Levobunolol hydrochloride
CAS No. 27912-14-7
Levobunolol hydrochloride( l-Bunolol hydrochloride )
Catalog No. M26738 CAS No. 27912-14-7
Levobunolol hydrochloride is a non-selective beta-blocker and is used topically to manage glaucoma.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 51 | In Stock |
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| 50MG | 98 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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Biological Information
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Product NameLevobunolol hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionLevobunolol hydrochloride is a non-selective beta-blocker and is used topically to manage glaucoma.
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DescriptionLevobunolol hydrochloride is a non-selective beta-blocker and is used topically to manage glaucoma.
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In Vitro——
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In Vivo——
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Synonymsl-Bunolol hydrochloride
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PathwayOthers
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TargetOther Targets
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RecptorMAO-B
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Research Area——
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Indication——
Chemical Information
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CAS Number27912-14-7
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Formula Weight327.85
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Molecular FormulaC17H26ClNO3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : ≥ 62.5 mg/mL (190.64 m)
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SMILESO=C1CCCC2=C1C=CC=C2OC[C@@H](O)CNC(C)(C)C.[H]Cl
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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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CPYPP
CPYPP is an inhibitor of DOCK2-Rac1 interaction. CPYPP binds to DOCK2 DHR-2 domain and inhibits the guanine nucleotide exchange factor (GEF) activity of DOCK2DHR-2 for Rac1 in a dose-dependent manner(IC50 : 22.8 μM).
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Gastric Inhibitory P...
GIP (1-30) amide, porcine is a full glucose-dependent insulinotropic polypeptide (GIP) receptor agonist with high affinity equal to native GIP(1-42). GIP (1-30) amide, porcine is a weak inhibitor of gastric acid secretion and potent stimulator of insulin.
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Simvastatin Hydroxy ...
Simvastatin hydroxy acid (Tenivastatin) sodium is a potent HMG-CoA reductase (HMGCR) inhibitor. Simvastatin hydroxy acid sodium reduces Indoxyl sulfate-mediated reactive oxygen species (ROS) production in human cardiomyocytes. Simvastatin hydroxy acid sodium can also modulates OATP3A1 expression in cardiomyocytes and HEK293 cells transfected with the OATP3A1 gene.
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