Did You Know...
...that the Eveready Battery began as an invention called the "electric flowerpot," which was a tube with a battery and light bulb inside? The idea was to fasten this gizmo to the side of a flowerpot so it would illuminate the flowers from the bottom. The idea died on the vine and the businessman who licensed the flower pot, Conrad Huber, was left with a pile of useless tubes -- until he found a way to market them as batteries to light the world!
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| Number | Title | Issue Date |
| 7534896 | Process for the synthesis of perindopril and its pharmaceutically acceptable salts Process for the synthesis of perindopril of formula (I): and its pharmaceutically acceptable salts. ... | 05/19/2009 |
| 7498330 | 4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrazine-6-carboxamide compounds Compound of formula (I): wherein: represents 1-oxidopyridyl substituted by the remainder of the molecule in any one of the positions 2, 3 and 4, | 03/03/2009 |
| 7470806 | Process for the synthesis of (7-methoxy-1-naphthyl) acetonitrile and its application in the synthesis of agomelatine A process for the industrial synthesis of the compound of formula (I) Application in the synthesis of agomelatine. ... | 12/30/2008 |
| 7459434 | Peptide interacting with anti-apoptotic proteins of the Bcl-2 family The invention relates to the identification of a new peptide interacting with the anti-apoptotic proteins Bcl-2, Bcl-W and/or Bcl-XL, and also to screening methods allowing identification of modifiers of those interactions. ... | 12/02/2008 |
| 7368580 | Method for the synthesis of perindopril and the pharmaceutically acceptable salts thereof Process for the synthesis of perindopril of formula (I): and its pharmaceutically acceptable salts. ... | 05/06/2008 |
| 7358395 | Crystalline form V of agomelatine, a process for its preparation and pharmaceutical compositions containing it Crystalline form V of the compound of formula (I): characterised by its powder X-ray diffraction diagram. Medicinal products containing the same which are useful in the treatment of melatoninergic disorders. ... | 04/15/2008 |
| 7358372 | Method for the synthesis of perindopril and the pharmaceutically acceptable salts thereof Process for the synthesis of perindopril of formula (I): and its pharmaceutically acceptable salts. ... | 04/15/2008 |
| 7323575 | Process for the synthesis of (2S)-indoline-2-carboxylic acid Process for the synthesis of (2S)-indoline-2-carboxylic acid of formula (I): Application in the synthesis of perindopril and its pharmaceutically acceptable salts. ... | 01/29/2008 |
| 7312213 | Substituted benzo[e][1,4]oxazino[3,2-g]isoindole compounds A compound selected from those of formula (I): wherein: W1, with the carbon atoms to which it is bonded, represents phenyl or pyridyl, Z represents a... | 12/25/2007 |
| 7265220 | Amino acid derivatives, method for production thereof and pharmaceutical compositions comprising said derivative Compound of formula (I): wherein: R1 represents aryl, heteroaryl or alkyl which is optionally substituted, or a group of formula —(CO)—CR6R7NR8R9 ... | 09/04/2007 |
| 7262191 | Benzothiadiazine compounds The invention relates to compounds of formula (I): wherein: X represents oxygen or sulphur, R1 represents linear or branched (C1-C6 | 08/28/2007 |
| 7214805 | Process for the industrial synthesis of strontium ranelate and its hydrates The process for the industrial The synthesis of strontium ranelate of formula (I): and its hydrates. ... | 05/08/2007 |
| 7214689 | Isoquinoline compounds The invention relatests compound of formula (I): wherein: n is 1, 2 or 3, A represents a group | 05/08/2007 |
| 7208607 | Process for synthesis of perindopril and pharmaceutically acceptable salts thereof Process for the synthesis of perindopril of formula (I): and pharmaceutically acceptable salts thereof. ... | 04/24/2007 |
| 7202255 | Substituted [1,4] benzodioxino[2,3-e] isoindole derivatives, method for preparing and pharmaceutical compositions containing same Compounds of formula (I): wherein: A is as defined in the description, Y represents a group selected from an oxygen atom and a methylene group, | 04/10/2007 |
| 7196204 | Method for the synthesis of s-indoline-2-carboxylic acid and application thereof in the synthesis of perindopril Process for the synthesis of (2S)-indoline-2-carboxylic acid of formula (I): Application in the synthesis of perindopril and its pharmaceutically acceptable salts. ... | 03/27/2007 |
| 7166633 | Method for synthesising perindopril and the pharmaceutically acceptable salt thereof Process for the synthesis of perindopril of formula (I): and pharmaceutically acceptable salts thereof. ... | 01/23/2007 |
| 7151108 | [3,4-a:3,4-c]carbazole compounds A compound selected from those of formula (I): wherein: W1 represents, together with carbon to which it is bonded, phenyl, pyridyl, Z represents a gr... | 12/19/2006 |
| 7074920 | Process for the synthesis of 1,3-dihydro-2H-3-benzazepin-2-one compounds, and to the application thereof in the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid Process for the synthesis of compounds of formula (I): wherein R1 and R2, which may be the same or different, each represent a linear or branched (C1–C8)alkoxy group ... | 07/11/2006 |
| 6992085 | Octahydro-2H-pyrido[1,2-a]pyrazine compounds A compound selected from those of formula (I): wherein: Ra represents linear or branched (C1–C6)alkylene, X represents a group selected from W | 01/31/2006 |
| 6872851 | Substituted cyclic compounds, preparation method and pharmaceutical compositions containing them The invention concerns compounds of formula (I): R—A—R′ wherein: A is as defined in the description; R represent, a group (V), wherein R′a and R″a are as defined in the description, or R forms with A a cyclic structure as defined in t... | 03/29/2005 |
| 6846833 | Vitronectin receptor antagonist bicyclic compounds, preparation method and compositions containing same Compounds of formula (1): wherein: G represents an optionally substituted phenyl or optionally substituted heterocycle, G1 and G2 being N or C, ... | 01/25/2005 |
| 6716852 | Amino acid derivatives and use thereof as NEP, ACE and ECE inhibitors The invention relates to compounds of formula (I): wherein 0≦n≦3, 0≦m≦6, R3 and R4 together form phenyl, B represents heteroaryl, R1 and R2... | 04/06/2004 |
| 6451789 | 1-aza-2-alky-6-aryl-cycloalkanes Compound of formula (I): ##STR1## wherein: n represents 0 or 1, R1 represents hydrogen, arylalkyl, alkyl, acyl, alkoxycarbonyl, arylalkoxycarbonyl or trifluoroacetyl, R2 represents alkyl, X represents oxygen, chlorine, OR3, SR | 09/17/2002 |
| 6441165 | Process for the preparation of 11-amino-3-chloro-6, 11-dihydro-5, 5-dioxo-6-methyl-dibenzo[c,f][1,2]thiazepine and application to the synthesis of tianeptine Process for the industrial synthesis of the compound of formula (I): ##STR1## and its addition salts. Application to the synthesis of tianeptine and its pharmaceutically acceptable salts.... | 08/27/2002 |
