Classifications

• • G—PHYSICS
  • G11—INFORMATION STORAGE
  • G11C—STATIC STORES
  • G11C16/00—Erasable programmable read-only memories
  • G11C16/02—Erasable programmable read-only memories electrically programmable
  • G11C16/06—Auxiliary circuits, e.g. for writing into memory
  • G11C16/10—Programming or data input circuits
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P17/00—Drugs for dermatological disorders
  • A61P17/14—Drugs for dermatological disorders for baldness or alopecia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P27/00—Drugs for disorders of the senses
  • A61P27/02—Ophthalmic agents
  • A61P27/06—Antiglaucoma agents or miotics
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
  • C07C59/40—Unsaturated compounds
  • C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
  • C07C59/56—Unsaturated compounds containing hydroxy or O-metal groups containing halogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
  • C07C59/40—Unsaturated compounds
  • C07C59/76—Unsaturated compounds containing keto groups
  • C07C59/90—Unsaturated compounds containing keto groups containing singly bound oxygen-containing groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
  • C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
  • C07C65/17—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups containing rings other than six-membered aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
  • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
  • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
  • C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
  • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
  • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom 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
  • C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
• • 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
  • 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
  • C07D333/40—Thiophene-2-carboxylic acid
• • 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
  • C07D417/12—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 linked by a chain containing hetero atoms as chain links

Definitions

• Ocular hypotensive agents are useful in the treatment of a number of various ocular hypertensive conditions, such as post-surgical and post-laser trabeculectomy ocular hypertensive episodes, glaucoma, and as presurgical adjuncts.
• Glaucoma is a disease of the eye characterized by increased intraocular pressure. On the basis of its etiology, glaucoma has been classified as primary or secondary. For example, primary glaucoma in adults (congenital glaucoma) may be either open-angle or acute or chronic angle-closure. Secondary glaucoma results from preexisting ocular diseases such as uveitis, intraocular tumor or an enlarged cataract.
• the underlying causes of primary glaucoma are not yet known.
• the increased intraocular tension is due to the obstruction of aqueous humor outflow.
• chronic open-angle glaucoma the anterior chamber and its anatomic structures appear normal, but drainage of the aqueous humor is impeded.
• acute or chronic angle-closure glaucoma the anterior chamber is shallow, the filtration angle is narrowed, and the iris may obstruct the trabecular meshwork at the entrance of the canal of Schlemm. Dilation of the pupil may push the root of the iris forward against the angle, and may produce pupilary block and thus precipitate an acute attack. Eyes with narrow anterior chamber angles are predisposed to acute anglecosure glaucoma attacks of various degrees of severity.
• Secondary glaucoma is caused by any interference with the flow of aqueous humor from the posterior chamber into the anterior chamber and subsequently, into the canal of Schlemm.
• Inflammatory disease of the anterior segment may prevent aqueous escape by causing complete posterior synechia in iris bombe, and may plug the drainage channel with exudates.
• Other common causes are intraocular tumors, enlarged cataracts, central retinal vein occlusion, trauma to the eye, operative procedures and intraocular hemorrhage.
• glaucoma occurs in about 2% of all persons over the age of 40 and may be asymptotic for years before progressing to rapid loss of vision.
• topical ⁇ -adrenoreceptor antagonists have traditionally been the drugs of choice for treating glaucoma.
• Eicosanoids and their derivatives are currently commercially available for use in glaucoma management.
• Eicosanoids and derivatives include numerous biologically important compounds such as prostaglandins and their derivatives.
• Prostaglandins can be described as derivatives of prostanoic acid which have the following structural formula:
• prostaglandins are known, depending on the structure and substituents carried on the alicyclic ring of the prostanoic acid skeleton. Further classification is based on the number of unsaturated bonds in the side chain indicated by numerical subscripts after the generic type of prostaglandin [e.g. prostaglandin E 1 (PGE 1 ), prostaglandin E 2 (PGE 2 )], and on the configuration of the substituents on the alicyclic ring indicated by ⁇ or ⁇ [e.g. prostaglandin F 2 ⁇ (PGF 2 ⁇ )].
• PGE 1 prostaglandin E 1
• PGE 2 prostaglandin E 2
• PPF 2 ⁇ prostaglandin F 2 ⁇
• Y is an organic acid functional group, or an amide or ester thereof comprising up to 14 carbon atoms; or Y is hydroxymethyl or an ether thereof comprising up to 14 carbon atoms; or Y is a tetrazolyl functional group;
• A is —CH 2 ) 6 —, cis CH 2 CH ⁇ CH—(CH 2 ) 3 —, or CH 2 C ⁇ C—(CH 2 ) 3 —, wherein 1 or 2 carbon atoms may be replaced by S or O; or
• A is —(CH 2 ) m —Ar—(CH 2 ) o — wherein Ar is interarylene or heterointerarylene, the sum of m and o is 1, 2, 3, or 4, and wherein one CH 2 may be replaced by S or O;
• J is C ⁇ O, CHOH, CHF, CHCl, CHBr, CF 2 , CCl 2 , CBr 2 , or CHCN;
• B is substituted aryl or substituted heteroaryl.
• carboxylic acid or a bioisostere thereof, said carboxylic acid having a structure
• A is —(CH 2 ) 6 —, cis —CH 2 CH ⁇ CH—(CH 2 ) 3 —, or —CH 2 C ⁇ C—(CH 2 ) 3 —, wherein 1 or 2 carbon atoms may be replaced by S or O; or A is —CH 2 ) m —Ar—(CH 2 ) o — wherein Ar is interarylene or heterointerarylene, the sum of m and o is 1, 2, 3, or 4, and wherein one CH 2 may be replaced by S or O;
• J is C ⁇ O, CHOH, CHF, CHCl, CHBr, CF 2 , CCl 2 , CBr 2 , or CHCN;
• B is substituted aryl or substituted heteroaryl.
• These compounds are useful for reducing intraocular pressure, treating glaucoma or intraocular pressure, growing hair, or improving the appearance of hair.
• Growing hair includes increasing the length or radius of individual hairs as well as increasing the number of hairs present in a given area.
• Improving the appearance of hair includes improving the color, such as darkening, or improving its gloss, shine, or other properties related to the reflection or dispersion of light.
• organic acid functional groups are bioisoteres of carboxylic acids.
• An organic acid functional group is an acidic functional group on an organic molecule.
• organic acid functional groups may comprise an oxide of carbon, sulfur, or phosphorous.
• Y is a carboxylic acid, sulfonic acid, or phosphonic acid functional group.
• an amide or ester of one of the organic acids shown above comprising up to 14 carbon atoms is also contemplated.
• a hydrocarbyl moiety replaces a hydrogen atom of an acid such as in a carboxylic acid ester, e.g. CO 2 Me, CO 2 Et, etc.
• an amine group replaces an OH of the acid.
• amides include CON(R 2 ) 2 , CON(OR 2 )R 2 , CON(CH 2 CH 2 OH) 2 , and CONH(CH 2 CH 2 OH) where R 2 is independently H, C 1 -C 6 alkyl, phenyl, or biphenyl.
• Moieties such as CONHSO 2 R 2 are also amides of the carboxylic acid notwithstanding the fact that they may also be considered to be amides of the sulfonic acid R 2 —SO 3 H.
• amides are also specifically contemplated, CONSO 2 -biphenyl, CONSO 2 -phenyl, CONSO 2 -heteroaryl, and CONSO 2 -naphthyl.
• the biphenyl, phenyl, heteroaryl, or naphthyl may be substituted or unsubstituted.
• Y may also be hydroxymethyl or an ether thereof comprising up to 14 carbon atoms.
• An ether is a functional group wherein a hydrogen of an hydroxyl is replaced by carbon, e.g., Y is CH 2 OCH 3 , CH 2 OCH 2 CH 3 , etc. These groups are also bioisosteres of a carboxylic acid.
• Up to 14 carbon atoms means that the entire Y moiety, including the carbonyl carbon of a carboxylic acid ester or amide, and both carbon atoms in the CH 2 O—C of an ether has 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 carbon atoms.
• Y may be a tetrazolyl functional group.
• a tetrazolyl functional group is another bioisostere of a carboxylic acid.
• An unsubstituted tetrazolyl functional group has two tautomeric forms, which can rapidly interconvert in aqueous or biological media, and are thus equivalent to one another. These tautomers are shown below.
• R 2 is C 1 -C 6 alkyl, phenyl, or biphenyl
• other isomeric forms of the tetrazolyl functional group such as the one shown below are also possible, unsubstituted and hydrocarbyl substituted tetrazolyl up to C 12 are considered to be within the scope of the term ‘tetrazolyl.’
• Y is CO 2 R 2 , CON(R 2 ) 2 , CON(OR 2 )R 2 , CON(CH 2 CH 2 OH) 2 , CONH(CH 2 CH 2 OH), CH 2 OH, P(O)(OH) 2 , CONHSO 2 R 2 , SO 2 N(R 2 ) 2 , SO 2 NHR 2 ,
• R 2 is independently H, C 1 -C 6 alkyl, unsubstituted phenyl, or unsubstituted biphenyl.
• the moieties shown below are also bioisosteres of a carboxylic acid.
• A is QCH 2 ) 6 —, cis CH 2 CH ⁇ CH—(CH 2 ) 3 —, or CH 2 C ⁇ C—(CH 2 ) 3 —, wherein 1 or 2 carbon atoms may be replaced with S or O; or A is —CH 2 ) m —Ar—(CH 2 ) o — wherein Ar is interarylene or heterointerarylene, the sum of m and o is 1, 2, 3, or 4, and wherein one CH 2 may be replaced with S or O.
• A may be —CH 2 ) 6 —, cis —CH 2 CH ⁇ CH—(CH 2 ) 3 —, or —CH 2 C ⁇ C—(CH 2 ) 3 —.
• A may be a group which is related to one of these three moieties in that any carbon is replaced with S and/or O.
• A may be a moiety where S replaces one or two carbon atoms such as one of the following or the like.
• A may be a moiety where O replaces one or two carbon atoms such as one of the following or the like.
• A may have an O replacing one carbon atom and an S replacing another carbon atom, such as one of the following or the like.
• A is —CH 2 ) m —Ar—(CH 2 ) o — wherein Ar is interarylene or heterointerarylene, the sum of m and o is 1, 2, 3, or 4, and wherein one CH 2 may be replaced with S or O.
• A comprises 1, 2, 3, or 4 CH 2 moieties and Ar, e.g. —CH 2 —Ar—, —(CH 2 ) 2 —Ar—, —CH 2 —Ar—CH 2 —, —CH 2 —Ar—(CH 2 ) 2 —, —(CH 2 ) 2 —Ar—(CH 2 ) 2 —, and the like; in another embodiment A comprises: 0; 0, 1, 2, or 3 CH 2 moieties; and Ar, e.g., —O—Ar—, Ar—CH 2 —O—, —O—Ar—(CH 2 ) 2 —, —O—CH 2 —Ar—, —O—CH 2 —Ar—(CH 2 ) 2 , and the like; or in another embodiment A comprises: S; 0, 1, 2, or 3 CH 2 moieties; and Ar, e.g., —S—Ar—, Ar—CH 2 —S—, —S—Ar—,
• the sum of m and o is 2, 3, or 4 wherein one CH 2 may be replaced with S or O.
• the sum of m and o is 3 wherein one CH 2 may be replaced with S or O.
• the sum of m and o is 2 wherein one CH 2 may be replaced with S or O.
• the sum of m and o is 4 wherein one CH 2 may be replaced with S or O.
• Interarylene or heterointerarylene refers to an aryl ring or ring system or a heteroaryl ring or ring system which connects two other parts of a molecule, i.e. the two parts are bonded to the ring in two distinct ring positions.
• Interarylene or heterointerarylene may be substituted or unsubstituted. Unsubstituted interarylene or heterointerarylene has no substituents other than the two parts of the molecule it connects. Substituted interarylene or heterointerarylene has substituents in addition to the two parts of the molecule it connects.
• Ar is substituted or unsubstituted interphenylene, interthienylene, interfurylene, interpyridinylene, interoxazolylene, and interthiazolylene.
• Ar is interphenylene (Ph).
• A is —CH 2 ) 2 —Ph-. While not intending to limit scope of the invention in any way, substituents may have 4 or less heavy atoms, wherein the heavy atoms are C, N, O, S, P, F, Cl, Br, and/or I in any stable combination. Any number of hydrogen atoms required for a particular substituent will also be included. A subsfftuent must be stable enough for the compound to be useful as described herein.
• a substituent may also have a metal cation or any other stable cation having an atom not listed above if the substituent is acidic and the salt form is stable.
• —OH may form an O—Na + salt or CO 2 H may form a CO 2 —K + salt. Any cation of the salt is not counted in the 4 or less heavy atoms.”
• the substituent may be hydrocarbyl having up to 4 carbon atoms, including alkyl up to G4, alkenyl, alkynyl, and the like;
• organic acid such as CO 2 H, SO 3 H, P(O)(OH) 2 , and the like, and salts thereof;
• halo such as F, Cl, or Br
• hydroxyl such as F, Cl, or Br
• NH 2 and alkylamine functional groups up to C 3 other N or S containing substituents such as CN, NO 2 , and the like; and the like.
• A is —CH 2 ) m —Ar—(CH 2 ) o — wherein Ar is interphenylene, the sum of m and o is 1, 2, or 3, and wherein one CH 2 may be repaced with S or O.
• A is —CH 2 Ar—OCH 2 —.
• A is CH 2 —Ar—OCH 2 — and Ar is interphenylene.
• Ar is attached at the 1 and 3 positions, otherwise known as m-interphenylene, such as when A has the structure shown below.
• A is —CH 2 ) 6 —, cis —CH 2 CH ⁇ CH—(CH 2 ) 3 —, or —CH 2 C ⁇ C—(CH 2 ) 3 —, wherein 1 or 2 carbon atoms may be replaced with S or O; or A is —CH 2 ) 2 -Ph- wherein one CH 2 may be replaced with S or O.
• A is —CH 2 ) 6 —, cis —CH 2 CH ⁇ CH—(CH 2 ) 3 —, or —CH 2 C ⁇ C—(CH 2 ) 3 —, wherein 1 or 2 carbon atoms may be replaced with S or O; or A is —CH 2 ) 2 -Ph-.
• A has one of the following structures, where Y is attached to the aromatic or heteroaromatic ring.
• A is —CH 2 OCH 2 Ar.
• A is —CH 2 SCH 2 Ar.
• A is —(CH 2 ) 3 Ar.
• A is —CH 2 O(CH 2 ) 4 .
• A is —CH 2 S(CH 2 ) 4 .
• A is —CH 2 ) 6 —.
• A is cis —CH 2 CH ⁇ CH—(CH 2 ) 3 —.
• A is —CH 2 C ⁇ C—(CH 2 ) 3 —.
• A is —S(CH 2 ) 3 S(CH 2 ) 2 —.
• A is —(CH 2 ) 4 OCH 2 —.
• A is cis —CH 2 CH ⁇ CH—CH 2 OCH 2 —.
• A is —CH 2 CH ⁇ CH—CH 2 OCH 2 —.
• A is —(CH 2 ) 2 S(CH 2 ) 3 —.
• A is —CH 2 -Ph-OCH 2 —, wherein Ph is interphenylene.
• A is —CH 2 -mPh-OCH 2 —, wherein mPh is m-interphenylene.
• A is —CH 2 —O—(CH 2 ) 4 —.
• A is —CH 2 —O—CH 2 —Ar—, wherein Ar is 2,5-interthienylene.
• A is —CH 2 —O—CH 2 —Ar—, wherein Ar is 2,5-interfurylene.
• A is (3-methylphenoxy)methyl.
• A is (4-but-2-ynyloxy)methyl.
• A is 2)-2-ethylthio)thiazolyl.
• A is 2-(3-propyl)thiazol-5-yl.
• A is 3-methoxymethyl)phenyl.
• A is 3-(3-propylphenyl.
• A is 3-methylphenethyl.
• A is 442-ethyl)phenyl.
• A is 4-phenethyl.
• A is 4-methoxybutyl.
• A is 5-(methoxymethyl)furan-2-yl.
• A is 5-(methoxymethyl)thiophen-2-yl.
• A is 5-(3-propyl)furan-2-yl.
• A is 5-(3-propyl)thiophen-2-yl.
• A is 6-hexyl
• A is (Z)-6-hex-4-enyl.
• A is —CH 2 ) 3 Ar—, —O(CH 2 ) 2 Ar—, —CH 2 OCH 2 Ar—, —(CH 2 ) 2 Ar—, —O(CH 2 ) 2 Ar—, —CH 2 OCH 2 Ar—, or —(CH 2 ) 2 OAr, wherein Ar is monocyclic interheteroarylene.
• Ar is interthienylene.
• Ar is interthiazolylene.
• Ar is interoxazolylene.
• J is C ⁇ O, CHOH, CHF, CHCl, CHBr, or CHCN.
• Aryl is an aromatic rng or ring system such as phenyl, naphthyl, biphenyl, and the like.
• Heteroaryl is aryl having one or more N, O, or S atoms in the ring, i.e. one or more ring carbons are substituted by N, O, and/or S. While not intending to be limiting, examples of heteroaryl include thienyl, pyrdinyl, furyl, benzothienyl, benzofuryl, imidizololyl, indolyl, and the like.
• a substituent of aryl or heteroaryl may have up to 20 non-hydrogen atoms each in any stable combination and as many hydrogen atoms as necessary, wherein the non-hydrogen atoms are C, N, O, S. P. F, Cl, Br, and/or I in any stable combination. However, the total number of non-hydrogen atoms on all of the substituents combined must also be 20 or less.
• a substituent must be sufficiently stable for the compound to be useful as described herein.
• a substituent may also have a metal cation or other stable cation having an atom not listed above if the substituent is acidic and the salt form is stable. For example, —OH may form an —O—Na + salt or CO 2 H may form a CO 2 —K + salt.
• a substituent may be:
• hydrocarbyl i.e. a moiety consisting of only carbon and hydrogen such as alkyl, alkenyl, alkynyl, and the like, including linear, branched or cyclic hydrocarbyl, and combinations thereof; hydrocarbyloxy, meaning O-hydrocarbyl such as OCH 3 , OCH 2 CH 3 , O-cyclohexyl, etc, up to 19 carbon atoms; other ether substituents such as CH 2 OCH 3 , (CH 2 ) 2 OCH(CH 3 ) 2 , and the like; thioether substituents including S-hydrocarbyl and other thioether substituents; hydroxyhydrocarbyl, meaning hydrocarbyl-OH such as CH 2 OH, C(CH 3 ) 2 OH, etc, up to 19 carbon atoms; nitrogen substituents such as NO 2 , CN, and the like, including amino, such as NH 2 , NH(CH 2 CH 3 OH), NHCH 3 , and the
• Substituted aryl or heteroaryl may have as many substituents as the ring or ring system will bear, and the substituents may be the same or different.
• an aryl ring or a heteroaryl ring may be substituted with chloro and methyl; methyl, OH, and F; CN, NO 2 , and ethyl; and the like including any conceivable substituent or combination of substituent possible in light of this disclosure.
• Substituted aryl or substituted heteroaryl also includes a bicyclic or polycyclic ring system wherein one or more rings are aromatic and one or more rings are not.
• indanonyl, indanyl, indanolyl, tetralonyl, and the like are substituted aryl.
• an aromatic or heteroaromatic ring, not a non-aromatic ring must be attached to the remainder of the molecule.
• the bond is a direct bond to an aromatic ring.
• B is substituted aryl or heteroaryl.
• B is substituted phenyl
• B has no halogen atoms.
• B is 4-(1-hydroxy-2,2-dimethylpropyl)phenyl.
• B is 4-(1-hydroxy-2-methylpropan-2-yl)phenyl.
• B is 4-(1-hydroxy-2-methylpropyl)phenyl.
• B is 4-(1-hydroxybutyl)phenyl.
• B is 4-(1-hydroxyheptyl)phenyl.
• B is 4-(1-hydroxyhexyl)phenyl.
• B is 4-(1-hydroxypentyl)phenyl.
• B is 4-(1-hydroxypropyl)phenyl.
• B is 4-(3-hydroxy-2-methylheptan-2-yl)phenyl.
• B is 4-(3-hydroxy-2-methyloctan-2-yl)phenyl.
• B is 1-hydroxy-2,3-dihydro-1 Hinden-5-yl.
• B is 2,3-dihydro-1 Hinden-5-yl.
• B is 4-(hydroxy(1-propylcyclobutyl)methyl)phenyl.
• B is 4-(1-hydroxy-5,5-dimethylhexyl)phenyl.
• B is 4-(hydroxy(1-propylcyclobutyl)methyl)phenyl.
• B is 4-tert-butylphenyl.
• B is 4-hexylphenyl.
• B is 4-(1-hydroxy-2-phenylethyl)phenyl.
• B is 4-(1-hydroxy-3-phenylpropyl)phenyl.
• B is 4-(1-hydroxycyclobutyl)phenyl.
• B is 4-(2-cyclohexyl-1-hydroxyethyl)phenyl.
• B is 4-(3-cyclohexyl-1-hydroxypropyl)phenyl.
• B is 4-(cyclohexyl(hydroxy)methyl)phenyl.
• B is 4-(cyclohexylmethyl)phenyl.
• B is 4-(hydroxy(phenyl)methyl)phenyl.
• Another embodiment is a compound according to the structure
• Another embodiment is a compound according to the structure
• Another embodiment is a compound according to the structure
• C1-10 hydrocarbyl is hydrocarbyl having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 carbon atoms.
• Hydrocarbyl is a moiety consisting of only carbon and hydrogen, and includes, but is not limited to alkyl, alkenyl, alkynyl, and the like, and in some cases aryl, and combinations thereof.
• Alkyl is hydrocarbyl having no double or triple bonds including: linear alkyl such as methyl, ethyl, propyl, nbutyl, n-pentyl, n-hexyl, and the like; branched alkyl such as isopropyl, branched butyl isomers (i.e. sec-butyl, tert-butyl, etc), branched pentyl isomers (i.e.
• alkenyl is hydrocarbyl having one or more double bonds including linear alkenyl, branched alkenyl, cyclic alkenyl, and combinations thereof in analogy to alkyl.
• Alkynyl is hydrocarbyl having one or more triple bonds including linear alkynyl, branched alkynyl, cyclic alkynyl and combinations thereof in analogy to alkyl.
• Aryl is an unsubstituted or substituted aromatic ring or ring system such as phenyl, naphthyl, biphenyl, and the like. Aryl may or may not be hydrocarbyl, depending upon whether it has substituents with heteroatoms.
• Arylalkyl is alkyl which is substituted with aryl. In other words alkyl connects aryl to the remaining part of the molecule. Examples are —CHaPhenyl, —CH 2 CH 2 -Phenyl, and the like.
• Arylalkyl may or may not be hydrocarbyl, depending upon whether it has substituents with heteroatoms.
• Unconjugated dienes or polyenes have one or more double bonds which are not conjugated. They may be linear, branched, or cyclic, or a combination thereof. Combinations of the above are also possible.
• each of the structures below is contemplated.
• These structures, or pharmaceutically acceptable salts thereof, or prodrugs thereof individually represent a compound which is an embodiment contemplated herein. In other words, each structure represents a different embodiment.
• x is 5, 6, or 7, and y+z is 2x+1.
• x is 5 and y+z is 11.
• x is 6 and y+z is 13.
• x is 7 and y+z is 15.
• Hypothetical examples of useful compounds are shown below.
• Y is an organic acid functional group, or an amide or ester thereof comprising up to 14 carbon atoms; or Y is hydroxymethyl or an ether thereof comprising up to 14 carbon atoms; or Y is a tetrazolyl functional group;
• A is —CH 2 ) 6 —, cis CH 2 CH ⁇ CH—(CH 2 ) 3 —, or —CH 2 C ⁇ C—(CH 2 ) 3 —, wherein 1 or 2 carbon atoms may be replaced by S or O; or
• A is —(CH 2 ) m —Ar—(CH 2 ) o , wherein Ar is interarylene or heterointerarylene, the sum of m and o is 1, 2, 3, or 4, and wherein one CH 2 may be replaced by S or O;
• J is C ⁇ O, CHOH, CHF, CHCl, CHBr, CF 2 , CC12, CBr 2 , or CHCN;
• B is substituted aryl or substituted heteroaryl.
• R 2 is independently H, C 1 -C 6 alkyl, unsubstituted phenyl, or unsubstituted biphenyl.
• R is hydrogen or C 1-10 hydrocarbyl.
• R is hydrogen or C 1-10 hydrocarbyl.
• compositions, kits, methods, uses, and medicaments employing the hypothetical compound examples are hypothetical examples of compositions, kits, methods, uses, and medicaments employing the hypothetical compound examples.
• a composition comprising a compound according to any one of compound examples 1 to 48, wherein said composition is a liquid which is ophthalmically acceptable.
• a medicament comprising a compound according to any one of compound examples 1 to 48, wherein said composition is a liquid which is ophthalmically acceptable.
• a method comprising administering a compound according to any one of compound examples 1 to 48 to a mammal for the treatment of glaucoma or ocular hypertension.
• a kit comprising a composition comprising compound according to any one of compound examples 1 to 48, a container, and instructions for administration of said composition to a mammal for the treatment of glaucoma or ocular hypertension.
• a “pharmaceutically acceptable salt” is any salt that retains the activity of the parent compound and does not impart any additional deleterious or untoward effects on the subject to which it is administered and in the context in which it is administered compared to the parent compound.
• a pharmaceutically acceptable salt also refers to any salt which may form in vivo as a result of administration of an acid, another salt, or a prodrug which is converted into an acid or salt.
• Pharmaceutically acceptable salts of acidic functional groups may be derived from organic or inorganic bases.
• the salt may comprise a mono or polyvalent ion.
• the inorganic ions lithium, sodium, potassium, calcium, and magnesium.
• Organic salts may be made with amines, particularly ammonium salts such as mono-, di- and trialkyl amines or ethanol amines. Salts may also be formed with caffeine, tromethamine and similar molecules.
• Hydrochloric acid or some other pharmaceutically acceptable acid may form a salt with a compound that includes a basic group, such as an amine or a pyridine ring.
• a “prodrug” is a compound which is converted to a therapeutically active compound after administration, and the term should be interpreted as broadly herein as is generally understood in the art. While not intending to limit the scope of the invention, conversion may occur by hydrolysis of an ester group or some other biologically labile group. Generally, but not necessarily, a prodrug is inactive or less active than the therapeutically active compound to which it is converted. Ester prodrugs of the compounds disclosed herein are specifically contemplated. An ester may be derived from a carboxylic acid of Cl (i.e.
• an ester may be derived from a carboxylic acid functional group on another part of the molecule, such as on a phenyl ring. While not intending to be limiting, an ester may be an alkyl ester, an aryl ester, or a heteroaryl ester.
• alkyl has the meaning generally understood by those skilled in the art and refers to linear, branched, or cyclic alkyl moieties.
• C 1-6 alkyl esters are particularly useful, where alkyl part of the ester has from 1 to 6 carbon atoms and includes, but is not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, secbutyl, iso-butyl, tbutyl, pentyl isomers, hexyl isomers, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and combinations thereof having from 1-6 carbon atoms, etc.
• a drug to be administered systemically it may be confected as a powder, pill, tablet or the like, or as a solution, emulsion, suspension, aerosol, syrup or elixir suitable for oral or parenteral administration or inhalation.
• non-toxic solid carriers include, but are not limited to, pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharin, the polyalkylene glycols, talcum, cellulose, glucose, sucrose and magnesium carbonate.
• the solid dosage forms may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period.
• a time delay material such as glyceryl monostearate or glyceryl distearate may be employed. They may also be coated by the technique described in the U.S. Pat. Nos.
• Liquid pharmaceutically administrable dosage forms can, for example, comprise a solution or suspension of one or more of the presently useful compounds and optional pharmaceutical adjutants in a carrier, such as for example, water, saline, aqueous dextrose, glycerol, ethanol and the like, to thereby form a solution or suspension.
• a carrier such as for example, water, saline, aqueous dextrose, glycerol, ethanol and the like, to thereby form a solution or suspension.
• the pharmaceutical composition to be administered may also contain minor amounts of nontoxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents and the like.
• auxiliary agents are sodium acetate, sorbitan monolaurate, triethanolamine, sodium acetate, triethanolamine oleate, etc.
• Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa., 16th Edition, 1980.
• the composition of the formulation to be administered, in any event contains a quantity of one or more of the presently useful compounds in an amount effective to provide the desired therapeutic effect.
• Parenteral administration is generally characterized by injection, either subcutaneously, intramuscularly or intravenously.
• Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol and the like.
• the injectable pharmaceutical compositions to be administered may also contain minor amounts of non-toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents and the like.
• the amount of the presently useful compound or compounds administered is dependent on the therapeutic effect or effects desired, on the specific mammal being treated, on the severity and nature of the mammal's condition, on the manner of administration, on the potency and pharmacodynamics of the particular compound or compounds employed, and on the judgment of the prescribing physician.
• the therapeutically effective dosage of the presently useful compound or compounds may be in the range of about 0.5 or about 1 to about 100 mg/kg/day.
• a liquid which is ophthalmically acceptable is formulated such that it can be administered topically to the eye.
• the comfort should be maximized as much as possible, although sometimes formulation considerations (e.g. drug stability) may necessitate less than optimal comfort.
• the liquid should be formulated such that the liquid is tolerable to the patient for topical ophthalmic use.
• an ophthalmically acceptable liquid should either be packaged for single use, or contain a preservative to prevent contamination over multiple uses.
• Preservatives that may be used in the pharmaceutical compositions of the present invention include, but are not limited to, benzalkonium chloride, chlorobutanol, thimerosal, phenylmercuric acetate and phenyomercuric nitrate.
• a useful surfactant is, for example, Tween 80.
• various useful vehicles may be used in the ophthalmic preparations of the present invention. These vehicles include, but are not limited to, polyvinyl alcohol, povidone, hydroxypropyl methyl cellulose, poloxamers, carboxymethyl cellulose, hydroxyethyl cellulose and purified water.
• Tonicity adjustors may be added as needed or convenient. They include, but are not limited to, salts, particularly sodium chloride, potassium chloride, mannitol and glycerin, or any other suitable ophthalmically acceptable tonicity adjustor.
• buffers include acetate buffers, citrate buffers, phosphate buffers and borate buffers. Acids or bases may be used to adjust the pH of these formulations as needed.
• an ophthalmically acceptable antioxidant for use in the present invention includes, but is not limited to, sodium metabisulfite, sodium thiosulfate, acetylcysteine, butylated hydroxyanisole and butylated hydroxytoluene.
• excipient components which may be included in the ophthalmic preparations are chelating agents.
• a useful chelating agent is edetate disodium, although other chelating agents may also be used in place or in conjunction with it.
• the ingredients are usually used in the following amounts:
• Ingredient Amount (% w/v) active ingredient about 0.001-5 preservative 0-0.10 vehicle 0-40 tonicity adjustor 1-10 buffer 0.01-10 pH adjustor q.s. pH 4.5-7.5 antioxidant as needed surfactant as needed purified water as needed to make 100%
• Topical formulations may generally be comprised of a pharmaceutical carrier, cosolvent, emulsifier, penetration enhancer, preservative system, and emollient.
• the actual dose of the active compounds of the present invention depends on the specific compound, and on the condition to be treated; the selection of the appropriate dose is well within the knowledge of the skilled artisan.
• the compounds disclosed herein are also useful in combination with other drugs useful for the treatment of glaucoma or other conditions.
• ⁇ -Blockers including carteolol, levobunolol, metiparanolol, timolol hemihydrate, timolol maleate, P1-selective antagonists such as betaxolol, and the like, or pharmaceutically acceptable salts or prodrugs thereof;
• Adrenergic Aqonists including non-selective adrenergic aqonists such as epinephrine borate, epinephrine hydrochloride, and dipivefrin, and the like, or pharmaceutically acceptable salts or prodrugs thereof; and ⁇ 2 -selective adrenergic agonists such as apraclonidine, brimonidine, and the like, or pharmaceutically acceptable salts or prodrugs thereof;
• Carbonic Anhydrase Inhibitors including acetazolamide, dichlorphenamide, methazolamide, brinzolamide, do
• these compounds can be administered topically, pedocularly, intraoculardy, or by any other effective means known in the art.
• prostaglandin EP2 selective agonists are believed to have several medical uses.
• U.S. Pat. No. 6,437,146 teaches the use of prostaglandin EP2 selective agonists “for treating or preventing inflammation and pain in joint and muscle (e.g., rheumatoid arthritis, rheumatoid spondylitis, osteoarthrtis, gouty arthritis, juvenile arthritis, etc.), inflammatory skin condition (e.g., sunburn, burns, eczema, dermatitis, etc.), inflammatory eye condition (e.g., conjunctivitis, etc.), lung disorder in which inflammation is involved (e.g., asthma, bronchitis, pigeon fancier's disease, farmers lung, etc.), condition of the gastrointestinal tract associated with inflammation (e.g., aphthous ulcer, Chrohn's disease, atrophic gastritis, gastritis varialo
• U.S. Pat. No. 6,710,072 teaches the use of EP2 agonists for the treatment or prevention of “osteoporosis, constipation, renal disorders, sexual dysfunction, baldness, diabetes, cancer and in disorder of immune regulation . . . various pathophysiological diseases including acute myocardial infarction, vascular thrombosis, hypertension, pulmonary hypertension, ischemic heart disease, congestive heart failure, and angina pectoris.”
• These compounds can also be used to treat or prevent conditions affecting the posterior part of the eye including maculopathies/retinal degeneration such as nonexudative age related macular degeneration (ARMD), exudative age related macular degeneration (ARMD), choroidal neovascularization, diabetic retinopathy, acute macular neuroretinopathy, central serous chorioretinopathy, cystoid macular edema, and diabetic macular edema; uveitis/retinitis/choroiditis such as acute multifocal placoid pigment epitheliopathy, Behcet's disease, birdshot retinochoroidopathy, infectious (syphilis, lyme, tuberculosis, toxoplasmosis), intermediate uveitis (pars planitis), multifocal choroiditis, multiple evanescent white dot syndrome (mewds), ocular sarcoidosis, posterior scleritis, serpiginous choroid
• the disease or condition is retinitis pigmentosa, proliferative vitreal retinopathy (PVR), age-related macular degeneration (ARMD), diabetic retinopathy, diabetic macular edema, retinal detachment, retinal tear, uveitus, or cytomegalovirus retinitis.
• PVR proliferative vitreal retinopathy
• ARMD age-related macular degeneration
• diabetic retinopathy diabetic macular edema
• retinal detachment retinal tear, uveitus
• cytomegalovirus retinitis cytomegalovirus retinitis
• These compounds are also useful in treating asthma.
• HEK-293 cells stably expressing the human or feline FP receptor, or EP 1 , EP 2 , or EP 4 receptors were washed with TME buffer, scraped from the bottom of the flasks, and homogenized for 30 sec using a Brinkman PT 10/35 polytron.
• TME buffer was added to achieve a final 40 ml volume in the centrifuge tubes (the composition of TME is 100 mM TRIS base, 20 mM MgCl 2 , 2M EDTA; 10 N HCl is added to achieve a pH of 7.4).
• the cell homogenate was centrifuged at 19000 r.p.m. for 20 min at 4° C. using a Beckman Ti-60 rotor. The resultant pellet was resuspended in TME buffer to give a final 1 mg/ml protein concentration, as determined by Biorad assay.
• Radioligand binding competition assays vs. [ 3 H]17-phenyl PGF 2 ⁇ (5 nM) were performed in a 100 ⁇ l volume for 60 min. Binding reactions were started by adding plasma membrane fraction. The reaction was terminated by the addition of 4 ml ice-cold TRIS-HCl buffer and rapid filtration through glass fiber GF/B filters using a Brandel cell harvester. The filters were washed 3 times with ice-cold buffer and oven dried for one hour.
• [ 3 ]H-1 PGE 2 (specific activity 180 Ci mmol) was used as the radioligand for EP receptors.
• [ 3 H] 17-phenyl PGF 2 ⁇ was employed for FP receptor binding studies. Binding studies employing EP1, EP2, EP4 and FP receptors were performed in duplicate in at least three separate experiments. A 200 ⁇ l assay volume was used. Incubations were for 60 min at 25° C. and were terminated by the addition of 4 ml of ice-cold 50 mM TRIS-HCl, followed by rapid filtration through Whatman GF/B filters and three additional 4 ml washes in a cell harvester (Brandel).
• HEK-293(EBNA) cells stably expressing one type or subtype of recombinant human prostaglandin receptors (prostaglandin receptors expressed: hDP/Gqs5; hEP 1 ; hEP 2 /Gqs 5 ; hEP 3A /Gqi5; hEP 4 /Gqs5; hFP; hIP; hTP), were cultured in 100 mm culture dishes in high-glucose DMEM medium containing 10% fetal bovine serum, 2 mM 1-glutamine, 250 ⁇ g/ml geneticin (G418) and 200 ⁇ g/ml hygromycin B as selection markers, and 100 units/ml penicillin G. 100 ⁇ g/ml streptomycin and 0.25 ⁇ g/ml amphotericin B.
• Cells were excited with an Argon laser at 488 nm, and emission was measured through a 510-570 nm bandwidth emission filter (FLIPRTM, Molecular Devices, Sunnyvale, Calif.). Drug solution was added in a 50 ⁇ l volume to each well to give the desired final concentration. The peak increase in fluorescence intensity was recorded for each well.
• FLIPRTM 510-570 nm bandwidth emission filter
• HBSS-HEPES buffer On each plate, four wells each served as negative (HBSS-HEPES buffer) and positive controls (standard agonists: BW245C (hDP); PGE2 (hEP 1 ; hEP 2 /Gqs5; hEP 3A /Gqi5; hEP 4 /Gqs5); PGF 2 ⁇ (hFP); carbacyclin (hIP); U-46619 (hTP), depending on receptor).
• standard agonists BW245C (hDP); PGE2 (hEP 1 ; hEP 2 /Gqs5; hEP 3A /Gqi5; hEP 4 /Gqs5); PGF 2 ⁇ (hFP); carbacyclin (hIP); U-46619 (hTP), depending on receptor).
• the peak fluorescence change in each drug-containing well was then expressed relative to the controls.
• HTS high-throughput
• CoRe concentration-response
• Treatment of inflammatory bowel disease may be accomplished by the administration of the compounds described herein to the suffering mammal.
• Inflammatory bowel disease describes a variety of diseases characterized by inflammation of the bowels including, but not limited to, ulcerative colitis and Crohn's disease.
• Treatment may be accomplished by oral administration, by suppository, or parenteral administration, or some other suitable method.
• these methods include 1) administration of a prodrug, including an azo or a carbohydrate based prodrug; 2) coating the drug with, or encapsulating or impregnating the drug into a polymer designed for delivery to the colon, 3) time released delivery of the dnug, 4) use of a bioadhesive system; and the like.
• intestinal microflora are capable of reductive cleavage of an azo bond leaving the two nitrogen atoms as amine functional groups.
• the azo prodrug approach has been used to deliver to 5-aminosalicylic acid to the colons of humans in dinical trials for the treatment of inflammatory bowel disease.
• bacteria of the lower GI also have enzymes which can digest glycosides, glucuronides, cyclodextrins, dextrans, and other carbohydrates, and ester prodrugs formed from these carbohydrates have been shown to deliver the parent active drugs selectively to the colon.
• glycoside conjugates may be useful for the delivery of steroids to the human colon.
• Other in vivo studies have suggested that glucouronide, cyclodextrin, and dextran prodnugs of steroids or non-steroidal anti-inflammatory drugs are useful for delivery of these drugs to the lower GI tract.
• An amide of salicylic acid and glutamic acid has been shown to be useful for the delivery of salicylic acid to the colon of rabbit and dog.
• carbohydrate polymers such as amylase, arabinogalactan, chitosan, chondroiton sulfate, dextran, guar gum, pectin, xylin, and the like, or azo-group containing polymers can be used to coat a drug compound, or a drug may be impregnated or encapsulated in the polymer. It is believed that after oral administration, the polymers remain stable in the upper GI tract, but are digested by the microflora of the lower GI thus releasing the drug for treatment.
• Polymers which are sensitive to pH may also be used since the colon has a higher pH than the upper GI tract.
• Such polymers are commercially available.
• Rohm Pharmaceuticals, Darmstadt, Germany commercially provides pH dependent methacrylate based polymers and copolymers which have varying solubilities over different pH ranges based upon the number of free carboxylate groups in the polymer under the tradename Eudragito.
• EudragitE dosage forms are currently used to deliver salsalazine for the treatment of ulcerative colitis and Crohn's disease. Time release systems, bioadhesive systems, and other delivery systems have also been studied.

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