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ClH/c18-6-8-26-9-7-19-11-3-1-2-10-14(11)17(25)21(16(10)24)12-4-5-13(22)20-15(12)23
INCB 028050
pseudo-irreversible orthosteric antagonist at the prostacyclin (IP)-receptor expressed by human airway epithelial cells: IP-receptor-mediated inhibition of CXCL9 and CXCL10 release
is also a potent scavenger of NADPH-oxidase-derived superoxide
AL 082D06 (D06) binds specifically to GR with nanomolar affinity
LY-2183240 nzophenone ClH/c18-6-8-26-9-7-19-11-3-1-2-10-14(11)17(25)21(16(10)24)12-4-5-13(22)20-15(12)23LY 2183240 is a potent, covalent inhibitor of the EC degrading enzyme fatty acid amide hydrolase (FAAH). LY 2183240 disrupts the cellular uptake of the lipid endocannabinoid (EC) anandamide and promote analgesia in vivo. LY 2183240 is also an inhibitor of monoacylgylcerol lipase (MGL). Product information CAS Number: 874902 19 9 Molecular Weight: 307. 35 Formula: C17H17N5O Chemical Name: 5 ([1,1' biphenyl] 4 ylmethyl) N,N dimethyl 1H tetrazole 1
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