Bizarre Patents
Crispy Chip Sandwich and Process of Producing a Sandwich Product
A food product comprising a multilayer cookie or snack having outer layers formed from a crispy type edible food product such as a potato chip or corn chip, etc. with an intermediate marshmallow layer being in contact with the inner surface of each crispy chip and one or more filler substances.
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| Number | Title | Issue Date |
| 7410969 | Antitumoral analogs of ET-743 Antitumor compounds have the five membered fused ring ecteinascidin structure of the formula (XIV). The present compounds lack a 1,4-bridging group as found in the ecteinascidins. They have at the C-1 position a substituent selected from an optionally protected or d... | 08/12/2008 |
| 7329746 | Macrocyclic beta-secretase inhibitors for the treatment of Alzheimer's disease The present invention is directed to compounds of formula I which are inhibitors of the beta-secretase enzyme and that are useful in the treatment or prevention of diseases in which the beta-secretase enzyme is involved, such as Alzheimer's disease. The invention is... | 02/12/2008 |
| 7323455 | 7-aryl 1,5-dihydro-4,1-benzoxazepin-2(3)-one derivatives and their use as progesterone receptor modulators This invention provides progesterone receptor modulators having the structure: wherein R1 to R7, X, and Q are as defined in the specification; or a pharmaceutically acceptable salt thereof. ... | 01/29/2008 |
| 7294631 | Substituted 8′-pyri(MI)dinyl-dihydrospiro-[cycloalkylamine]-pyrimido[1,2-]pyrimidin-6-one derivatives The invention relates to a dihydrospiro-[cycloalkylamine]-pyrimidone derivative represented by formula (I) or a salt thereof: wherein X, Y, R1, R2, R3, R4, o, m, n, p and q are as defined herein. The invention rela... | 11/13/2007 |
| 7247629 | Antitumoral analogs of et-743 Antitumour compounds have the five membered fused ring ecteinascidin structure of the formula (XIV). The present compounds lack a 1,4-bridging group as found in the ecteinascidins. They have at the C-1 position a substituent selected from an optionally protected or ... | 07/24/2007 |
| 7241892 | Hemisynthetic method and new compounds Methods are provided for preparing a compound with a fused ring structure of formula (XIV) which comprises one or more reactions starting from a 21-cyano compound of formula (XVI) where typically: R1 is an amidomethylene group or an acyloxymethylene group... | 07/10/2007 |
| 7202246 | Spiro-rifamycin derivatives targeting RNA polymerase Compounds of the current invention relate to rifamycin derivatives having antimicrobial activities, including activities against drug-resistant microorganisms. More specifically, compounds of the current invention relate to a series of novel spiro rifamycin derivati... | 04/10/2007 |
| 7122677 | NK1 antagonists A NK1 antagonist having the formula (I), wherein Ar1 and Ar2 are optionally substituted phenyl or heteroaryl, X1 is an ether, thio or imino linkage, R4 and R5... | 10/17/2006 |
| 7122662 | Tricyclic compound having spiro union This invention relates to tricyclic compounds having spiro union represented by the following formula (I) or its salt which is useful as a drug, and in particular, as an inhibitor for activated blood coagulation factor X, which can be administered orally and which e... | 10/17/2006 |
| 6939855 | Anti-inflammatory compositions and method The disclosed invention includes pharmaceutical compositions and methods for treating inflammatory conditions, particularly those that are characterized by increased binding of alpha-9 integrin to one or more of its ligands. Also disclosed are methods for selecting ... | 09/06/2005 |
| 6790954 | Mutant Actinosynnema pretiosum strain with increased maytansinoid production A microorganism that is a mutant bacterial strain of the species Actinosynnema pretiosum, designated PF4-4, (ATCC PTA-3921), being capable of producing maytansinoid ansamitocins such as ansamitocin P-3 in improved yield compared to previous known strains, and... | 09/14/2004 |
| 6545038 | Heterocyclic metalloprotease inhibitors The invention provides compounds of formula ##STR1## as described in the claims, or an optical isomer, diastereomer or enantiomer thereof, or a pharmaceutically-acceptable salt, or biohydrolyzable amide, ester, or imide thereof are useful as inhibitors of... | 04/08/2003 |
| 6281352 | Macrocyclic compounds as metalloprotease inhibitors This invention relates to macrocyclic molecules which inhibit metalloproteinases, including aggrecanase, and the production of tumor necrosis factor (TNF). In particular, the compounds are inhibitors of metalloproteinases involved in tissue degradation an... | 08/28/2001 |
| 6265572 | Pyrrolidincarbonylamino cyclic disulfide anti-inflammatory agents Compounds of the formula: ##STR1## are described which have activity as anti-inflammatory agents. Cyclic disulfide compounds are provided which inhibit of binding of cells to endothelium. Such compounds are useful for treating inflammatory diseases, ... | 07/24/2001 |
| 6207668 | Substituted pyridines/pyrimidines, their preparation, and their use as pesticides The present invention relates to novel substituted pyridines/pyrimidines of the formula I ##STR1## where A is CH or N; X is NH, oxygen or S(O)q where q is 0, 1 or 2; Y is a direct bond or CH2 ; Z is oxygen, NR7 or S(O) | 03/27/2001 |
| 6180619 | Prenyl transferase inhibitors A family of compounds capable of inhibiting the activity of prenyl transferases. The compounds are covered by the four following formulas ##STR1## Each of the R groups is defined in the disclosure.... | 01/30/2001 |
| 6124453 | Macrolides A novel class of macrolides in which i) positions 2 to 6 inclusive of the macrocyclic ring are provided by a piperidazinyl carboxylic acid residue; and/or ii) positions 7 to 9 inclusive of the macrocyclic ring are provided by an aromatic -amino acid res... | 09/26/2000 |
| 6100394 | Long-lived homogenous oxidation catalysts A robust chelate complex is provided having the formula: ##STR1## wherein: M is a metal, preferably a transition metal; Z is an anionic donor atom, three of which are nitrogen, and the other is oxygen; L1 is a labile ligand; Ch1... | 08/08/2000 |
| 5952320 | Macrocyclic inhibitors of matrix metalloproteinases and TNF secretion Macrocyclic compounds of formula ##STR1## are potent inhibitors of matrix metalloproteinase and are useful in the treatment of diseases in which matrix metalloproteinase play a role. Also disclosed are matrix metalloproteinase inhibiting compositions... | 09/14/1999 |
| 5877312 | Method for preparing alkylating agents for their use for alkylating cyclic ureas This invention relates to methods for preparing alkylating agents and use of the agents prepared. In particular, this invention relates to preparation methods for hydroxy halide and organooxy halide alkylating agents and their use for alkylating cyclic ur... | 03/02/1999 |
| 5856476 | Processes for preparing azepiones useful as intermediates in the preparation of inhibitors of angiotensin converting enzyme and neutral endopeptidase Processes are disclosed for preparing the azepine intermediates of the formula ##STR1## These intermediates can be reacted with acylmercaptocarboxylic acids of the formula ##STR2## to give the pharmaceutically active products.... | 01/05/1999 |
| 5726307 | Benzo-fused lactams promote release of growth hormone There are disclosed certain novel compounds identified as benzo-fused lactams which promote the release of growth hormone in humans and animals. This property can be utilized to promote the growth of food animals to render the production of edible meat pr... | 03/10/1998 |
| 5721362 | Process for producing ecteinascidin compounds The present invention is directed to a synthetic process for the formation of ecteinascidin compounds and related structures, such as the saframycins. In one particularly preferred embodiment, the present invention provides a synthetic route for the forma... | 02/24/1998 |
| 5627283 | Amidinophenylalanine derivatives, a process for the preparation thereof, use thereof and agents containing these as anticoagulants Amidinophenylalanine derivatives of the formula I ##STR1## the synthesis of these compounds, the use thereof and pharmaceutical agents which contain these compounds are described.... | 05/06/1997 |
| 5457114 | Amidinophenylalanine derivatives, a process for the preparation thereof, use thereof and agents containing these as anticoagulants Amidinophenylalanine derivatives of the formula I ##STR1## the synthesis of these compounds, the use thereof and pharmaceutical agents which contain these compounds are described.... | 10/10/1995 |
| 5362726 | Compound and method of treatment for falciparum malaria This invention deals with the spirononacyclic indoloquinoline alkaloid known as cryptospirolepine and its use as an anti-malarial.... | 11/08/1994 |
| 5326782 | Salts derived from 26-(dialkylaminoalkylsulphonyl)pristinamycin IIB Di-p-toluoyl tartrate, di-t-butylacetyl tartrate, di-butyryl tartrate and di-i-valeryl tartrate of (dialkylamino-2 alkyl)sulphonyl-26 pristinamycin IIB having general formula (I) wherein Alk represents a straight or branched alkylene radical an... | 07/05/1994 |
| 5244888 | 5-HT selective agents Substituted 8-alkoxy-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrroles; 5-alkoxy-2,3,4,4a,9,9a-hexahydro-1-H-indeno[2,1-c]pyridines; and 9-alkoxy-2,3,3a,4,5,9a-hexahydro-1H-benz[e]isoindoles are selective 5-HT receptor agents and are thus useful in the treatme... | 09/14/1993 |
| 5242911 | Bridged bicyclic imides as anxiolytics and antidepressants A series of bridged bicyclic imide compounds having a 4-(4-[2-pyrimidinyl]-1-piperazinyl)butyl group attached to the imide nitrogen are useful for alleviating the symptoms of anxiety and depression in human subjects.... | 09/07/1993 |
| 5149823 | Sulfonamide substituted spirodilactams A novel class of sulfonamoyl-substituted 1,6-diaza[4.4]spirodilactams, having a sulfonamoyl substituent on the hydrocarbyl group attached to each spiro ring nitrogen atom, is useful for the preparation of polymers, including polyamides and as latent curin... | 09/22/1992 |
| 5141930 | Fused thiophene compounds and uses thereof A fused thiophene compound of the formula: ##STR1## or a pharmaceutically acceptable acid addition salt thereof. In the above formula, one of E1, E2 and E3 is sulfur atom and other two of them are C--R1 and... | 08/25/1992 |
| 5128466 | Cyclic compounds for complexing with cations Cyclic molecules having oriented groups are capable of forming stable complexes with cations.... | 07/07/1992 |
| 4771044 | Tetraoxo compounds and pharmaceutical compositions Tetraoxo compounds of the Formula (I) ##STR1## wherein R1 is an alkyl, alkenyl, phenylalkyl or cycloalkylalkyl group, R2 and R3 are each independently an alkyl or phenyl group or together denote an alkylene group, W i... | 09/13/1988 |
| 4764512 | Benzodiazinone-pyridone compounds, cardiotonic compositions including the same, and their uses This invention relates to substituted benzodiazinone-pyridone compounds and their use as cardiotonic agents including methods for increasing cardiac contractility, pharmaceutical compositions including the same and methods for the preparation thereof.... | 08/16/1988 |
| 4709027 | Bicyclic spirosulfonimides with psychotropic activity There are disclosed compounds of the formula ##STR1## wherein R1 and R2 are each, independently, hydrogen or lower alkyl, or R1 and R2 taken together represent ##STR2## A is O or NR3 ; B is ... | 11/24/1987 |
| 4372961 | Derivatives of rifamycins, their preparation and pharmaceutical compositions thereof The present invention provides compounds of the general formula: ##STR1## wherein Y is a hydrogen atom or an acetyl radical, R is a hydrogen atom, a straight-chained or branched, saturated or unsaturated aliphatic hydrocarbon radical containing up to... | 02/08/1983 |
| 4309541 | Piperidinyl-lactams N-[1-(4-amino-2-quinazolinyl)-3 or 4-piperidinyl]-lactams, e.g., those of the formula ##STR1## and salts thereof are antihypertensive agents.... | 01/05/1982 |
| 4297497 | Synthesis of 2-keto-1,4-diazacycloalkanes Several novel syntheses have been discovered for preparation of 2-keto-1,4-diazacycloalkanes and their derivatives. Trans isomers of polysubstituted quinoxalin-2-ones may now be prepared.... | 10/27/1981 |
| 4261990 | N-alkyleneiminoalkyl-dicarboximides as antiallergics and antiasthmatics N-(diphenylmethoxy-mono- or bicyclic-alkyleneiminoalkyl)-dicarboximides, e.g. those of the formula ##STR1## A=aliphatic or cycloaliphatic radical R,R'=H, alkyl, halogen or CF3 R"=H or both are ethylene q=2-4 and salts thereof are antiallergics ... | 04/14/1981 |
| 4255429 | N-Quinazolinylpiperidinyl-lactams N-[1-(4-amino-2-quinazolinyl)-3- or 4-piperidinyl]-lactams, e.g., those of the formula ##STR1## and salts thereof are antihypertensive agents.... | 03/10/1981 |
