| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 81 | PREBIOTIC INULIN BASED PREPARATION | PCT/IB2015/057265 | 2015-09-21 | WO2016046727A1 | 2016-03-31 | TERENZIO, Domenico; RASTRELLI, Luca; PARISELLA, Chiara |
The present invention relates to an inulin-based prebiotic complex enriched with vitamin B12 and selenium, which finds use in the field of food, nutraceutical, herbal, pharmaceutical preparations. |
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| 82 | 신규한 유기염료 및 이의 제조방법 | PCT/KR2010/003947 | 2010-06-18 | WO2010147425A2 | 2010-12-23 | 배호기; 안현철; 이종찬 |
본 발명은 신규한 염료증감 광전변환소자용 유기염료 및 이의 제조방법에 관한 것으로, 본 발명에 따른 유기염료는 염료감응태양전지(dye-sensitized solar cell, DSSC)에 염료증감 광전변환소자로서 사용되어 종래의 염료보다 향상된 몰흡광계수, Jsc(단회로 광전류 밀도) 및 광전기 변환효율을 나타내어 태양전지의 효율을 크게 향상시킬 수 있다. |
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| 83 | DYES FOR POLYMER COLORATION, THEIR PREPARATION AND THEIR USE | PCT/EP2009065430 | 2009-11-19 | WO2010060849A3 | 2010-07-29 | BARBIERU ROXANA; RUSS WERNER; HARFMANN CARSTEN |
| The present invention relates to a compound of formula (I) where X, Y, S and T are each as defined in claim 1, to its preparation and to its use. | ||||||
| 84 | DYES FOR POLYMER COLORATION, THEIR PREPARATION AND THEIR USE | PCT/EP2009065681 | 2009-11-24 | WO2010063606A2 | 2010-06-10 | BARBIERU ROXANA; HARFMANN CARSTEN; RUSS WERNER |
| The present invention relates to a compound of formula (I), where X, Y, T and Z are each as defined in claim 1, to its preparation and to its use. | ||||||
| 85 | SULFIDE DYES | PCT/EP2006063179 | 2006-06-14 | WO2006136516A3 | 2007-11-01 | CREMER CHRISTIAN; WALLQUIST OLOF |
| Disclosed are compounds of formula. Method of dyeing keratin-containing fibers comprising treating the fiber with at least one sulfide dye of formula (1), their salts, isomers, hydrates and other solvates, wherein R1, R2, R3 and R4 independently from each other are hydrogen; C1-C20alkyl; C1-C20alkoxy; C3-C6cycloalkyl; halogen; NO2; OH; SH; or a radical of formula (1a) wherein R5 is hydrogen; or C1-C20alkyl; R6, R7 and R8 independently from each other are hydrogen, C1-C20alkyl, C4-C12cycloalkyl, C6-C13aralkyl; phenyl- C1-C5alkyl; or R6 and R7 together with the linking nitrogen atom form a C4-C12-membered heterocyclic ring which may be interrupted by one or more than one- O- or -NH- goups; Y1 is C1-C10alkylene; C5-C10cycloalkylene; C5-C10arylene; or C5-C10arylene-( C1-C10alkylene); T1 is a radical of formula (1b); or -O-(X3)s; Q1 is a cationic biradical of a saturated, aromatic or heteroaromatic group; or a radical of formula (1c); Z1 is -C(O)-; -(CH2CH2-O)1-5-; -C(O)O-; -OCO-; CON(R9)-; -X4-CON(R9)-; -(R9)NC(O)-; - O-; -S-; -S(O)-; or -S(O)2-; R9, R10 and R11 each independently from each other are hydrogen; C1-C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl- C1-C10alkyl; or C1-C10alkyl(C5-C10aryl); X1, X2, X3 and X4 independently from each other are C1-C18alkylene; -(CO)- C1-C18alkylene, C1-C18arylene; C6-C18arylene- C1-C12alkylene; or -(OCH2CH2)n-O-; n is a number from 1 to 5; p, r, s, t and u independently from each other are a 0 or 1; m is 1; or 2; U is hydrogen, if m is 1; and U is the direct bond, if m is 2. The compounds are useful for the dyeing of organic materials, such as keratin fibers, preferably human hair. The dyes are distinguished by deep dying having good fastness properties with respect to washing, light, shampooing and rubbing. | ||||||
| 86 | DERIVATIVES OF CEPHALOSPORIN AND CLAVULANIC ACID FOR DETECTING BETA-LACAMASE IN A SAMPLE | PCT/US2005001901 | 2005-01-21 | WO2005071096A3 | 2005-12-15 | CORRY SCHUYLER; DOWNEY WILLIAM; FILANOSKI BRIAN; GEE KYLE; GREENFIELD I LAWRENCE; HIRSCH JAMES; JOHNSON IAIN; RUKAVISHNIKOV ALEKSEY |
| The present invention relates to compounds which are derivative of cephalosporin and for clavulanic acid that are substrates for an enzyme, and upon reaction with the enzyme provide a detectable response, such as an optically detectable response. In particular, the compounds have utility in detecting the presence of a ß-lactamase in a sample. In addition to the compounds methods are disclosed for analyzing a sample for the presence of a ß-lactmase, for example, as an indicator of expression of a nucleic acid sequence coding for a ß-lactmase. Kits are disclosed that include the disclosed compounds and additional components, for example, cells, antibodies, a ß-lactmase or instructions for using the components in an assay. | ||||||
| 87 | PIGMENTS HAVING A VIEWING ANGLE DEPENDENT SHIFT OF COLOR, METHOD FOR PRODUCING SAID PIGMENTS, USE OF SAID PIGMENTS IN SECURITY APPLICATIONS, COATING COMPOSITION COMPRISING SAID PIGMENTS AND A DETECTING DEVICE | PCT/EP2001/001644 | 2001-02-14 | WO01060924A2 | 2001-08-23 | |
| The invention describes luminescent optically variable pigments (OVP), methods for obtaining such pigments, as well as the use of such pigments as security elements in inks, coatings and articles. The luminescence centers are preferably incorporated into the dielectric material of the OVP's optical Fabry-Perot resonance cavity, allowing for the machine-discrimination of luminescent OVP from simple mixtures of luminescents and non-luminescent OVP. | ||||||
| 88 | SQUARAINE DYES | PCT/GB0001223 | 2000-03-30 | WO0058405A3 | 2001-02-01 | WEST RICHARD MARTIN; CUMMINS WILLIAM JONATHAN; NAIRNE ROBERT JAMES DOMETT; BULL MATTHEW GRAHAM |
| Compounds having the structure: W = Sq - A where A has the formula: -NR<1>R<2>, where R<1> and R<2> are the same or different and each is H or C1-C20 hydrocarbon or a group -L-G, or one of R<1> and R<2> is -OR<5> or -NR<6>R<7> or -COR<7> or -NR<6> COR<7> or -N =R<8> or R<1> and R<2> together form a single ring or fused ring system, saturated or unsaturated and unsubstituted or substituted, or an azacrown or a metal-binding group, Sq represents formula (A) or formula (B) where m is 1, 2 or 3, W represents a wing moiety having structure (C), L' is a linker of 0-3 moieties selected from carbon atoms and arylene groups, the dotted line represents a single ring or fused ring system, aromatic or heterocyclic, unsubstituted or substituted, containing or joined to a tertiary or quaternary N atom, and having unsaturation co-ordinated with that of L' = Sq, each of R<5>, R<6>, R<7> and R<8> is H or C1-C20 hydrocarbon or a group -L-G, R<9> is a negative charge or a group -L-G, L is a linker chain of 0 to 30 moieties, branched or unbranched which optionally contains one or more arylene groups, or O or N or N<+> or S or S<+> or P or P<+> or Se atoms, and G is a functional or a reactive group by means of which the compound may be covalently linked to a biomolecule, or a group which enhances or reduces water solubility or provides electron donating or withdrawing properties to modify the spectral characteristics of the compound, and homo-dimers and -oligomers and hetero-dimers and -oligomers of the compounds. | ||||||
| 89 | SQUARAINE DYES | PCT/GB2000/001223 | 2000-03-30 | WO00058405A2 | 2000-10-05 | |
| Compounds having the structure: W = Sq - A where A has the formula: -NR<1>R<2>, where R<1> and R<2> are the same or different and each is H or C1-C20 hydrocarbon or a group -L-G, or one of R<1> and R<2> is -OR<5> or -NR<6>R<7> or -COR<7> or -NR<6> COR<7> or -N =R<8> or R<1> and R<2> together form a single ring or fused ring system, saturated or unsaturated and unsubstituted or substituted, or an azacrown or a metal-binding group, Sq represents formula (A) or formula (B) where m is 1, 2 or 3, W represents a wing moiety having structure (C), L' is a linker of 0-3 moieties selected from carbon atoms and arylene groups, the dotted line represents a single ring or fused ring system, aromatic or heterocyclic, unsubstituted or substituted, containing or joined to a tertiary or quaternary N atom, and having unsaturation co-ordinated with that of L' = Sq, each of R<5>, R<6>, R<7> and R<8> is H or C1-C20 hydrocarbon or a group -L-G, R<9> is a negative charge or a group -L-G, L is a linker chain of 0 to 30 moieties, branched or unbranched which optionally contains one or more arylene groups, or O or N or N<+> or S or S<+> or P or P<+> or Se atoms, and G is a functional or a reactive group by means of which the compound may be covalently linked to a biomolecule, or a group which enhances or reduces water solubility or provides electron donating or withdrawing properties to modify the spectral characteristics of the compound, and homo-dimers and -oligomers and hetero-dimers and -oligomers of the compounds. | ||||||
| 90 | PYRIDINE DYES AND QUINOLINE DYES USED AS MARKERS FOR BIOMOLECULES, POLYMERS, MEDICAMENTS, AND PARTICLES | PCT/EP9909471 | 1999-12-03 | WO0034394A2 | 2000-06-15 | WOLFBEIS OTTO SAMUEL; PROBST MARIO; LEHMANN FRANK |
| The invention relates to water-soluble marker dyes which are derived from the quinoline or pyridine heterocyclic compound. They are able to bond with biomolecules such as proteins, lipids, polynucleotides, DNA, medicaments or pharmaceutical products and with polymer particles. They are provided for dying, especially for fluorescence marking of these materials. The molecules or particles marked in this manner can be subsequently used in optical, especially fluorescence-optical, determination methods. Typical methods include the reaction of dye-marked antigens, antibodies, or DNA segments with the complementary species. | ||||||
| 91 | SOLUBLE CHROMOPHORES HAVING IMPROVED SOLUBILISING GROUPS | PCT/EP1998/000248 | 1998-01-17 | WO98032802A1 | 1998-07-30 | |
| Compounds of formula (I): A(B)x wherein x is an integer from 1 to 8; A is the radical of a chromophore of the quinacridone, anthraquinone, perylene, indigo, quinophthalone, indanthrone, isoindolinone, isoindoline, dioxazine, azo, phthalocyanine or diketopyrrolopyrrole series that is bonded to x groups B via one or more hetero atoms, those hetero atoms being selected from the group consisting of N, O and S and forming part of the radical A; each group B independently of any other(s) is hydrogen or a group of formula alpha , at least one group B being a group of said formula, wherein Q is p, q-C2-C12alkylene that is unsubstituted or mono- or poly-substituted by C1-C12alkoxy, C1-C12alkylthio or by C2-C24dialkylamino, p and q being different position numbers; X is a hetero atom selected from the group consisting of N, O and S, m being the number 0 when X is O or S and m being the number 1 when X is N, and L1 and L2 are each independently of the other [-(p',q'-C2-C12alkylene)-Z-]n-C1-C12alkyl or C1-C12alkyl that is unsubstituted or mono- or poly-substituted by C1-C12alkoxy, C1-C12alkylthio, C2-C24dialkylamino, C6-C12aryloxy, C6-C12arylthio, C7-C24arylalkylamino or by C12-C24diarylamino, wherein n is a number from 1 to 1000, p' and q' are different position numbers, each Z independently of any other(s) is a hetero atom O, S or C1-C12alkyl-substituted N, and C2-C12alkylene in the repeating units [-C2-C12alkylene-Z-] may be identical or different; and L1 and L2 may be saturated or one- to ten-fold unsaturated, uninterrupted or interrupted at any desired points by from 1 to 10 groups selected from the group consisting of -(C=O)- and -C6H4-, and may carry no substituents or may carry from 1 to 10 further substituents selected from the group consisting of halogen, cyano and nitro; with the proviso that when -Q- is -(CH2)r-, wherein r is a number from 2 to 12, and X is S, L2 may not be unsubstituted, saturated and uninterrupted C1-C4alkyl. The compounds according to the invention are used in high-molecular-weight organic materials, thermo-, photo- or chemo-sensitive recording materials, light-sensitive negative or positive resist compositions, ink compositions for ink-jet printing and colour tapes for thermal transfer printing. | ||||||
| 92 | Method for producing a pigment, the pigment having a color shift which depends on the viewing angle, use in pigment security applications, coating composition and the detection device comprising a pigment | JP2001560298 | 2001-02-14 | JP4916636B2 | 2012-04-18 | ミューラー，エドガー; ロズメク，オリヴィエ |
| 93 | Pigment composition, pigment dispersions and ink | JP2006053626 | 2006-02-28 | JP4678316B2 | 2011-04-27 | 順 佐武; 勝彦 澤村; 篤 遠藤; 浩 長曽我部 |
| 94 | Ink composition for ink jet printing and printing method | JP2009077180 | 2009-03-26 | JP2010229251A | 2010-10-14 | SAO AKIHITO; IKEDA HIRONARI |
| PROBLEM TO BE SOLVED: To provide an ink composition for ink jet printing, having preferable water solubility, stability, printing characteristics, color, sharpness, light resistance and other kinds of solidity. SOLUTION: The ink composition used for an ink jet printing method includes at least a water-soluble dye having an anthraquinone skeleton with solubility to water at 30°C of 50 g/L or less, and one or more kinds of polyoxyethylene alkyl ethers of a 11.4-18.8 HLB value, represented by formula (I): HO(-CH 2CH 2O-) nRa, wherein n is 4-100, and Ra is a 8-24C saturated alkyl group. COPYRIGHT: (C)2011,JPO&INPIT | ||||||
| 95 | Soluble chromophores having improved solubility groups | JP53154998 | 1998-01-17 | JP4558106B2 | 2010-10-06 | オール−グール，ベロニク; ビゼ，アリーヌ |
| 96 | Pigment composition and colorant composition | JP2009041624 | 2009-02-25 | JP2010195906A | 2010-09-09 | SUGAMO HITOSHI; FURUBAYASHI RYUSAKU; MOCHIZUKI AKIMITSU; TOBA YASUMASA |
| <P>PROBLEM TO BE SOLVED: To provide a pigment composition which is favorably used for a colorant composition such as an inkjet ink and has excellent vividness, coloring power and dispersion stability on storage. <P>SOLUTION: The pigment composition is obtained by adding 0.05-20.0 wt.% of at least one kind selected from among pigment derivatives, anthraquinone derivatives, and triazine derivatives to a naphthol red pigment, in particular, C.I. Pigment Red 31, 147, 150, 185, 245, 269. The colorant composition such as an inkjet ink is obtained by using the pigment composition. <P>COPYRIGHT: (C)2010,JPO&INPIT | ||||||
| 97 | Ink composition for inkjet printing and textile printing method | JP2008281018 | 2008-10-31 | JP2010106174A | 2010-05-13 | SAO AKIHITO; IKEDA HIRONARI |
| PROBLEM TO BE SOLVED: To provide an ink composition for inkjet printing having good color, sharpness and fastness such as light fastness. SOLUTION: The ink composition for inkjet printing contains an anthraquinone-based water-soluble dye and a sorbitan fatty acid ester having a specific HLB value and being expressed by the formula (wherein l+m+n is 0-40; and R is a 8-24C saturated alkyl). COPYRIGHT: (C)2010,JPO&INPIT | ||||||
| 98 | Two-photon absorption dye discoloration material, three-dimensional refractive index modulation material, three-dimensional absorption index modulation material and three-dimensional optical recording material | JP2004199005 | 2004-07-06 | JP4411153B2 | 2010-02-10 | 裕雄 滝沢 |
| 99 | Polycyclic compound and a method of manufacturing the same | JP2002309814 | 2002-10-24 | JP4252788B2 | 2009-04-08 | ダブリュ．ボデ ジェフリー; 鈴木 啓介 |
| 100 | Natural non-polar fluorescent dye from a non-bioluminescent marine invertebrate, compositions containing the dye and the use thereof | JP2003580430 | 2003-03-24 | JP2006504808A | 2006-02-09 | アヌトシュ・ガングリー; ウシャ・ゴスヴァミ |
| 本発明は、非生物発光の海生棘皮動物Holothuria scabraから天然の、環境にやさしい無毒性の、細胞透過性の多色蛍光タンパク質染料を抽出、精製および特性決定する方法、この染料を含む組成物、ならびにこの染料の様々な応用を開示する。 | ||||||
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