WO1999002165A1 - Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma - Google Patents
Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma Download PDFInfo
- Publication number
- WO1999002165A1 WO1999002165A1 PCT/SE1998/001368 SE9801368W WO9902165A1 WO 1999002165 A1 WO1999002165 A1 WO 1999002165A1 SE 9801368 W SE9801368 W SE 9801368W WO 9902165 A1 WO9902165 A1 WO 9902165A1
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- WIPO (PCT)
- Prior art keywords
- cycloalkyl
- alkyl
- prostaglandin
- aryl
- prostaglandin analogue
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- 0 Cc1cccc(CCC(CC[C@](C(CC(C2)=O)C2C2)C2=*)O)c1 Chemical compound Cc1cccc(CCC(CC[C@](C(CC(C2)=O)C2C2)C2=*)O)c1 0.000 description 4
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/557—Eicosanoids, e.g. leukotrienes or prostaglandins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/557—Eicosanoids, e.g. leukotrienes or prostaglandins
- A61K31/5575—Eicosanoids, e.g. leukotrienes or prostaglandins having a cyclopentane, e.g. prostaglandin E2, prostaglandin F2-alpha
-
- 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
Definitions
- the invention is related to a method of treating glaucoma and ocular hypertension utilizing prostaglandin analogues or derivatives that are devoid of, or have reduced melanogenic effect in the eye.
- the invention also relates to ophthalmic compositions containing prostaglandin compounds devoid of, or have reduced melanogenic effect in the eye.
- Glaucoma is an eye disorder characterized by increased intraocular pressure, excavation of the optic nerve head, and gradual loss of the visual field.
- An abnormally high intraocular pressure is commonly known to be detrimental to the eye, and there are clear indications that in glaucoma the intraocular pressure is the most important factor causing degenerative changes in the retina and the optic nerve head.
- the exact pathophysiological mechanism of open angle glaucoma is, however, still unknown. Unless treated, glaucoma may lead to blindness, the course of the disease typically being slow with progressive loss of vision.
- the intraocular pressure (IOP) can be defined according to the formula (1):
- IOP Pe + (Ft - Fu) x R
- Pe is the episcleral venous pressure
- Ft the formation of aqueous humor
- Fu the part of the aqueous humor which exits the eye through the uveoscleral outflow pathway
- R is the resistance in the trabecular outflow pathway.
- the aqueous humor in the anterior and posterior chambers of the eye is produced by the ciliary processes behind the iris. It then flows through the pupil into the anterior chamber, and normally exits the eye through the trabecular meshwork and Schlemm's canal into the episcleral veins outside the eye globe. However, part of the aqueous humor may leave the eye through the uveoscleral outflow route.
- the flow in this route is regarded as only minimally influenced by the intraocular pressure (Bill, 1975).
- the intraocular pressure in humans is normally in the range of 12-22 mmHg. At higher pressures, e.g. above 22 mmHg, there is an increased risk that the eye may be damaged. In one particular form of glaucoma, normal tension glaucoma, damage may, however, occur at intraocular pressure levels that are within the normal physiological range.
- the opposite situation is also known, i.e. some individuals may exhibit an abnormally high intraocular pressure without any manifest defects in the visual field or the optic nerve head. Such conditions usually are referred to as ocular hypertension.
- Glaucoma treatment can be given by means of drugs, laser or surgery.
- drug treatment the purpose is to reduce either the formation of aqueous humor (Ft), or the resistance to outflow of aqueous humor (R), which according to formula (1) above will result in reduced intraocular pressure; alternatively to increase the outflow of aqueous humor through the uveoscleral route which according to formula (1) also reduces the intraocular pressure.
- the use of prostaglandins and their derivatives is described in several patents and patent applications, for instance in US 4,599,353 (Bito), US 4,952,581 (Bito), WO89/03384 (Resul and Stjemschantz), EP 170258 (Cooper), EP 253094 (Goh), and in EP 308135 (Ueno).
- Prostaglandins are fatty acids usually derived from the precursors eicosatrienoic, eicosatetraenoic and eicosapentaneoic acid through metabolic steps involving oxygenation. Naturally occurring prostaglandins typically have the general structure shown in Fig. 1.
- the prostaglandins accordingly carry a cyclopentane ring to which two carbon chains link, the upper chain usually being called the alpha chain and the lower chain usually being called the omega chain.
- the prostaglandins are classified in subgroups A, B, C, D, E, F, G, H, I and J depending on the stmcture and substituents in the cyclopentane ring as shown in Fig. 2.
- the alpha chain is a 7 carbon carboxy-terminated aliphatic chain whereas the omega chain is an 8 carbon methyl-terminated aliphatic chain.
- subscripts of 1 to 3 are given.
- the double bond is situated between carbons 13 and 14 in the omega chain, and it exhibits trans configuration in naturally occurring prostaglandins.
- prostaglandins with subscript 2 ⁇ an additional double bond in the cis configuration is situated between carbons 5 and 6 in the alpha chain, and finally in prostaglandins with subscript 3, a third double bond is situated between carbons 17 and 18 in the omega chain. This double bond also exhibits cis configuration in naturally occurring prostaglandins. All naturally occurring prostaglandins carry a hydroxyl group on carbon 15, which is essential for biological activity.
- the receptor system for the naturally occurring prostaglandins has only recently been elucidated. Thus most of the prostaglandin receptors have been pharmacologically characterized and their molecular stmcture identified by molecular biological techniques (Coleman et al., 1994). There are specific receptors for the naturally occurring prostaglandins.
- the receptors for PGD, PGE, PGF, PGI 2 (prostacyclin) and TxA (thromboxane) being abbreviated DP, EP, FP, IP, and TP, respectively.
- the EP receptor can be subdivided into four receptors, namely the EPi, EP 2 , EP 3 , and EP 4 receptors.
- Specific tissues or cells may express only a few or many of these receptors, depending on the evolutionary development of this autacoid system in different species.
- the cat iris sphincter muscle expresses predominantly FP receptors that are functionally coupled and mediate constriction of the pupil, while the corresponding smooth muscle of the bovine eye expresses EPj and TP receptors, activation of either of which will result in contraction of the muscle.
- a compound which binds to a specific receptor and activates it is called an agonist while a compound that only binds to a receptor without activating it is called an antagonist.
- a limiting factor may be their property of causing increased pigmentation of the iris in the eye (Stjemschantz and Aim, 1996).
- the colour of the iris during chronic treatment in monkeys and in man tends to become darker, turning into brown. While this apparently has no negative medical consequences, it is a clear disadvantage from a cosmetic point of view, particularly in patients undergoing treatment only in one eye. It would thus be desirable to identify prostaglandins which effectively reduce the intraocular pressure without causing the side-effect of increased iridial pigmentation.
- prostaglandin derivatives and analogues which are selective agonists for the EPi subgroup of prostanoid receptors fulfil the criteria for a prostaglandin analogue which effectively reduces the intraocular pressure without causing increased production of pigment (melanogenesis) in the iris.
- the background of this finding is that in a study to identify the prostanoid receptor subtypes in the human iridial melanocytes we have found that these cells express in their cell membranes the FP, EP 2 , and EP 3 receptors, but not the EP t and TP receptors.
- intraocular pressure reducing effect of several relatively selective EPi agonists we have investigated the intraocular pressure reducing effect of several relatively selective EPi agonists and found that these prostaglandin analogues effectively and potently reduce the intraocular pressure both in cats and monkeys.
- high selectivity or specificity to the EPi receptor compared to other prostaglandin receptors in the eye characterizes the compounds to be used in the method or compositions according to the present invention. It need not to be said that the more selective the compound is for the EPj receptor, the better results are obtained but a certain advantage is of course achieved also in cases of some interaction with other receptors.
- High selectivity in this connection means that the effect on the EPi receptor is a least more than 5 times, especially more than 10 times, and in particular more than 100 or 1000 times the effect on the other prostaglandin receptors.
- the specific prostaglandin analogues that we have used for exemplifying and proving this invention were PGF 2 p (1), PGF p isopropyl ester (2), 17-phenyl-18,19,20-trinor- PGE 2 (3), 17-phenyl-18,19,20-trinor-PGE 2 isopropyl ester (4), 15(R,S)-16,16- trimethylene-PGE 2 (5), 15(R,S)-16,16-trimethylene-PGE 2 methyl ester (6), and 13,14- dihydro-17-(3-fluorophenyl)-18, 19, 20 trinor-PGE 2 -isopropyl ester (7). All these analogues are relatively selective EPi receptor agonists. The receptor profiles of the test compounds are presented in Table I.
- the invention relates to the use of selective prostaglandin EPi receptor agonists devoid of melanogenic effect for the treatment of glaucoma or ocular hypertension.
- the method for treating glaucoma or ocular hypertension comprises contacting the surface of the eye with an effective intraocular pressure reducing amount of a composition, containing an EPj selective prostaglandin as aforesaid, in order to reduce the intraocular pressure and to maintain said pressure at a reduced level.
- the composition usually contains about 0.1-100 ⁇ g, especially 1-30 ⁇ g per application of the active substance.
- the composition is applied topically on the eye 1- 3 times daily.
- the prostaglandin derivative is mixed with an ophthalmologically compatible vehicle known per se.
- the vehicle which may be employed for preparing compositions of this invention comprises aqueous solutions, e.g. physiological saline, oil solutions, or ointments.
- the vehicle may furthermore contain ophthalmologically compatible preservatives such as e.g. benzalkonium chloride, surfactants, such as polysorbate 80, liposomes or polymers, for example methyl cellulose, polyvinyl alcohol, polyvinyl pyrrolidone and hyaluronic acid; these may be used for increasing the viscosity.
- ophthalmologically compatible preservatives such as e.g. benzalkonium chloride, surfactants, such as polysorbate 80, liposomes or polymers, for example methyl cellulose, polyvinyl alcohol, polyvinyl pyrrolidone and hyaluronic acid; these may be used for increasing the viscosity.
- surfactants such as polysorbate 80
- liposomes or polymers for example methyl
- the invention in another aspect, relates to ophthalmological compositions for medical treatment of glaucoma or ocular hypertension which comprise an effective intraocular pressure reducing amount of a prostaglandin analogue which is a selective agonist of EP ! receptors as defined above and an ophthalmologically compatible carrier.
- the effective amount usually comprises a dose of about 0.1-100 ⁇ g in about 10-50 ⁇ l of the composition.
- the compositions according to the present invention are clear improvements over the prior art prostaglandin compositions due to the selectivity of the active compound for EPI receptors compared to other prostaglandin receptors with the risk for pigmentation eliminated or at least substantially reduced.
- the invention relates to the use of the prostaglandin analogue for the preparation of a medicament for treatment of glaucoma and ocular hypertension.
- the prostaglandin analogue is derived from PGF or PGE type prostaglandins.
- the prostaglandin analogue is a compound of the general formula: wherein: the wavy bonds represent the ⁇ or ⁇ configuration, and the dashed bonds represent a single bond, a triple bond or a double bond in the cis or trans configuration;
- R is hydrogen, saturated or unsaturated alkyl, preferably C ⁇ -10 alkyl, cycloalkyl, preferably C 3-8 cycloalkyl, aryl, arylalkyl, preferably aryl-C 2-5 alkyl, or heteroaryl;
- Rl is a saturated or unsaturated alkyl group having 2-5 carbon atoms, optionally interrupted by heteroatoms selected from oxygen, sulfur and nitrogen, cycloalkyl, preferably C 3- cycloalkyl, cycloalkenyl, preferably C 3-7 cycloalkenyl, aryl or heteroaryl;
- R2 is hydrogen, hydroxy, methyl, ethyl, methoxy or OCOR4, where R4 is a straight or branched chain saturated or unsaturated alkyl group, preferably Cj.io alkyl, especially C ⁇ -6 alkyl, or a cycloalkyl, preferably C 3 . 8 cycloalkyl, or aryl group;
- R3 is a straight or branched chain saturated or unsaturated alkyl group, preferably having 3-8 carbon atoms, especially 3-5 carbon atoms, optionally interrupted by one or more heteroatoms selected from oxygen, sulfur and nitrogen, each carbon atom optionally being substituted with a substituent selected from C1.5 alkyl, hydroxy and carbonyl groups, hydroxy and carbonyl preferentially being attached to carbon 15 of the prostaglandin stmcture, and said alkyl group optionally containing a cycloalkyl, preferably C 3-8 cycloalkyl, aryl or heteroaryl group, which may be mono- or independently multi-substituted with C ⁇ . 3 alkyl, C ⁇ -3 alkoxy, hydroxy, nitro, trifluoromethyl or halogen; or a pharmaceutically acceptable salt or ester thereof.
- Aryl is preferably substituted or unsubstituted phenyl.
- exemplary heteroaryl groups are thiophene, furan, thiazole, isothiazole, oxazole, isoxazole, pyridine, pyrazine, pyrimidine, pyridazine.
- Aryl, heteroaryl and cycloalkyl may be mono- or independently di- or multi- substituted by C ⁇ -3 alkyl, C ⁇ -3 alkoxy, hydroxy, nitro, trifluoromethyl or halogen.
- Unsaturated alkyl may contain one or more double and/or triple bonds.
- Halogen is fluorine, chlorine, bromine or iodine, especially fluorine, chlorine or bromine.
- the prostaglandins may be in epimeric mixtures as well as in the form of the individual epimers.
- the prostaglandin receptors were identified using the reversed transcriptase polymerase chain reaction (RT-PCR) technique. Specific primers were designed for the FP, EPi, EP 2 , EP 3 , and TP receptors. The primers used in the assays are presented in Table II.
- RT-PCR was performed on mRNA isolated from human iridial melanocytes in culture. The cultured cells were used for preparing mRNA. The RT-PCR mix was analysed on agarose gel and bands of expected size were cloned and sequenced. The deduced sequences were analysed for similarity to each prostaglandin receptor sequence.
- Human iridial melanocytes were isolated and cultured according to Hu et al. (1993) and used in early passages. Cells were grown to confluence and harvested for the mRNA enrichment.
- mRNA was isolated using Dynals mRNA Direct System (Dynal A/S, Norway) according to the manufacturer's instructions. 100.000-200.000 human melanocyte cells were used in the enrichment. mRNA is covalently bound to an oligo-dT labeled Dynabead. Using reverse transcriptase the first strand cDNA is synthesized directly on the Dynabeads with the oligo-dT as a reverse transcriptase primer. The second strand cDNA is synthesized using a known 3' sequence primer from respective prostaglandin receptor, resulting in double stranded cDNA. The same set of Dynabeads was used for each receptor RT-PCR.
- Receptor specific primers were used for PCR amplifying DNA from Dynabead bound cDNA according to the manufacturer's instmctions.
- the PCR was performed in 50 ⁇ l final volume with 5% DMSO, 200 ⁇ M dNTPs and 20 pmoles of each primer.
- the other receptors hot start with AmpliWax pellets Perkin Elmer, USA was used in a final volume of 75 ⁇ l with 5% DMSO, 200 ⁇ M dNTPs and 20 pmoles of each primer.
- EPi primers primary primers; TGT GGC ATG GCC GTG GAG and ACC AAC ACC AGC ATT
- GGG C secondary primers CTG CAG GGA GGT AGA GCT C and GGC ACG TGG TGC
- TTC ATC G EP 2 primers primary primers; CAA CCA TGC CTA TTT CTA CAG C and TCT CGC TCC AAA
- EP 3 primers primary primers; GGG ATC CAA GAT CTG GTT CAG and GCC TTC CCG ATC
- TP primers primary primers; CTG GTG ACC GGT ACC ATC GTG GTG T and GTA GAT CTA
- PCR mix from these reactions was analyzed on a 1% LMP agarose gel (BioRad Laboratories, USA).
- DNA fragments of the expected size were TA-cloned using a TA-cloning kit according to the manufacturer's instmctions (Invitrogen Inc., USA), and sequenced on an Applied Biosystem Model 373A DNA sequencing system (Applied Biosystems Inc., USA) according to Applied Biosystems' protocol for their Taq Dye Dioxy Terminator cycle sequencing kit.
- the generated primary data were processed on a VAX computer using the sequence analysis programs from Genetics Computer Group Inc., Madison, USA (Devereux, J., et al., Nucleic Acids Research 12 (1): 387-395 (1984).
- Example 4 17-Phenyl-18,19,20-trinor-PGE isopropyl ester (compound 4) DBU (43.5 mg, 0.29 mmol) in acetonitrile (1 ml) was added dropwise to a stirred solution of compound 3 (22.1 mg, 0.057 mmol) in acetonitrile (3 ml) at 0 °C. The mixture was allowed to warm to room temperature whereupon isopropyl iodide (78.0 mg, 0.46 mmol) in acetonitrile (2 ml) was added dropwise.
- Example 5 15RS-16,16-trimethylene-PGE 2 (compound 5) To a stirred solution of 15RS-16,16-trimethylene-PGE 2 methyl ester (52 mg, 0.13 mmol) in acetone (0.4 ml) and phosphate buffer pH 7 (4 ml) was added lipase VII (40 mg). The mixture was stirred at room temperature for 24 h (TLC monitoring). The mixture was quenched with ethanol (3 ml) and extracted with ethyl acetate (2x10 ml). The organic layer was washed with brine, dried (sodium sulfate), and concentrated in vacuo furnishing 46 mg of the product as an oil.
- E-Tributyltin-4,4-trimethylene- 1 -octene-3-ol (13) A mixture of 4,4-trimethylene-l-octyn-3-ol (12) (5.0 g, 30 mmol), tributyltin hydride (14.6 ml, 54.2 mmol), and AEBN (30 mg) was stirred at 130 °C for 24 h (TLC monitoring). The residue was chromatographed on silicagel using hexane and hexane:ether 9: 1 , respectively, as eluent, to give the title compound (13) (12.54 g, 91.4%) as an oil.
- E-Tributyltin-4,4-trimethylene-3-trimethylsilyloxy- 1 -octene (14) To the mixture of E-tributyltin-4,4-trimethylene-l-octene-3-ol (13) (7 g, 15.3 mmol) in DMF (100 ml) was added imidazole (2.1 g, 30.6 mmol) and trimethylsilyl chloride (2.5 g, 23.0 mmol). The reaction mixture was stirred at room temperature for 1 h (TLC monitoring). The mixture was partitioned between water (200 ml) and ether (200 ml). The organic phase was dried and evaporated in vacuo. The residue was chromatographed on silica gel using hexane as eluent to give 14 (5.53 g).
- the water layer was acidified with 5% aqueous solution of citric acid to pH 4 and extracted with EtOAc (2x50 ml). The organic phase was washed with brine (30 ml), dried on sodium sulfate, and filtered. The solvent was removed in vacuo, and the slurry 26 was used directly without isolation for the next step.
- Intraocular pressure reducing effect of he test compounds in cats and monkeys The compounds were tested for intraocular pressure reducing effect in animal models. The intraocular pressure was measured with a calibrated pneumotonometer. European domestic cats and cynomolgus monkeys were used as experimental animals. The cornea was anaesthetized with oxibuprocain before the measurement.
- TableV Intraocular pressure reducing effect of the test compounds, with effect on the EPi . receptor, in monkeys.
- the dose of PGF 2 p-isopropyl ester was 30 ⁇ g, while that of 17-phenyl-18,19,20-trinor-PGE 2 -isopro ⁇ yl ester, and 15RS-16,16-trimethylene-PGE 2 - isopropyl ester was 3 ⁇ g.
- the present invention discloses that compounds with selective stimulatory effect on EPi receptors reduce the intraocular pressure, and that such compounds cannot have any melanogenic effect, or at least have significantly reduced effect in the eye since the pigment producing cells, the melanocytes, lack the EPi receptor in man.
- the common side-effect of increased iridial pigmentation can be avoided during chronic therapy with prostaglandins selective for EPi receptors.
- Reagents a.N-isopropylcyclohexyl amine / THF, n-BuLi, ethylcyclobutanecarboxylate/ DMSO b.DIBAL-H, / toluene c.DCC/ DME, DMSO, H3P04, d.Lithium-acetylide-ethylene diamine, DMSO e.tributyltin hydride, AIBN f.Trimethylsilyl chloride (TMSCI), imidazole/ DMF g.Li2CuCN(CH3)2, TMSCI, triethylamine, 4-t-butyl-dimethylsilyloxy-2-cyclopentenone, 1 -tributyltin-4,4,-trimethylene-3-trimethylsilyloxy-1 -octene, methyl-2-yn-8-octanoate h.Pd-BaS04, quinoline, i.HF
Abstract
Description
Claims
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL13387198A IL133871A (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma |
AU83683/98A AU739828B2 (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma |
KR1020007000240A KR20010021682A (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment 0f glaucoma |
JP50856099A JP2002509543A (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives without side effects for the treatment of glaucoma |
CA002294779A CA2294779A1 (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma |
SK1834-99A SK183499A3 (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma |
EP98934082A EP1014991A1 (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma |
NZ501834A NZ501834A (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives 13,14-dihydro-17-(3-fluorophenyl)-18,19,20-trinor-PGF2 for the treatment of glaucoma without increased melanin concentration in the eyes (iris) |
BR9815501-6A BR9815501A (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives free of side effects for the treatment of glaucoma |
NO20000062A NO20000062L (en) | 1997-07-11 | 2000-01-06 | Prostaglandin derivatives free of side effects for the treatment of glaucoma |
IS5333A IS5333A (en) | 1997-07-11 | 2000-01-07 | Prostaglandin derivatives without side effects to treat glaucoma |
HK01100916A HK1029942A1 (en) | 1997-07-11 | 2001-02-09 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9702706-4 | 1997-07-11 | ||
SE9702706A SE9702706D0 (en) | 1997-07-11 | 1997-07-11 | Prostaglandin derivatives devoid of side effects for the treatment of glaucoma |
Publications (1)
Publication Number | Publication Date |
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WO1999002165A1 true WO1999002165A1 (en) | 1999-01-21 |
Family
ID=20407743
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/SE1998/001368 WO1999002165A1 (en) | 1997-07-11 | 1998-07-10 | Prostaglandin derivatives devoid of side-effects for the treatment of glaucoma |
Country Status (19)
Country | Link |
---|---|
EP (1) | EP1014991A1 (en) |
JP (1) | JP2002509543A (en) |
KR (1) | KR20010021682A (en) |
CN (1) | CN1169528C (en) |
AU (1) | AU739828B2 (en) |
BR (1) | BR9815501A (en) |
CA (1) | CA2294779A1 (en) |
HK (1) | HK1029942A1 (en) |
HU (1) | HUP0003106A3 (en) |
IL (1) | IL133871A (en) |
IS (1) | IS5333A (en) |
NO (1) | NO20000062L (en) |
NZ (1) | NZ501834A (en) |
PL (1) | PL337940A1 (en) |
RU (1) | RU2207858C2 (en) |
SE (1) | SE9702706D0 (en) |
SK (1) | SK183499A3 (en) |
TR (1) | TR200000008T2 (en) |
WO (1) | WO1999002165A1 (en) |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000025771A1 (en) * | 1998-11-04 | 2000-05-11 | Synphora Ab | Method for preventing increased iridial pigmentation during prostaglandin treatment |
WO2003002755A2 (en) * | 2001-06-26 | 2003-01-09 | Allergan, Inc. | Glaucoma treatments with reduced hyperpigmentation |
JP2004530687A (en) * | 2001-05-17 | 2004-10-07 | アラーガン、インコーポレイテッド | Prostanoic acid derivatives as intraocular pressure reducing agents |
WO2006112742A3 (en) * | 2005-04-18 | 2006-12-28 | Inst Farmaceutyczny | PROCESS FOR PREPARATION OF 13,14-DIHYDRO-PGF2α DERIVATIVES |
US7268239B2 (en) | 2001-05-24 | 2007-09-11 | Resolution Chemicals Limited | Process for the preparation of prostaglandins and analogues thereof |
US7456274B2 (en) * | 2002-09-16 | 2008-11-25 | Texas Tech University System | Inhibition of metallo-β-lactamase |
WO2009133863A1 (en) | 2008-04-28 | 2009-11-05 | 国立大学法人浜松医科大学 | Immunopotentiating agent comprising ep1 agonist |
US8084501B2 (en) | 2005-01-20 | 2011-12-27 | Breath Limited | Stable prostaglandin-containing compositions |
USRE43372E1 (en) | 1999-03-05 | 2012-05-08 | Duke University | C16 unsaturated FP-selective prostaglandins analogs |
EP2488508A1 (en) * | 2009-10-16 | 2012-08-22 | Cayman Chemical Company, Incorporated | Process for the preparation of f-series prostaglandins |
WO2013143663A1 (en) | 2012-03-28 | 2013-10-03 | Merck Patent Gmbh | Bicyclic pyrazinone derivatives |
WO2014144781A1 (en) | 2013-03-15 | 2014-09-18 | Aerie Pharmaceuticals, Inc. | Combination therapy |
US8906962B2 (en) | 2000-03-31 | 2014-12-09 | Duke University | Compositions and methods for treating hair loss using non-naturally occurring prostaglandins |
US9346837B2 (en) | 2000-03-31 | 2016-05-24 | Duke University | Cosmetic and pharmaceutical compositions and methods using 2-decarboxy-2-phosphinico derivatives |
US9643927B1 (en) | 2015-11-17 | 2017-05-09 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
US10112920B2 (en) | 2008-07-25 | 2018-10-30 | Aerie Pharmaceuticals, Inc. | Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds |
US10174017B2 (en) | 2009-05-01 | 2019-01-08 | Aerie Pharmaceuticals, Inc. | Dual mechanism inhibitors for the treatment of disease |
US10472327B2 (en) | 2007-01-10 | 2019-11-12 | Aerie Pharmaceuticals, Inc. | 6-aminoisoquinoline compounds |
US10858339B2 (en) | 2017-03-31 | 2020-12-08 | Aerie Pharmaceuticals, Inc. | Aryl cyclopropyl-amino-isoquinolinyl amide compounds |
US11389441B2 (en) | 2016-08-31 | 2022-07-19 | Aerie Pharmaceuticals, Inc. | Ophthalmic compositions |
US11427563B2 (en) | 2018-09-14 | 2022-08-30 | Aerie Pharmaceuticals, Inc. | Aryl cyclopropyl-amino-isoquinolinyl amide compounds |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012246301A (en) * | 2012-08-10 | 2012-12-13 | Cayman Chemical Co Inc | Method for preparing prostaglandins f |
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WO1994008585A1 (en) * | 1992-10-13 | 1994-04-28 | Alcon Laboratories, Inc. | Combinations of prostaglandins and clonidine derivatives for the treatment of glaucoma |
-
1997
- 1997-07-11 SE SE9702706A patent/SE9702706D0/en unknown
-
1998
- 1998-07-10 RU RU2000103224/14A patent/RU2207858C2/en not_active IP Right Cessation
- 1998-07-10 TR TR2000/00008T patent/TR200000008T2/en unknown
- 1998-07-10 BR BR9815501-6A patent/BR9815501A/en not_active IP Right Cessation
- 1998-07-10 JP JP50856099A patent/JP2002509543A/en not_active Withdrawn
- 1998-07-10 SK SK1834-99A patent/SK183499A3/en unknown
- 1998-07-10 HU HU0003106A patent/HUP0003106A3/en unknown
- 1998-07-10 IL IL13387198A patent/IL133871A/en not_active IP Right Cessation
- 1998-07-10 PL PL98337940A patent/PL337940A1/en unknown
- 1998-07-10 CA CA002294779A patent/CA2294779A1/en not_active Abandoned
- 1998-07-10 CN CNB988070456A patent/CN1169528C/en not_active Ceased
- 1998-07-10 WO PCT/SE1998/001368 patent/WO1999002165A1/en not_active Application Discontinuation
- 1998-07-10 KR KR1020007000240A patent/KR20010021682A/en not_active Application Discontinuation
- 1998-07-10 AU AU83683/98A patent/AU739828B2/en not_active Ceased
- 1998-07-10 NZ NZ501834A patent/NZ501834A/en unknown
- 1998-07-10 EP EP98934082A patent/EP1014991A1/en not_active Ceased
-
2000
- 2000-01-06 NO NO20000062A patent/NO20000062L/en unknown
- 2000-01-07 IS IS5333A patent/IS5333A/en unknown
-
2001
- 2001-02-09 HK HK01100916A patent/HK1029942A1/en not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
---|---|
EP1014991A1 (en) | 2000-07-05 |
CA2294779A1 (en) | 1999-01-21 |
IL133871A0 (en) | 2001-04-30 |
JP2002509543A (en) | 2002-03-26 |
NO20000062D0 (en) | 2000-01-06 |
PL337940A1 (en) | 2000-09-11 |
TR200000008T2 (en) | 2000-05-22 |
IS5333A (en) | 2000-01-07 |
AU739828B2 (en) | 2001-10-18 |
NO20000062L (en) | 2000-01-06 |
KR20010021682A (en) | 2001-03-15 |
HK1029942A1 (en) | 2001-04-20 |
BR9815501A (en) | 2001-07-17 |
AU8368398A (en) | 1999-02-08 |
RU2207858C2 (en) | 2003-07-10 |
CN1169528C (en) | 2004-10-06 |
NZ501834A (en) | 2002-05-31 |
SK183499A3 (en) | 2000-07-11 |
SE9702706D0 (en) | 1997-07-11 |
CN1262623A (en) | 2000-08-09 |
HUP0003106A2 (en) | 2001-01-29 |
IL133871A (en) | 2004-09-27 |
HUP0003106A3 (en) | 2002-12-28 |
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