MK-7288
CAS No. 936626-07-2
MK-7288 ( MK7288;MK 7288 )
Catalog No. M16708 CAS No. 936626-07-2
A novel histamine H3 receptor inverse agonist for the treatment of sleep apnoea syndrome.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 873 | Get Quote |
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50MG | 1782 | Get Quote |
|
100MG | 2250 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameMK-7288
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NoteResearch use only, not for human use.
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Brief DescriptionA novel histamine H3 receptor inverse agonist for the treatment of sleep apnoea syndrome.
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DescriptionA novel histamine H3 receptor inverse agonist for the treatment of sleep apnoea syndrome; significantly prolongs MWT sleep latency, and improves car driving simulation standard deviation of lane position in clinical trials.Sleep Disorder Phase 1 Clinical
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SynonymsMK7288;MK 7288
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PathwayGPCR/G Protein
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TargetHistamine Receptor
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RecptorHistamine Receptor
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Research AreaNeurological Disease
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IndicationSleep Disorder
Chemical Information
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CAS Number936626-07-2
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Formula Weight401.51
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Molecular FormulaC22H31N3O4
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Purity>98% (HPLC)
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Solubility——
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SMILESCN(CCN1CCCCC1)C(=O)C2CCC3(CC2)C4=C(C(=O)O3)N=C(C=C4)OC
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Chemical Name(1r,4r)-2'-methoxy-N-methyl-7'-oxo-N-(2-(piperidin-1-yl)ethyl)-7'H-spiro[cyclohexane-1,5'-furo[3,4-b]pyridine]-4-carboxamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Hydroxyzine free bas...
Hydroxyzine is an antagonist of histamine H1-receptor. Hydroxyzine is an antihistaminic with sedative properties used in the control of anxiety and emesis.
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Orphenadrine hydroch...
Orphenadrine is an anticholinergic drug of the ethanolamine antihistamine class with prominent central nervous system (CNS) and peripheral actions used to treat painful muscle spasms and other similar conditions, as well as the treatment of some aspects of Parkinson's disease.
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JNJ-5207852 dihydroc...
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor. JNJ-5207852 is a potent dibasic amine antagonist that binds potently to rat H3 receptors (Ki=1.2?nm), and has good brain penetration. In ex vivo binding studies in mice, the compound had an ED50 of 0.13?mg?kg?1, subcutaneously.