IP Library Granted Patent US 9,249,307
Granted Patent B2
US 9,249,307 · App. 13/571,858 · Granted Feb 2, 2016

Benzocyanine compounds

Inventors: Greg Hermanson (Loves Park, IL); Peter T. Czerney (Weimar, DE); Surbhi Desai (Rockford, IL); Matthias S. Wenzel (Jena, DE); Boguslawa Dworecki (Rockford, IL); Frank G. Lehmann (Jena, DE); Marie Christine Nlend (Rockford, IL)
Assignee: Pierce Biotechnology, Inc.
C09B23/083A61K49/0034A61K49/0058
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Quick Facts
Patent No.
US 9,249,307
App. No.
13/571,858
Granted
Feb 2, 2016
Kind
B2
Abstract

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.

Claims (15)

1. A compound selected from the group consisting of

where

each of R 1 , R 2 , R 5 , and R 6 is the same or different and is independently 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 polyethylene glycol group, where the polyethylene 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 carboxamide 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 independently 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 polyethylene glycol group, where the polyethylene 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, CH 3 , a CH 3 group, an alkyl group, or a heteroalkyl group;

X is selected from —OH, —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, imidazole, azide, —O-carbodiimide, —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, —NR-L-NH—CO—CH 2 —I, or —NR-L-NH—CO—CH 2 —Br wherein R is —H or an aliphatic or heteroaliphatic group;

L is selected from 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; p is an integer from 1 to 6 inclusive;

each of R3 and R4 is the same or different and is independently hydrogen, an aliphatic group, a heteroaliphatic group, or a PEG group P—Z where P is selected from an ethylene glycol group, a diethylene glycol group, and a polyethylene glycol group, where the polyethylene glycol group is (CH 2 CH 2 O) s , where s is an integer from 3-6 inclusive, and Z is selected from H, a CH 3 group, an alkyl group, or a heteroalkyl group; or R3 and R4 together form a cyclic structure where R3 and R4 are joined using a divalent structural element selected from the group consisting of —(CH 2 ) q —, —(CH 2 ) q O(CH 2 ) q′ —, —(CH 2 ) q S(CH 2 ) q′ —, —(CH 2 ) q CH═CH—, —OCH═CH— where each of q and q′ is the same or different and is a integer from 2 to 6 inclusive; and

Y is selected from the group consisting of hydrogen, alkyl, sulfoalkyl, fluorine, chlorine, bromine, a substituted or unsubstituted aryl-, phenoxy-, phenylmercapto function, and a PEG group P—Z where P is selected from an ethylene glycol group, a diethylene glycol group, and a polyethylene glycol group, where the polyethylene glycol group is (CH 2 CH 2 O) s , where s is an integer from 3-6 inclusive, and Z is selected from H, a CH 3 group, an alkyl group, or a heteroalkyl group.

2. The compound of claim 1 wherein each of R13 and R14 is sulfo.

3. The compound of claim 1 wherein each of R7, R8, R11, and R12 is sulfo.

4. A compound selected from the group consisting of compound V10-04152

and compound V08-15173

5. A kit for detecting 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.

6. The kit of claim 5 wherein the compound is V10-04152 or V08-15173.

Assignments (2)
MERGER Recorded Mar 11, 2026
From: PIERCE BIOTECHNOLOGY, INC.
To: LIFE TECHNOLOGIES CORPORATION
Reel/Frame 075052/0213 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2012
From: HERMANSON, GREG; CZERNEY, PETER T.; DESAI, SURBHI; WENZEL, MATTHIAS S.; DWORECKI, BOGUSLAWA; LEHMANN, FRANK G.; NLEND, MARIE CHRISTINE
To: PIERCE BIOTECHNOLOGY, INC.; DYOMICS GMBH
Reel/Frame 028894/0436 →
Continuity (4)
Provisional Application 61524167 · Aug 16, 2011
Provisional Application 61604232 · Feb 28, 2012
Provisional Application 61607737 · Mar 7, 2012
Related Publication 20130045488A1 · Feb 21, 2013