Xenbase Image ID: 124190

Figure 3. Relative activity of AaOR8 towards (R)-(—)-1-octen-3-ol and related compounds.Changes relative to (R)-(—)-1-octen-3-ol are shaded in grey. Presence and absence of a specific chemical feature are indicated by + and -, respectively. The formula of racemic compounds does not assume the 3 dimensional orientation of the residues attached to the chiral center. Note that the least active isomers are those lacking the proper chirality at the 3-position (C3*). Relative activities of each odorant (EC50s) are reflected by area of solid circles. Image published in: Bohbot JD and Dickens JC (2009) Image downloaded from an Open Access article in PubMed Central. This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. Larger Image Printer Friendly View

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