Arotinolol hydrochloride
CAS No. 68377-91-3
Arotinolol hydrochloride( —— )
Catalog No. M34506 CAS No. 68377-91-3
Arotinolol hydrochloride(Arotinolol HCl) is a non-selective α/β-adrenergic receptor blocker.Arotinolol hydrochloride inhibits the binding of the radioligand 125I-ICYP to the 5HT1B-hydroxytryptamine receptor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 103 | In Stock |
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| 10MG | 154 | In Stock |
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| 25MG | 255 | In Stock |
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| 50MG | 365 | In Stock |
|
| 100MG | 547 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 1163 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameArotinolol hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionArotinolol hydrochloride(Arotinolol HCl) is a non-selective α/β-adrenergic receptor blocker.Arotinolol hydrochloride inhibits the binding of the radioligand 125I-ICYP to the 5HT1B-hydroxytryptamine receptor.
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DescriptionArotinolol hydrochloride(Arotinolol HCl) is a non-selective α/β-adrenergic receptor blocker.Arotinolol hydrochloride inhibits the binding of the radioligand 125I-ICYP to the 5HT1B-hydroxytryptamine receptor. Arotinolol hydrochloride is an antihypertensive and anti-obesity agent that improves aortic stiffness in rats and is used to study obesity-related diseases.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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TargetAdrenergic Receptor
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RecptorAdrenergic Receptor | 5-HT Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number68377-91-3
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Formula Weight408
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Molecular FormulaC15H22ClN3O2S3
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Purity>98% (HPLC)
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Solubility——
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SMILESCl.CC(C)(C)NCC(O)CSc1nc(cs1)-c1ccc(s1)C(N)=O
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Chemical Name——
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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TAK-259
A potent and selective human α1D adrenoceptor (α1D-AR) antagonist with Ki of 1.1 nM; displays 200-fold and 800-fold selectivity against α1A- and α1B-AR, respectively.
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L748337
L748337 is a competitive and potent β3-adrenoceptor antagonist that inhibits the action of β3-, β2-, and β1-adrenoceptors, activates MAPK signaling, promotes phosphorylation of Erk1/2, and inhibits the protective effects of CL316243, and is used in the study of disorders caused by abnormalities of the β3-adrenoceptors.
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BODIPY FL prazosin
BODIPY FL prazosin is a fluorescent α1-adrenergic antagonist with binding affinities of Ki: 14.5 nM for α1a-AR and Ki: 43.3 nM for α1b-AR, used to study subcellular localization differences in α1-adrenoceptor subtypes.
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