Fosciclopirox
CAS No. 1380539-06-9
Fosciclopirox( CPX-POM )
Catalog No. M28675 CAS No. 1380539-06-9
Fosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 50 | In Stock |
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| 2MG | 29 | In Stock |
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| 5MG | 46 | In Stock |
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| 10MG | 79 | In Stock |
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| 25MG | 164 | In Stock |
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| 50MG | 254 | In Stock |
|
| 100MG | 375 | In Stock |
|
| 200MG | 533 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameFosciclopirox
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NoteResearch use only, not for human use.
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Brief DescriptionFosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration.
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DescriptionFosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration.
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In Vitro——
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In Vivo——
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SynonymsCPX-POM
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PathwayNeuroscience
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TargetGamma-secretase
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number1380539-06-9
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Formula Weight317.278
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Molecular FormulaC13H20NO6P
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (315.19 mM)
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SMILESCc1cc(C2CCCCC2)n(OCOP(O)(O)=O)c(=O)c1
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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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Jagged-1 188-204
This peptide is a fragment of the JAG-1 protein. JAG-1 is Notch ligand, a peptide that is the most conspicuously expressed ligand in skin. JAG-1 induces epidermal maturation. Exposing submerged keratinocytes monolayers to JAG-1 with elevated calcium concentration produces stratification with loricrin expression and NF-αB activation.
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RBPJ Inhibitor-1
RBPJ Inhibitor-1 (RIN1), a compound that impedes the functional interaction between RBPJ and SHARP, effectively inhibits NOTCH-dependent tumor cell proliferation.
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γ-Secretase-IN-1
γ-Secretase-IN-1 is a potent γ-secretase inhibitor that displays partial antiproliferative activity on T-47D cells and inhibits β-amyloid(40), β-amyloid(42), and Notch γ-secretase cleavage.
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