Home - Products - Neuroscience - Gamma-secretase - Fosciclopirox

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
2MG	29	In Stock
5MG	46	In Stock
10MG	79	In Stock
25MG	164	In Stock
50MG	254	In Stock
100MG	375	In Stock
200MG	533	In Stock
500MG	Get Quote	In Stock
1G	Get Quote	In Stock

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

Fosciclopirox
Note

Research use only, not for human use.
Brief Description

Fosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration.
Description

Fosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration.
In Vitro

——
In Vivo

——
Synonyms

CPX-POM
Pathway

Neuroscience
Target

Gamma-secretase
Recptor

——
Research Area

——
Indication

——

Chemical Information

CAS Number

1380539-06-9
Formula Weight

317.278
Molecular Formula

C13H20NO6P
Purity

>98% (HPLC)
Solubility

In Vitro:?DMSO : 100 mg/mL (315.19 mM)
SMILES

Cc1cc(C2CCCCC2)n(OCOP(O)(O)=O)c(=O)c1
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1.Faria DB, et al. Effects of lidocaine and droxicainide on myocardial necrosis: a comparative study. J Am Coll Cardiol. 1983 Jun;1(6):1447-52.

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

PEAQX

PEAQX(NVP-AAM 077) is an effective and orally available NMDA antagonist. It can inhibit human NMDA receptors for 1A/2A(IC50: 270 nM), rather than 1A/2B(29, 600 nM).
Compound W

The compound is an inhibitor of γ-secretase. It also causes a decrease in the released levels of Aβ42 and notch-1 Aβ-like peptide 25 (Nβ25).
LY900009

LY900009 is a small molecule inhibitor of Notch signalling via selective inhibition of the γ-secretase protein.?

Sign In Join Free