Most natural odors are complex mixtures of many volatile components, competing to bind odorant receptors (ORs) expressed in olfactory sensory neurons (OSNs) of the nose. To date surprisingly little is known about how OR antagonism shapes neuronal representations in the periphery of the olfactory system. Here, we investigated its prevalence, the degree to which it disrupts OR ensemble activity, and its conservation across related ORs. Calcium imaging microscopy of dissociated OSNs revealed significant inhibition, often complete attenuation, of responses to indole, a commonly occurring volatile associated with both floral and fecal odors, by a set of 36 tested odorants. To confirm an OR mechanism for the observed inhibition, we performed single-cell transcriptomics on OSNs that exhibited specific response profiles to a diagnostic panel of odorants and identified the receptor Olfr743 which, when tested in vitro, recapitulated ex vivo responses. We screened ten ORs from the Olfr743 clade with 800 perfumery-related odorants spanning a range of chemical scaffolds and functional groups, over half of which (430) antagonized at least one of the ten ORs. Furthermore, OR activity outcomes were divergent rather than redundant, even for the most closely related paralogs. OR activity fitted a mathematical model of competitive receptor binding and suggests that normalization of OSN ensemble responses to odorant mixtures is the rule rather than the exception. In summary, we observed OR antagonism, inverse agonism and partial agonism occurring frequently and in a combinatorial manner. Thus, extensive receptor-mediated computation of mixture information appears to occur in the olfactory epithelium prior to transmission of odor information to the olfactory bulb. 2 3 heterologous expression systems and the lack of a protein structure [41] have impeded systematic exploration of the full range of possible receptor-ligand interactions for ORs. As such, it is not well understood to what extent classical GPCR interactions, like antagonism, partial agonism and inverse agonism shape odor representations before they are propagated to the olfactory bulb.This lack of information on the prevalence of non-agonist interactions, and on correlations between ORs severely limits our ability to understand fundamental aspects of mixture encoding by the olfactory system. For example, infrequent, but strong antagonism would simply prevent the activation of a limited number of ORs in the presence of an antagonist. Alternatively, widespread antagonism could lead to extensive normalization of inputs [29] and decoupling of similarity between mixture compositions and their resulting OSN activity ensembles. With the rise of mathematical models of olfaction demonstrating wide varieties of possible encoding strategies, it has become important to provide data which can help test parameter values and rule out certain classes of model.In this study, we investigated the prevalence of antagonism, quantified its ability to disrupt OSN activity, and examined its cons...