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Product introduction
PF-03654764 has pK i values of 8.98 and 8.10 for human H 3 and rat H 3 in whole cell assay, respectively. PF-03654764 has pK i values of 8.84, 7.73 and K i values of 1.4 nM and 19 nM for human H 3 and rat H 3 in HEK-293 cells, respectively. PF-03654764 has >1000-fold selectivity for the H3 receptor over the other histamine receptor subtypes. PF-03654764 has a human liver microsomes (HLM) T 1/2 of 120 min and a HLM CL h In Vivo PF-03654764 (10 mL/kg; oral; 14 days) has a C max of 8057 ng/mL and an AUC 0-24 of 67400 ng•h/mL in Sprague-Dawley rats . PF-03654764 (1 mL/kg; oral; 7 days) has a C max of 6302 ng/mL and an AUC 0-24 of 18175 ng•h/mL in beagle dogs . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:human H 3 receptor 1.2 nM (Ki) rat H 3 receptor 7.9 nM (Ki) human H 3 receptor 8.98 (pKi) rat H 3 receptor 8.10 (pKi)
Chinese name
PF-03654764, 组胺 H3 受体拮抗剂
English name
PF-03654764
Chinese alias
-
English alias
H3 receptor antagonist 1 | Cyclobutanecarboxamide, 3-fluoro-3-[3-fluoro-4-(1-pyrrolidinylmethyl)phenyl]-N-(2-methylpropyl)-, trans-
CAS number
935840-35-0
molecular formula
C20H28F2N2O
molecular weight
350.45 g/mol
Exact mass
≥98%
PSA
32.299 Ų
Logp
3.400
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Research chemical 1mg; ≥98%

Research chemical 1mg; ≥98%; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1mg; ≥98%.

item number:P650652-1mg
Product model:1mg
level: 1mg; ≥98%
Lead Time:30days
sold 638 Items
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1mg

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