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. Author manuscript; available in PMC: 2014 Oct 23.
Published in final edited form as: Nat Methods. 2007 Aug;4(8):619–628. doi: 10.1038/nmeth1072

Table 1. Properties of selected commercially available caged compounds.

Caged compound Φ ε(M–1 cm–1) Φ × ε Rate (s–1) Stability
Calcium chelators
DM-nitrophena,b 0.18 4,300 774 3.8 × 104 Complete
NP-EGTAa 0.23 970 194 6.8 × 104 Complete
nitr-5b 0.012 5,500 66 2.5 × 103 Complete
diazo-2a 0.03 22,800 1,596 2.3 × 103 Complete
Neurotransmitters
CNB-Glua 0.14 500 70 4.8 × 104 Fair
CNB-GABAa 0.16 500 70 3.6 × 104 Fair
CNB- 0.8 430 344 1.7 × 104 Excellent
carbamoylcholinea
MNI-Gluc 0.085 4,300 366 ∼105 Excellent
Phosphates
NPE-IP3a,b 0.65 430 280 225 and 280 Excellent
NPE-cAMPb 0.51 430 219 200 Fair
DMNPE-cAMPa 0.05 5,000 250 300 Poor
NPE-cADPribosea 0.11 430 271 18 Excellent
NPE-ATP-a,b 0.63 430 271 90 Excellent
DMNPE-ATP a 0.07 5,000 350 18 Fair
Fluorophores
bis-CMNB-fluoresceina ND 2,000 ND ND Complete
DMNB-HPTS a ND ∼5,000 ND ND Complete
a

From Invitrogen (Molecular Probes).

b

From Calbiochem.

c

From Tocris. ε, extinction coefficient; Φ, quantum yield. ND, not determined.