Luminescent compounds, reactive intermediates used to synthesize luminescent compounds, and methods of synthesizing and using luminescent compounds. These compounds may be based on squaric, croconic, and rhodizonic acid, and their analogs, among others, and relate generally to the structure: where
Luminescent compounds, reactive intermediates used to synthesize luminescent compounds, and methods of synthesizing and using luminescent compounds. These compounds may be based on squaric, croconic, and rhodizonic acid, and their analogs, among others, and relate generally to the structure: where Z is a four, five, or six-member aromatic ring, and A, B, C, D, E, and F are substituents of Z, in any order, that may include O, S, Se, Te, C(Ra)(Rb), N--Rc,N(Rd)(Re), W1,and W2. Generally, each compound includes at least one of W1or W2,where W1and W2have the structures: respectively. The compounds may include a reactive group and/or a carrier. The luminescent compounds may be useful in both free and conjugated forms as probes, labels, and/or indicators.
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Luminescent compounds, reactive intermediates used to synthesize luminescent compounds, and methods of synthesizing and using luminescent compounds. These compounds may be based on squaric, croconic, and rhodizonic acid, and their analogs, among others, and relate generally to the structure: where
Luminescent compounds, reactive intermediates used to synthesize luminescent compounds, and methods of synthesizing and using luminescent compounds. These compounds may be based on squaric, croconic, and rhodizonic acid, and their analogs, among others, and relate generally to the structure: where Z is a four, five, or six-member aromatic ring, and A, B, C, D, E, and F are substituents of Z, in any order, that may include O, S, Se, Te, C(Ra)(Rb), N--Rc,N(Rd)(Re), W1,and W2. Generally, each compound includes at least one of W1or W2,where W1and W2have the structures: respectively. The compounds may include a reactive group and/or a carrier. The luminescent compounds may be useful in both free and conjugated forms as probes, labels, and/or indicators. P 56147860 of Nov. 1981. Patent Abstracts of Japan of JP 02276874 of Nov. 1990. Patent Abstracts of Japan of JP 08259869 of Oct. 1996. Patent Abstracts of Japan of JP 07278479 of Oct. 1995. Patent Abstracts of Japan of JP 05320276 of Dec. 1993. Patent Abstracts of Japan of JP 10316909 of Dec. 1998. Patent Abstracts of Japan of JP 09031360 of Feb. 1997. Patent Abstracts of Japan of JP 56147861 of Nov. 1981. Patent Abstracts of Japan of JP 03240557 dated Oct. 1991. Patent Abstracts of Japan of JP 03240558 dated Oct. 1991.
Brynes Paul J. (Libertyville IL) Johnson Donald D. (Lindenhurst IL) Molina Cynthia M. (Deerfield IL) Flentge Charles A. (Lake Villa IL) Jonas Patrick F. (Waukegan IL), Reagents for an amphetamine-class fluorescence polarization immunoassay.
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