Title : Pharmacological differences between the human and rat vanilloid receptor 1 (VR1).

Pub. Date : 2001 Mar

PMID : 11226139






4 Functional Relationships(s)
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Protein Name
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1 Capsazepine and ruthenium red were both more potent at blocking the capsaicin response of human VR1 than rat VR1. capsazepine transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
2 Capsazepine and ruthenium red were both more potent at blocking the capsaicin response of human VR1 than rat VR1. Ruthenium Red transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
3 Capsazepine blocked the human but not the rat VR1 response to low pH. capsazepine transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
4 Capsazepine was also more effective at inhibiting the noxious heat response of human than of rat VR1. capsazepine transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus