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Class 544/88 - 1,3-Oxazines


Subclass of Class 544 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein the six-membered hetero ring has oxygen
No. of applications: 23
Last issue date: 11/22/2012


Application No.Application TitleIssue Date
201202959001,3-OXAZINES AS BACE 1 AND/OR BACE2 INHIBITORS
The present invention provides compounds of formula I

having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active subs...

11/22/2012
201202589621,3-OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS
The present invention provides 4-(3-Amino-phenyl)-5,6-dihydro-4H-[1,3]oxazin-2-ylamines of formula I

having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing th...

10/11/2012
20120245157OXAZINE DERIVATIVES
The present invention provides, for example, a compound mentioned below as a medicament for treating or preventing the diseases induced by production, secretion or deposition of amyloid-β proteins.

A compound of the formula (I):

09/27/2012
20120165521LOW-VOC POLYAMINO ALCOHOLS
A method for producing a polyamino-polyalcohol. The method comprises steps of: (a) combining an aminoalcohol of formula (I)

with a nitro-diol of formula (II)

06/28/2012
20110165101PHOTO-LABILE PRO-FRAGRANCE CONJUGATES
The present invention relates to photo-labile pro-fragrance conjugates comprising:
  • a) a photo-labile unit which upon exposure to electromagnetic radiation is capable of releasing a pro-fragrance unit...
07/07/2011
201101440972-AMINO-5,5-DIFLUORO-5,6-DIHYDRO-4H-[1,3]OXAZIN-4-YL)-PHENYL]-AMIDES
The present invention relates to 2-Amino-5,5-difluoro-5,6-dihydro-4H-[1,3]oxazin-4-yl)-phenyl]-amides of formula I

having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions...

06/16/2011
20110028367PHOTO-LABILE PRO-FRAGRANCE CONJUGATES
The present invention relates to photo-labile pro-fragrance conjugates comprising:
    • a) a photo-labile unit which upon ex...
02/03/2011
20100256114Amido Compounds And Their Use As Pharmaceuticals
The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases ass...
10/07/2010
20100048545Compounds and Compositions for Use in the Prevention and Treatment of Disorders of Fat Metabolism and Obesity
The invention relates to 4-hydroxyisoleucine, isomers, analogs, lactones, salts, and prodrugs thereof, to processes for their preparation, and to pharmaceutical compositions comprising the same. More particularly, the invention relates to the use of those compounds in t...
02/25/2010
20090281309METHOD FOR PRODUCING 2-OXAZOLINE ANALOGUE OR 1,3-OXAZINE ANALOGUE
The present invention is a method for producing a 2-oxazoline analogue or a 1,3-oxazine analogue represented by the following general formula (3) by reacting a 1,2-aminoalcohol compound or a 1,2-aminothiol compound with an α,α-dihaloamine compound.

11/12/2009
20090104116COMPOUNDS FOR THE INHIBITION OF INTEGRINS AND USE THEREOF
The present invention is related to a compound of formula (I), wherein A is a nonaromatic heterocyclic ring, Ar is either absent or phenylene; Ψ is a radical of formula (II), R2 is a hydrophobic moiety; and G is a radical containing one or more moieties sel...
04/23/2009
20090069533Benzoxazine monomers, polymers and compositions
Benzoxazine monomers comprising at least one pendant group are described. (Co)Polymers comprising at least one benzoxazine monomer having at least one pendant group are also described. In a preferred embodiment, the pendant group is located in a side chain of the benzox...
03/12/2009
20080318905Prodrugs and methods of making and using the same
Prodrugs of parent drugs and methods of making and using the same are described. The prodrugs comprise an amine-containing parent drug moiety and a prodrug moiety, such as methoxyphosphonic acid or ethoxyphosphonic acid. The prodrugs may be employed in therapy for the t...
12/25/2008
20080171681Photo-labile pro-fragrance conjugates
The present invention relates to photo-labile pro-fragrance conjugates comprising:
  • a) a photo-labile unit which upon exposure to electromagnetic radiation is capable of releasing a pro-fragrance unit...
07/17/2008
20080146797PROCESS FOR SYNTHESIZING HETEROCYCLIC COMPOUNDS
The invention provides the process illustrated in scheme 1 for synthesizing heterocyclic compounds of formula I.

In the process, an isothiocyanate of formula II is initially reacted with a primary amine or fo...

06/19/2008
20080027211Enantiopure Heterocyclic Compound Useful for the Preparation of Peptides Which Can Be Potentially Used as Medicaments
Enantiopure heterocyclic compound Enantiopure heterocyclic compound of formula (I) in which J is chosen from C, N, O and S; Z is H or a group for protecting the amino functional group, R3 denotes H or an organic residue, m is 0, 1 or 2 and n is 0, 1 or 2, and...
01/31/2008
20070281930Novel Insecticides
Compounds of the formula in which
    • Z1 is an oxygen atom; or a sulfur atom;
    • 12/06/2007
20070264217Photo-labile pro-fragrance conjugates
The present invention relates to photo-labile pro-fragrance conjugates comprising: a) a photo-labile unit which upon exposure to electromagnetic radiation is capable of releasing a pro-fragrance unit; and b) a pro-fragrance unit, which when so released is either i) a pr...
11/15/2007
20070208014NOVEL 2-SUBSTITUTED BENZIMIDAZOLES AS SELECTIVE ANDROGEN RECEPTOR MODULATORS (SARMS)
The present invention is directed to a novel 2-substituted benzimidazole derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by the androgen receptor. ...
09/06/2007
20070082895Novel mycobacterial inhibitors
The present invention relates to novel substituted quinoline derivatives according to the general formula (Ia) or the general formula (Ib)
salts, quaternary amines, stereochemically isomeric forms, tautomeric forms and N-oxide forms thereof, wherein R1
04/12/2007
20050227969EP4 receptor agonist, compositions and methods thereof
This invention relates to potent selective agonists of the EP4 subtype of prostaglandin E2 receptors, their use or a formulation thereof in the treatment of glaucoma and other conditions, which are related to elevated intraocular pressure in the eye of a pati...
10/13/2005
20050119260Inhibitors of cellular necrosis
The present invention relates to compounds and pharmaceutical preparations and their use in therapy for preventing or treating trauma, ischemia, stroke and degenerative diseases associated with cell death. Methods and compositions of the invention are particularly usefu...
06/02/2005
20050020505R-isomer of beta amino acid compounds as integrin receptor antagonists derivatives
The present invention relates to a class of compounds represented by the Formula I
or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of the Formula I, and methods of selectively inhibiting or antagonizing the α
01/27/2005
 
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