...Chester Carlson was a patent agent who tired of having to make multiple copies of patent applications using the only duplication method available at the time: carbon paper. In 1959 he came up with a new copying system and took it to IBM for evaluation. The "experts" at IBM determined potential sales to be only 5,000 units because people wouldn't want to use a bulky machine when they had carbon paper. Carlson's invention was the xerography process, the company founded on the system is Xerox.
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| Number | Title | Issue Date |
| 6900193 | Structural modification of 19-norprogesterone I: 17-α-substituted-11-β-substituted-4-aryl and 21-substituted 19-norpregnadienedione as new antiprogestational agents The present invention relates, inter alia, to compounds having the general formula: in which: R1 is a member selected from the group consisting of —OCH3, —SCH3, —N(CH3)... | 05/31/2005 |
| 6861415 | 21-substituted progesterone derivatives as new antiprogestational agents A compound having the general formula: in which: R1 is a member selected from the group consisting of —OCH3, —SCH3, —N(CH3)2, —NHCH3, —CHO, â€... | 03/01/2005 |
| 5994335 | 17-azolyl steroids useful as androgen synthesis inhibitors Androgen synthesis inhibitors, as well as methods for the use of the same to reduce plasma levels of testosterone and/or dyhydrotestosterone, and to treat prostate cancer and benign prostatic hypertrophy, are disclosed.... | 11/30/1999 |
| 5994333 | Pregnane and cholane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical compositions and methods The invention relates to a method of altering hypothalamic function in an individual. The method comprises nasally administering a human vomeropherin, e.g. a pregnane or cholane steroid, or a pharmaceutical composition containing a vomeropherin, such that... | 11/30/1999 |
| 5827842 | 14, 17-C2 -bridged norprogesterone derivatives The invention describes 14,17-C2 -bridged steroids of general formula (I), ##STR1## wherein the various R groups are as defined in the specification, and wherein said steroids are, in contrast with the disclaimed compound 14,17-ethano... | 10/27/1998 |
| 5824670 | 17-deoxycorticosteroid-21-›O!carboxylic esters, processes for their preparation and pharmaceuticals containing these compounds 17-Deoxycorticoid-21-carboxylic esters of the formula I ##STR1## are described, in which A is CHOH and CHCl, CH2, C.dbd.O or 9(11) double bond; Y is H, F or Cl; Z is H, F or CH3 ; R(1) is aryl or hetaryl and R(2) is H or methyl.... | 10/20/1998 |
| 5760256 | Process for the production of 21-acyloxy-4,9 (11),16-pregnatriene-3,20-diones A process for the production of a compound of the formula ##STR1## wherein R1 is acyl of 1 to 8 carbon atoms,. The compound is formed by the reduction of an intermediary to form an alcohol, epoxidation and hydrolyzation of the alcohol to f... | 06/02/1998 |
| 5616743 | 16-methyl-ÆŠ1,4 -pregnadiene-3,20-diones A compound having the formulae selected from the group consisting of ##STR1## wherein R2 and R3 are hydrogen or R2 is fluorine and R3 is formyloxy or acetyloxy, the dotted line in 9(11) position indicates a... | 04/01/1997 |
| 5502223 | Process for preparation of ÆŠ4,9(11),16 pregnatriene-3,20-diones A process for the preparation of a compound of the formula ##STR1## wherein R1 is acyl of an organic carboxylic acid of 1 to 8 carbon atoms useful as intermediates for synthesis of therapeutically active steroids.... | 03/26/1996 |
| 5401864 | Process for preparing 21 acyloxy-ÆŠ4,9(11),16 pregnatrienes 3-20-dione A process for the preparation of a compound of the formula ##STR1## wherein R1 is acyl of 1 to 8 carbon atoms, by reducing an intermediary to form an alcohol, oxidizing the alcohol to form an aidehyde, which is subjected to the action of a... | 03/28/1995 |
| 5352808 | Process for steroid preparation A process for the preparation of a compound of the formula ##STR1## wherein R1 is selected from the group consisting of hydrogen, alkyl of 1 to 4 carbon atoms optionally substituted by halogen or a nitrogen or oxygen function and alkenyl a... | 10/04/1994 |
| 5294704 | 4,9(11),17(20)-pregnatriene-3-ones A process for the production of a compound of the formula ##STR1## wherein R is an acyl group of 1 to 8 carbon atoms. The compound is formed through an intermediate compound of the formula ##STR2## wherein R1 is selected from the grou... | 03/15/1994 |
| 5264427 | 20-substituted pregnene derivatives and their use as androgen synthesis inhibitors Novel 20-substituted-pregnene derivatives, compositions containing such derivatives and methods for their use and manufacture are disclosed. The 20-substituted-pregnene derivatives inhibit the androgen biosynthesis enzymes 17(alpha)-hydroxylase/C17 | 11/23/1993 |
| 5248773 | 16-methyl-ÆŠ1,4-pregnadiene-3,20-diones A compound of the formula ##STR1## in which ##STR2## is either a 3-keto-ÆŠ4-system or a 3-keto -ÆŠ1,4-system or a 3-OR4 -ÆŠ5-system in which R4 is hydrogen or a protector group of hydroxy, R is methyl, --CH2... | 09/28/1993 |
| 5169966 | Process for producing an -acyloxy-, ଲ-unsaturated carbonyl compound and a 20-acyloxy-17(20)-methylen-21-al-steroid compound There are disclosed a process for producing an -acyloxy-,ଲ-unsaturated carbonyl compound represented by the general formula (VI): ##STR1## wherein R1, R2 and R4 are independently hydrogen atoms or ... | 12/08/1992 |
| 5116830 | Stereoisomerically pure 17-ethynyl-estra-2-en-17ଲ-ol and the 17ଲ esters thereof, methods of preparation and uses This invention relates to a stereoisomerically pure ÆŠ2 compound of the formula (I): ##STR1## wherein: R1 is hydrogen or --(C.dbd.O)--R2, wherein: R2 is an organic substituent selected from the group consisting ... | 05/26/1992 |
| 4948533 | 11a-hydroxy steroid diester The present invention relates to 21-(3-carboxy-1-oxopropoxy) -17-hydroxy-11-(3,3-dimethyl-1-oxobutoxy)pregna-1,4-diene-3, 20 dione and pharmaceutically acceptable salts thereof which are useful steroid prodrugs.... | 08/14/1990 |
| 4929395 | 16-methylation process C16 -unsaturated corticoids are readily transformed to the corresponding 16-methyl-17-hydroxy corticoids by use of a ÆŠ17 (20)-20-silyl ether.... | 05/29/1990 |
| 4920114 | 19-fluoro- or cyano-21-hydroxyprogesterone derivatives useful as 19-hydroxylase inhibitors 19-Fluoro- and cyano- substituted 21-hydroxyprogesterone derivatives and related compounds which are active as 19-hydroxylase inhibitors and useful as antihypertensive agents are described herein. The compounds are prepared using appropriate synthetic pat... | 04/24/1990 |
| 4917827 | Process for the preparation of 9(11)-dehydro steroids 9(11)-dehydroandrostanes and 9(11)-dehydropregnanes are prepared by dehydrating the corresponding 9-alpha-hydroxy steroid in the presence of a Lewis acid. The corresponding 8(9)-dehydro-isomer was not detectable. The resulting products are valuable interm... | 04/17/1990 |
| 4913852 | Compounds obtained from the associative synthesis of sulfur-containing or sulfur-free amino acids with pregnane derivatives Compounds obtained from the associative synthesis of sulfur-containing or sulfur-free amino acids with derivatives of ÆŠ-4-pregnene-3,20-dione or with derivatives of ÆŠ-1,4-pregnadiene-3,20-dione of the general formulas (I), (II) and (III), having glucoco... | 04/03/1990 |
| 4871724 | Novel 11-aryloestrane and 11-arylpregnane derivatives The present invention is concerned with 11-aryloestrane and 11-arylpregnane derivatives, characterized in that these derivatives have the following structure: ##STR1## wherein R1 is an aryl group with an ##STR2## group as substit... | 10/03/1989 |
| 4870069 | 11ଲ-alkynyl-estrenes and -estradienes, their production and pharmaceutical preparations containing them 11ଲ-substituted steroids of the formula ##STR1## wherein A and B together represent a second bond between the 6-position and 7-position carbon atoms, or, respectively, are each H; X is O, two H atoms or hydroximino; Z is the residue of a pentagonal ... | 09/26/1989 |
| 4668437 | Novel 20 benzcylamino pregnene derivatives and process for preparing same The invention relates to new pregnene derivatives of the general formula (I), ##STR1## wherein R1 stands for a C1-4 alkyl group; R2 stands for a hydrogen atom or a C2-4 alkanoyl group; R3 stands for a... | 05/26/1987 |
| 4634695 | Steroid derivatives Novel 19-nor steroids and 19-nor-D-homo-steroids of the formula ##STR1## wherein R1 is an organic radical of 1 to 18 carbon atoms containing at least one atom selected from the group consisting of nitrogen, phosphorous and silicon with the... | 01/06/1987 |
| 4603128 | Mineralocorticoid hormone antagonists 7-acylthio-4-pregnene-3,20-diones, active as mineralocorticoid hormone antagonists, of the formula: ##STR1## in which R1 is hydrogen, hydroxyl or acyloxy --OR2, R2 is an acyl group derived from a straight or br... | 07/29/1986 |
| 4588718 | Carboxy containing ester prodrugs of corticosteroids A compound of the formula ##STR1## wherein St represents a corticosteroid moiety bonded to the carbonyl via the 21-hydroxy group of said corticosteroid; wherein Z is a bond or --O--; wherein n is an integer from 4 to 9; wherein Q is (1) Y--CH2 ... | 05/13/1986 |
| 4551278 | Preparation of 20-keto-ÆŠ16 -steroids A novel process for the preparation of 20-keto-ÆŠ16 -steroids comprising reacting a 17-(isocyanosulfonylmethylene)-steroid with an alkylating agent QR4 wherein R4 is an organic group and Q is a group or atom readily displa... | 11/05/1985 |
| 4548749 | Process for the preparation of 21-hydroxy-20-keto-ÆŠ16 -steroids and new intermediate compounds formed in this process A novel process for the preparation of 21-hydroxy-20-keto-ÆŠ16 -steroids comprising reacting a 17-(isocyanosulfonylmethylene)-steroid with an aldehyde and an alcohol to form a 17-(2-alkoxy-3-oxazolin-4-yl)-ÆŠ16 -steroid and subjectin... | 10/22/1985 |
| 4547493 | Novel 11ଲ-substituted-19-nor-steroids Novel 19-nor-steroids of the formula ##STR1## wherein R1 is an organic group of 1 to 18 carbon atoms optionally containing at least one heteroatom with the atom immediately adjacent the 11-carbon atom being carbon, R2 is a hydro... | 10/15/1985 |
| 4519949 | Steroid-20-carboxylic acid compounds and a process for their production New ÆŠ1,4,9(11)-pregnatrien-3-one-2o-carboxlic acid compounds are described, corresponding to general formula I below: ##STR1## in which X represents halogen, particularly chlorine or bromine or NH2. There is also described the process for... | 05/28/1985 |
| 4515787 | Steroids Novel 9,11ଲ-dichloro-16-methyl-ÆŠ1,4 -pregnadiene 3,20-diones of the formula ##STR1## wherein R is selected from the group consisting of trimethylsilylphenyl, cyclododecyloxy, dicyclopentylmethoxy and cyclohexylmethoxy ... | 05/07/1985 |
| 4477445 | 3-Keto-19-nor-ÆŠ4,9-steroids Novel 3-keto-19-nor-ÆŠ4,9-steroids of the formula ##STR1##... | 10/16/1984 |
| 4472392 | Sulfonate containing ester prodrugs of corticosteroids Novel solution stable ester prodrugs of corticosteroids of the formula ##STR1## and their salts.... | 09/18/1984 |
| 4469689 | Sulfonate containing ester prodrugs of corticosteroids Novel solution stable ester prodrugs of corticosteroids of the formula ##STR1## and their salts.... | 09/04/1984 |
| 4464302 | 17-[(Hydroxymethyl)formamido-methylene]-steroids Novel 17-[(hydroxymethyl)formamido methylene]-steroids of the formula ##STR1## wherein R1 is selected from the group consisting of hydrogen, alkyl of 1 to 4 carbon atoms optionally substituted with halogen or an oxygen or nitrogen function... | 08/07/1984 |
| 4456602 | Amine containing ester prodrugs of corticosteroids Novel solution stable ester prodrugs of corticosteroids of the formula ##STR1##... | 06/26/1984 |
| 4447424 | Steroid derivatives Novel 19-nor steroids and 19-nor-D-homo-steroids of the formula ##STR1## wherein R1 is an organic radical of 1 to 18 carbon atoms containing at least one atom selected from the group consisting of nitrogen, phosphorous and silicon with the... | 05/08/1984 |
| 4443440 | Amine containing ester prodrugs of corticosteroids Novel solution stable ester prodrugs of corticosteroids of the formula ##STR1##... | 04/17/1984 |
| 4440684 | Process for the preparation of 6-methyl-ÆŠ4,6 -3-keto steroids A process for preparing 6-methyl-ÆŠ4,6 -3-keto steroids of the formula ##STR1## comprises reacting a corresponding ÆŠ4 -3-keto steroid with methoxymethyl acetate (CH3 --O--CH2 --OAc) in an inert solvent ... | 04/03/1984 |