Celebrity Inventors
Actor Zeppo Marx patented a "Cardiac Pulse Rate Monitor" in 1969.
PatentStorm News
Make the Most of Our Site
See this month's Top Inventors and Most Cited Patents.
Stay on top of the latest innovations by subscribing to an RSS feed.
Registered users: Manage your profile.
| Number | Title | Issue Date |
| 7423155 | N-sulfonyldicarboximide containing tethering compounds Compounds having two reactive functional groups are described that can be used as a tethering compound to immobilize an amine-containing material to a substrate. The first reactive functional group can be used to provide attachment to a surface of a substrate. The s... | 09/09/2008 |
| 7361767 | N-sulfonyldicarboximide containing tethering compounds Compounds having two reactive functional groups are described that can be used as a tethering compound to immobilize an amine-containing material to a substrate. The first reactive functional group can be used to provide attachment to a surface of a substrate. The s... | 04/22/2008 |
| 7351838 | N-sulfonyldicarboximide containing tethering compounds Compounds having two reactive functional groups are described that can be used as a tethering compound to immobilize an amine-containing material to a substrate. The first reactive functional group can be used to provide attachment to a surface of a substrate. The s... | 04/01/2008 |
| 6291507 | Chemical compounds A pharmaceutical composition which comprises a compound of formula (I) ##STR1## or a pharmaceutically acceptable salt, ester or amide thereof, which is an inhibitor of monocyte chemoattractant protein-1, and wherein A and B form an optionally substituted ... | 09/18/2001 |
| 6251931 | Inhibitors of gap junction communication Oleamide is an endogenous fatty acid primary amide that possesses sleep-inducing properties in animals and has been shown to effect seratonergic systems and block gap junction communication in a structurally specific manner. Certain agents can serve both ... | 06/26/2001 |
| 5919790 | Hydroxamate inhibitors of interleukin-1ଲ converting enzyme The present invention relates to compounds that are inhibitors of interleukin-1ଲ converting enzyme that have the Formula II ##STR1## This invention also relates to a method of treatment of stroke, inflammatory diseases, septic shock, reperfusio... | 07/06/1999 |
| 5824804 | Method for the preparation of a N-alkoxy-(tetra-or hexahydro)-phthalimide and method for the preparation of a N-alkoxyamine Method for the preparation of N-alkoxy-(tetra- or hexahydro)-phthalimide according to formula I ##STR1## R1 being methyl or ethyl and R2 and R3 being each independently of one another hydrogen or alkyl with 1-4 C atom... | 10/20/1998 |
| 5719144 | Fibrinogen receptor antagonists Fibrinogen receptor antagonists having the formula ##STR1## where L is L is (CH2)p, where p is 1 or 2; and Z is --CR1 .dbd.CR2 --; which are useful for inhibiting platelet aggregation for example ##STR... | 02/17/1998 |
| 5414089 | Long chain carboxylic acid imide ester Provided is a long chain carboxylic acid imide ester (I) represented by the following general formula (I) ##STR1## wherein W is a divalent long chain hydrocarbon group which may optionally be interrupted by one or more groups each independently selec... | 05/09/1995 |
| 5350743 | Bisphosphonic acid derivatives, as bone resorption inhibitors A bisphosphonic acid derivative of the formula (I) or a pharmaceutically acceptable salt thereof: ##STR1## wherein A is ##STR2## each of R3 and R4, which may be the same or different, is (i) a hydrogen atom, (ii) a C | 09/27/1994 |
| 5349001 | Cyclic imide thione activated polyalkylene oxides Water-soluble cyclic imide thione activated polyalkylene oxides having improved hydrolytic stability are disclosed. Methods of forming and conjugating the activated polyalkylene oxides with biologically active nucleophiles are also disclosed.... | 09/20/1994 |
| 5346879 | Plant growth regulator containing a phthalimide derivative Plant growth regulators comprising, as an active ingredient, a substituted dicarboxylic acid derivative having the formula: ##STR1## wherein R1, R2, R3 and R4 are the same as defined in the present specific... | 09/13/1994 |
| 5081301 | Hydroxylamine derivatives which are intermediates for making herbicidal compounds Hydroxylamine derivatives have the general formula I Aryl--A--O--B I where Aryl is an unsubstituted or substituted, mononuclear or binuclear, isocyclic radical; A is a 1,4-butenylene group of the general formulae IIa or ... | 01/14/1992 |
| 4853149 | Heterocyclic liquid crystal compounds Heterocyclic liquid crystal compounds containing the structural element ##STR1## wherein M is H, CN,, NCS, halogen or an alkyl group with 1-5 C atoms, X is CR4 or N, Y is CHR4, O, S or NR5, R4 is H, alkyl with 1-15 C... | 08/01/1989 |
| 4684660 | Mercaptoacyldepeptides Compounds having the formula ##STR1## and alkyl esters and salts thereof. R1 is hydrogen, alkanoyl or ##STR2## R2 is hydrogen, alkyl, or phenylalkyl; n is 0 or 1; and A1 and A2 each is an -amino or &... | 08/04/1987 |
| 4642353 | Photocrosslinkable polymers having thioetherimidyl side groups Photocrosslinkable polymers having an average molecular weight of at least 1,000 and side groups of the formula Ia and/or Ib ##STR1## in which R, R', R1, R2, A, E, Y and n are as defined in claim 1, are suitable, for example, fo... | 02/10/1987 |
| 4563535 | Process for producing tetrahydrophthalimides A compound of the formula: ##STR1## wherein R is an isoproyl group or an n-amyloxycarbonylmethyl group, useful as a herbicide, is effectively produced by reacting a compound of the formula: ##STR2## wherein R is as defined above, with sulfu... | 01/07/1986 |
| 4508657 | Peptide synthesis and amino acid blocking agents Process for the preparation of peptides including higher polypeptides utilizing indenylmethoxycarbonyl blocking groups and products produced thereby.... | 04/02/1985 |
| 4469874 | Fragrant prevulcanization inhibitors Alkyl thiosalicylate prevulcanization inhibitors having a pleasant odor are described. Claimed compounds include those of the formula: ##STR1## in which X is an amide inhibitor moiety attached through the nitrogen atom derived from the group consisti... | 09/04/1984 |
| 4423243 | Process for the preparation of 2,2-dimethyl-3-vinyl-cyclopropanecarboxylic acids and esters A process for the production of 2,2-dimethyl-3-vinyl-cyclopropanecarboxylic acid derivative of the formula ##STR1## in which R1 is a hydrogen atom, an alkyl group or a radical of an alcohol which can be used in pyrethroids, and X1 | 12/27/1983 |
| 4298613 | Agricultural heterocyclic sulfenamides Heterocyclic sulfenamides, such as N-[2-chloro-5-(trifluoromethyl)phenyl]-N-[2,4-dinitro-6-trifluoromethyl)ph enyl]-3-nitro-2-pyridinesulfenamide, are useful as miticides, insecticides, fungicides and ovicides.... | 11/03/1981 |
| 4275214 | Substituted alkoxy carbonyl-3-oxo--phthalimido-5-isoxozolidineacetic acids Analogs of tricholomic acids and process for preparing them.... | 06/23/1981 |
| 4219393 | Process for producing sulfenimides Sulfenimides are prepared by electrolytic oxidation of organic disulfides or mercaptans and imides. The electrolytic oxidation is accelerated by a halide compound.... | 08/26/1980 |
| 4148901 | N-phenyl or n-pyridyl sulfamides and methanesulfonamides The invention provides novel fluoro-imides/amides of the formula: ##STR1## IN WHICH AT LEAST TWO OF X1, X2, X3 and X4 are fluorine and any of X1, X2, X3 and X4 which i... | 04/10/1979 |
| 4131611 | Azabicyclohexanes Substituted 3-azabicyclo[3.1.0]hexanes, acid addition salts, method of use and method of preparation are described. The compounds have anxiolytic and analgesic activity.... | 12/26/1978 |
| 3956331 | N-(Salicyloylamino)imides and process for the preparation of the same Novel N-(salicyloylamino)imides which can act as excellent stabilizers for polyolefins are disclosed. A process for the preparation of the same which comprises the reaction of salicyloylhydrazine with a cyclic acid anhydride is also disclosed.... | 05/11/1976 |
