CA2665616A1 - Effective delivery of cross-species a3 adenosine-receptor antagonists toreduce intraocular pressure - Google Patents

Effective delivery of cross-species a3 adenosine-receptor antagonists toreduce intraocular pressure Download PDF

Info

Publication number
CA2665616A1
CA2665616A1 CA002665616A CA2665616A CA2665616A1 CA 2665616 A1 CA2665616 A1 CA 2665616A1 CA 002665616 A CA002665616 A CA 002665616A CA 2665616 A CA2665616 A CA 2665616A CA 2665616 A1 CA2665616 A1 CA 2665616A1
Authority
CA
Canada
Prior art keywords
mrs
intraocular pressure
eye
iop
adenosine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002665616A
Other languages
English (en)
French (fr)
Inventor
Civan M. Mortimer
Kenneth A. Jacobson
Marcel Y. Avila
Richard Stone
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University of Pennsylvania Penn
US Department of Health and Human Services
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2665616A1 publication Critical patent/CA2665616A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Ophthalmology & Optometry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Saccharide Compounds (AREA)
CA002665616A 2006-10-06 2007-10-05 Effective delivery of cross-species a3 adenosine-receptor antagonists toreduce intraocular pressure Abandoned CA2665616A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US85017506P 2006-10-06 2006-10-06
US60/850,175 2006-10-06
PCT/US2007/021409 WO2008045330A2 (en) 2006-10-06 2007-10-05 Effective delivery of cross-species a3 adenosine-receptor antagonists to reduce intraocular pressure

Publications (1)

Publication Number Publication Date
CA2665616A1 true CA2665616A1 (en) 2008-04-17

Family

ID=39283379

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002665616A Abandoned CA2665616A1 (en) 2006-10-06 2007-10-05 Effective delivery of cross-species a3 adenosine-receptor antagonists toreduce intraocular pressure

Country Status (8)

Country Link
US (1) US20090258836A1 (https=)
EP (1) EP2076267A4 (https=)
JP (1) JP2010505848A (https=)
AU (1) AU2007307157A1 (https=)
BR (1) BRPI0715318A2 (https=)
CA (1) CA2665616A1 (https=)
MX (1) MX2009003750A (https=)
WO (1) WO2008045330A2 (https=)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG182285A1 (en) 2010-01-11 2012-08-30 Inotek Pharmaceuticals Corp Combination, kit and method of reducing intraocular pressure
EA201290958A1 (ru) * 2010-03-26 2013-04-30 Инотек Фармасьютикалз Корпорейшн Способ снижения внутриглазного давления у людей с применением n6-циклопентиладенозина (cpa), производных cpa или их пролекарств
BR112014018413A8 (pt) 2012-01-26 2017-07-11 Inotek Pharmaceuticals Corp Polimorfos anidros de nitrato de metila [(2r,3s,4r,5r)-5-(6-(ciclopentilamino)-9h-purin-9-il)-3,4-diidroxitetraidrofuran-2-il)] e processos de preparação do mesmo
CA2903114A1 (en) 2013-03-15 2014-09-25 Inotek Pharmaceuticals Corporation Ophthalmic formulations
ES2578363B1 (es) 2015-01-22 2017-01-31 Palobiofarma, S.L. Moduladores de los receptores A3 de adenosina
HK1254892A1 (zh) 2016-01-14 2019-08-02 韩德株式会社 拮抗a3腺苷受体的化合物、其制备方法、及其医学用途
ES2676535B1 (es) 2017-01-20 2019-04-29 Palobiofarma Sl Moduladores de los receptores a3 de adenosina
KR101805400B1 (ko) 2017-03-21 2017-12-07 퓨쳐메디신 주식회사 아데노신 유도체를 포함하는 녹내장 예방 및 치료용 약학적 조성물
CN109666053A (zh) * 2017-10-16 2019-04-23 张家口华健致远生物科技有限公司 一种a3腺苷受体激动剂及其用途
KR102007640B1 (ko) * 2017-11-29 2019-08-07 퓨쳐메디신 주식회사 아데노신 유도체를 포함하는 망막 질환 또는 시신경 질환 예방 및 치료용 약학적 조성물
US11395597B2 (en) * 2018-06-26 2022-07-26 General Electric Company System and method for evaluating blood flow in a vessel

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2244774C (en) * 1996-01-29 2006-10-17 The United States Of America, Represented By The Secretary, Department Of Health And Human Services Dihydropyridine derivatives, their preparation and their use as adenosine receptor antagonists
ATE290910T1 (de) * 1998-07-16 2005-04-15 Univ Pennsylvania Verwendung von a3-adenosine antagonisten zur herstellung eines arzneimittels zur senkung des augeninnendrucks
IL133680A0 (en) * 1999-09-10 2001-04-30 Can Fite Technologies Ltd Pharmaceutical compositions comprising an adenosine receptor agonist or antagonist

Also Published As

Publication number Publication date
AU2007307157A1 (en) 2008-04-17
EP2076267A4 (en) 2013-07-31
BRPI0715318A2 (pt) 2013-07-16
EP2076267A2 (en) 2009-07-08
WO2008045330A3 (en) 2008-06-26
JP2010505848A (ja) 2010-02-25
WO2008045330A2 (en) 2008-04-17
MX2009003750A (es) 2009-06-18
US20090258836A1 (en) 2009-10-15

Similar Documents

Publication Publication Date Title
US20090258836A1 (en) Effective delivery of cross-species a3 adenosine-receptor antagonists to reduce intraocular pressure
US6528516B1 (en) Methods for reducing intraocular pressure using A3 adenosine receptor antagonists
Guha et al. Lysosomal alkalinization, lipid oxidation, and reduced phagosome clearance triggered by activation of the P2X7 receptor
Koseki et al. A placebo-controlled 3-year study of a calcium blocker on visual field and ocular circulation in glaucoma with low-normal pressure
Kent et al. Vitreous concentration of topically applied brimonidine tartrate 0.2%
Nuyen et al. Steroid-induced glaucoma in the pediatric population
Sigurdsson et al. Cyclodextrin formulation of dorzolamide and its distribution in the eye after topical administration
Wang et al. Nucleoside-derived antagonists to A3 adenosine receptors lower mouse intraocular pressure and act across species
Grosenbaugh et al. Stiripentol is anticonvulsant by potentiating GABAergic transmission in a model of benzodiazepine-refractory status epilepticus
Donnenfeld et al. Global experience with Xibrom (bromfenac ophthalmic solution) 0.09%: the first twice-daily ophthalmic nonsteroidal anti-inflammatory drug
US12102640B2 (en) Use of dopamine and serotonin receptor antagonists for treatment in a subject with retinal degeneration
EP3749322A1 (en) Compounds and methods for treating addiction and related disorders
Chien et al. Ocular pharmacokinetics and pharmacodynamics of phenylephrine and phenylephrine oxazolidine in rabbit eyes
CN112888312A (zh) 用于预防或降低短暂性脑缺血发作发病率的组合物及方法
Brubaker et al. Topical forskolin (colforsin) and aqueous flow in humans
Walker Pharmacokinetic-pharmacodynamic correlations of analgesics
JP7816716B2 (ja) 強膜菲薄化治療用点眼剤及び強膜菲薄化治療剤のスクリーニング方法
Sponsel et al. Periocular accumulation of timolol and betaxolol in glaucoma patients under long-term therapy
KR20180094879A (ko) 망막 질환을 치료하기 위한 미라베그론
Wang et al. Barrier qualities of the mouse eye to topically applied drugs
US20090054412A1 (en) Treatment of Sleep Disorders
Maltese et al. Pharmacokinetic profile of topical flunarizine in rabbit eye and plasma
US10370378B2 (en) Treatment of sleep disorders
Schoenwald et al. The ocular pharmacokinetics of ketanserin and its metabolite, ketanserinol, in albino rabbits
Manzoni et al. P-9-1 Effect of ceftriaxone, gabapentin and lamotrigine on [3H] glutamate uptake in an animal model of amyotrophic lateral sclerosis

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued

Effective date: 20141007