VDM11 is a potent and selective inhibitor of fatty acid amide hydrolase (FAAH), serving as a key modulator in endocannabinoid signaling. By inhibiting FAAH, VDM11 enhances the levels of anandamide, which can contribute to various physiological effects, including pain modulation and neuroprotection. This compound is beneficial for research applications examining endocannabinoid pathways and developing therapeutics for related disorders.
VDM11 is a potent and selective inhibitor of fatty acid amide hydrolase (FAAH), serving as a key modulator in endocannabinoid signaling. By inhibiting FAAH, VDM11 enhances the levels of anandamide, which can contribute to various physiological effects, including pain modulation and neuroprotection. This compound is beneficial for research applications examining endocannabinoid pathways and developing therapeutics for related disorders.
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