Chemiluminescent acridinium compounds and analogues thereof as substrates of hydrolytic enzymes
View Patent ↗A chemiluminescent substrate of a hydrolytic enzyme having the following general Formula I is disclosed, as follows: Lumi-M-PFormula I where “Lumi” is a chemiluminescent moiety capable of producing light (a) by itself, (b) with MP attached and (c) with M attached. Examples of Lumi include chemiluminescent acridinium compounds, benzacridinium compounds, quinolinium compounds, isoquinolinium compounds, phenanthridinium compounds, and lucigenin compounds, spiroacridan compounds, luminol compounds and isoluminol compounds. M is a multivalent heteroatom having at least one lone pair of electrons selected from oxygen, nitrogen and sulfur, directly attached to the light emitting moiety of Lumi at one end and to P at the other end. P is a group that can be readily removed by hydrolytic enzymes. An enzymatic reaction utilizing the above compound is the following: where HE is a hydrolytic enzyme. Lumi-M is a chemiluminescent product having physical and/or chemical properties different from those of Lumi-M-P.
1. A chemiluminescent substrate of a hydrolytic enzyme, said substrate having the structure
wherein
P is PO 3 B wherein B is a divalent cation selected from cations of the group consisting of Ca and Mg, or two monovalent cations selected from the group consisting of Na, H, K
M is oxygen;
R 1 is an alkyl, alkenyl, alkynyl or aralkyl containing 0 to 20 heteroatoms;
R 2a , R 2b , R 2c , R 3a , R 3b , R 3c and R 3d can be the same or different and are selected from the group consisting of hydrogen, methyl, methoxy, halide and cyano (—CN);
R 12 , R 13 , R 14 and R 15 can be the same or different and are selected from the group consisting of hydrogen, —R, substituted or unsubstituted aryl, halides, nitro, sulfonate, sulfate, phosphonate, —CO 2 H, —C(O)OR, cyano (—CN), —SCN, —OR, —SR, —SSR, —C(O)R, —C(O)NHR, ethylene glycol and polyethylene glycol, where R is an alkyl group having 1 to 6 carbon atoms;
A − is a counter ion for the electroneutrality of the quaternary nitrogen of the acridinium compound, said A − not being present if said R 1 substituent contains a strongly ionizable group that can form an anion and pair with the quaternary ammonium cationic moiety; and
X is selected from the group consisting of O, N and S, such that,
when X is O or S, Y is selected from the group consisting of phenyl, (2′-methyl)phenyl, (2′-methoxy)phenyl, (2′,6′-dimethyl)phenyl, (2′,6′-dimethoxy)phenyl, (2′-methyl-6′-methoxy)phenyl, (2′,6′-dimethyl-4′-benzyloxycarbonyl)phenyl, (2′,6′-dimethoxy-4′-benzyloxycarbonyl)phenyl, (4′-methyl)phenyl, (2′-methyl-6′-methoxy-4′-benzyloxycarbonyl)phenyl, (2′,6′-dimethyl-4′-carboxyl)phenyl, (2′,6′-dimethoxy-4′-carboxyl)phenyl and (2′-methyl-6′-methoxy-4′-carboxyl)phenyl, and Z is omitted, and
when X is nitrogen, Z is —SO 2 —Y′, Y is as defined above, Y′ being defined the same as Y above, or Y and Y′ can each be a branched or straight-chain alkyl containing 0 to 20 carbons, halogenated or unhalogenated, a substituted aryl or heterocyclic ring system, and Y and Y′ can be the same or different.
2. The chemiluminescent substrate of claim 1 wherein any adjacent two groups of R 12 , R 13 , R 14 and R 15 can form one or more additional fused hydrocarbon aromatic rings or heteroaromatic rings with or without substitutions, said rings selected from the group consisting of benzene, naphthlene, pyridine, thiophene, furan and pyrrole.
3. The chemiluminescent substrate of claim 1 wherein said counter ion A − is selected from the group consisting of CH 3 SO 4 − , FSO 3 − , CF 3 SO 3 − , C 4 F 9 SO 3 − , CH 3 C 6 H 4 SO 3 − , halide, CF 3 COO − , CH 3 COO − , and NO 3 − .
4. The chemiluminescent substrate of claim 1 wherein R 1 is selected from the group consisting of methyl, carboxymethyl and sulfoalkyl.
5. The chemiluminescent substrate of claim 4 wherein R 1 is selected from the group consisting of sulfopropyl and sulfobutyl.
6. The chemiluminescent substrate of claim 1 wherein P is PO 3 B.
7. The chemiluminescent substrate of claim 1 wherein R 2a , R 2b , R 2c , R 3a , R 3b , R 3c and R 3d are hydrogen.
8. The chemiluminescent substrate of claim 1 having the structure
wherein A − is selected from the group consisting of CH 3 SO 4 − , FSO 3 − , CF 3 SO 3 − , C 4 F 9 SO 3 − , CH 3 C 6 H 4 SO 3 − , halide, CF 3 COO − , CH 3 COO − and NO 3 − .
9. The chemiluminescent substrate of claim 1 having the structure
wherein A − is selected from the group consisting of CH 3 SO 4 − , FSO 3 − , CF 3 SO 3 − , C 4 F 9 SO 3 − , CH 3 C 6 H 4 SO 3 − , halide, CF 3 COO − , CH 3 COO − and NO 3 − .
10. The chemiluminescent substrate of claim 1 having the structure
wherein A − is selected from the group consisting of CH 3 SO 4 − , FSO 3 − , CF 3 SO 3 − , C 4 F 9 SO 3 − , CH 3 C 6 H 4 SO 3 − , halide, CF 3 COO − , CH 3 COO − and NO 3 − .
11. The chemiluminescent substrate of claim 1 having the structure
12. The chemiluminescent substrate of claim 1 having the structure