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Review

Current and emerging “at-site” pain medications: a review

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Pages 279-286 | Published online: 08 Sep 2011

Figures & data

Figure 1 Summary of pain pathophysiology and some pain targets.

Abbreviations: CB, cannabinoid; COX, cyclooxygenase; NMDA, N-Methyl-D-aspartate.
Figure 1 Summary of pain pathophysiology and some pain targets.

Figure 2 Chemical structures of some nonselective CB receptor modulators.

Abbreviations: CB, cannabinoid; Ki, inhibition constant.
Figure 2 Chemical structures of some nonselective CB receptor modulators.

Figure 3 Chemical structures of some selective CB2 receptor modulators.

Abbreviations: CB, cannabinoid; Ki, inhibition constant.
Figure 3 Chemical structures of some selective CB2 receptor modulators.

Figure 4 Chemical structures of some selective CB2 receptor modulators.

Abbreviations: CB, cannabinoid; EC50, half-maximal effective concentration; Ki, inhibition constant.
Figure 4 Chemical structures of some selective CB2 receptor modulators.

Figure 5 Chemical structures of some TRPV1 receptor antagonists.

Abbreviations: EC50, half-maximal effective concentration; IC50, half-maximal inhibitory concentration; TRPV1, transient receptor potential vanilloid-1.
Figure 5 Chemical structures of some TRPV1 receptor antagonists.

Figure 6 Chemical structures of some P2X7 receptor antagonists.

Abbreviation: pIC50, negative logarithm of the half-maximal inhibitory concentration.
Figure 6 Chemical structures of some P2X7 receptor antagonists.

Figure 7 Chemical structures of some glial cell modulators.

Figure 7 Chemical structures of some glial cell modulators.