Tetrahydrozoline HCl
CAS No. 522-48-5
Tetrahydrozoline HCl( Tetryzoline hydrochloride )
Catalog No. M18718 CAS No. 522-48-5
Tetrahydrozoline HCl is an imidazoline derivative with alpha receptor agonist activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | 27 | In Stock |
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Biological Information
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Product NameTetrahydrozoline HCl
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NoteResearch use only, not for human use.
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Brief DescriptionTetrahydrozoline HCl is an imidazoline derivative with alpha receptor agonist activity.
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DescriptionTetrahydrozoline HCl is an imidazoline derivative with alpha receptor agonist activity.(In Vitro):Tetrahydrozoline hydrochloride (0.05% HCl-tetrahydrozoline diluted with DMEM to 1:20 concentration; 24 hours) induces the synthesis of collagen types I and III in primary human gingival fibroblasts.
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In VitroTetrahydrozoline hydrochloride (0.05% HCl-tetrahydrozoline diluted with DMEM to 1:20 concentration; 24 hours) induces the synthesis of collagen types I and III in primary human gingival fibroblasts. They are for reference only.
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In Vivo——
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SynonymsTetryzoline hydrochloride
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PathwayOthers
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TargetOther Targets
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Recptorα-adrenergic receptor
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number522-48-5
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Formula Weight236.74
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Molecular FormulaC13H16N2·HCl
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Purity>98% (HPLC)
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SolubilityH2O : ≥ 50 mg/mL 211.20 mM DMSO : 16.67 mg/mL 70.41 mM
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SMILESCl.C1CN=C(N1)C1CCCC2=CC=CC=C12
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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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Osteocalcin (human) is a vitamin K-dependent bone specific protein. Osteocalcin (human) is chemotactic for several of the cell types frequently found at bone remodeling surfaces.
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Bacterial Sortase Su...
The Staphylococcus aureus transpeptidase Sortase A (SrtA) anchors virulence and colonization-associated surface proteins to the cell wall. SrtA selectively recognizes a C-terminal LPXTG motif. SrtA readily reacts with its native substrate Abz-LPETG-Dap(DNP)-NH2, cleaving it and catalyzing the formation of an amide bond between the carboxyl group of threonine and the amino group of cell-wall crossbridges.
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