Bizarre Patents
Method and apparatus for making a drink hop along a bar or counter
A method for generating a drink which appears to hop from a remote spot on the bar or counter and take one or more leaps, before landing in a patron's glass.
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| Number | Title | Issue Date |
| 7763740 | Method for the production of mumbaistatin derivatives The present invention relates to a process for preparing mumbaistatin derivatives (I), where the anthraquinone skeleton is constructed via a Diels-Alder reaction and the central methylene bridge via a transition metal-catalyzed reaction, and to the intermediates use... | 07/27/2010 |
| 7745646 | Bicyclic heteroaryl inhibitors of PDE4 The present invention relates to compounds and methods which may be useful as inhibitors of phosphodiesterase 4 (PDE4) for the treatment or prevention of inflammatory diseases and other diseases involving elevated levels of cytokines and proinflammatory mediators. | 06/29/2010 |
| 7374749 | Amino substituted hydroxyphenyl benzophenone derivatives Described are amino substituted hydroxyphenyl benzophenone derivatives of formula (I), wherein R1, and R2 independently from each other are; C1-C20alkyl; C2-C20-alken... | 05/20/2008 |
| 7329654 | Heteroatom containing tetracyclic derivatives as selective estrogen receptor modulators The present invention is directed to novel heteroatom containing tetracyclic derivatives, pharmaceutical compositions containing them, their use in the treatment and/or prevention of disorders mediated by one or more estrogen receptors and processes for their prepar... | 02/12/2008 |
| 7314942 | Methylenelactones syntheses in supercritical fluids Alpha-methylenelactone is produced from butyrolactone and valerolactone by the addition of formaldehyde in a supercritical fluid. ... | 01/01/2008 |
| 7312200 | 9-ketospinosyn derivatives The present invention relates to derivatives of 9-keto spinosyns, which are substituted by a ═N—(O, NH or NRx)—Ry moiety in the C-9 position, to methods for their manufacture, and to their use for controlling animal pests. ... | 12/25/2007 |
| 7176234 | Derivatives of gambogic acid and analogs as activators of caspases and inducers of apoptosis The present invention is directed to derivatives of gambogic acid and analogs thereof. Exemplary gambogic acid derivatives of the present invention include, among others, derivatives substituted in the C10 and C28 positions of gambogic acid. The present invention al... | 02/13/2007 |
| 7115651 | Macrocycles and uses thereof The present invention relates to compounds having the structure (and pharmaceutically acceptable derivatives thereof) wherein R0–R4, Z, X, A—B, D—E, G—J, and... | 10/03/2006 |
| 7105684 | Lactone compounds An object of the present invention is to provide a novel monomer compound having a lactone structure which gives polymers having more excellent feature as resist material, etc. The present invention relates to a compound represented by the following formula [... | 09/12/2006 |
| 6979721 | Substituted cyclohexene endcaps for polymers with thermal-oxidative stability This invention relates to polyimides having improved thermal-oxidative stability, to the process of preparing said polyimides, and the use of polyimide prepolymers in the preparation of prepregs and composites. The polyimides are particularly useful in the preparati... | 12/27/2005 |
| 6936402 | MONOMERS CONTAINING AN OXEPAN-2-ONE GROUP, PHOTORESIST COMPOSITIONS COMPRISING POLYMERS PREPARED FROM THE MONOMERS, METHODS FOR PREPARING THE COMPOSITIONS, AND METHODS FOR FORMING PHOTORESIST PATTERNS USING THE COMPOSITIONS Disclosed herein is a novel norbornene, acrylate or methacrylate monomer as a photoresist monomer containing an oxepan-2-one group. Further disclosed are photoresist compositions comprising a polymer prepared from the monomer, methods for preparing the photoresist c... | 08/30/2005 |
| 6919464 | Synthetic derivatives of 21-butenyl and related spinosyns Macrolide compounds produced by synthetic modification of factors produced by NRRL 30141 have insecticidal and acaricidal activity and are useful intermediates for preparing additional insecticidal and acaricidal compounds ... | 07/19/2005 |
| 6900339 | Bryostatin composition and bryostatin acquisition methodologies Methods for obtaining bryostatins from the marine bryozoans of the Bugula neritina species complex are provided wherein the methods involve the extraction and purification of bryostatins from the larvae of Bugula neritina organisms. Further, the presen... | 05/31/2005 |
| 6818667 | Eurotinones, and derivatives thereof, processes for preparing them, and their use The present invention relates to novel compounds of the formula I in which R(1), R(2), R(3) and R(4) are, independently of each other, hydrogen or an alkyl radical. The compounds of the formula I are inhibitors of KDR ... | 11/16/2004 |
| 6815463 | Laulimalide derivatives Laulimalide compounds, intermediates thereto and methods for their preparation, and methods for their use in the treatment of diseases characterized by cellular hyperproliferation. ... | 11/09/2004 |
| 6808724 | Artemisolide compound isolated from the aerial parts of Artemisia sylvatica, isolation method, and use thereof The present invention relates to a novel compound isolated from Artemisia Sylvatica, expressed by the formula 1, a method of isolation, and its use thereof, and more particularly to a novel compound isolated from Artemisia Sylvatica, a method of isolat... | 10/26/2004 |
| 6670389 | Laulimalide derivatives Laulimalide compounds, intermediates thereto and methods for their preparation, and methods for their use in the treatment of diseases characterized by cellular hyperproliferation. ##STR1##... | 12/30/2003 |
| 6670348 | Methods and compositions for destruction of selected proteins Compounds having an ansamycin anitibiotic, or other moiety which binds to hsp90, coupled to a targeting moiety which binds specifically to a protein, receptor or marker can provide effective targeted delivery of the ansamycin antibiotic leading to the deg... | 12/30/2003 |
| 6617304 | Method for producing macrocyclic lactone The invention discloses a method for the production of a macrocyclic lactone represented by a formula (2), which comprises subjecting a hydroxycarboxylic acid ester represented by a formula (1) to intramolecular esterification reaction. ##STR1## In t... | 09/09/2003 |
| 6610736 | 16-Halogen-epothilone derivatives, method for producing them and their pharmaceutical use The invention relates to novel epothilone derivatives of general formula (I), wherein R8 means a halogen atom, especially a fluorine or chlorine atom, and the remaining substituents have the meanings given in the description. The novel compound... | 08/26/2003 |
| 6504035 | 3-deoxy-desmycosin derivatives and process for their preparation The present invention relates to derivatives of 3-deoxy desmycosin of the formula I, wherein, starting from triply protected desmycosin, there are performed an oxidation at C-3 in the first step and then, optionally, a hydrogenation of double bonds and an... | 01/07/2003 |
| 6369099 | Method of locking 1 -OH of vitamin D compounds in axial orientation A method of modifying or altering the structure of a 1-hydroxylated vitamin D compound to increase its biological activity by altering the conformational equilibrium of the A-ring to favor a chair conformation that presents the 1-hydroxyl in... | 04/09/2002 |
| 6307065 | Processes for producing epsilon caprolactones and/or hydrates and/or esters thereof This invention relates in part to processes for producing one or more substituted or unsubstituted epsilon caprolactones and/or hydrates and/or esters thereof which comprise subjecting one or more substituted or unsubstituted penten-1-ols to carbonylation... | 10/23/2001 |
| 6222048 | Diaryl-2-(5H)-furanones as Cox-2 inhibitors The invention encompasses the novel compound of Formula (I) as well as a method of treating cyclooxygenase-2 mediated diseases comprising administration to a patient in need of such treatment of a non-toxic therapeutically effective amount of a compound o... | 04/24/2001 |
| 6184391 | Processes for producing epsilon caprolactones and/or hydrates and/or esters thereof This invention relates in part to processes for producing one or more substituted or unsubstituted epsilon caprolactones and/or hydrates and/or esters thereof which comprise subjecting one or more substituted or unsubstituted penten-1-ols to carbonylation... | 02/06/2001 |
| 6100293 | Tetracyclic triterpene derivatives with immunosuppressant activity The compounds of Formula I ##STR1## are useful as immunosuppressive agents.... | 08/08/2000 |
| 6090952 | (2R, 3S, 22R, 23R)-2,3,22,23-tetrahydroxy-24-ethyl-ଲ-homo-7-oxa-5-cholesta n-6-one and a process for preparing the same The invention discloses a process for the preparation of a compound, having molecular formula C29 H50 O6 and isomeric structural formulae (2R, 3S, 22R, 23R) -2, 3, 22, 23 -tetrahydroxy-24- ethyl-ଲ-homo-7-oxa -5³... | 07/18/2000 |
| 6063731 | Brassinosteroid analogs useful as plant growth regulators Disclosed are compositions and methods for promoting plant growth. The compounds are cyclopropyl- and cyclobutyl-substituted brassinosteroids having high growth promoting ability. They may be used alone or in combination with other plant growth regulating... | 05/16/2000 |
| 6011058 | Seco-cholestane derivatives and methods of making the same The present invention is directed to novel seco-cholestane derivatives, as well as to pharmaceutical compositions thereof, and methods of making the same. More particularly, the invention relates to C5- and C8-substituted seco-cholestane derivatives. The ... | 01/04/2000 |
| 6008380 | (2R,3S,24S)-2,3-diacetoxy-22,23-epoxy -24-ethyl-ଲ-homo-7-oxa-5-cholestan-6-one and a process for preparing the same The present invention relates to a novel compound namely (2R,3S,24S)-2,3-diacetoxy-22,23-epoxy-24-ethyl-ଲ-homo-7-oxa-5- cholestan-6-one and a process for the preparation thereof. The said compound is represented by the structural formula ... | 12/28/1999 |
| 5998408 | Triterpene derivatives with immunosuppressant activity The compounds of Formula I ##STR1## are useful as immunosuppressive agents.... | 12/07/1999 |
| 5977165 | Radicicol derivatives The present invention relates to radicicol derivatives represented by the following formula (I) or pharmacologically acceptable salts thereof: ##STR1## wherein R1 and R2 are the same or different and each represents hydrogen, al... | 11/02/1999 |
| 5883119 | Triterpene derivatives with immunosuppressant activity The compounds of Formula I ##STR1## are useful as immunosuppressive agents.... | 03/16/1999 |
| 5786492 | Halichondrins Halichondrin derivatives, isolatable from a marine sponge of the Lissodendoryx Sp., have cytotoxic preparations and are of the formula: ##STR1## wherein R1 and R2 together form a spiro attached ring system selected from the grou... | 07/28/1998 |
| 5763478 | Triterpene derivatives with immunosuppressant activity The compounds of Formula I ##STR1## are useful as immunosuppressive agents.... | 06/09/1998 |
| 5763366 | Brassinosteroid derivative and plant growth regulator using the same Brassinosteroid derivatives expressed in formula (I) and formula (II) ##STR1## and a plant growth regulator containing one type or two types of these brassinosteroid derivatives as active ingredient. The invention thereby presents novel brassinosteroid an... | 06/09/1998 |
| 5741814 | Cyclooctadiene derivatives Cyclooctadiene derivative of the following formula (1): ##STR1## wherein A1, A2, A3 and A4 each independently represent COOR5 (where R5 represents a hydrogen atom, a C1 -C10... | 04/21/1998 |
| 5696156 | Triterpene derivatives with immunosuppressant activity The compounds of Formula I ##STR1## are useful as immunosuppressive agents.... | 12/09/1997 |
| 5679705 | Triterpene derivatives with immunosuppressant activity The compounds of Formula I ##STR1## are useful as immunosuppressive agents.... | 10/21/1997 |
| 5650430 | Radicicol derivatives, their preparation and their anti-tumor activity Radicicol derivatives in which one or both hydroxy groups are acylated have valuable anti-tumor activity or may be used as chemical intermediates.... | 07/22/1997 |
