Benzocyanine compounds

US10526317B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10526317-B2
Application numberUS-201715641376-A
CountryUS
Kind codeB2
Filing dateJul 5, 2017
Priority dateFeb 28, 2012
Publication dateJan 7, 2020
Grant dateJan 7, 2020

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Compounds useful as labels with properties comparable to known fluorescent compounds. The compounds are conjugated to proteins and nucleic acids for biological imaging and analysis. Synthesis of the compounds, formation and use of the conjugated compounds, and specific non-limiting examples of each are provided.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound of general formula IIc where each of R 1 , R 2 , R 5 , and R 6 is the same or different and is selected from the group consisting of an aliphatic, heteroaliphatic, sulfoalkyl, heteroaliphatic with terminal SO 3 —, a PEG group P—Z where P is selected from an ethylene glycol group, a diethylene glycol group, and a (poly)ethylene glycol group, where the (poly)ethylene glycol group is (CH 2 CH 2 O) s , where s is an integer from 3-6 inclusive, a sulfonamide group -L-SO 2 NH—P—Z, and a caboxamide group -L-CONH—P—Z, where Z is selected from H, CH 3 , a CH 3 group, an alkyl group, or a heteroalkyl group; each of R 7 , R 8 , R 11 , R 12 , R 13 , and R 14 is the same or different and is selected from the group consisting of H, SO 3 —, a PEG group P—Z where P is selected from an ethylene glycol group, a diethylene glycol group, and a (poly)ethylene glycol group, where the (poly)ethylene glycol group is (CH 2 CH 2 O) s , where s is an integer from 3-6 inclusive, a sulfonamide-containing group -L-SO 2 NH—P—Z, and a carboxamide-containing group -L-CONH—P—Z, where Z is selected from H, a CH 3 group, an alkyl group, or a heteroalkyl group; each of R 9 and R 10 is the same or different and is a PEG group P-L-Z where P is selected from an ethylene glycol group, a diethylene glycol group, and a (poly)ethylene glycol group, where the (poly)ethylene glycol group is (CH 2 CH 2 O) s , where s is an integer from 3-6 inclusive, a PEG group P-L-X; X is selected from the group consisting of —SH, —NH 2 , —NH—NH 2 , —F, —Cl, —Br, I, —NHS (hydroxysuccinimidyl/sulfosuccinimidyl), —O-TFP (2,3,5,6-tetrafluorophenoxy), —O-STP (4-sulfo-2,3,5,6-tetrafluorophenoxy), —O-benzotriazole, -benzotriazole, —NR-L-OH, —NR-L-O-phosphoramidite, —NR-L-SH, —NR-L-NH 2 , —NR-L-NH—NH 2 , —NR-L-CO 2 H, —NR-L-CO—NHS, —NR-L-CO-STP, —NR-L-CO-TFP, —NR-L-CO-benzotriazole, —NR-L-CHO, —NR-L-maleimide, and —NR-L-NH—CO—CH 2 —I, where R is —H or an aliphatic or heteroaliphatic group; L is selected from the group consisting of a divalent linear (—(CH 2 ) t —, t=0 to 15), crossed, or cyclic alkyl group optionally substituted by at least one oxygen atom and/or sulfur atom; Kat is a number of Na + , K + , Ca 2+ , ammonia, or other cation(s) needed to compensate the negative charge brought by the cyanine; m is an integer from 0 to 5 inclusive; o is an integer from 0 to 12 inclusive; and n is an integer from 1 to 3 inclusive; with the proviso that at least one of R 1 , R 2 , R 5 , R 6 , R 7 , R 8 , R 11 , R 12 , R 13 or R 14 is a PEG group. 2. A method of labeling at least one biomolecule, the method comprising combining at least one biomolecule with a composition comprising at least one excipient and the compound of claim 1 in an effective concentration to bind to at least one biomolecule under conditions sufficient for labeling the biomolecule with the compound. 3. The method of claim 2 wherein the biomolecule is selected from the group consisting of a protein, antibody, enzyme, nucleoside triphosphate, oligonucleotide, biotin, hapten, cofactor, lectin, antibody binding protein, carotenoid, carbohydrate, hormone, neurotransmitter, growth factors, toxin, biological cell, lipid, receptor binding drug, fluorescent proteins, organic polymer carrier material, inorganic polymeric carrier material, and combinations thereof. 4. A method of detecting at least one biomolecule, the method comprising combining at least one biomolecule with a composition comprising at least one excipient and the compound of claim 1 in an effective concentration to bind to at least one biomolecule under conditions sufficient for binding the compound to the biomolecule, and detecting the biomolecule-bound compound. 5. The method of claim 4 wherein the biomolecule is selected from a protein, antibody, enzyme, nucleoside triphosphate, oligonucleotide, biotin, hapten, cofactor, lectin, antibody binding protein, carotenoid, carbohydrate, hormone, neurotransmitter, growth factors, toxin, biological cell, lipid, receptor binding drug, fluorescent proteins, organic polymer carrier material, inorganic polymeric carrier material, and combinations thereof. 6. The method of claim 4 wherein the at least one biomolecule is detected in an assay selected from fluorescence microscopy, flow cytometry, in vivo imaging, immunoassay, hybridization, chromatographic assay, electrophoretic assay, microwell plate based assay, fluorescence resonance energy transfer (FRET) system, bioluminescence resonance energy transfer (BRET), high throughput screening, or microarray. 7. The method of claim 4 wherein the biomolecule is detected by in vivo imaging comprising providing the biomolecule-bound compound to at least one of a biological sample, tissue, or organism, and detecting the biomolecule within the at least one of a biological sample, tissue, or organism. 8. A kit for detecting and/or labeling at least one biomolecule in a sample, the kit comprising the compound of claim 1 and at least one excipient, and instructions for use of the compound to detect a biomolecule in a sample. 9. A method of in vivo imaging using a compound of claim 1 , comprising combining at least one biomolecule with a composition comprising at least one excipient and the compound of claim 1 in an effective concentration to bind to at least one biomolecule under conditions sufficient for binding the compound to the biomolecule; providing the biomolecule-bound compound to an organism; and detecting the biomolecule within the organism. 10. A kit for in vivo imaging, the kit comprising the compound of claim 1 and at least one excipient, and instructions for use of the compound to image a tissue, organ, or body of an organism.

Assignees

Inventors

Classifications

  • Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles · CPC title

  • Methine dyes, e.g. cyanine dyes · CPC title

  • C07D403/14Primary

    containing three or more hetero rings · CPC title

  • Nanoparticles · CPC title

  • with fluorescent label · CPC title

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Frequently asked questions

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What does patent US10526317B2 cover?
Compounds useful as labels with properties comparable to known fluorescent compounds. The compounds are conjugated to proteins and nucleic acids for biological imaging and analysis. Synthesis of the compounds, formation and use of the conjugated compounds, and specific non-limiting examples of each are provided.
Who is the assignee on this patent?
Pierce Biotechnology Inc, Dyomics Gmbh
What technology area does this patent fall under?
Primary CPC classification C07D403/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 07 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).