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Product introduction
JNJ-1661010是一种有效的,选择性的FAAH抑制剂,IC50分别为10 nM(大鼠)和12 nM (人类),作用于FAAH-1比作用于FAAH-2选择性高100倍以上。A selective and reversible inhibitor of fatty acid amide hydrolase (FAAH). JNJ-1661010 is a potent and selective FAAH inhibitor with IC50 of 10 nM (rat) and 12 nM (human), exhibits >100-fold selectivity for FAAH-1 when compared to FAAH-2. A selective and reversible inhibitor of fatty acid amide hydrolase (FAAH).
Chinese name
JNJ-1661010,FAAH抑制剂, 脂肪酸酰胺水解酶抑制剂
English name
JNJ-1661010
Chinese alias
-
English alias
AKOS024457512 | 1-Piperazinecarboxamide, N-phenyl-4-(3-phenyl-1,2,4-thiadiazol-5-yl)- | N1-phenyl-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide | HMS3651L15 | N-phenyl-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide | Oprea1_746619
CAS number
681136-29-8
molecular formula
C19H19N5OS
molecular weight
365.45 g/mol
Exact mass
-
PSA
89.600 Ų
Logp
3.500
Technical Documents
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JNJ-1661010 10mM in DMSO 1ml

JNJ-1661010 10mM in DMSO 1ml; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1ml.

item number:J408111-1ml
Product model:1ml
level: 1ml
Lead Time:-
sold 120 Items
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