4 Results for "

Rat cerebral cortex H

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "Rat cerebral cortex H" in MCE Product Catalog:

Cat. No.: HY-107563
CAS No.: 184576-87-2
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

ROS 234 is a potent H3 antagonist, with a pKB of 9.46 for Guinea-pig ileum H3-receptor, a pKi of 8.90 for Rat cerebral cortex H3-receptor, and a ED50 of 19.12 mg/kg (ip) in ex vivo of Rat cerebral cortex. ROS 234 diaplays poor central access .
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Cat. No.: HY-107563A
CAS No.: 1781941-93-2
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

ROS 234 dioxalate is a potent H3 antagonist, with a pKB of 9.46 for Guinea-pig ileum H3-receptor, a pKi of 8.90 for Rat cerebral cortex H3-receptor, and a ED50 of 19.12 mg/kg (ip) in ex vivo of Rat cerebral cortex. ROS 234 dioxalate diaplays poor central access .
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Cat. No.: HY-105115
CAS No.: 111841-85-1
Synonyms: ZK 112119
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Abecarnil (ZK 112119) is a ligand or a partial agonist for benzodiazepine (BZ) receptor. Abecarnil possesses anxiolytic and anticonvulsant properties. Abecarnil can act as a positive allosteric modulator of GABAA receptor. Abecarnil inhibits the binding of the BZ [3H]lormetazepam to rat cerebral cortex membranes, with an IC50 of 0.82 nM. Abecarnil can be used for epilepsy research .
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Cat. No.: HY-136693
CAS No.: 98719-20-1
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

L-654284 is an α2-adrenergic receptor antagonist with significant selectivity. L-654284 competes with the binding of 3H-clonidine and 3H-rauwolscine in vitro and shows Ki values of 0.8 nM and 1.1 nM, respectively. L-654284 can block the protrusion effect of clonidine in isolated vas deferens in rats, with a pA2 value of 9.1. L-654284 exhibits remarkable selectivity for α2 and α1 adrenergic receptors, and exhibits a Ki of 110 nM in inhibiting 3H-prazosin binding. L-654284 can significantly increase the turnover rate of norepinephrine in rat cerebral cortex in vivo, showing α2-adrenergic receptor blocking activity in the central nervous system .
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