Zinc-selective fluorescent probes for emission-ratiometric imaging
The compounds relate to zinc-sensitive fluorescent probes, compositions and methods utilizing the same. Such compounds provide an emission-ratiometric fluorescence response upon binding of an analyte. In some embodiments, compounds can be used for two-photon excitation microscopy or conventional fluorescence microscopy. The compounds described herein can also contain one or more functional groups to improve the emission-ratiometric fluorescence response.
1. A compound according to Formula I:
wherein Z is
Y 1 is selected from —NR 4 — and —S—;
Y 2 is selected from —NR 5 —, —S—, and —O—;
R c is Ar, —OR 4 , or —N((CH 2 ) q —Ar) 2 ;
R 1 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, substituted or unsubstituted heteroaryl, —OCH 3 , —OCH 2 COOR 9 , —OCH 2 CH 2 COOR 9 , —OCH 2 CH 2 CH 2 SO 2 R 9 , —NH 2 , —NHR 9 , and —N(R 9 ) 2 ; R 2 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, and substituted or unsubstituted heteroaryl; or in the alternative, R 1 and R 2 join together to form a moiety selected from substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, and substituted or unsubstituted heteroaryl;
R 3 and R 4 are each independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, and substituted or unsubstituted heteroaryl;
R 5 is selected from C 1-3 -alkyl optionally substituted with —OR 4 or Ar;
R 9 is selected from —CH 3 , —C 2 H 5 , substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, and substituted or unsubstituted heteroaryl;
n is 1, 2, or 3;
q is 1, 2, or 3;
Ar is independently at each occurrence a substituted or unsubstituted six-membered heteroaryl selected from:
and
m is any integer from 0 to 3.
2. The compound of claim 1 , wherein:
Z is selected from:
and
s is 1, 2, or 3.
3. The compound of claim 1 , wherein:
Z is selected from:
4. The compound of claim 1 , wherein Ar is the same at each occurrence.
5. A compound according to the following formula:
wherein:
Y 1 is selected from —NR 4 — and —S—;
R 1 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, substituted or unsubstituted heteroaryl, —OCH 3 , —OCH 2 COOR 9 , —OCH 2 CH 2 COOR 9 , —OCH 2 CH 2 CH 2 SO 2 R 9 , —NH 2 , —NHR 9 , and —N(R 9 ) 2 ; R 2 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, and substituted or unsubstituted heteroaryl; or in the alternative, R 1 and R 2 join together to form a moiety selected from substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, and substituted or unsubstituted heteroaryl;
R 3 and R 4 are each independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted heterocycloalkenyl, and substituted or unsubstituted heteroaryl;
R 7 and R 8 are each independently selected from —H, —CH 3 , —OR 4 , —CF 3 , —F, —Cl, —CN, —COOR 4 , and —SO 2 R 4 ; and
R 9 is selected from —CH 3 , —C 2 H 5 , substituted or unsubstituted heteroalkyl, substituted or unsubstituted heteroalkenyl, substituted or unsubstituted heteroalkynyl, and substituted or unsubstituted heteroaryl.
6. A compound having a formula selected from:
7. A compound having a formula selected from:
8. A fluorescent complex comprising the compound of claim 1 and zinc(II) in a 1:1 stoichiometric ratio.
9. The fluorescent complex of claim 8 , wherein the fluorescent complex further comprises a ligand.
10. The fluorescent complex of claim 8 , wherein a maximum absorption wavelength of the fluorescent complex is from about 15 nm to about 50 nm greater than a maximum absorption wavelength of the compound of Formula I.
11. The fluorescent complex of claim 8 , wherein a maximum emission wavelength of the fluorescent complex is from about 40 nm to about 60 nm greater than a maximum emission wavelength of the compound of Formula I.
12. A method of detecting zinc in a sample comprising:
treating the sample with the compound according to claim 1 ,
detecting a first wavelength emission intensity of the sample at a first wavelength and a second wavelength emission intensity of the sample at a second wavelength, wherein the first wavelength emission intensity is associated with the compound not being bonded to zinc and the second wavelength emission intensity is associated with the compound being bonded to zinc; and
comparing the first wavelength emission intensity to the second wavelength emission intensity to determine the concentration of zinc in the sample.
13. The method of claim 12 , wherein the first wavelength is from about 380 nm to about 700 nm;
wherein the second wavelength is about 40 nm to about 80 nm greater than the first wavelength; and
wherein the sample is a biological sample.
14. A method of detecting zinc in a sample comprising:
treating a sample with the compound according to claim 7 ;
detecting a first wavelength emission intensity of the sample at a first wavelength and a second wavelength emission intensity of the sample at a second wavelength, wherein the first wavelength emission intensity is associated with the compound not being bonded to zinc and the second wavelength emission intensity is associated with the compound being bonded to zinc; and
detecting zinc in the sample by comparing the first wavelength emission intensity to the second wavelength emission intensity.
15. The method according to claim 14 further comprising determining the concentration of zinc in the sample.