WO2007027468A1 - Ep2 receptor agonists for treating glaucoma - Google Patents
Ep2 receptor agonists for treating glaucoma Download PDFInfo
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- WO2007027468A1 WO2007027468A1 PCT/US2006/032670 US2006032670W WO2007027468A1 WO 2007027468 A1 WO2007027468 A1 WO 2007027468A1 US 2006032670 W US2006032670 W US 2006032670W WO 2007027468 A1 WO2007027468 A1 WO 2007027468A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
- C07D213/71—Sulfur atoms to which a second hetero atom is attached
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Definitions
- the present invention relates to novel EP2 Receptor agonists that are useful for treating glaucoma and other conditions and indications in man.
- 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 pre-existing 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 pupillary block and thus precipitate an acute attack. Eyes with narrow anterior chamber angles are predisposed to acute angle-closure 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.
- glaucoma as a disorder of increased intraocular pressure (lOP) oversimplifies the clinical situation.
- Another possible factor in the etiology of glaucoma may be regulation of the regional microvasculature of the anterior optic nerve.
- microvascular factors are important is that many microvascular diseases are associated with glaucomatous optic neuropathy.
- Cioffi, et al. Matusi published a paper on the Ophthalmologic aspects of Systemic Vasculitis" [Nippon Rinsho. 52 (8), p. 2158-63, August 1994] and added further support to the assertion that many microvascular diseases are associated with glaucomatous optic neuropathy.
- systemic vasculitis such as polyarteritis nodosa, giant cell angitis and aortitis syndrome were reviewed.
- Systemic lupus erythematosus is not categorized as systemic vasculitis, however its ocular findings are microangiopathic. Therefore, review of its ocular findings was included in this paper.
- the most common fundus finding in these diseases is ischemic optic neuropathy or retinal vascular occlusions. Therefore several points in diagnosis or pathogenesis of optic neuropathy and retinal and choroidal vaso-occlusion were discussed.
- Choroidal ischemia was able to be diagnosed clinically, since fluorescein angiography was applied in these lesions.
- choroidal arteries When choroidal arteries are occluded, overlying retinal pigment epithelium is damaged. This causes disruption of barrier function of the epithelium and allows fluid from choroidal vasculatures to pass into subsensory retinal spaces. This is a pathogenesis of serous detachment of the retina. The retinal arterial occlusion resulted in non- perfused retina. Such hypoxic retina released angiogenesis factors which stimulate retinal and iris neovascularizations and iris neovascularizations may cause neovascular glaucoma.
- Fluorescein defects are significantly correlated with visual field loss and retinal nerve fiber layer loss.
- the second circulatory defect is a decrease of flow of fluorescein in the retinal vessels, especially the retinal veins, so that the greater the age, diastolic blood pressure, ocular pressure and visual field loss , the less the flow.
- Both the optic disk and retinal circulation defects occur in untreated ocular hypertensive eyes. These observations indicate that circulatory defects in the optic disk and retina occur in ocular hypertension and open-angle glaucoma and increase with the progression of the disease.
- Prostaglandins were earlier regarded as potent ocular hypertensives; however, evidence accumulated in the last two decades shows that some prostaglandins are highly effective ocular hypotensive agents and are ideally suited for the long-term medical management of glaucoma.
- Some prostaglandins are highly effective ocular hypotensive agents and are ideally suited for the long-term medical management of glaucoma.
- Bito, L. Z. Biological Protection with Prostaglandins Cohen, M. M., ed., Boca Raton, FIa, CRC Press Inc., 1985, pp. 231-252; and Bito, L. Z., Applied Pharmacology in the
- Such prostaglandins include PGF 2 ⁇ , PGF 1 ⁇ , PGE 2 , and certain lipid-soluble esters, such as C 1 to Cg alkyl esters, e.g. 1-isopropyl ester, of such compounds.
- the present invention provides a method of treating ocular hypertension or lowering elevated intraocular pressure (lOP) by administering to a mammal having ocular hypertension a therapeutically effective amount of N, N' dibenzyl pyridyl sulfonamide compound having EP 2 receptor agonist activity which compound may be represented by
- R is hydrogen or an aliphatic straight chain or branched radical comprised of 1 to 20 carbon atoms, or R is a polar esterifying group which may be represented by the formula (CHR 1 CYHX) n H wherein X is O or S; Y is selected from the group consisting of H,
- R is selected from the group consisting of
- R 1 is selected from the group consisting of hydrogen and alky] radicals comprised of from 1 to 20 carbon atoms.
- the present invention relates to an ophthalmic solution comprising a therapeutically effective amount of a compound of the above formula or a pharmaceutically-acceptable salt thereof, in admixture with a non-toxic, ophthalmically acceptable liquid vehicle, packaged in a container suitable for metered application.
- the present invention relates to a pharmaceutical product, comprising a container adapted to dispense its contents in a metered form; and an ophthalmic solution therein, as hereinabove defined.
- Figure 1 shows the effect on the IOP of dogs by the administration of a compound of the invention.
- Figure 2 shows the effect on the ocular surface hyperemia of dogs by the administration of a compound of the invention.
- Figure 3 shows the effect on the IOP of monkeys by the administration of a solution comprising 0.01% w/v of a compound of the invention.
- Figure 4 shows the effect on the IOP of monkeys by the administration of a solution comprising 0.03% w/v of a compound of the invention.
- Figure 5 shows the effect on the IOP of monkeys by the administration of a solution comprising 0.1% w/v of a compound of the invention.
- Figure 6 shows the effect on the IOP of dogs by the administration of a compound, as an isopropyl ester, of the invention.
- Figure 7 shows the effect on the ocular surface hyperemia of dogs by the administration of a compound, as an isopropyl ester, of the invention.
- Figure 8 shows the effect on the IOP of monkeys by the administration of a solution comprising 0.1% w/v of a compound, as an isopropyl ester, of the invention.
- the present invention relates to the use of N, N'dibenzyl pyridyl sulfonamides having EP 2 -receptor agonist activity for treating ocular hypertension in and/or providing neuroprotection to a mammal, e.g. a human, in need of such treatment.
- the compounds used in accordance with the present invention are encompassed by the following structural formula:
- R is an aliphatic straight chain or branched radical comprised of from 1 to 20 carbon atoms, or R is a polar esterifying group which may be represented by the formula (CHR 1 CYHX) n H wherein X is O or S; Y is selected from the group consisting of H, -OH, - COOH, CONH 2 , SO 3 H and PO 3 H 2 and n is an integer of from 1 to 10, or R is selected from the group consisting of (i) acyl sulfonamide radicals represented by the formula NSO 2 R 1
- R 1 is selected from the group consisting of hydrogen and alkyl radicals comprised of from 1 to 20 carbon atoms, and pharmaceutically-acceptable salts thereof.
- R is a lower alkyl radical, i.e. a Ci to C 7 alkyl, e.g. a C 1 to C 4 alkyl radical such as methyl, ethyl, isopropyl, isobutyl, etc. More preferably, R is a methyl or ethyl or isopropyl radical, e.g. a methyl or isopropyl radical. Most preferably R is a isopropyl radical.
- R 1 is H or a lower alkyl radical, i.e. a Ci to C 7 alkyl, e.g. a Ci to C 4 alkyl radical such as methyl, ethyl, isopropyl, isobutyl, etc. More preferably, R is a methyl or ethyl or isopropyl radical, e.g. a methyl or isopropyl radical. Most preferably R is a isopropyl radical.
- a Ci to C 7 alkyl e.g. a Ci to C 4 alkyl radical such as methyl, ethyl, isopropyl, isobutyl, etc.
- R is a methyl or ethyl or isopropyl radical, e.g. a methyl or isopropyl radical.
- R is a isopropyl radical.
- X is O.
- Y is hydrogen
- R is a polar esterifying group it may be (CH 2 CH 2 O) n H, e.g. C 2 H 4 OH.
- a pharmaceutically-acceptable salt is any salt which retains the activity of the parent compound and does not impart any deleterious or undesirable effect on the subject to whom it is administered and in the context in which it is administered.
- salts formed with inorganic ions such as sodium, potassium, calcium, magnesium and zinc.
- compositions including the above compounds may be prepared by combining a therapeutically effective amount of at least one compound according to the present invention, or a pharmaceutically-acceptable salt thereof, as an active ingredient, with conventional ophthalmically acceptable pharmaceutical excipients, and by preparation of unit dosage forms suitable for topical ocular use.
- the therapeutically efficient amount typically is between about 0.0001 and about 5% (w/v), preferably about 0.001 to about 1.0% (w/v) in liquid formulations.
- solutions are prepared using a physiological saline solution as a major vehicle.
- the pH of such ophthalmic solutions should preferably be maintained between 4.5 and 8.0 with an appropriate buffer system, a neutral pH being preferred but not essential.
- the formulations may also contain conventional, pharmaceutically-acceptable preservatives, stabilizers and surfactants.
- Preferred 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 phenylmercuric nitrate.
- a preferred surfactant is, for example, Tween 80.
- various preferred 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 cyclodextrin and purified water.
- Tonicity adjusters 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.
- the preferred chelating agent is edentate disodium, although other chelating agents may also be used in place of or in conjunction with it.
- the ingredients are usually used in the following amounts:
- Inqredient Amount (% w/v) active ingredient about 0.001-5 preservative 0-0.10 vehicle 0-40 tonicity adjustor 0-10 buffer 0.01-10 pH adjustor q.s. pH 4.5-8.0 antioxidant as needed surfactant as needed purified water as needed to make 100%
- 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 ophthalmic formulations for use in the method of the present invention are conveniently packaged in forms suitable for metered application, such as in containers equipped with a dropper, to facilitate application to the eye.
- Containers suitable for dropwise application are usually made of suitable inert, non-toxic plastic material, and generally contain between about 0.5 and about 15 ml solution.
- One package may contain one or more unit doses.
- Especially preservative-free solutions are often formulated in non-resealable containers containing up to about ten, preferably up to about five units doses, where a typical unit dose is from one to about 8 drops, preferably one to about 3 drops.
- the volume of one drop usually is about 20-35 ⁇ .
- Cynomolgus monkeys (Macaca fascicularis) were used for the intraocular pressure studies. Each animal was unilaterally laser-treated by circumferential laser photocoagulation to induce ocular hypertension in one eye. Conscious female animals were trained sit in custom design chairs and to accept applanation pneumatonometry. The drug was administered topically to one eye using a dropper bottle to deliver approximately a 35 ⁇ volume, the other eye received vehicle (1 % polysorbate 80 in 5 mM Tris HCI) as a control. Proparacaine at 0.25% was used for corneal anesthesia during tonometry. Intraocular pressure was determined just before drug administration and at 2, 4, 6, and 24 hours.
- Figures 1 and 2 show that a single daily dose of (3- ⁇ [(4-tert-butyl-benzyl)-(pyridine-3- sulfonyl)-amino]-methyl ⁇ -phenoxy)-acetic acid over a 5 day period is effective for reducing IOP of the dogs with mild ocular surface hyperemia that diminishes over time.
- Figures 3 through 5 show that a single dose of 0.01%, 0.03% or 0.1% (3- ⁇ [(4-tert-butyl- benzyl)-(pyridine-3-sulfonyl)-amino]-methyl ⁇ -phenoxy)-acetic acid t° the eye of a monkey lowers the elevated IOP over 24 hours, almost to the level of the control normotensive eye for the two higher doses.
- Figures 6 and 7 show that a single dose of the isopropyl ester of (3- ⁇ [(4-tert-butyl-benzyl)- (pyridine-3-sulfonyl)-amino]-methyl ⁇ -phenoxy)-acetic acid over a 5 day period is effective for reducing IOP of the dogs with minimal ocular surface hyperemia.
- Figure 8 shows that a single dose of the isopropyl ester of (3- ⁇ [(4-tert-butyl-benzyl)- (pyridine-3-sulfonyl)-amino]-methyl ⁇ -phenoxy)-acetic acid to the eye of a monkey lowers the elevated IOP over 24 hours almost to the level of the control normotensive eye.
- the present invention may utilize any other N, N' dibenzyl pyridyl sulfonamide compound having EP 2 receptor agonist activity in addition to the compounds represented by the above general formula to treat ocular hypertension or provide neuroprotection to the eyes of a mammal, e.g. a human.
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- Health & Medical Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Ophthalmology & Optometry (AREA)
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- Bioinformatics & Cheminformatics (AREA)
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- Heart & Thoracic Surgery (AREA)
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Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2006285177A AU2006285177A1 (en) | 2005-08-29 | 2006-08-21 | EP2 receptor agonists for treating glaucoma |
EP06813615A EP1919870A1 (en) | 2005-08-29 | 2006-08-21 | Ep2 receptor agonists for treating glaucoma |
CA002602442A CA2602442A1 (en) | 2005-08-29 | 2006-08-21 | Ep2 receptor agonists for treating glaucoma |
BRPI0615245-7A BRPI0615245A2 (en) | 2005-08-29 | 2006-08-21 | ep2 receptor agonists for treatment of glaucoma |
JP2008529107A JP2009506113A (en) | 2005-08-29 | 2006-08-21 | EP2 receptor agonists for the treatment of glaucoma |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US71258605P | 2005-08-29 | 2005-08-29 | |
US60/712,586 | 2005-08-29 | ||
US11/472,145 US7696235B2 (en) | 2005-08-29 | 2006-06-21 | EP2 receptor agonists for treating glaucoma |
US11/472,145 | 2006-06-21 |
Publications (1)
Publication Number | Publication Date |
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WO2007027468A1 true WO2007027468A1 (en) | 2007-03-08 |
Family
ID=37529305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/032670 WO2007027468A1 (en) | 2005-08-29 | 2006-08-21 | Ep2 receptor agonists for treating glaucoma |
Country Status (7)
Country | Link |
---|---|
US (1) | US7696235B2 (en) |
EP (1) | EP1919870A1 (en) |
JP (1) | JP2009506113A (en) |
AU (1) | AU2006285177A1 (en) |
BR (1) | BRPI0615245A2 (en) |
CA (1) | CA2602442A1 (en) |
WO (1) | WO2007027468A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010113957A1 (en) | 2009-03-30 | 2010-10-07 | 宇部興産株式会社 | Pharmaceutical composition for treating or preventing glaucoma |
WO2011030871A1 (en) * | 2009-09-11 | 2011-03-17 | 宇部興産株式会社 | N-substituted heteroaryl compounds |
WO2011030868A1 (en) * | 2009-09-11 | 2011-03-17 | 宇部興産株式会社 | Substituted carbonyl compounds |
US8063240B2 (en) | 2007-11-14 | 2011-11-22 | Cayman Chemical Company, Incorporated | Prostaglandin E1 and E2 analogs for the treatment of various medical conditions |
US8648097B2 (en) | 2008-03-12 | 2014-02-11 | Ube Industries, Ltd. | Pyridylaminoacetic acid compound |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0714683A2 (en) * | 2006-07-28 | 2013-03-26 | Pfizer Prod Inc | ep2 agonists |
CN102498101A (en) * | 2009-09-11 | 2012-06-13 | 宇部兴产株式会社 | Aniline compounds |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999019300A1 (en) * | 1997-10-10 | 1999-04-22 | Pfizer Inc. | Prostaglandin agonists and their use to treat bone disorders |
WO2004078169A1 (en) * | 2003-03-04 | 2004-09-16 | Pfizer Products Inc. | Use of ep2 selective receptor agonists in medical treatment |
US20050065133A1 (en) * | 2003-09-19 | 2005-03-24 | Pfizer Inc | Pharmaceutical compositions and methods comprising combinations of 2-alkylidene-19-nor-vitamin D derivatives and an EP2 or EP4 selective agonist |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020115695A1 (en) * | 2000-11-07 | 2002-08-22 | Paralkar Vishwas M. | Combination therapies for the stimulation of bone growth |
-
2006
- 2006-06-21 US US11/472,145 patent/US7696235B2/en not_active Expired - Fee Related
- 2006-08-21 EP EP06813615A patent/EP1919870A1/en not_active Withdrawn
- 2006-08-21 AU AU2006285177A patent/AU2006285177A1/en not_active Abandoned
- 2006-08-21 WO PCT/US2006/032670 patent/WO2007027468A1/en active Application Filing
- 2006-08-21 JP JP2008529107A patent/JP2009506113A/en active Pending
- 2006-08-21 BR BRPI0615245-7A patent/BRPI0615245A2/en not_active IP Right Cessation
- 2006-08-21 CA CA002602442A patent/CA2602442A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999019300A1 (en) * | 1997-10-10 | 1999-04-22 | Pfizer Inc. | Prostaglandin agonists and their use to treat bone disorders |
WO2004078169A1 (en) * | 2003-03-04 | 2004-09-16 | Pfizer Products Inc. | Use of ep2 selective receptor agonists in medical treatment |
US20050065133A1 (en) * | 2003-09-19 | 2005-03-24 | Pfizer Inc | Pharmaceutical compositions and methods comprising combinations of 2-alkylidene-19-nor-vitamin D derivatives and an EP2 or EP4 selective agonist |
Non-Patent Citations (4)
Title |
---|
BITO, L. Z.: "Applied Pharmacology in the Medical Treatment of Glaucomas", 1984, GRUNE & STRATTON, pages: 477 - 505 |
BITO, L. Z.: "Bioloaical Protection with Prostaglandins", 1985, CRC PRESS INC., pages: 231 - 252 |
PARALKAR VM ET AL., PROC. NAT. ACAD. SCI., vol. 100, 2003, pages 6736 - 6740 |
STARR, M.S., EXP. EVE RES, vol. 11, 1971, pages 170 - 177 |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8063240B2 (en) | 2007-11-14 | 2011-11-22 | Cayman Chemical Company, Incorporated | Prostaglandin E1 and E2 analogs for the treatment of various medical conditions |
US8648097B2 (en) | 2008-03-12 | 2014-02-11 | Ube Industries, Ltd. | Pyridylaminoacetic acid compound |
WO2010113957A1 (en) | 2009-03-30 | 2010-10-07 | 宇部興産株式会社 | Pharmaceutical composition for treating or preventing glaucoma |
US8685986B2 (en) | 2009-03-30 | 2014-04-01 | Ube Industries, Ltd. | Medical composition for treatment or prophylaxis of glaucoma |
WO2011030871A1 (en) * | 2009-09-11 | 2011-03-17 | 宇部興産株式会社 | N-substituted heteroaryl compounds |
WO2011030868A1 (en) * | 2009-09-11 | 2011-03-17 | 宇部興産株式会社 | Substituted carbonyl compounds |
JPWO2011030868A1 (en) * | 2009-09-11 | 2013-02-07 | 宇部興産株式会社 | Substituted carbonyl compounds |
Also Published As
Publication number | Publication date |
---|---|
AU2006285177A1 (en) | 2007-03-08 |
JP2009506113A (en) | 2009-02-12 |
EP1919870A1 (en) | 2008-05-14 |
BRPI0615245A2 (en) | 2011-05-10 |
US7696235B2 (en) | 2010-04-13 |
US20070049625A1 (en) | 2007-03-01 |
CA2602442A1 (en) | 2007-03-08 |
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