkoxyisothiazole derivatives as herbicides
WO1996014843A2 (en) * 1994-11-10 1996-05-23 Cor Therapeutics, Inc. Pharmaceutical pyrazole compositions useful as inhibitors of protein kinases
US5773459A (en) * 1995-06-07 1998-06-30 Sugen, Inc. Urea- and thiourea-type compounds
WO1998052559A1 (en) * 1997-05-23 1998-11-26 Bayer Corporation Raf kinase inhibitors
WO1998054116A1 (en) * 1997-05-28 1998-12-03 Cadus Pharmaceutical Corporation Synthesis and use of thiophene- and pyrrole-based heteroaromatic compounds
WO1999062890A1 (en) * 1998-06-04 1999-12-09 Pfizer Products Inc. Isothiazole derivatives useful as anticancer agents

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1950990A1 (en) * 1968-10-17 1970-05-14 Ciba Geigy Process for the preparation of new triazacyclic compounds
GB1355513A (en) * 1971-04-07 1974-06-05 May & Baker Ltd Isothiazole derivatives
DE2408234A1 (en) * 1974-02-21 1975-09-04 Celamerck Gmbh & Co Kg 1-Alkyl-3-(substd 5-isothiazolyl)-ureas - with herbicidal, fungicidal and algicidal activity
US4075001A (en) * 1976-06-18 1978-02-21 Fmc Corporation 3-Aminoisothiazole derivatives as herbicides
DE3529247A1 (en) * 1985-05-17 1986-11-20 Bayer Ag, 5090 Leverkusen USE OF THIENYL UREAS AND ISOHARNS AS AN PERFORMANCE DRIVER IN ANIMALS, NEW THIENYL URINS AND ISOHARNS AND THEIR PRODUCTION
DE3540377A1 (en) * 1985-11-14 1987-05-21 Bayer Ag THIENOOXAZINONE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PERFORMANCE PROVIDER
DE3541631A1 (en) * 1985-11-26 1987-05-27 Bayer Ag SELECTIVE-FUNGICIDAL USE OF THIENYL URINE DERIVATIVES
US4859699A (en) * 1987-07-20 1989-08-22 Sandoz Ltd. Substituted N-benzoyl-N'-thienylureas
US6177401B1 (en) 1992-11-13 2001-01-23 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis
DE4328425A1 (en) * 1993-08-24 1995-03-02 Basf Ag Acylamino-substituted isoxazole or isothiazole derivatives, processes for their preparation and their use
TW276256B (en) * 1993-08-26 1996-05-21 Takeda Pharm Industry Co Ltd
US5792767A (en) * 1995-01-27 1998-08-11 Abbott Laboratories Bicyclic substituted hexahydrobenz e! isoindole alpha-1 adrenergic antagonists

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4057416A (en) * 1976-06-18 1977-11-08 Fmc Corporation 3-Alkylthio-, 3-alkylsulfinyl-, and 3-alkylsulfonylisothiazole derivatives as herbicides
US4059433A (en) * 1976-06-18 1977-11-22 Fmc Corporation 3-Alkoxyisothiazole derivatives as herbicides
WO1996014843A2 (en) * 1994-11-10 1996-05-23 Cor Therapeutics, Inc. Pharmaceutical pyrazole compositions useful as inhibitors of protein kinases
US5773459A (en) * 1995-06-07 1998-06-30 Sugen, Inc. Urea- and thiourea-type compounds
WO1998052559A1 (en) * 1997-05-23 1998-11-26 Bayer Corporation Raf kinase inhibitors
WO1998054116A1 (en) * 1997-05-28 1998-12-03 Cadus Pharmaceutical Corporation Synthesis and use of thiophene- and pyrrole-based heteroaromatic compounds
WO1999062890A1 (en) * 1998-06-04 1999-12-09 Pfizer Products Inc. Isothiazole derivatives useful as anticancer agents

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
CHIN. J. CHEM. (1997), 15(6), 541-547 *
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; LU, RONG-JIAN ET AL: "Regioselective addition of 5-amino-3-benzylthio-1,2,4-triazole and its analogs with aryl isocyanates", XP002142821, retrieved from STN Database accession no. 128:217329 *
WERBS, H. ET AL: "Reactions of 4-ethoxycarbonyl-3-amino-2-aminocarbonyl-5- methylthiopyrazole with isocyanates and isothiocyanates", PHARMAZIE (1974), 29(10-11), 687-9, XP002142820 *

Cited By (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897623B2 (en) 1999-01-13 2011-03-01 Bayer Healthcare Llc ω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US8841330B2 (en) 1999-01-13 2014-09-23 Bayer Healthcare Llc Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US6482842B2 (en) 2000-02-07 2002-11-19 Bristol-Myers Squibb Company 3-aminopyrazole inhibitors of cyclin dependent kinases
US6610724B2 (en) 2000-02-07 2003-08-26 Bristol-Myers Squibb Company 3-Aminopyrazole inhibitors of cyclin dependent kinases
US7358376B2 (en) 2000-02-12 2008-04-15 Astrazeneca Ab Substituted Thiophene compounds
WO2002068406A3 (en) * 2001-01-12 2003-04-24 Amgen Inc Substituted amine derivatives and their use for the treatment of angiogenesis
US7514564B2 (en) 2001-01-12 2009-04-07 Amgen Inc. Substituted amine derivatives and methods of use
US7102009B2 (en) 2001-01-12 2006-09-05 Amgen Inc. Substituted amine derivatives and methods of use
US7105682B2 (en) 2001-01-12 2006-09-12 Amgen Inc. Substituted amine derivatives and methods of use
US7956084B2 (en) 2001-07-25 2011-06-07 Astrazeneca Ab Phenyl thiophene carboxamide compounds as inhibitors of the enzyme IKK-2
US7098240B2 (en) 2001-07-25 2006-08-29 Astrazeneca Ab Compounds
US7125896B2 (en) 2001-07-25 2006-10-24 Astrazeneca Ab Thiophene carboxamide compounds as inhibitors of enzyme IKK-2
WO2003010158A1 (en) * 2001-07-25 2003-02-06 Astrazeneca Ab Novel compounds
WO2003010163A1 (en) * 2001-07-25 2003-02-06 Astrazeneca Ab Novel compounds
US8242147B2 (en) 2002-02-11 2012-08-14 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity
US7678811B2 (en) 2002-02-11 2010-03-16 Bayer Healthcare Llc Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
US8618141B2 (en) 2002-02-11 2013-12-31 Bayer Healthcare Llc Aryl ureas with angiogenesis inhibiting activity
US8071616B2 (en) 2002-02-11 2011-12-06 Bayer Healthcare Llc Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
US7838541B2 (en) 2002-02-11 2010-11-23 Bayer Healthcare, Llc Aryl ureas with angiogenesis inhibiting activity
WO2003105843A1 (en) * 2002-06-13 2003-12-24 Kinetek Pharmaceuticals, Inc. Methods of using isothiazole derivatives to treat cancer or inflammation
WO2004011461A1 (en) * 2002-07-25 2004-02-05 Pfizer Products Inc. Isothiazole derivatives useful as anticancer agents
JP2005536523A (en) * 2002-07-25 2005-12-02 ファイザー・プロダクツ・インク Isothiazole derivatives useful as anticancer drugs
EP1581309A4 (en) * 2002-11-15 2009-07-29 Exelixis Inc Kinase modulators
EP1581309A2 (en) * 2002-11-15 2005-10-05 Exelixis, Inc. Kinase modulators
US7572826B2 (en) 2003-01-15 2009-08-11 Astrazeneca Ab Thiophene-carboxamide derivatives and their use as inhibitors of the enzyme IKK-2
US7553868B2 (en) 2003-01-15 2009-06-30 Astrazeneca Ab Thiophene carboxamides as inhibitors of the enzyme IKK-2
CN1315820C (en) * 2003-01-15 2007-05-16 阿斯利康(瑞典)有限公司 Thiophene carboxamides as inhibitors of the enzyme IKK-2
EP2527326B1 (en) * 2003-03-07 2014-10-08 Santen Pharmaceutical Co., Ltd Novel compounds having 4-pyridylalkylthio group as substituent
US8796250B2 (en) 2003-05-20 2014-08-05 Bayer Healthcare Llc Diaryl ureas for diseases mediated by PDGFR
US8637553B2 (en) 2003-07-23 2014-01-28 Bayer Healthcare Llc Fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
US7803832B2 (en) 2004-03-18 2010-09-28 Pfizer Inc. N-(1-arylpyrazol-4L)sulfonamides and their use as parasiticides
US7687533B2 (en) 2004-03-18 2010-03-30 Pfizer Inc. N-(1-arylpyrazol-4l) sulfonamides and their use as parasiticides
US8207166B2 (en) 2004-04-30 2012-06-26 Bayer Healthcare Llc Substituted pyrazolyl urea derivatives useful in the treatment of cancer
US7932390B2 (en) 2006-06-29 2011-04-26 Hoffman-La Roche Inc. Substituted thieno[3,2-C]pyridine carboxylic acid derivatives
EP2116530A1 (en) * 2007-02-26 2009-11-11 Santen Pharmaceutical Co., Ltd Novel pyrrole derivative having ureide group and aminocarbonyl group as substituents
US7977371B2 (en) 2007-02-26 2011-07-12 Santen Pharmaceutical Co., Ltd. Pyrrole derivative having ureido group and aminocarbonyl group as substituents
EP2116530A4 (en) * 2007-02-26 2010-08-11 Santen Pharmaceutical Co Ltd Novel pyrrole derivative having ureide group and aminocarbonyl group as substituents
US7968554B2 (en) 2007-08-14 2011-06-28 Hoffman-La Roche Inc. Pyrazolo[3,4-d]pyrimidine derivatives
US8916555B2 (en) 2012-03-16 2014-12-23 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
US9346792B2 (en) 2012-03-16 2016-05-24 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
US9365556B2 (en) 2012-03-16 2016-06-14 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
US9382237B2 (en) 2012-03-16 2016-07-05 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
US9540351B2 (en) 2013-09-18 2017-01-10 Axikin Pharmaceuticals, Inc. Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors
US9546163B2 (en) 2014-12-23 2017-01-17 Axikin Pharmaceuticals, Inc. 3,5-diaminopyrazole kinase inhibitors
US9730914B2 (en) 2014-12-23 2017-08-15 Axikin Pharmaceuticals 3,5-diaminopyrazole kinase inhibitors

Also Published As

Publication number Publication date
DZ3042A1 (en) 2004-03-27
CA2374247A1 (en) 2000-11-30
US6380214B1 (en) 2002-04-30
ES2276681T3 (en) 2007-07-01
AU4137400A (en) 2000-12-12
BR0010746A (en) 2002-02-13
JP2003500401A (en) 2003-01-07
JP2005008641A (en) 2005-01-13
EP1187826B1 (en) 2006-12-27
DE60032601T2 (en) 2007-11-15
PA8494101A1 (en) 2003-09-05
DE60032601D1 (en) 2007-02-08
CA2374247C (en) 2008-01-22
MA26733A1 (en) 2004-12-20
JP3692041B2 (en) 2005-09-07
GT200000069A (en) 2001-11-08
ATE349440T1 (en) 2007-01-15
CO5170417A1 (en) 2002-06-27
EP1187826A1 (en) 2002-03-20
MXPA01011920A (en) 2002-05-06
PE20010152A1 (en) 2001-02-08
AR029634A1 (en) 2003-07-10
HN2000000051A (en) 2001-02-02
UY26143A1 (en) 2000-12-29
TNSN00104A1 (en) 2005-11-10

Similar Documents

Publication Publication Date Title
US6380214B1 (en) Heterocyclic derivatives useful as anticancer agents
JP4971946B2 (en) Isothiazole-4-carboxamide salts and their use as antiproliferative hyperagents
JP5258790B2 (en) RHO kinase inhibitor
US6653320B2 (en) Imidazopyridine derivatives
EA004935B1 (en) Isothiazole derivatives useful as anticancer agents
JP2010516698A (en) MEK inhibitor
WO2005123089A2 (en) Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease
AU2002214204A1 (en) Salts of a isothiazole-4-carboxamide and their use as anti-hyperproliferation agents
JPWO2007043568A1 (en) S1P3 receptor antagonist
CN110066276A (en) Heteroaromatic compound, wherein mesosome, preparation method, pharmaceutical composition and application
EP1590347A1 (en) Isothiazole derivatives
WO2004011461A1 (en) Isothiazole derivatives useful as anticancer agents
JP7021356B2 (en) Pyrimidine derivative kinase inhibitors
US6319915B1 (en) Benzazepine derivatives as inhibitors of hyperproliferation diseases
CN114634503A (en) Heterocyclic substituted-1, 3-thiazolidone derivative containing indole alkaloid and preparation method and application thereof

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2000920969

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2374247

Country of ref document: CA

Ref country code: CA

Ref document number: 2374247

Kind code of ref document: A

Format of ref document f/p: F

ENP Entry into the national phase

Ref country code: JP

Ref document number: 2000 619789

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: PA/a/2001/011920

Country of ref document: MX

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 2000920969

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 2000920969

Country of ref document: EP