UA82684C2 - Гідрофільні, реакційні відносно тіол-групи ціанінові барвники, спосіб їх одержання, їх кон'югати з біомолекулами, спосіб одержання останніх та їх застосування, а також діагностичний набір - Google Patents
Гідрофільні, реакційні відносно тіол-групи ціанінові барвники, спосіб їх одержання, їх кон'югати з біомолекулами, спосіб одержання останніх та їх застосування, а також діагностичний набір Download PDFInfo
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- UA82684C2 UA82684C2 UAA200508207A UA2005008207A UA82684C2 UA 82684 C2 UA82684 C2 UA 82684C2 UA A200508207 A UAA200508207 A UA A200508207A UA 2005008207 A UA2005008207 A UA 2005008207A UA 82684 C2 UA82684 C2 UA 82684C2
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- 241001122767 Theaceae Species 0.000 description 1
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- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 description 1
- RXLAFGWEFKFVAF-UHFFFAOYSA-M [4-[(2-methylpropan-2-yl)oxy]-4-oxobutyl]-triphenylphosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCC(=O)OC(C)(C)C)C1=CC=CC=C1 RXLAFGWEFKFVAF-UHFFFAOYSA-M 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- LEKJTGQWLAUGQA-UHFFFAOYSA-N acetyl iodide Chemical compound CC(I)=O LEKJTGQWLAUGQA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
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- 239000000298 carbocyanine Substances 0.000 description 1
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- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
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- 239000012141 concentrate Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- YKFKEYKJGVSEIX-UHFFFAOYSA-N cyclohexanone, 4-(1,1-dimethylethyl)- Chemical compound CC(C)(C)C1CCC(=O)CC1 YKFKEYKJGVSEIX-UHFFFAOYSA-N 0.000 description 1
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- JOXWSDNHLSQKCC-UHFFFAOYSA-N ethenesulfonamide Chemical group NS(=O)(=O)C=C JOXWSDNHLSQKCC-UHFFFAOYSA-N 0.000 description 1
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- WBJINCZRORDGAQ-UHFFFAOYSA-N ethyl formate Chemical compound CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
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- 125000000524 functional group Chemical group 0.000 description 1
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- 239000003102 growth factor Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- MOFVSTNWEDAEEK-UHFFFAOYSA-M indocyanine green Chemical compound [Na+].[O-]S(=O)(=O)CCCCN1C2=CC=C3C=CC=CC3=C2C(C)(C)C1=CC=CC=CC=CC1=[N+](CCCCS([O-])(=O)=O)C2=CC=C(C=CC=C3)C3=C2C1(C)C MOFVSTNWEDAEEK-UHFFFAOYSA-M 0.000 description 1
- 229960004657 indocyanine green Drugs 0.000 description 1
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
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- PGLTVOMIXTUURA-UHFFFAOYSA-N iodoacetamide Chemical compound NC(=O)CI PGLTVOMIXTUURA-UHFFFAOYSA-N 0.000 description 1
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- 238000005304 joining Methods 0.000 description 1
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- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 1
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- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
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- QWYZFXLSWMXLDM-UHFFFAOYSA-M pinacyanol iodide Chemical class [I-].C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=[N+]1CC QWYZFXLSWMXLDM-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BGUWFUQJCDRPTL-UHFFFAOYSA-N pyridine-4-carbaldehyde Chemical compound O=CC1=CC=NC=C1 BGUWFUQJCDRPTL-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
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- 239000013049 sediment Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
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- ZXUCBXRTRRIBSO-UHFFFAOYSA-L tetrabutylazanium;sulfate Chemical compound [O-]S([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC ZXUCBXRTRRIBSO-UHFFFAOYSA-L 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/0008—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/0066—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain being part of a carbocyclic ring,(e.g. benzene, naphtalene, cyclohexene, cyclobutenene-quadratic acid)
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
- C09B23/08—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines
- C09B23/086—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines more than five >CH- groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2003102787 DE10302787A1 (de) | 2003-01-24 | 2003-01-24 | Hydrophile, Thiol-reaktive Cyaninfarbstoffe und deren Konjugate mit Biomolekülen für die Fluoreszenzdiagnostik |
| PCT/EP2003/012735 WO2004065491A1 (en) | 2003-01-24 | 2003-11-14 | Hydrophilic, thiol-reactive cyanine dyes and conjugates thereof with biomolecules for fluorescence diagnosis |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA82684C2 true UA82684C2 (uk) | 2008-05-12 |
Family
ID=32694952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UAA200508207A UA82684C2 (uk) | 2003-01-24 | 2003-11-14 | Гідрофільні, реакційні відносно тіол-групи ціанінові барвники, спосіб їх одержання, їх кон'югати з біомолекулами, спосіб одержання останніх та їх застосування, а також діагностичний набір |
Country Status (6)
| Country | Link |
|---|---|
| CN (1) | CN1742057A (no) |
| DE (1) | DE10302787A1 (no) |
| NO (1) | NO20053919L (no) |
| RS (1) | RS20050561A (no) |
| UA (1) | UA82684C2 (no) |
| ZA (1) | ZA200506759B (no) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102498177B (zh) * | 2009-07-16 | 2014-12-24 | 贝克曼考尔特公司 | 新荧光染料及其用途 |
| EP3001197A1 (en) * | 2014-09-23 | 2016-03-30 | Universität Heidelberg | Fluorescent protein stains |
| CN107488657A (zh) * | 2017-08-15 | 2017-12-19 | 苏州泽科生物科技有限公司 | 核酸的活性染料偶联标记、检测及提纯方法 |
| US10968386B2 (en) | 2018-01-09 | 2021-04-06 | Shenzhen University | Pentamethine cyanine dye and preparation method therefor |
| CN108192376A (zh) * | 2018-01-09 | 2018-06-22 | 深圳大学 | 一种五甲川菁染料及制备方法 |
| CN108727245B (zh) * | 2018-07-02 | 2021-09-28 | 广州中医药大学(广州中医药研究院) | 一种水杨酸类化合物及其制备方法和应用 |
| CN110201189B (zh) * | 2019-06-03 | 2021-12-07 | 沈阳药科大学 | 白蛋白结合型近红外荧光染料-马来酰亚胺共轭物 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6225050B1 (en) * | 1986-04-18 | 2001-05-01 | Carnegie Mellon University | Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods |
| US6002503A (en) * | 1997-10-23 | 1999-12-14 | Ciena Corporation | Optical add/drop multiplexer |
| US6217848B1 (en) * | 1999-05-20 | 2001-04-17 | Mallinckrodt Inc. | Cyanine and indocyanine dye bioconjugates for biomedical applications |
| US6180085B1 (en) * | 2000-01-18 | 2001-01-30 | Mallinckrodt Inc. | Dyes |
-
2003
- 2003-01-24 DE DE2003102787 patent/DE10302787A1/de not_active Ceased
- 2003-11-14 CN CN 200380109197 patent/CN1742057A/zh active Pending
- 2003-11-14 UA UAA200508207A patent/UA82684C2/uk unknown
- 2003-11-14 RS YUP-2005/0561A patent/RS20050561A/sr unknown
-
2005
- 2005-08-23 ZA ZA200506759A patent/ZA200506759B/en unknown
- 2005-08-23 NO NO20053919A patent/NO20053919L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| RS20050561A (en) | 2007-09-21 |
| ZA200506759B (en) | 2007-01-31 |
| DE10302787A1 (de) | 2004-08-12 |
| NO20053919L (no) | 2005-10-24 |
| NO20053919D0 (no) | 2005-08-23 |
| CN1742057A (zh) | 2006-03-01 |
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