Self Containing Enclosure for Protection from Killer Bees
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| Number | Title | Issue Date |
| 7538250 | Pyrene compound and organic light emitting device An object of the present invention is to provide a novel pyrene compound. Provided is a pyrene compound represented by the following general formula (I): wherein: R1 and R2 each represent a substituted... | 05/26/2009 |
| 7288678 | Process for preparing terbinafine by using platinum as catalyst A process for the preparation of terbinafine, comprising the reaction of a compound of formula (II), or a salt thereof, wherein X is a leaving group, with tert-butylacetylene, in the presence of a platinum catalyst ... | 10/30/2007 |
| 7244703 | Pharmaceutical compositions and methods for peptide treatment Compositions and methods for treating a patient with a pharmaceutically active peptide that combines a pharmaceutically active peptide, a permeation enhancer, and a carrier, are disclosed. ... | 07/17/2007 |
| 7122184 | Specific monoclonal antibody against terbinafine The invention concerns momoclonal antibodies to terbinafine in free base or salt form, immunogenic conjugates suitable for preparing them, hybridoma capable of producing them, and corresponding assay kits. The antibodies can be prepared by administering to an approp... | 10/17/2006 |
| 7112561 | Pharmaceutical compositions and methods for insulin treatment Compositions and methods for treating a patient with insulin that combines insulin, a permeation enhancer, and a carrier that maintains an acidic pH, are disclosed. ... | 09/26/2006 |
| 7022883 | Preparation of aryl intermediates Disclosed are methods of making aryl intermediate compounds of the formula (A) which are useful in the production of heteroaryl ureas, Y and P are defined herein below. ... | 04/04/2006 |
| 6919317 | Pharmaceutical composition comprising squalene epoxidase inhibitor and macrolide immunomodulator Synergistic combinations of a squalene epoxidase inhibitor such as terbinafine and a macrolide T-cell immunomodulator or immunosuppressant such as 33-epichloro, 33-desoxyascomycin are provided, which are useful in particular in the treatment of diseases involving fu... | 07/19/2005 |
| 6787570 | Substituted N-cycloalkyl-N-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity The invention relates to substituted N-Alkyl/Alkenyl/Cycloalkyl/Heterocycyl N-Aryl/Heteroaryl tertiary-Heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and metho... | 09/07/2004 |
| 6710089 | Substituted N-fused-phenyl-N-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity The invention relates to substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating atheroscle... | 03/23/2004 |
| 6689913 | Process for preparing terbinafine and HCI salt thereof Provided is a process for preparing terbinafine or its HCl salt comprising: reacting a furan derivative with a base to form a second compound; performing a reductive alkylation of the second compound obtained in the step with N-methyl-1-naphthalenemethyla... | 02/10/2004 |
| 6583183 | Substituted n-phenyl-n-fused-benzyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity The invention relates to substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating... | 06/24/2003 |
| 6515181 | Process for the preparation of terbinafine A process for the preparation of terbinafine which comprises the reaction of tert-butylacetylene with a compound of formula (II) ##STR1## characterized in that the reaction is carried out in the presence of copper (I) salts and of a base, in the absence o... | 02/04/2003 |
| 6495496 | Hydroxy aromatic mannich base condensation products and the use thereof as soot dispersants in lubricating oil compositions Low molecular weight Mannich base condensates of hydroxy aromatic compounds, an aldehyde; and an amine, wherein the combined number of substituent carbon atoms does not exceed 80. Such compounds are useful as soot dispersants in lubricating oils when used... | 12/17/2002 |
| 6448295 | Use of substituted N-fused-phenyl-N-benzyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity The invention relates to substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating... | 09/10/2002 |
| 6252114 | Process for preparing novel biologically active synthetic molecule 4-(p-methoxyphenyl)-2-amino-butane The invention provides a process for the preparation of 4-(p-methoxyphenyl)-2-aminobutane represented by structural formula (1) as shown herein below: ##STR1## [C11 H17 ON=4-(p-methoxy phenyl)-2-amino butane] said process comprising ... | 06/26/2001 |
| 6114394 | Polyamine derivatives as radioprotective agents The present invention relates to polyamine derivatives of the formula RHN-(CH2)m -NH-(CH2)n -NHR wherein m is an integer from 2 to 4, n is an integer from 3 to 10 and R is C2 -C6 alkyl or -... | 09/05/2000 |
| 6001884 | Calcium receptor-active molecules The present invention features molecules which can modulate one or activities of an inorganic ion receptor. Preferably, the molecule can mimic or block the effect of extracellular Ca2+ on a calcium receptor. The preferred use of such molecules... | 12/14/1999 |
| 5981599 | Inorganic ion receptor active compounds The present invention features compounds able to modulate one or more activities of an inorganic ion receptor and methods for treating diseases or disorders using such compounds. Preferred compounds can mimic or block the effect of extracellular calcium o... | 11/09/1999 |
| 5817875 | Methods for the manufacture of terbinafine Process for the manufacture of naphthylmethylamine derivatives and among them terbinafine as potential antimycotic agents.... | 10/06/1998 |
| 5808098 | Optically active beta-aminoalkoxyborane complex 1. An optically active ଲ-aminoalkoxyborane complex of the formula (I): ##STR1## wherein R1 is C1 -C8 alkyl, C3 -C7 cycloalkyl, C7 -C11 aralkyl or C6 -C10 | 09/15/1998 |
| 5686616 | Process for preparing an optically active amine A novel process for preparing an optically active amine by asymmetric hydrogenation of an imine compound, such as an imine compound prepared by condensing benzylamine and acetophenone, in the presence of a catalytic amount of an iridium-optically active p... | 11/11/1997 |
| 5633405 | Asymmetric synthesis of (-)-6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1- benzoxanzin-2-one An improved synthesis of a highly potent HIV reverse transcription inhibitor is disclosed, involving an acetylide and a trifluoromethyl ketone which produces a chiral product in the presence of a chiral amino alcohol.... | 05/27/1997 |
| 5571942 | Ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes and 3-aminochromanes The present invention provides novel ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes and 3-aminochromanes which exhibit binding activity at the serotonin 1A receptor.... | 11/05/1996 |
| 5508306 | Aromatic amine derivatives This invention relates to novel aromatic amine compounds having the structure: ##STR1## where each W, Z1 and Z2 is independently H, C1 -C6 alkyl, C1 -C6 alkoxy, OH, F, Cl, Br, I, NO | 04/16/1996 |
| 5436354 | Intermediates for producing enyne derivatives (E)-N-(3-Chloro-2-propenyl)-N-methyl-1naphthylenemethanamine and (E)-3-chloro-N-(3-chloro-2-propenyl)-N-methylbenzo[b]thiophene-7-methanami ne which are useful as intermediates in the production of enyne compounds which exhibit squalene epoxidase inhibitin... | 07/25/1995 |
| 5430063 | Phenoxyphenyl derivatives, compositions thereof and methods for their use The invention concerns a phenoxyphenyl compound having the formula ##STR1## wherein R is one or two halogen atoms; and A is CH2 NR1 R2 or 4,5-dihydro-1H-imidazole, in which R1 and R2 are independently... | 07/04/1995 |
| 5359091 | Intermediates for producing enyne derivatives A compound of the formula: ##STR1## wherein R11 is hydrogen, lower alkyl, haloloweralkyl, lower alkenyl, lower alkynyl or cycloalkyl; R21 is a group of the formula: ##STR2## wherein each of R3, R31, an... | 10/25/1994 |
| 5334628 | Amine derivatives, processes for preparing the same and fungicides containing the same Amine derivatives having the general formula (I): ##STR1## wherein X is selected from the group consisting of ##STR2## wherein Q is oxygen, sulfur or nitrogen atom, and ##STR3## wherein Q is as above; Y is selected from the group consisting... | 08/02/1994 |
| 5296612 | Process for producing enyne derivatives A process for producing an enyne derivative, and intermediate, which is useful for preparing compounds showing strong inhibiting activities against squalane epoxidase of Eumycetes and strong anti-cholesterol activities. The process comprises reacting a co... | 03/22/1994 |
| 5276053 | Polycyclic amines useful as cerebrovascular agents A novel series of polycyclic amines, derivatives, methods of making the compounds, novel intermediates, compositions containing them, and methods for using them in the treatment and prevention of cerebrovascular disorders are disclosed.... | 01/04/1994 |
| 5245028 | Process for preparing tetracyclic amines useful as cerebrovascular agents Processes for the preparation of a series of tetracyclic amines useful in the treatment and/or prevention of cerebrovascular disorders are disclosed.... | 09/14/1993 |
| 5231183 | Process for producing enyne derivatives A process for producing an enyne derivative, and intermediate, which is useful for preparing compounds showing strong inhibiting activities against squalane.epoxidase of Eumycetes and strong anti-cholesterol activities. The process comprises reacting a co... | 07/27/1993 |
| 5216178 | Process of reducing olefins Novel aminoalkylthiodibenzoxepins, physiologically tolerable acid addition salts thereof, a method of preparing same, pharmaceutical and veterinary preparations including same and methods of treating by administering same are disclosed. These compounds ar... | 06/01/1993 |
| 5202486 | Tetrahydroethanonaphthaleneamine derivatives Tetrahydronaphthaleneamine derivatives having the formula ##STR1## wherein R, R', R1 and R2 are as defined herein, are novel calcium channel blockers.... | 04/13/1993 |
| 5180746 | Aralkylamine compounds An aralkylamine compound of the formula ##STR1## wherein R1 means a hydrogen atom or a lower alkyl group; R2 means an aromatic group which may be substituted; R3 means a hydrogen atom, a lower alkyl group or an aromat... | 01/19/1993 |
| 5166438 | 1,3-pentadiene derivatives and electrophotographic photoconductor using the same A charge transporting material comprising a 1,3-pentadiene derivative having formula (I): A--CH.dbd.CH--CH.dbd.CH--CH2 --A (I) wherein A represents a 9-anthryl group which may have a substituent, a N-substituted carbazolyl group... | 11/24/1992 |
| 5149714 | Antidepressants The present invention provides novel aryloxy indanamines of the formula ##STR1## wherein n, p and q are each independently 0, 1 or 2, Y and X are each independently lower alkyl, lower alkoxy, hydroxy, CF3, halogeno or when p or q are 2 and each... | 09/22/1992 |
| 5132459 | Propenylamines, processes for their production, pharmaceutical compositions containing them and their use as pharmaceuticals Compounds of formula I ##STR1## wherein R1 represents a group of formula ##STR2##... | 07/21/1992 |
| 5117062 | Aromatic tertiary amines, enamines, deoxybenzoins and benzils A novel synthesis of aromatic tertiary amines involves reacting an aromatic anil and an aromatic ether in a molar ratio of 1:1; adjusting the ratio to 2:1 produces novel enamines and by employing a two step process for enamine production, various unsymmet... | 05/26/1992 |
| 5032616 | 4-substituted cyclohexylamine derivatives, fungicides containing these and a method of controlling fungi 4-trans-substituted cyclohexylamine derivatives of the formula ##STR1## where R1 is the group CR5 R6 R7, in which R5, R6 and R7 are hydrogen, unsubstituted or substituted alkyl, ... | 07/16/1991 |