WO2006121822B1 - USE OF β-LACTAMS FOR THE TREATMENTOF IBD AND GLAUCOMA - Google Patents
USE OF β-LACTAMS FOR THE TREATMENTOF IBD AND GLAUCOMAInfo
- Publication number
- WO2006121822B1 WO2006121822B1 PCT/US2006/017336 US2006017336W WO2006121822B1 WO 2006121822 B1 WO2006121822 B1 WO 2006121822B1 US 2006017336 W US2006017336 W US 2006017336W WO 2006121822 B1 WO2006121822 B1 WO 2006121822B1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- prodrug
- acceptable salt
- formula
- pharmaceutically acceptable
- Prior art date
Links
- OFHVFLHQBXKZMW-QGZVFWFLSA-N CC(C)(C)c1ccc([C@@H](C2)N(CCCCCCC(O)=O)C2=O)cc1 Chemical compound CC(C)(C)c1ccc([C@@H](C2)N(CCCCCCC(O)=O)C2=O)cc1 OFHVFLHQBXKZMW-QGZVFWFLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- 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
- A61P27/08—Mydriatics or cycloplegics
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ophthalmology & Optometry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The use of compounds of the general formula (I) or a pharmaceutically acceptable salt or a prodrug thereof for the treatment of IBD and glaucoma is disclosed, wherein Y, A, R, D, and n are as described. Methods, compositions, and medicaments related thereto are also disclosed.
Claims
AMENDED CLAIMS received by the International Bureau on 20 November 2006
1. A compound of the formula
or a pharmaceutically acceptable salt or a prodrug thereof, wherein a dashed line represents the presence or absence of a eovulcπt bond;
Y is a carboxylic acid, sulfonic acid, or phosphoric acid; or an amide or ester thereof comprising from 0 to 12 carbon atoms; or Y is a hydroxymethyl, or tctrazolyl functional group;
A is -(CH2)6-, cis -CH2CH=CH-(CH2)3-, or -CH2C≡C-(CH2)3- , whereirι 1 or 2 carbon atoms may be substituted with S or O; or A is -(CH2)m-Ar-(CH2)0- wherein Ar is substituted or uαsubstituted phenyl or monocyclic heteroaryl, the sum of m and o is from 1 to 4, and wherein one CH2 may be substituted with S or O;
X is S or O;
R is a hydrocarbyl or a hydroxyhydrocarbyl moiety comprising from 1 to 12 carbon atoms;
D is independently a moiety comprising from 1 to 6 non-hydrogen atoms; and n is an integer from 0 to 4.
2. The compound of claim 1, wherein n is 0.
3. The compound of claim 1 , wherein R comprises from 6 to 9 carbon atoms and a cyclic structure.
4. The compound of claim 3 of the formula
or a pharmaceutically acceptable salt, or a prodrug thereof. 5, The compound of claim 3 of the formula
or a pharmaceutically acceptable salt, or a prodrug thereof. 6, The compound of claim 1 of the formula
or a pharmaceutically acceptable salt, or a prodrug thereof. 7. The compound of claim 1 of the formula
S. The compound of claim 1 wherein A is -(CH2)6-, cis -CH2CH=CH-(CH2)3-, or -CH2C= C-(CH2)3- 9. The compound of claim 2 of the formula
or a pharmaceutically acceptable salt or a prodrug thereof. 10. The compound of claim 2 of the formula
or a pharmaceutically acceptable salt or a prodrug thereof;
wherein R3, R4, and R5 are independently H or C1-6 alkyl
11. The compound of claim .10 wherein R" and R4 are methyl.
12. The compound of claim 11 of the formula
13. The compound of claim 2, wherein A is -(CH2)m -Ar-(CH2)o- wherein Ar is phenyl, the sum of m and o is from 1 to 4, and wherein one CH2 may be substituted with S or O.
14. The compound of claim 3 wherein A is -CH2-Ar-O-CH2-.
15. The compound of claim 1 of the formula
16. Use of a compound according to any one of claims 1 to 15 in the manufacture of a medicament for the treatment of glaucoma or ocular hypertension in a mammal.
17. A. composition comprising a compound, according to any one of claims 1 to 15, wherein said composition is a liquid which is ophthalmically acceptable.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/569,696 US7674786B2 (en) | 2005-05-06 | 2006-05-02 | Therapeutic β-lactams |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67840305P | 2005-05-06 | 2005-05-06 | |
US60/678,403 | 2005-05-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006121822A1 WO2006121822A1 (en) | 2006-11-16 |
WO2006121822B1 true WO2006121822B1 (en) | 2007-01-18 |
Family
ID=37011956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/017336 WO2006121822A1 (en) | 2005-05-06 | 2006-05-02 | USE OF β-LACTAMS FOR THE TREATMENTOF IBD AND GLAUCOMA |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006121822A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8063033B2 (en) | 2008-01-18 | 2011-11-22 | Allergan, Inc. | Therapeutic beta-lactams |
US7956051B2 (en) * | 2008-01-24 | 2011-06-07 | Allergan, Inc. | Therapeutic amides and related compounds |
US8440819B2 (en) | 2008-02-22 | 2013-05-14 | Allergan, Inc. | Therapeutic substituted beta-lactams |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5462968A (en) * | 1994-01-19 | 1995-10-31 | Allergan, Inc. | EP2 -receptor agonists as agents for lowering intraocular pressure |
US5698598A (en) * | 1995-08-04 | 1997-12-16 | Allergan | EP2 -receptor agonists as agents for lowering intraocular pressure |
US6090847A (en) * | 1997-11-21 | 2000-07-18 | Allergan Sales, Inc. | EP2 -receptor agonists as neuroprotective agents for the eye |
MXPA04005555A (en) * | 2002-03-18 | 2005-05-16 | Pfizer Prod Inc | Methods of treatment with selective ep4 receptor agonists. |
-
2006
- 2006-05-02 WO PCT/US2006/017336 patent/WO2006121822A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2006121822A1 (en) | 2006-11-16 |
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