| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 101 | Tetra-substituted fulvalene derivatives | US855105 | 1986-04-23 | US4691028A | 1987-09-01 | Hiroo Inokuchi; Gunji Saito; Kazuhiko Seki; Takehiko Mori |
| A fulvalene derivative represented by formula (1) below. ##STR1## where A.sup.1 -A.sup.8 are at least one atom or a combination of two or more atoms selected from S atom, Se atom, and Te atom; and R.sup.1 -R.sup.4 are alkyl or alkene having 3 to 22 carbon atoms.The fulvalene derivative of this invention has electric conductivity as it is at normal temperature and under normal pressure. It is useful as a semiconductor, which has an electrical conductance greater than 10.sup.-9 Scm.sup.-1 and a minimum specific resistance of 10.sup.5 .OMEGA..multidot.cm order. | ||||||
| 102 | Choline Esters | US16791265 | 2020-02-14 | US20200352903A1 | 2020-11-12 | William GARNER; Margaret GARNER; George MINNO; David GOODEN |
| Compounds, formulations, and methods are provided containing the choline ester of a reducing agent, especially lipoic acid or derivatives thereof. The compounds may be administered via a topical ocular route to treat or prevent oxidative damage. | ||||||
| 103 | Thiazolidin-4-one derivatives | US13570956 | 2012-08-09 | US08524752B2 | 2013-09-03 | Christoph Binkert; Martin Bolli; Boris Mathys; Claus Mueller; Michael Scherz; Oliver Nayler |
| The invention relates to pharmaceutical compositions containing at least one thiazolidin-4-one derivative to prevent or treat disorders associated with an activated immune system. Furthermore, the invention relates to novel thiazolidin-4-one derivatives notably for use as pharmaceutically active compounds. Said compounds particularly act also as immunosuppressive agents. | ||||||
| 104 | Development of molecular imaging probes for carbonic anhydrase-IX using click chemistry | US12862955 | 2010-08-25 | US08354092B2 | 2013-01-15 | Hartmuth C. Kolb; Joseph C. Walsh; Dhanalakshmi Kasi; Vani P. Mocharla; Bing Wang; Umesh B. Gangadharmath; Brian A. Duclos; Kai Chen; Wei Zhang; Gang Chen; Henry Clifton Padgett; Farhad Karimi; Peter J. H. Scott; Zhiyong Gao; Qianwa Liang; Thomas Lee Collier; Tieming Zhao; Chunfang Xia |
| The present application discloses methods for identifying inhibitors with high binding-affinity for the carbonic anhydrase-IX (CA-IX) enzyme using click chemistry and uses the candidates thereof as positron emission tomography (PET) imaging agents. | ||||||
| 105 | Thiazolidin 4-one derivatives | US12496945 | 2009-07-02 | US08273779B2 | 2012-09-25 | Christoph Binkert; Martin Bolli; Boris Mathys; Claus Mueller; Michael Scherz; Oliver Nayler |
| The invention relates to pharmaceutical compositions containing at least one thiazolidin-4-one derivative to prevent or treat disorders associated with an activated immune system. Furthermore, the invention relates to novel thiazolidin-4-one derivatives notably for use as pharmaceutically active compounds. Said compounds particularly act also as immunosuppressive agents. | ||||||
| 106 | 1,3 dithiolane-2-thione additives for lubricants and fuels | US12409827 | 2009-03-24 | US08048832B2 | 2011-11-01 | Robert G. Rowland |
| Fuels, especially hydrocarbon fuels, and lubricants, especially lubricating oils, contain a class of anti-corrosion, anti-wear, anti-fatigue, and extreme pressure additives that are derived from 1,3-dithiolane-2-thiones. | ||||||
| 107 | Sulfonium compound, photosensitive composition containing the compound and pattern-forming method using the photosensitive composition | US11703100 | 2007-02-07 | US08021819B2 | 2011-09-20 | Yasutomo Kawanishi |
| A photosensitive composition, which comprises a compound represented by formula (I): wherein R1 to R13 each independently represents a hydrogen atom or a substituent, and at least one of R1 to R13 is a substituent containing an alcoholic hydroxyl group; Z represents a single bond or a divalent linking group; and X− represents a counter anion; and a pattern-forming method using the photosensitive composition. | ||||||
| 108 | Development of molecular imaging probes for carbonic anhydrase-IX using click chemistry | US12099135 | 2008-04-07 | US07829063B2 | 2010-11-09 | Hartmuth C. Kolb; Joseph C. Walsh; Dhanalakshmi Kasi; Vani P. Mocharla; Bing Wang; Umesh B. Gangadharmath; Brian A. Duclos; Kai Chen; Wei Zhang; Gang Chen; Henry Clifton Padgett; Farhad Karimi; Peter J. H. Scott; Zhiyong Gao; Qianwa Liang; Thomas Lee Collier; Tieming Zhao; Chunfang Xia |
| The present application discloses methods for identifying inhibitors with high binding-affinity for the carbonic anhydrase-IX (CA-IX) enzyme using click chemistry and uses the candidates thereof as positron emission tomography (PET) imaging agents. | ||||||
| 109 | Dithiol Compounds, Derivatives, and Uses Therefor | US12390928 | 2009-02-23 | US20090192212A1 | 2009-07-30 | William Garner; Margaret Garner; Ronald D. Blum |
| Dithiol compounds and derivatives thereof are disclosed. The agents are useful for treating ocular disease, especially presbyopia and cataract. | ||||||
| 110 | Neuroprotective benzo 1 3 oxathiol 2 ones | US10564941 | 2004-07-29 | US20060234987A1 | 2006-10-19 | James Jaquith |
| This invention relates to benzo[1,3]oxathiol-2-ones, derivatives, and precursors thereof, and their use as neuroprotective agents in the treatment and prevention of neuronal disorders of the central and peripheral nervous systems. | ||||||
| 111 | Dioxolanes and thio analogs, derivatives thereof and lubricants and fuels containing same | US770692 | 1991-10-03 | US5268007A | 1993-12-07 | Reed H. Walsh |
| Dioxolanes, thio analogs thereof, and derivatives of these and methods of preparation are described. These materials are useful as additives in lubricants and fuels. Methods for reducing fuel consumption in internal combustion engines employing the lubricating compositions are described. | ||||||
| 112 | Photographic element containing a macrocyclic ether compound | US77131 | 1987-07-23 | US4782013A | 1988-11-01 | Arthur H. Herz; Roger L. Klaus |
| This invention is directed to a photographic element containing a radiation-sensitive silver halide emulsion layer and a macrocyclic thia or selena ether compound which also comprises oxygen atoms. These macrocyclic compounds are improved silver halide ripening agents. | ||||||
| 113 | High pressure synthesis of sulfur-selenium fulvalenes | US372058 | 1982-04-26 | US4465845A | 1984-08-14 | Yoshiyuki Okamoto; Piotr S. Wojciechowski |
| A process is disclosed for one-step preparation of sulfur-selenium fulvalenes by reaction of an acetylenic compound with carbon selenide sulfide or with a mixture of carbon diselenide and carbon disulfide under pressures of at least about 1,000 atmospheres. Fulvalene compounds made by the process are characterized in having at least one sulfur atom and at least one selenium atom in the ring structure of the fulvalene compound. Substituted diselenadithiafulvalenes made by this process are precursors to very pure diselenadithiafulvalene which is useful in preparing charge-transfer salts. | ||||||
| 114 | Substituted heterofulvalenes | US74927 | 1979-09-13 | US4312992A | 1982-01-26 | Dennis C. Green |
| Substituted derivatives of tetrathiafulvalene, tetraselenafulvalene and dithiadiselenafulvalene having the general formulae ##STR1## where Z is S and Y is S; Z is S and Y is Se; and Z is Se and Y is Se, and R can be CO.sub.2 H, R'R"COH, R'CHOH, COR', SCH.sub.3, SO.sub.2.sup.- Li.sup.+, SnR.sub.3 ', SiR.sub.3, --CH.sub.2 OH --CO.sub.2 R', R'CHOH, CHO, CR.sub.2 ' CR.sub.2 'OH, TTF, TSeF and DTDSeF, R' and R" can be the same or different and is selected from the group consisting of alkyls, aryls, alkaryls, ether substituted alkyls, halogen substituted alkyls and halogens, are prepared. A novel method for their preparation is also described. | ||||||
| 115 | 4,5-benzo-3h-1,2-thiaselenol-5-one and production thereof | US3511853D | 1967-11-28 | US3511853A | 1970-05-12 | KLINGSBERG ERWIN |
| 116 | Highly chlorinated aryl sulfides and process for the manufacture thereof | US12507761 | 1961-07-19 | US3217044A | 1965-11-09 | HELMUT KLUG |
| 117 | SELENOPHENES AND SELENOPHENE-BASED POLYMERS, THEIR PREPARATION AND USES THEREOF | EP08808020.5 | 2008-09-10 | EP2190832A2 | 2010-06-02 | BENDIKOV, Michael; PATRA, Asit; WIJSBOOM, Yair-Haim; LI, Mao; SHEYNIN, Yana; ZAMOSHCHIK, Natalia; ZADE, Sanjio S. |
| This invention is directed to selenophene compounds, selenophene-based polymers (polyselenophene), processes for the preparation of the same and uses thereof. The polyselenophenes of this invention have high conductivity and can be used as electrodes in various devices such as in electrochromic devices, batteries, solar cells, optical amplifiers, organic light emitting diodes, and the like. | ||||||
| 118 | SPECIFIC KINASE INHIBITORS | EP05799606 | 2005-09-26 | EP1794137A4 | 2009-12-02 | SANTI DANIEL V; REID RALPH C; HUTCHINSON RICHARD C; SUNDERMANN KURT F; LAU JANICE |
| 119 | SPECIFIC KINASE INHIBITORS | EP05799606.8 | 2005-09-26 | EP1794137A2 | 2007-06-13 | SANTI, Daniel, V.; REID, Ralph, C.; HUTCHINSON, Richard, C.; SUNDERMANN, Kurt, F.; LAU, Janice |
| Resorcylic acid lactones having a C5-C6 cis double bond and a ketone at C7 and other compounds capable of Michael adduct formation are potent and stable inhibitors of a subset of protein kinases having a specific cysteine residue in the ATP binding site. | ||||||
| 120 | THIA- AND/OR SELENAFULVALENYL COMPOUND | EP91900354 | 1990-11-21 | EP0454874A4 | 1992-04-22 | MIZUTANI, MAKOTO IDEMITSU KOSAN CO., LTD.; KAWABATA, KAZUSHIGE IDEMITSU KOSAN CO., LTD.; TANAKA, KEIJI IDEMITSU KOSAN CO., LTD. |
| A thia- and/or selenafulvalenyl compound having an excellent thermal stability and represented by general formula (I), wherein X1 to X4 and X1' to X4' are each independently S or Se; Y is a substituent not inhibiting overlapping of the molecule; m is an integer of 0 to 4; Z1, Z2, Z1' and Z2' are each independently a hydrogen atom, CnH2n+1 wherein n is an integer of 1 to 5 or XCnH2n+1 wherein X is S or Se, n is an integer of 1 to 5, or Z1 and Z2 are combined to Z1' and Z2' to form CnH2n wherein n is an integer of 1 to 5, or X(CnH2n)n'X wherein X is S or Se and n' is an integer of 1 to 3; and R1 to R3 and R1' to R3' are each independently a hydrogen atom or CnH2n+1 wherein n is an integer of 1 to 5, and a conductive complex comprising a compound represented by general formula (I) as an electron donor. | ||||||
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